AU2004275937A1

AU2004275937A1 - Bicyclic imino acid derivatives used as inhibitors of matrix-metalloproteinases

Info

Publication number: AU2004275937A1
Application number: AU2004275937A
Authority: AU
Inventors: Armin Hofmeister; Hans Matter; Manfred Schudok
Original assignee: Sanofi Aventis Deutschland GmbH
Current assignee: Sanofi Aventis Deutschland GmbH
Priority date: 2003-09-27
Filing date: 2004-09-14
Publication date: 2005-04-07
Also published as: RS20060194A; AR046165A1; JP4861179B2; IL174040A0; TW200520755A; RU2335494C2; JP2007506690A; KR20060086367A; CN1856478B; RU2006114352A; MXPA06002927A; EP1670766A1; NZ546158A; BRPI0414594A; EP1670766B1; WO2005030728A1; ATE550327T1; MEP33008A; DE10344936A1; MY139830A

Description

IN THE MATTER OF an Australian Application corresponding to PCT Application PCT/EP2004/010248 RWS Group Ltd, of Europa House, Marsham Way, Gerrards Cross, Buckinghamshire, England, hereby solemnly and sincerely declares that, to the best of its knowledge and belief, the following document, prepared by one of its translators competent in the art and conversant with the English and German languages, is a true and correct translation of the PCT Application filed under No. PCT/EP2004/010248. Date: 6 January 2006 S. ANTHONY Director For and on behalf of RWS Group Ltd WO 2005/030728 1 PCT/EP2004/010248 Bicyclic imino acid derivatives used as inhibitors of matrix metalloproteinases 5 The invention relates to novel derivatives of saturated bicyclic imino acids, such as, in particular, decahydroisoquinoline-1-carboxylic acid, to methods for preparing them, and to the use thereof as pharmaceuticals. In diseases such as osteoarthritis and rheumatism, destruction of the joint 10 takes place, with this destruction being caused, in particular, by the proteolytic breakdown of collagen due to collagenases. Collagenases belong to the metalloproteinase (MP) or matrix metalloproteinase (MMP) superfamily. The MMPs form a group of Zn-dependent enzymes which are involved in the biological breakdown of the extracellular matrix (D. Yip et al. 15 in Investigational New Drugs 17 (1999), 387-399 and Michaelides et al. in Current Pharmaceutical Design 5 (1999) 787 - 819). These MMPs are, in particular, able to break down fibrillar and nonfibrillar collagen and also proteoglycans, both of which are important matrix constituents. MMPs are involved in processes of wound healing, tumor invasion and metastasis 20 migration, and also in angiogenesis, multiple sclerosis and heart failure (Michaelides, page 788; see above). In particular, they play an important role in the breakdown of the joint matrix in arthrosis and arthritis, whether this be osteoarthrosis, osteoarthritis or rheumatoid arthritis. 25 The activity of the MMPs is furthermore essential for many of the processes which play a role in atherosclerotic plaque formation, such as the infiltration of inflammatory cells and smooth muscle cell migration, as well as proliferation and angiogenesis (S.J. George, Exp. Opin. Invest. Drugs (2000), 9 (5), 993-1007). Furthermore, the degradation of matrix by MMPs 30 can cause anything from plaque instabilities through to ruptures, with these conditions being able to give rise to the clinical symptoms of atherosclerosis, unstable angina pectoris, myocardial infarction or stroke (E.J.M. Creemers et al., Circulation Res. 89, 201-210 (2001)). All in all, the MMP family as a whole is able to break down all the components of the 35 extracellular matrix of the blood vessels; in normal blood vessels, therefore, their activity is to a very great degree subject to regulatory mechanisms. The increase in MMP activity during plaque formation and plaque instability is caused by an increase in cytokine-stimulated and growth factor stimulated gene transcription, an increase in zymogen activation and an 2 imbalance in the MMP/TIMP (tissue inhibitors of metalloproteases) ratio. It therefore seems plausible that an MMP inhibition or the reattainment of the MMP-TIMP balance, would be helpful in treating atherosclerotic diseases. It is likewise becoming ever more clear that an increase in MMP activity is at 5 least partially responsible for other cardiovascular diseases in addition to atherosclerosis, such as restenosis, dilated cardiomyopathy and the previously mentioned myocardial infarction. It has been shown that administering synthetic inhibitors to experimental animal models of these diseases is able to achieve marked improvements, for example in regard to 10 the formation of atherosclerotic lesions, neointima formation, left ventricular remodeling, pump performance malfunction or infarction healing. In various preclinical studies using MMP inhibitors, detailed tissue analyses indicated a reduction in collagen damage, an improvement in extracellular matrix remodeling and an improvement in the structure and function of cardiac 15 muscle and blood vessels. Among these processes, matrix remodeling processes and MMP-regulated fibroses, in particular, are regarded as being important components in the progression of heart diseases (infarction) (Drugs 61, 1239-1252 (2001)). 20 Under physiological conditions, MMPs cleave matrix proteins such as collagen, laminin, proteoglycans, elastin or gelatine, and also process (i.e. activate or inactivate), by means of cleavage, a large number of other proteins and enzymes, which means that they play an important role in the entire body, with this role being particularly significant in the connective 25 tissue and bones. A large number of different MMP inhibitors are known (EP 0 606 046; WO 94/28889; WO 96/27583; cf. reviews such as Current Medicinal Chemistry 8, 425-74 (2001) as well). Following the first clinical studies in humans, it 30 has now been found that MMPs give rise to side-effects. The side-effects to be mentioned are musculoskeletal pain or anthralgias. The prior art makes it clear that it is expected that more selective inhibitors would be able to reduce these side-effects (Yip, page 387, see above). Specificity towards MMP-1 is particularly to be emphasized in this connection since these 35 unwanted side-effects evidently appear to an increased extent when MMP 1 is inhibited. A disadvantage of the known MMP inhibitors is therefore that they frequently lack specificity. Most MMP inhibitors inhibit many MMPs 3 simultaneously because the catalytic domains of the MMPs possess similar structures. As a consequence, the inhibitors also undesirably affect the enzymes which have a vital function (Massova I, et al., The FASEB Journal (1998) 12, 1075-1095). 5 In the endeavor to find effective compounds for treating connective tissue diseases, it has now been found that the derivatives which are employed in accordance with the invention are powerful inhibitors of the matrix metalloproteinases MMP-2, MMP-3, MMP-8, MMP-9 and MMP-13 while 10 only having a weak inhibitory effect on MMP-1. The invention therefore relates to a compound of the formula I n2 n1 R2 I '2 N.S- A-ring 1 -B-ring-D-ring3-E-ring 4 R4t 0 R5 R1 R3 )X O 0 15 and/or to all the stereoisomeric forms of the compound of the formula I and/or to mixtures of these forms in any ratio, and/or to a physiologically tolerated salt of the compound of the formula I, wherein 20 A is -(Co-C 4 )-alkylene, B, D and E are identical or different and are, independently of each other, -(Co-C4)-alkylene or the radical -B1-B2-B3- in which B1 is -(CH 2 )n-, in which n is the integer zero, 1 or 2, B3 is -(CH 2 )m-, in which m is the integer zero, 1 or 2, 25 with the proviso that the sum of n and m amounts to zero, 1 or 2, and B2 is 1) -C(0) 2) -(C 2

-C

4 )-alkenylene, 3) -S(0)o-, where o is the integers zero, 1 or 2, 30 4) -N(R6)-, in which R6 is hydrogen atom, methyl or ethyl, 5) -N(R6)-C(Y)-, in which Y is oxygen atom or sulfur atom and R6 is defined as above, 4 6) -C(Y)-N(R6)-, in which Y is oxygen atom or sulfur atom and R6 is defined as above, 7) -N(R6)-SO 2 -, in which R6 is defined as above, 8) -SO 2 -N(R6)-, in which R6 is defined as above, 5 9) -N(R6)-SO 2 -N(R6)-, in which R6 is defined as above, 10) -N(R6)-C(Y)-N(R6)-, in which Y is oxygen atom or sulfur atom and R6 is defined as above, 11) -O-C(O)-N(R6)-, 12) -NH-C(O)-O-, 10 13) -0-, 14) -C(0)-O-, 15) -O-C(0)-, 16) -O-C(0)-O-, 17) -O-CH 2 -C(0)-, 15 18) -O-CH 2 -C(0)-O-, 19) -O-CH 2 -C(0)-N(R6)-, in which R6 is defined as above, 20) -C(0)-CH 2 -O-, 21) -O-C(0)-CH 2 -O-, 22) -N(R6)-C(O)-CH 2 -O-, in which R6 is defined as above, 20 23) -O-(CH 2 )n-O-, in which n is the integer 2 or 3, or 24) -O-(CH 2 )m-N(R6)-, in which m is the integer 2 or 3 and R6 is defined as above, 25) -N(R6)-(CH 2 )m-O-, in which m is the integer 2 or 3 and R6 is defined as above, 25 26) -N(R6)-N(R6)-, in which R6 is defined as above, 27) -N=N-, 28) -N(R6)-CH=N-, in which R6 is defined as above, 29) -N=CH-N(R6)-, in which R6 is defined as above, 30) -N(R6)-C(R7)=N-, in which R6 is defined as above and R7 is 30 -NH-R6, 31) -N=C(R7)-N(R6)-, in which R6 is defined as above and R7 is -NH-R6, or 32) -(C2-C 6 )-alkynylene, ring1, ring2 and ring3 are identical or different and are, independently of 35 each other, 1) covalent bond, 2) -(C 6

-C

1 4 )-aryl, in which aryl is unsubstituted or substituted, independently of each other, once, twice or three times, by G, or 5 3) 4- to 15-membered Het ring, in which Het ring is unsubstituted or substituted, independently of each other, once, twice or three times, by G, ring4 is 5 1) -(C6-C 14 )-aryl, in which aryl is unsubstituted or substituted, independently of each other, once, twice or three times, by G, 2) 4- to 15-membered Het ring, in which the Het ring is unsubstituted or substituted, independently of each other, once, twice or three times, by G, or 10 3) is one of the following radicals O OO 0 O 0 N 00 N 0 H H and these radicals are unsubstituted or substituted once by 15 G, G is 1) hydrogen atom, 2) halogen, 3) =O, 4) -(C 1

-C

6 )-alkyl, in which alkyl is unsubstituted or substituted, 20 once, twice or three times, by halogen, -(C 3

-C

6 )-cycloalkyl, (C 2

-C

6 )-alkynyl, -(C 6

-C

1 4)-aryl or Het ring, 5) -(C 6

-C

1 4 )-aryl, 6) Het ring, 7) -C(0)-O-R1 0, in which R10 is 25 a) -(CO-Cs)-alkyl, in which alkyl is unsubstituted or substituted, once or twice, by -(C3-C 6 )-cycloalkyl,

-(C

2

-C

6 )-alkynyl, -(C6-C 1 4 )-aryl or Het ring, or b) -(C6-C 14 )-aryl or Het ring, 8) -C(S)-O-R10, in which R10 is defined as above, 30 9) -C(0)-NH-R 11, in which R11 is a) -(CO-C 6 )-alkyl, in which alkyl is unsubstituted or substituted, once or twice, by -(C 3

-C

6 )-cycloalkyl,

-(C

6

-C

1 4)-aryl or Het ring, or b) -(C 6

-C

14 )-aryl or Het ring, 35 10) -C(S)-NH-R11, in which R11 is defined as above, 11) -O-R12, in which R12 is 6 a) hydrogen atom, b) -(C 1

-C

6 )-alkyl, in which alkyl is unsubstituted or substituted, once, twice or three times, by halogen, -(C 3

-C

6 )-cycloalkyl, -(C2-C 6 )-alkynyl, 5 (C 6

-C

1 4)-aryl or Het ring, c) -(C 6 -0 1 4 )-aryl, d) Het ring, e) -C(O)-O-R13, in which R13 is e)1) -(C 1 -Ce)-alkyl, in which alkyl is 10 unsubstituted or substituted, once or twice, by -(C 3

-C

6 )-cycloalkyl, -(C 2

-C

6

)

alkynyl, -(C 6

-C

14 )-aryl, or Het ring, or e)2) -(C 6

-C

1 4 )-aryl or Het ring, f) -C(S)-O-R13, in which R13 is defined as above, 15 g) -C(O)-NH-R14, in which R14 is g)1) -(C-C 6 )-alkyl, in which alkyl is unsubstituted or substituted, once or twice, by -(C 3

-C

6 )-cycloalkyl, -(C 2

-C

6

)

alkynyl, -(C 6 -0 14 )-aryl or Het ring, or 20 g)2) -(C 6

-C

14 )-aryl or Het ring, or h) -C(S)-NH-R14, in which R14 is defined as above, 12) -C(O)-R1 0, in which R10 is defined as above, 13) -S(O)p-R12, in which R12 is defined as above and p is the integers zero, 1 or 2, 25 14) -NO 2 , 15) -CN, or 16) -N(R15)-R12, in which R15 is 16)1) hydrogen atom, 16)2) -(C 1

-C

6 )-alkyl, or 30 16)3) -SO 2

-(C

1

-C

6 )-alkyl, in which alkyl is unsubstituted or substituted, once or twice, by -(C 3

-C

6 )-cycloalkyl, (C 2

-C

6 )-alkynyl, -(C 6

-C

14 )-aryl or Het ring, and R12 is defined as above, or 17) -SO 2 -N(R12)-R1, in which R12 is defined as above and R1 is 35 defined as below, X is -OH or -NH-OH, n1 is the integer zero, 1, 2 or 3, n2 is the integer zero, 1, 2, 3 or 4, with the proviso that the sum of n1 and n2 amounts to 1, 2, 3, 4, 5, 6 or 7, 7 R1, R2, R3, R4 and R5 are identical or different and are, independently of each other, 1) hydrogen atom, 2) -(C 1

-C

6 )-alkyl, in which alkyl is unsubstituted or substituted, 5 once or twice, by -(C 3

-C

6 )-cycloalkyl, -(C2-C 6 )-alkynyl, -(C6 C1 4 )-aryl or Het ring, 3. -C(O)-O-R8, in which R8 is 3)1) hydrogen atom, 3)2) -(C 1

-C

6 )-alkyl, in which alkyl is unsubstituted or 10 substituted, once or twice, by -(C 3

-C

6 )-cycloalkyl,

-(C

2

-C

6 )-alkynyl, -(C6-C14)-aryl or Het ring, or substituted once to five times, by fluorine, or 3)3) -(C 6 -C14)-aryl or Het ring, 4) -O-R8, in which R8 has the abovementioned meaning, or 15 5) -(C 3

-C

6 )-cycloalkyl. The invention also relates to the compound of the formula I where A is -(Co-C 4 )-alkylene, B, D and E are identical or different and are, independently of each other, 20 -(Co-C 4 )-alkylene or the radical -B1-B2-B3- in which B1 is -(CH 2 )n-, in which n is the integer zero, 1 or 2, B3 is -(CH 2 )m-, in which m is the integer zero, 1 or 2, with the proviso that the sum of n and m amounts to zero, 1 or 2, and B2 is 25 1) -C(0) 2) -(C 2

-C

4 )-alkenylene, 3) -S(0)o-, where o is the integers zero, 1 or 2, 4) -N(R6)-, in which R6 is hydrogen atom, methyl or ethyl, 5) -N(R6)-C(Y)-, in which Y is oxygen atom or sulfur atom and 30 R6 is defined as above, 6) -C(Y)-N(R6)-, in which Y is oxygen atom or sulfur atom and R6 is defined as above, 7) -N(R6)-SO 2 -, in which R6 is defined as above, 8) -SO 2 -N(R6)-, in which R6 is defined as above, 35 9) -N(R6)-SO 2 -N(R6)-, in which R6 is defined as above, 10) -N(R6)-C(Y)-N(R6)-, in which Y is oxygen atom or sulfur atom and R6 is defined as above, 11) -O-C(0)-N(R6)-, 12) -NH-C(0)-O-, 8 13) -0-, 14) -C(O)-O-, 15) -O-C(0)-, 16) -O-C(0)-O-, 5 17) -O-CH 2 -C(0)-, 18) -O-CH 2 -C(0)-O-, 19) -O-CH 2 -C(0)-N(R6)-, in which R6 is defined as above, 20) -C(0)-CH 2 -O-, 21) -O-C(0)-CH 2 -O-, 10 22) -N(R6)-C(0)-CH 2 -O-, in which R6 is defined as above, 23) -O-(CH 2 )n-O-, in which n is the integer 2 or 3, or 24) -O-(CH 2 )m-N(R6)-, in which m is the integer 2 or 3 and R6 is defined as above, 25) -N(R6)-(CH 2 )m-O-, in which m is the integer 2 or 3 and R6 is 15 defined as above, 26) -N(R6)-N(R6)-, in which R6 is defined as above, 27) -N=N-, 28) -N(R6)-CH=N-, in which R6 is defined as above, 29) -N=CH-N(R6)-, in which R6 is defined as above, 20 30) -N(R6)-C(R7)=N-, in which R6 is defined as above and R7 is -NH-R6, 31) -N=C(R7)-N(R6)-, in which R6 is defined as above and R7 is -NH-R6, or 32) -(C 2

-C

6 )-alkynylene, 25 ring1, ring2 and ring3 are identical or different and are, independently of each other, 1) covalent bond, 2) phenyl or naphthyl and are unsubstituted or substituted, independently of each other, once, twice or three times, by G, 30 or 3) 4- to 15-membered Het ring, in which the Het ring is a radical from the series acridinyl, azepinyl, azetidinyl, aziridinyl, benzimidazalinyl, benzimidazolyl, benzofuranyl, benzothiofuranyl, benzothiophenyl, benzoxazolyl, 35 benzothiazolyl, benzotriazolyl, benzotetrazolyl, benzisoxazolyl, benzisothiazolyl, carbazolyl, 4aH-carbazolyl, carbolinyl, quinazolinyl, quinolinyl, 4H-quinolizinyl, quinoxalinyl, quinuclidinyl, chromanyl, chromenyl, cinnolinyl, deca-hydroquinolinyl, dibenzofuranyl, dibenzothiophenyl, 9 dihydrofuran[2,3-b]tetrahydrofuranyl, dihydrofuranyl, dioxolyl, dioxanyl, 2H,6H-1,5,2-dithiazinyl, furanyl, furazanyl, imidazolidinyl, imidazolinyl, imidazolyl, 1H-indazolyl, indolinyl, indolizinyl, indolyl, 3H-indolyl, isobenzofuranyl, isochromanyl, 5 isoindazolyl, isoindolinyl, isoindolyl, isoquinolinyl (benzimidazolyl), isothiazolidinyl, 2-isothiazolinyl, isothiazolyl, isoxazolyl, isoxazolidinyl, 2-isoxazolinyl, morpholinyl, naphthyridinyl, octahydroisoquinolinyl, oxadiazolyl, 1,2,3 oxadiazolyl, 1,2,4-oxadiazolyl, 1,2,5-oxadiazolyl, 1,3,4 10 oxadiazolyl, oxazolidinyl, oxazolyl, oxothiolanyl, pyrimidinyl, phenanthridinyl, phenanthrolinyl, phenazinyl, phenothiazinyl, phenoxathiinyl, phenoxazinyl, phthalazinyl, piperazinyl, piperidinyl, pteridinyl, purinyl, pyranyl, pyrazinyl, pyroazolidinyl, pyrazolinyl, pyrazolyl, pyridazinyl, 15 pyridooxazolyl, pyridoimidazolyl, pyridothiazolyl, pyridothiophenyl, pyridinyl, pyridyl, pyrimidinyl, pyrrolidinyl, pyrrolinyl, 2H-pyrrolyl, pyrrolyl, tetrahydrofuranyl, tetrahydroisoquinolinyl, tetrahydroquinolinyl, tetrahydro pyridinyl, 6H-1,2,5-thiadazinyl, 1,2,3-thiadiazolyl, 1,2,4-thia 20 diazolyl, 1,2,5-thiadiazolyl, 1,3,4-thiadiazolyl, thianthrenyl, thiazolyl, thienyl, thienothiazolyl, thienooxazolyl, thienoimidazolyl, thiomorpholinyl, thiophenyl, triazinyl, 1,2,3 triazolyl, 1,2,4-triazolyl, 1,2,5-triazolyl, 1,3,4-triazolyl and xanthenyl, and these radicals are unsubstituted or 25 substituted, independently of each other, once, twice or three times, by G, ring4 is 1) -(C 6

-C

1 4 )-aryl, in which aryl is a radical from the series phenyl, naphthyl, 1-naphthyl, 2-naphthyl, anthryl and fluorenyl, and 30 these radicals are unsubstituted or substituted, independently of each other, once, twice or three times, by G, 2) 4- to 15-membered Het ring, in which the Het ring is a radical from the series acridinyl, azepinyl, azetidinyl, aziridinyl, benzimidazalinyl, benzimidazolyl, benzofuranyl, 35 benzothiofuranyl, benzothiophenyl, benzoxazolyl, benzothiazolyl, benzotriazolyl, benzotetrazolyl, benzisoxazolyl, benzisothiazolyl, carbazolyl, 4aH-carbazolyl, carbolinyl, quinazolinyl, quinolinyl, 4H-quinolizinyl, quinoxalinyl, quinuclidinyl, chromanyl, chromenyl, cinnolinyl, 10 deca-hydroquinolinyl, dibenzofuranyl, dibenzothiophenyl, dihydrofuran[2,3-b]tetrahydrofuranyl, dihydrofuranyl, dioxolyl, dioxanyl, 2H,6H-1,5,2-dithiazinyl, furanyl, furazanyl, imidazolidinyl, imidazolinyl, imidazolyl, 1H-indazolyl, indolinyl, 5 indolizinyl, indolyl, 3H-indolyl, isobenzofuranyl, isochromanyl, isoindazolyl, isoindolinyl, isoindolyl, isoquinolinyl (benzimidazolyl), isothiazolidinyl, 2-isothiazolinyl, isothiazolyl, isoxazolyl, isoxazolidinyl, 2-isoxazolinyl, 2'-methylbiphenyl 2-ol, morpholinyl, naphthyridinyl, octahydroisoquinolinyl, 10 oxadiazolyl, 1,2,3-oxadiazolyl, 1,2,4-oxadiazolyl, 1,2,5 oxadiazolyl, 1,3,4-oxadiazolyl, oxazolidinyl, oxazolyl, oxothiolanyl, pyrimidinyl, phenanthridinyl, phenanthrolinyl, phenazinyl, phenothiazinyl, phenoxathiinyl, phenoxazinyl, phthalazinyl, piperazinyl, piperidinyl, pteridinyl, purinyl, 15 pyranyl, pyrazinyl, pyroazolidinyl, pyrazolinyl, pyrazolyl, pyridazinyl, pyridooxazolyl, pyridoimidazolyl, pyridothiazolyl, pyridothiophenyl, pyridinyl, pyridyl, pyrimidinyl, pyrrolidinyl, pyrrolinyl, 2H-pyrrolyl, pyrrolyl, tetrahydrofuranyl, tetrahydroisoquinolinyl, tetrahydroquinolinyl, tetrahydro 20 pyridinyl, 6H-1,2,5-thiadazinyl, 1,2,3-thiadiazolyl, 1,2,4-thia diazolyl, 1,2,5-thiadiazolyl, 1,3,4-thiadiazolyl, thianthrenyl, thiazolyl, thienyl, thienothiazolyl, thienooxazolyl, thienoimidazolyl, thiomorpholinyl, thiophenyl, triazinyl, 1,2,3 triazolyl, 1,2,4-triazolyl, 1,2,5-triazolyl, 1,3,4-triazolyl and 25 xanthenyl, and are unsubstituted or substituted, independently of each other, once, twice or three times, by G, or 3) is one of the following radicals O O O O.4 N N 30 H H and these radicals are unsubstituted or substituted once by G, G is 1) hydrogen atom, 35 2) halogen, 3) =O, 11 4) -(C 1

-C

6 )-cycloalkyl, (C 2

-C

6 )-alkynyl, -(C 6

-C

1 4)-aryl or Het ring, where aryl and Het ring are defined as above, 5 5) -(C 6

-C

1 4)-aryl, where aryl is defined as above, 6) Het ring, where Het ring is defined as above, 7) -C(O)-O-R10, in which R10 is a) -(C-C 6 )-alkyl, in which alkyl is unsubstituted or substituted, once or twice, by -(C 3

-C

6 )-cycloalkyl, 10 -(C 2

-C

6 )-alkynyl, -(C 6

-C

14 )-aryl or Het ring, where aryl and Het ring are defined as above, or b) -(C 6

-C

14 )-aryl or Het ring, where aryl and Het ring are defined as above, 8) -C(S)-O-R10, where R10 is defined as above, 15 9) -C(O)-NH-R11, in which R11 is a) -(C 1 -Cs)-alkyl, in which alkyl is unsubstituted or substituted, once or twice, by -(C 3

-C

6 )-cycloalkyl,

-(C

2

-C

6 )-alkynyl, -(C 6

-C

14 )-aryl or Het ring, where aryl and Het ring are defined as above, or 20 b) -(C 6

-C

14 )-aryl or Het ring, where aryl and Het ring are defined as above, 10) -C(S)-NH-R 11, in which R11 is defined as above, 11) -O-R12, in which R12 is a) hydrogen atom, 25 b) -(C-C 6 )-alkyl, in which alkyl is unsubstituted or substituted, once, twice or three times, by halogen, -(C 3

-C

6 )-cycloalkyl, -(C 2

-C

6 )-alkynyl, (C 6

-C

1 4 )-aryl or Het ring, where aryl and Het ring are defined as above, 30 c) -(C 6

-C

14 )-aryl, where aryl is defined as above, d) Het ring, where Het ring is defined as above, e) -C(O)-O-R13, in which R13 is e)l1) -(CO-C 6 )-alkyl, in which alkyl is unsubstituted or substituted, once or 35 twice, by -(C 3

-C

6 )-cycloalkyl, -(C2-C6) alkynyl, -(C6-C14)-aryl, or Het ring, where aryl and Het ring are defined as above, or e)2) -(C6-C14)-aryl or Het ring, where aryl and Het ring are defined as above, 12 f) -C(S)-O-R1 3, in which R13 is defined as above, g) -C(O)-NH-R14, in which R14 is g)1) -(C1-C 6 )-alkyl, in which alkyl is unsubstituted or substituted, once or 5 twice, by -(C 3

-C

6 )-cycloalkyl, -(C2-C6) alkynyl, -(C 6

-C

1 4)-aryl or Het ring, where aryl and Het ring are defined as above, or g)2) -(C 6

-C

14 )-aryl or Het ring, where aryl and Het ring are defined as above, or 10 h) -C(S)-NH-R14, in which R14 is defined as above, 12) -C(O)-R10, in which R10 is defined as above, 13) -S(O)p-R12, in which R12 is defined as above and p is the integers zero, 1 or 2, 14) -NO 2 , 15 15) -CN, or 16) -N(R15)-R12, in which R15 is 16)1) hydrogen atom, or 16.2) -(Cl-C 6 )-alkyl and R12 is defined as above, 16.3) -SO 2 -(C0 1

-C

6 )-alkyl, in which alkyl is unsubstituted or 20 substituted, once or twice, by -(C 3

-C

6 )-cycloalkyl, (C 2

-C

6 )-alkynyl, -(C6-C 1 4)-aryl or Het ring, 17) -SO 2 -N(R12)-R1, in which R12 is defined as above and R1 is defined as below, X is -OH or -NH-OH, 25 nl is the integer 1 or 2, n2 is the integer 2 or 3, R1, R2, R3, R4 and R5 are identical or different and are, independently of each other, 1 ) hydrogen atom, 30 2) -(C0 1

-C

6 )-cycloalkyl, -(C 2

-C

6 )-alkynyl, -(C6 C1 4 )-aryl or Het ring, 3) -C(O)-O-R8, in which R8 is 3)1) hydrogen atom, 35 3)2) -(C 1

-C

6 )-cycloalkyl,

-(C

2

-C

6 )-alkynyl, -(C 6 -0 14 )-aryl or Het ring, or is substituted once to five times by fluorine, or 3)3) -(C6-C 14 )-aryl or Het ring, 13 4) -O-R8, in which R8 has the abovementioned meaning, or 5) -(C 3

-C

6 )-cycloalkyl. The invention furthermore relates to the compound of the formula I wherein 5 A is -(Co-C 4 )-alkylene, B, D and E are identical or different and are, independently of each other, -(Co-C4)-alkylene or the radical -B1-B2-B3- in which B1 is -(CH 2 )n-, in which n is the integer zero, 1 or 2, B3 is -(CH 2 )m-, in which m is the integer zero, 1 or 2, 10 with the proviso that the sum of n and m amounts to zero, 1 or 2, and B2 is 1) -(Co-C 2 )-alkylene, 2) ethenylene, 3) ethynylene, 15 4) -C(0) 5) -N(R6)-C(0)-, in which R6 is hydrogen atom, methyl or ethyl, 6) -C(0)-N(R6)-, in which R6 is defined as above, 7) -0-, or 8) -S-, 20 ring1, ring2 and ring3 are identical or different and are, independently of each other, 1) covalent bond, 2) phenyl or naphthyl and are unsubstituted or substituted, independently of each other, once or twice, by G, or 25 3) Het ring, in which the Het ring is a radical from the series dihydrofuranyl, furanyl, pyridinyl, pyrimidinyl, pyrrolyl, thiadiazolyl, thiazolyl or thiophenyl, and the radicals are unsubstituted or substituted, independently of each other, once or twice, by G, 30 ring4 is 1) phenyl or naphthyl and is unsubstituted or substituted, independently of each other, once or twice, by G, 2) Het ring, in which the Het ring is a radical from the series benzofuranyl, dihydrofuranyl, dibenzofuranyl, 35 dibenzothiophenyl, furanyl, 2'-methylbiphenyl-2-ol, morpholinyl, piperazinyl, piperidinyl, pyridinyl, pyrimidinyl, pyridothiophenyl, pyrrolyl, pyrrolidinyl, thiazolyl or thiophenyl and is unsubstituted or substituted, independently of each other, once or twice, by G, or 14 3) the following radical Noo 5 and this radical is unsubstituted or substituted once by G, G is 1) hydrogen atom, 2) Br, CI or F, 3) -(C 1

-C

4 )-alkyl, in which alkyl is unsubstituted or substituted once or twice by F, phenyl, -C 3 -cycloalkyl or Het ring, where 10 Het ring is defined as above, 4) phenyl, 5) Het ring, where Het ring is defined as above, 6) -C(O)-O-RO10, in which R10 is a) -(C 1

-C

6 )-alkyl, in which alkyl is unsubstituted or 15 substituted, once or twice, by cyclopropyl, phenyl or Het ring, where Het ring is defined as above, b) phenyl, or c) Het ring, where Het ring is defined as above, 7) -C(O)-NH-R11, in which R11 is 20 a) -(Cl-Cs)-alkyl, in which alkyl is unsubstituted or substituted, once or twice, by cyclopropyl, phenyl or Het ring, where Het ring is defined as above, b) phenyl, or c) Het ring, where Het ring is defined as above, 25 8) -O-R12, in which R12 is a) hydrogen atom, b) -(C 1

-C

6 )-alkyl, in which alkyl is unsubstituted or substituted, once, twice or three times, by halogen, cyclopropyl, phenyl or Het ring, where 30 Het ring is defined as above, c) phenyl, d) Het ring, where Het ring is defined as above, e) -C(O)-O-R13, in which R13 is e)l1) -(C 1

-C

6 )-alkyl, in which alkyl is 35 unsubstituted or substituted, once or twice, by cyclopropyl, phenyl or Het ring, where Het ring is defined as above, or 15 e)2) phenyl or Het ring, where Het ring is defined as above, f) -C(S)-O-R13, in which R13 is defined as above, or 5 g) -C(O)-NH-R14, in which R14 is g)1) -(C 1

-C

6 )-alkyl, in which alkyl is unsubstituted or substituted, once or twice, by phenyl or Het ring, where Het ring is defined as above, or 10 g)2) phenyl or Het ring, where Het ring is defined as above, 9) -C(O)-R10, in which R10 is defined as above, 10) -S(O)p-R12, in which R12 is defined as above and p is the integers 1 or 2, 15 11) -NO 2 , 12) -CN, or 13) -N(R15)-R12, in which R15 is 13)1) hydrogen atom, or 13)2) -(Cl-C 6 )-alkyl and R12 is defined as above, 20 X is -OH or -NH-OH, nl is the integer 1 or 2, n2 is the integer 2 or 3, R1, R2 and R3 are in each case hydrogen atom, R4 and R5 are identical or different and are, independently of each other, 25 1) hydrogen atom, 2) methyl, 3) ethyl, or 4) -OH. 30 The invention furthermore relates to the compound of the formula I wherein A is -(Co-C4)-alkylene, B, D and E are identical or different and are, independently of each other, -(Co-C4)-alkylene or the radical -B1-B2-B3- in which B1 is -(CH 2 )n-, in which n is the integer zero, 1 or 2, 35 B3 is -(CH 2 )m-, in which m is the integer zero, 1 or 2, with the proviso that the sum of n and m amounts to zero, 1 or 2, and B2 is 1) -(Co-C 2 )-alkylene, 2) ethenylene, or 16 3) ethynylene, ring, ring2 and ring3 are identical or different and are, independently of each other, 1) covalent bond, 5 2) phenyl, and are unsubstituted or substituted, independently of each other, once or twice, by G, or 3) Het ring, in which the Het ring is a radical from the series dihydrofuranyl, furanyl, morpholinyl, piperazinyl, piperidinyl, pyridinyl, pyrimidinyl, pyrrolyl, thiazolyl or thiophenyl, and are 10 unsubstituted or substituted, independently of each other, once or twice, by G, ring4 is 1) phenyl, and is unsubstituted or substituted, independently of each other, once or twice, by G, 15 2) Het ring, in which the Het ring is a radical from the series benzofuranyl, dihydrofuranyl, dibenzofuranyl, dibenzothiophenyl, furanyl, 2'-methylbiphenyl-2-ol, morpholinyl, piperazinyl, piperidinyl, pyridinyl, pyrimidinyl, pyridothiophenyl, pyrrolyl, pyrrolidinyl, thiazolyl or thiophenyl 20 and is unsubstituted or substituted, independently of each other, once or twice, by G, or 3) the following radical Noo 25 and this radical is unsubstituted or substituted once by G, G is 1) hydrogen atom, 2) Br, Cl or F, 3) -(C1-C 4 )-alkyl, in which alkyl is unsubstituted or substituted 30 once, twice or three times, by Br, CI, F, -C 3 -cycloalkyl, phenyl or Het ring, where Het ring is defined as above, 4) phenyl, 5) Het ring, where Het ring is defined as above, 6) -C(0)-O-R10, in which R10 is 35 a) -(C 1

-C

6 )-alkyl, in which alkyl is unsubstituted or substituted, once or twice, by cyclopropyl, phenyl or Het ring, where Het ring is defined as above, 17 b) phenyl, or c) Het ring, where Het ring is defined as above, 7) -C(O)-NH-R 11, in which R11 is a) -(C 1

-C

6 )-alkyl, in which alkyl is unsubstituted or 5 substituted, once or twice, by cyclopropyl, phenyl or Het ring, where Het ring is defined as above, b) phenyl or naphthyl, or c) Het ring, where Het ring is defined as above, 8) -O-R12, in which R12 is 10 a) hydrogen atom, b) -(C 1

-C

6 )-alkyl, in which alkyl is unsubstituted or substituted, once, twice or three times, by halogen, cyclopropyl, phenyl or Het ring, where Het ring is defined as above, 15 c) phenyl, d) Het ring, where Het ring is defined as above, e) -C(O)-O-R13, in which R13 is e)1) -(CO-C 6 )-alkyl, in which alkyl is unsubstituted or substituted, once or 20 twice, by cyclopropyl, phenyl, naphthyl, or Het ring, where Het ring is defined as above, or e)2) phenyl or Het ring, where Het ring is defined as above, 25 f) -C(S)-O-R13, in which R13 is defined as above, or g) -C(O)-NH-R14, in which R14 is g)1) -(C1-C 6 )-alkyl, in which alkyl is unsubstituted or substituted, once or 30 twice, by phenyl or Het ring, where Het ring is defined as above, or g)2) phenyl or Het ring, where Het ring is defined as above, 9) -C(O)-R1 0, in which R10 is defined as above, 35 10) -S(O)p-R12, in which R12 is defined as above and p is the integers 1 or 2, 11) -NO 2 , 12) -CN, or 13) -N(R15)-R12, in which R15 is 18 13)1) hydrogen atom, or 13)2) -(C 1

-C

6 )-alkyl and R12 is defined as above, X is -OH or -NH-OH, n1 is the integer 2, 5 n2 is the integer 3, R1, R2, R3, R4 and R5 are in each case hydrogen atom. The invention furthermore relates to the compound of the formula I wherein A is a covalent bond or -CH 2

-CH

2 -, 10 B, D and E are identical or different and are, independently of each other, -(Co-C 4 )-alkylene or the radical -B1-B2-B3- in which B1 is -(CH 2 )n-, in which n is the integer zero, 1 or 2, B3 is -(CH 2 )m-, in which m is the integer zero, 1 or 2, with the proviso that the sum of n and m amounts to zero, 1 or 2, and 15 B2 is 1) -C(0) 2) -(C 2

-C

4 )-alkynylene, 3) -S(O)o-, where o is the integers zero or 1, 4) -N(R6)-C(Y)-, in which Y is oxygen atom and R6 is hydrogen 20 atom, 5) -C(Y)-N(R6)-, in which Y is oxygen atom and R6 is hydrogen atom, or 6) -0-, ring1, ring2 and ring3 are identical or different and are, independently of 25 each other, 1) covalent bond, 2) phenyl and are unsubstituted or substituted, independently of each other, once or twice, by G, or 3) Het ring, in which the Het ring is a radical from the series 30 furanyl, pyridinyl, pyrimidinyl or thiophenyl, and are unsubstituted or substituted, independently of each other, once or twice, by G, ring4 is 1) phenyl and is unsubstituted or substituted, independently of 35 each other, once or twice, by G, 2) Het ring, in which the Het ring is a radical from the series benzofuranyl, dibenzofuranyl, furanyl, 2'-methylbiphenyl-2-ol, morpholinyl, piperazinyl, piperidinyl, pyridinyl, pyrimidinyl, pyridothiophenyl, pyrrolyl, pyrrolidinyl, thiazolyl or thiophenyl 19 and is unsubstituted or substituted, independently of each other, once or twice, by G, or 3) the following radical 5 N and this radical is unsubstituted or substituted once by G, G is 1) hydrogen atom, 2) Br, CI or F, 3) -(C 1 -C4)-alkyl, in which alkyl is unsubstituted or once, twice or 10 three times, by Br, CI, F, -C 3 -cycloalkyl, phenyl or Het ring, where Het ring is defined as above, 4) phenyl, 5) Het ring, where Het ring is defined as above, 6) -C(O)-O-R10, in which R10 is 15 a) -(C 1

-C

6 )-alkyl, in which alkyl is unsubstituted or substituted, once or twice, by cyclopropyl, phenyl or Het ring, where Het ring is defined as above, b) phenyl, or c) Het ring, where Het ring is defined as above, 20 7) -C(O)-NH-R1 1, in which R11 is a) -(C 1

-C

6 )-alkyl, in which alkyl is unsubstituted or substituted, once or twice, by cyclopropyl, phenyl or Het ring, where Het ring is defined as above, b) phenyl, or 25 c) Het ring, where Het ring is defined as above, 8) -O-R12, in which R12 is a) hydrogen atom, b) -(C 1

-C

6 )-alkyl, in which alkyl is unsubstituted or substituted, once; twice or three times, by 30 halogen, cyclopropyl, phenyl or Het ring, where Het ring is defined as above, c) phenyl, d) Het ring, where Het ring is defined as above, e) -C(O)-O-R13, in which R13 is 35 e)1) -(C1-C 6 )-alkyl, in which alkyl is unsubstituted or substituted, once or 20 twice, by cyclopropyl, phenyl or Het ring, where Het ring is defined as above, or e)2) phenyl or Het ring, where Het ring is defined as above, 5 f) -C(S)-O-R13, in which R13 is defined as above, or g) -C(O)-NH-R14, in which R14 is g)1) -(C 1

-C

6 )-alkyl, in which alkyl is unsubstituted or substituted, once or 10 twice, by phenyl or Het ring, where Het ring is defined as above, or g)2) phenyl or Het ring, where Het ring is defined as above, 9) -C(O)-R1 0, in which R10 is defined as above, 15 10) -S(O)p-R12, in which R12 is defined as above and p is the integers zero, 1 or 2, 11) -NO 2 , 12) -CN, or 13) -N(R15)-R12, in which R15 is 20 13)1) hydrogen atom, or 13)2) -(Cl-C 6 )-alkyl and R12 is defined as above, Xis -NH-OH, n1 is the integer 2, n2 is the integer 3, and 25 R1, R2, R3, R4 and R5 are in each case hydrogen atom. The invention also relates to the compound of the formula I from the series 2-(4'-nitrobiphenyl-4-sulfonyl)decahydroisoquinoline-1 -(N hydroxy)carboxamide, 30 2-(4'-chlorobiphenyl-4-sulfonyl)decahydroisoquinoline-1l-carboxylic acid, 2-(4'-chlorobiphenyl-4-sulfonyl)decahydroisoquinoline-1 -(N-hydroxy) carboxamide, 2-(6-phenoxypyridine-3-sulfonyl)decahydroisoquinoline-1 -carboxylic acid; trifluoroacetate, 35 2-(6-phenoxypyridine-3-sulfonyl)decahydroisoquinoline-1 -(N-hydroxy) carboxamide; trifluoroacetate, 2-[2-(4'-chlorobiphenyl-4-yl)ethanesulfonyl]decahydroisoquinoline-1 carboxylic acid, 21 2-[2-(4'-chlorobiphenyl-4-yl)ethanesulfonyl]decahydroisoquinoline-1 -(N hydroxy)carboxamide, 2-[4-(pyridin-4-yloxy)benzenesulfonyl]decahydroisoquinoline-1 -carboxylic acid; trifluoroacetate, 5 2-[4-(pyridin-4-yloxy)benzenesulfonyl]decahydroisoquinoline-1 -(N-hydroxy) carboxamide; trifluoroacetate, 2-[4-(4-methoxyphenoxy)benzenesulfonyl]decahydroisoquinoline-1 carboxylic acid, 2-[4-(4-methoxyphenoxy)benzenesulfonyl]decahydroisoquinoline-1l-(N 10 hydroxy)carboxamide, 2-{4-[4-(2,2,2-trifluoroethoxy)phenoxy]benzenesulfonyl}decahydro isoquinoline-1-carboxylic acid, 2-{4-[4-(2,2,2-trifluoroethoxy)phenoxy]benzenesulfonyl}decahydro isoquinoline-1l-(N-hydroxy)carboxamide, 15 2-[4'-(2,2,2-trifluoroethoxy)biphenyl-4-sulfonyl]decahydroisoquinoline-1 carboxylic acid, 2-(4'-isopropoxycarbonylaminobiphenyl-4-sulfonyl)decahydroisoquinoline 1- carboxylic acid, [4'-(1-hydroxycarbamoyloctahydroisoquinoline-2-sulfonyl)biphenyl-4 20 yl]carboxamide isopropyl ester, 2-[4'-(2,2,2-trifluoroethoxy)biphenyl-4-sulfonyl]decahydroisoquinoline-1 -(N hydroxy)carboxamide, 2-(4'-trifluoromethoxybiphenyl-4-sulfonyl)decahydroisoquinoline-1 -(N hydroxy)carboxamide, 25 2-[4-(4-fluorophenoxy)benzenesulfonyl]decahydroisoquinoline-1

-(N

hydroxy)carboxamide, 2-[4-(4-trifluoromethoxyphenoxy)benzenesulfonyl]decahydroisoquinoline-1 (N-hydroxy)carboxamide, 2-[4-(4-trifluoromethoxyphenoxy)benzenesulfonyl]decahydroisoquinoline-1 30 carboxylic acid, 2-(biphenyl-4-sulfonyl)decahydroisoquinoline-1 -(N-hydroxy)carboxamide, 2-(biphenyl-4-sulfonyl)decahydroisoquinoline-1l-carboxylic acid, 2-[4-(4-cyanophenoxy)benzenesulfonyl]decahydroisoquinoline-1 -(N hydroxy)carboxamide, 35 2-(dibenzofuran-2-sulfonyl)decahydroisoquinoline-1l-carboxylic acid, 2-(dibenzofuran-2-sulfonyl)decahydroisoquinoline-1 -(N hydroxy)carboxamide, or 22 2-[4-(4-fluorophenoxy)benzenesulfonyl]-6-methoxydecahydroisoquinoline 1-(N-hydroxy)carboxamide, and also all the isomeric forms of the abovementioned compounds. 5 The term "(Cl-C 6 )alkyl" is understood as meaning hydrocarbon radicals whose carbon chain is straight-chain or branched and contains from 1 to 6 carbon atoms, for example methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tertiary butyl, pentyl, isopentyl, neopentyl, hexyl, 2,3-dimethylbutane or neohexyl. 10 The term "-(Co-C 4 )alkylene" is understood as meaning hydrocarbon radicals whose carbon chain is straight-chain or branched and contains from 1 to 4 carbon atoms, for example methylene, ethylene, propylene, isopropylene, isobutylene, butylene or tertiary butylene. "-Co-Alkylene" is a covalent bond. 15 The term "-(CH 2 )n-, in which n is the integer zero, 1 or 2" is understood as meaning a covalent bond, where n is zero, the radical methylene, where n is 1 and the radical ethylene where n is 2. The term "-(C 2 -C4)-alkenylene" is understood as meaning hydrocarbon radicals whose carbon chain is straight-chain or branched and contains 20 from 2 to 4 carbon atoms and which, depending on chain length, possess one or two double bonds, for example ethenylene, propenylene, isopropenylene, isobutenylene or butenylene; insofar as the possibility exists in principle, the substituents at the double bond can be arranged in the E position or Z position. 25 The term "-(C 2

-C

6 )-alkynylene" is understood as meaning hydrocarbon radicals whose carbon chain is straight-chain or branched and contains from 2 to 6 carbon atoms and which, depending on chain length, possess one or two triple bonds, for example ethynylene, propenylene, isopropynylene, isobutynyl, butynylene, pentynylene or isomers of 30 pentynylene, or hexynyl or isomers of hexynylene. The term "(C 3

-C

6 )-cycloalkyl" is understood as meaning radicals such as compounds which are derived from 3- to 6-membered monocycles such as cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl. The radicals 35 23 n2 , n1 or are in each case understood as meaning -OH 2 - radicals in the ring of the formula I, where the variables n1l or n2 in each case specify the number of 5 the -OH 2 - radicals in the ring of the formula I. When n1l has the value zero, a covalent bond ensues and the resulting part ring has a total of 4 ring atoms. When n2 has the value zero, a covalent bond ensues and the resulting part ring has a total of 3 ring atoms. When n1 has the value 1, a

-OH

2 - radical ensues and the resulting part ring has a total of 5 ring atoms. 10 When n1 has the value 2, a -CH 2

-CH

2 - radical ensues and the resulting part ring has a total of 6 ring atoms. When n1 has the value 3, a -CH 2

-CH

2 CH 2 - radical ensues and the resulting part ring has a total of 7 ring atoms. Corresponding part rings ensue in the case of n2. The term "-(C6-C 1 4 )-aryl" is understood as meaning aromatic hydrocarbon 15 radicals having from 6 to 14 carbon atoms in the ring. -(C 6

-C

14 )-Aryl radicals are, for example, phenyl, naphthyl, for example 1-naphthyl or 2 naphthyl, anthryl or fluorenyl. Naphthyl radicals and, in particular, phenyl radicals are preferred aryl radicals. The term "4- to 15-membered Het ring" or "Het ring" is understood as 20 meaning ring systems which have from 4 to 15 carbon atoms, which are present in one, two or three ring systems which are linked to each other, and which contain one, two, three or four identical or different heteroatoms from the series oxygen, nitrogen or sulfur. Examples of these ring systems are the radicals acridinyl, azepinyl, azetidinyl, aziridinyl, benzimidazalinyl, 25 benzimidazolyl, benzofuranyl, benzothiofuranyl, benzothiophenyl, benzoxazolyl, benzothiazolyl, benzotriazolyl, benzotetrazolyl, benzisoxazolyl, benzisothiazolyl, carbazolyl, 4aH-carbazolyl, carbolinyl, quinazolinyl, quinolinyl, 4H-quinolizinyl, quinoxalinyl, quinuclidinyl, chromanyl, chromenyl, cinnolinyl, decahydroquinolinyl, dibenzofuranyl, 30 dibenzothiophenyl, dihydrofuran[2,3-b]tetrahydrofuranyl, dihydrofuranyl, dioxolyl, dioxanyl, 2H, 6H-1,5,2-dithiazinyl, furanyl, furazanyl, imidazolidinyl, imidazolinyl, imidazolyl, 1H-indazolyl, indolinyl, indolizinyl, indolyl, 3H-indolyl, isobenzofuranyl, isochromanyl, isoindazolyl, isoindolinyl, isoindolyl, isoquinolinyl (benzimidazolyl), isothiazolidinyl, 2-isothiazolinyl, 35 isothiazolyl, isoxazolyl, isoxazolidinyl, 2-isoxazolinyl, 2'-methylbiphenyl-2- 24 ol, morpholinyl, naphthyridinyl, octahydroisoquinolinyl, oxadiazolyl, 1,2,3 oxadiazolyl, 1,2,4-oxadiazolyl, 1,2,5-oxadiazolyl, 1,3,4-oxadiazolyl, oxazolidinyl, oxazolyl, oxothiolanyl, pyrimidinyl, phenanthridinyl, phenanthrolinyl, phenazinyl, phenothiazinyl, phenoxathiinyl, phenoxazinyl, 5 phthalazinyl, piperazinyl, piperidinyl, pteridinyl, purinyl, pyranyl, pyrazinyl, pyroazolidinyl, pyrazolinyl, pyrazolyl, pyridazinyl, pyridooxazolyl, pyridoimidazolyl, pyridothiazolyl, pyridothiophenyl, pyridinyl, pyridyl, pyrimidinyl, pyrrolidinyl, pyrrolinyl, 2H-pyrrolyl, pyrrolyl, tetrahydrofuranyl, tetrahydroisoquinolinyl, tetrahydroquinolinyl, tetrahydropyridinyl, 6H-1,2,5 10 thiadiazinyl, 1,2,3-thiadiazolyl, 1,2,4-thiadiazolyl, 1,2,5-thiadiazolyl, 1,3,4 thiadiazolyl, thianthrenyl, thiazolyl, thienyl, thienothiazolyl, thienooxazolyl, thienoimidazolyl, thiomorpholinyl, thiophenyl, triazinyl, 1,2,3-triazolyl, 1,2,4-triazolyl, 1,2,5-triazolyl, 1,3,4-triazolyl and xanthenyl. 15 Preferred Het rings are the radicals benzofuranyl, benzimidazolyl, benzoxazolyl, benzothiazolyl, benzothiophenyl, 1,3-benzodioxolyl, quinazolinyl, quinolinyl, quinoxalinyl, chromanyl, cinnolinyl, furanyl such as 2-furanyl and 3-furanyl; imidazolyl, indolyl, indazolyl, isoquinolinyl, isochromanyl, isoindolyl, isothiazolyl, isoxazolyl, 2'-methylbiphenyl-2-ol, 20 oxazolyl, phthalazinyl, pteridinyl, pyrazinyl, pyrazolyl, pyridazinyl, pyridoimidazolyl, pyridopyridinyl, pyridopyrimidinyl, pyridyl; such as 2 pyridyl, 3-pyridyl or 4-pyridyl; pyrimidinyl, pyrrolyl; such as 2-pyrrolyl and 3 pyrrolyl; purinyl, thiazolyl, tetrazolyl or thienyl; such as 2-thienyl and 3 thienyl. 25 The term "halogen" is understood as meaning fluorine, chlorine, bromine or iodine. The invention furthermore relates to a process for preparing the compound 30 of the formula I and/or a stereoisomeric form of the compound of formula I and/or a physiologically tolerated salt of the compound of the formula I, which comprises a) reacting a compound of the formula IV, O n2 R2 ,Re O R4 NH(IV) 35 R5 R3 25 in which Re is a hydrogen atom or an ester-protecting group, with a compound of the formula V, O II Rz-- A -ring 1 - B-ring2-D-ringy-E-ring 4 (V) II 5 O in which A, B, D, E and ring, ring2, ring3 and ring4 are defined as in formula I, and in which Rz is chlorine atom, imidazoyl or OH, 10 in the presence of a base or following silylation with a suitable silylating agent, or using a suitable dehydrating agent when Rz = OH, to give a compound of the formula VI, n2 R2 ,Re 0 R4 N,0 R5R3 -& A-ring,-B-ring-D-ring3-E-ring 4 (VI) O 15 in which A, B, D, E, Re and ring, ring2, ring3 and ring4 are defined as above, and b) when Re = ester reacting a compound of the formula VI prepared as 20 described in a) with a solution of alkali such as NaOH or LiOH, and then treating the product with acid, to give the carboxylic acid according to the invention of the formula I, in which X = OH (corresponding to VII), with modifications in one of the side chains of the rings ringl-ring4 also having previously been made, where 25 appropriate; or converting said ester, by treating it with a mineral acid, such as hydrochloric acid, into the free carboxylic acid VII 26 n2 R2 OH R4 N\O R5R3 ' - A-ring 1 - B-ring2-D-rinlg -E-ring 4 (VII) 5 and then converting this into the hydroxamic acid according to the invention, in which X = NH-OH, of the formula I, c) using salt formation with enantiomerically pure acids or bases, chromatography on chiral stationary phases, or derivatization with 10 chiral, enantiomerically pure compounds such as amino acids, separation of the resulting diastereomers and elimination of the chiral auxiliary groups, to separate a compound of formula I prepared as described in procedure a), or a suitable precursor of the formula I, which arises in enantiomeric forms due to its chemical structure, into 15 the pure enantiomers, or d) either isolating the compound of the formula I prepared as described in procedures b) or c) in free form, or, when acid or basic groups are present, converting it into physiologically tolerated salts. 20 Compounds of the formula IV to VII type are compounds which are only presented by way of example; in accordance with formula I, it is also possible to adduce four-membered rings, six-membered rings and seven membered rings instead of the five-membered ring. 25 Compounds of the formula IV type can be prepared using known protocols. For example, compounds in which nj = 1 and n 2 = 0 (methanoprolines) can be prepared using a number of known methods. The description of a recent synthesis can be found, for example, in Tetrahedron 53, 14773-92 (1997). 30 For example, the bicyclic skeletons of the formula IV in which nj = 2 and n 2 = 3 in accordance with formula I can be prepared by hydrogenation of isoquinoline-1-carboxylic acid or suitable derivatives of isoquinoline-1 carboxylic acid, such as methyl ester or ethyl ester. This hydrogenation is 35 described, for example, in US 5430023, US 5726159 and EP 643073.

27 In the same way, it is possible to use 1,2,3,4-tetrahydroisoquinoline-1 carboxylic acid and its derivatives to prepare these compounds by hydrogenation. This procedure has the advantage that it is possible to use 5 a broad range of methods for synthesizing the 1,2,3,4-tetrahydro isoquinoline-1 -carboxylic acids. For example, Pictet-Spengler-type cyclizations, such as described in US 4902695, are particularly well known and broadly applicable. Depending on the nature of the starting compounds employed, such methods can be used, for example, to obtain substituted 10 compounds, i.e. compounds in which the substituents R1, R4 and R5 are not H atoms. A novel example of ring-substituted compounds can be found in WO 2003041641. Innumerable examples of R1 and/or R4 and R5 not being H exist and are readily available to the skilled person. 15 Other possible methods for preparing the cyclic skeletons use free radical cyclization reactions, for example, and are described in Tetrahedron 48, 4659-76 (1992). Other methods can be used for synthesizing compounds of the IV type 20 when n, = 1 and n 3 = 3. For example, described syntheses are to be found in Tetrahedron 55, 8025 (1999) and Tetrahedron Lett. 24, 5339 (1983) or in the laid-open specifications DE 3322530 and DE 3211676. Methods for synthesizing compounds of the IV type in which nj = 1 and n 2 25 = 2 are likewise to be found in Tetrahedron 55, 8025 (1999) and DE 3322530 or DE 3211676. Methods for synthesizing the skeletons of related compounds, for example in which n, = 1 and n 2 = 4, are also described. For example, J. Org. Chem. 30 61, 7125 (1996) describes syntheses of 1-lactams which contain said skeleton. The substituted basic structures in analogy with formula IV can also be prepared from these compounds by opening the P3-lactam. Methods for synthesizing the skeletons in which n, = 2 and n 2 = 4 are 35 likewise known and well described, for example in EP 0672665 and the abovementioned references. The groups used as protecting groups for esters in "Protective Groups in Organic Synthesis", T.H. Greene, P.G.M. Wuts, Wiley-lnterscience, 1999, 28 can be used as the ester-protecting group Re. Examples of preferred ester protecting groups are methyl, ethyl, isopropyl, tert-butyl and benzyl. Under certain conditions, it can be useful to employ compounds of the IV 5 type in the N-protected state. For example, it is easier to purify compounds which are protected in this way than it is to purify the free imino acids; in the same way, these protected compounds can sometimes also be more readily used for preparing the enantiomerically pure or diastereomerically pure compounds. The groups described in "Protective Groups in Organic 10 Synthesis", T.H. Greene, P.G.M. Wuts, Wiley-Interscience, 1999, can be employed as protecting groups for the amino group. Examples of preferred amino-protecting or imino-protecting groups are Z, Boc, Fmoc, Aloc, acetyl, trifluoroacetyl, benzoyl, benzyl and the like. 15 The starting compounds and reagents employed can either be prepared using known methods or obtained commercially. The reactions are carried out as described, for example, in WO 97/18194. The reaction as described in procedural step a) takes place in the presence 20 of a base, such as KOH, NaOH, LiOH, N-methylmorpholine (NMM), N ethylmorpholine (NEM), triethylamine (TEA), diisopropylethylamine (DIPEA), pyridine, collidin, imidazole or sodium carbonate, in solvents such as tetrahydrofuran (THF), dimethylformamide (DMF), dimethylacetamide, dioxane, acetonitrile, toluene, chloroform or methylene chloride, or else in 25 the presence of water. If the reaction is being carried out using silylating agents, N,O-bis(trimethylsilyl)acetamide (BSA) or N,O-bis(trimethylsilyl) trifluoroacetamide (BSTFA) is used, for example, for silylating the imino acid in order to subsequently carry out the sulfonamide formation. 30 Modifications in the side chain F mean that, for example, a nitro group is hydrogenated using the metal catalyst Pd/C, or reacted with SnCI 2 or Zn under standard conditions, and the resulting amino group can then be subjected to further modification, for example by reacting it with carbonyl chlorides, sulfonyl chlorides, chloroformic esters, isocyanates, 35 isothiocyanates or other reactive or activatable reagents in order to arrive at the precursors of the compounds of formula I according to the invention. In this case, it is frequently advantageous for Re in compound VI to be an ester since side reactions can be expected when the carboxylic acid is unprotected.

29 In procedural step c), the compound of the formula I is separated, insofar as it arises as a mixture of diastereomers or enantiomers, or accrues in the chosen synthesis as their mixtures, into the pure stereoisomers, either by 5 means of chromatography on a support material, which is chiral where appropriate, or, provided the racemic compound of formula I is capable of salt formation, by means of fractional crystallization of the diastereomeric salts which are formed with an optically active base or acid used as auxiliary substance. Examples of chiral stationary phases which are 10 suitable for separating enantiomers by means of thin layer chromatography or column chromatography are modified silica gel supports (what are termed Pirkle phases) and also high molecular weight carbohydrates such as triacetylcellulose. For analytical purposes, it is also possible, following appropriate derivatization known to the skilled person, to use gas 15 chromatographic methods on chiral stationary phases. In order to resolve the racemic carboxylic acids into their enantiomers, an optically active base, which is as a rule commercially available, such as (-)-nicotine, (+) and (-)-phenylethylamine, quinine bases, L-lysine or L- and D-arginine, are used to form the differently soluble diastereomeric salts, the more difficulty 20 soluble component is isolated as a solid, the more readily soluble diastereomer is removed from the mother liquor, and the pure enantiomers are obtained from the diastereomeric salts which have thus been isolated. In what is in principle the same way, the racemic compounds of the formula I which contain a basic group such as an amino group can be converted 25 into the pure enantiomers using optically active acids, such as (+)-camphor-10-sulfonic acid, D- and L-tartaric acid, D- and L-lactic acid and also (+)- and (-)-mandelic acid. It is also possible to convert chiral compounds which contain alcohol or amine functions into the corresponding esters or amides using appropriately activated and, where 30 appropriate, N-protected enantiomerically pure amino acids or, vice versa, to convert chiral carboxylic acids into the amides using carboxyl-protected enantiomerically pure amino acids or to convert them into the corresponding chiral esters using enantiomerically pure hydroxycarboxylic acids such as lactic acid. The chirality of the amino acid radical or alcohol 35 radical which has been introduced in enantiomerically pure form can then be used for separating the isomers by carrying out a separation of the diastereomers, which are now present, by means of crystallization or by means of chromatography on suitable stationary phases and, after that, 30 using suitable methods to once again eliminate the entrained chiral molecule moiety. In addition, the possibility arises, in the case of some of the compounds 5 according to the invention, of using diastereomerically pure or enantiomerically pure starting compounds for preparing the skeletal structures. This then makes it possible, where appropriate, to also use other methods, or simplified methods, for purifying the end products. These starting compounds were prepared beforehand in enantiomerically pure 10 form or diastereomerically pure form using methods known from the literature. For example, it is possible, as mentioned and cited above, to use isoquinoline-1-carboxylic acid either directly in the method for preparing decahydroisoquinoline-1-carboxylic acid. As a result of 3 heterocenters being present, it is possible, in this case, to form a maximum of 8 15 stereoisomers (4 enantiomeric diastereomer pairs). However, the nature of the preparation, for example hydrogenation, strongly favors certain stereoisomers. Thus, it should be possible, as described in the literature, to achieve strong preference for hydrogen attachment at the positions of the ring linkage, for example, by selecting the hydrogenation conditions 20 (catalyst, pressure, solvent and temperature) appropriately. Thus, it is possible, under the specified conditions, to achieve formation of the cis linked rings. It would then consequently only remain a matter of determining the position of the carboxylic acid since the number of possible stereoisomers would already be restricted to 4. As a result of the nature of 25 the hydrogenation mechanism, it is particularly easy to attach the hydrogens on the same side as that of the bridgehead hydrogens, i.e. a further restriction in the possibility of isomer formation is thereby to be expected. It would consequently be possible, in the most favorable case, to assume that only one enantiomer pair would be formed. It ought then to be 30 possible to use the abovementioned methods to resolve this pair into the enantiomers. However, in connection with these considerations, it has also to be assumed that complete stereoselection will never take place and that, on the contrary, varying proportions of the other isomers will virtually always also be formed or will be detectable, even in very small quantities, 35 when suitable methods are used. When enantiomerically pure 1,2,3,4-tetrahydroisoquinoline-1l-carboxylic acid derivatives are used, it would be expected that, if the reaction conditions were identical or similar to those used during the hydrogenation of isoquinoline-1-carboxylic acid, analogous considerations would apply 31 and it would once again to a large extent only be preferred stereoisomers which were formed; in this said case, there should be strong preference for only one single enantiomer since, when carrying out the hydrogenation process under conditions which were analogous to those which lead to the 5 cis ring linkage when hydrogenating isoquinoline-1-carboxylic acid, the H atoms can once again only be attached from the one side and, as a consequence, analogous products will be formed. The identity of the structures can be established by means of suitable 2D NMR experiments, X ray methods such as cocrystallization and others, as well as reference 10 analysis or chemical derivatization and suitable analysis or chemical derivatization which leads to known and described isomers. Another possibility for synthesizing enantiomerically pure or diastereomerically pure compounds is that of using suitably chirally 15 substituted starting compounds in order, by means of the chiral substituent, to achieve induction of chirality at other chiral centers. For example, chiral glyoxylic esters could be used in Pictet-Spengler cyclizations in order to obtain chiral Tic derivatives and then to hydrogenate these derivatives, as already mentioned above. 20 Acid or basic products of the compound of formula I can be present in the form of their salts or in free form. Preference is given to pharmacologically tolerated salts, for example alkali metal or alkaline earth metal salts, or hydrochlorides, hydrobromides, sulfates, hemisulfates and all possible 25 phosphates, as well as salts of the amino acids, natural bases or carboxylic acids. Physiologically tolerated salts are prepared in a manner known per se, in accordance with procedural step d), from compounds of formula I, including their stereoisomeric forms, which are capable of salt formation. The compounds of formula I form stable alkali metal salts, alkaline earth 30 metal salts, or optionally substituted ammonium salts, with basic reagents such as hydroxides, carbonates, hydrogen carbonates or alkoxides, as well as ammonia or organic bases, for example trimethylamine, triethylamine, ethanolamine, diethanolamine, triethanolamine or trometamol, or else basic amino acids, for example lysine, ornithine or arginine. Provided the 35 compounds of formula I possess basic groups, it is also possible to prepare stable acid addition salts using strong acids. Both inorganic and organic acids, such as hydrochloric acid, hydrobromic acid, sulfuric acid, hemisulfuric acid, phosphoric acid, methanesulfonic acid, benzenesulfonic acid, p-toluenesulfonic acid, 4-bromobenzenesulfonic acid, 32 cyclohexylamidosulfonic acid, trifluoromethylsulfonic acid, 2-hydroxyethanesulfonic acid, acetic acid, oxalic acid, tartaric acid, succinic acid, phosphoglyceric acid, lactic acid, malic acid, adipic acid, citric acid, fumaric acid, maleic acid, gluconic acid, glucuronic acid, palmitic acid or 5 trifluoroacetic acid are suitable for this purpose. The invention also relates to pharmaceuticals which are characterized by an effective content of at least one compound of the formula I and/or a physiologically tolerated salt of the compound of formula I and/or an 10 optionally stereoisomeric form of the compound of formula I, together with a pharmaceutically suitable and physiologically tolerated carrier substance, additive and/or other active compounds and auxiliary substances. On account of their pharmacological properties, the compounds according 15 to the invention are suitable for the selective prophylaxis and therapy of all those diseases whose course involves an increase in the activity of the metalloproteinases. These diseases include degenerative joint diseases such as osteoarthroses, spondyloses and chondrolysis following joint trauma or a relatively long period of joint immobilization following meniscus 20 injuries or patella injuries or ligament ruptures. They furthermore also include diseases of the connective tissue such as collagenoses, periodontal diseases, wound healing disturbances and chronic diseases of the locomotory apparatus such as inflammatory, immunologically determined or metabolism-determined acute and chronic arthritides, 25 arthropathies, myalgias and disturbances of bone metabolism. The compounds of the formula I are furthermore suitable for the treatment of ulceration, atherosclerosis and stenoses. In addition, the compounds of the formula I are suitable for the treatment of inflammations, cancer diseases, tumor metastases formation, cachexia, anorexia, heart failure and septic 30 shock. The compounds are also suitable for the prophylaxis of myocardial and cerebral infarctions. The pharmaceuticals according to the invention can be administered by means of oral, inhalative, rectal or transdermal administration or by means 35 of subcutaneous, intraarticular, intraperitoneal or intravenous injection. Oral administration is preferred. The invention also relates to a process for producing a pharmaceutical, which comprises bringing at least one compound of the formula I, together 33 with a pharmaceutically suitable and physiologically tolerated excipient and, where appropriate, other suitable active compounds, additives or auxiliary substances, in a suitable form of administration. 5 Examples of suitable solid or galenic preparation forms are granules, powders, sugar-coated tablets, tablets, (micro)capsules, suppositories, syrups, juices, suspensions, emulsions, drops or injectable solutions, as well as preparations giving a protracted release of active compound, the production of which makes use of customary adjuvants such as carrier 10 substances, disintegrants, binders, coating agents, swelling agents, glidants, lubricants, flavorings, sweeteners and solubilizers. Frequently employed auxiliary substances which may be mentioned are magnesium carbonate, titanium dioxide, lactose, mannitol and other sugars, talc, milk protein, gelatin, starch, cellulose and its derivatives, animal and vegetable 15 oils, such as cod liver oil, sunflower oil, groundnut oil or sesame oil, polyethylene glycol and solvents such as sterile water and monohydric or polyhydric alcohols, such as glycerol. The pharmaceutical preparations are preferably produced and 20 administered in dosage units, with each unit containing, as the active constituent, a defined dose of the compound of the formula I according to the invention. This dose can be up to about 1000 mg, preferably, however, from about 50 to 300 mg, in the case of solid dosage units, such as tablets, capsules, sugar-coated tablets or suppositories, and be up to about 300 25 mg, preferably, however, from about 10 to 100 mg, in the case of injection solutions in ampoule form. Daily doses of from about 2 mg to 1000 mg of active compound, preferably of from 50 mg to 500 mg, are indicated, in dependence on the activity of 30 the compound of the formula I, for treating an adult patient weighing about 70 kg. However, higher or lower daily doses may sometimes also be appropriate. The daily dose can be administered either by means of a once-only administration in the form of a single dosage unit or of several smaller dosage units or else by means of the multiple administration of 35 subdivided doses at defined intervals. End products are as a rule determined by means of mass-spectroscopic methods (FAB-MS and ESI-MS) and 1 H-NMR (400 MHz, in DMSO-D6); the main peak or the two main peaks are given in each case. Temperatures 34 are given in degrees centigrade, RT denotes room temperature (210C to 240C). The abbreviations employed are either explained or in conformity with the customary conventions. The invention is clarified below with the aid of examples. 5 General protocol 1: Sulfonamide from sulfonyl chloride and carboxylic acid The carboxylic acid (6.45 mmol) was dissolved in 20 ml of dimethylform amide (DMF), and 3 equivalents of a 3N solution of NaOH (6.45 ml) were 10 added at 000C. After 10 min, a solution of the arylsulfonyl chloride (1.1 equivalents, 7.1 mmol) in from 10 to 15 ml of DMF was slowly added dropwise; after room temperature (RT) has been reached, the mixture continues to be stirred for a maximum of 12 hours (h) at temperatures between 200C and 80*C. The precise time depends on when conversion is 15 complete, with this being established by mass spectroscopy. After that, the solvent was removed under reduced pressure. Aqueous working-up (extracting by shaking with 1N HCI and a saturated solution of NaCI, drying of the organic phase such as ethyl acetate, methylene chloride or chloroform with magnesium sulfate or sodium sulfate, and after that 20 concentrating) subsequently took place. The crude product was either subjected directly to further reaction or purified by chromatography. General protocol 2: Sulfonamide from sulfonyl chloride and carboxylic acid 25 The carboxylic acid was dissolved in 0.5-2 molar NaOH, where appropriate in the added presence of 10-50% tetrahydrofuran (THF) or DMF. Acid chloride (1-1.2 equivalents, preferably 1.1) was dissolved in THF (concentration, from 0.05 to 1 M) and this solution was slowly added dropwise. 2 N NaOH was automatically added at RT, using an autotitrator, 30 for the purpose of maintaining a constant pH. The set pH was: from 8 to 12, preferably from 9 to 11. After the termination of the reaction, recognizable by no further NaOH being consumed, the organic cosolvent was removed on a rotary evaporator and the aqueous solution or suspension was treated with ethyl acetate and acidified with 1N HCL After the organic phase had 35 been separated off, and the aqueous phase had been extracted once again with ethyl acetate, the organic phases were combined and dried over sodium sulfate; the solvent was subsequently removed under reduced pressure. The crude product was either subjected directly to further reaction or purified by chromatography.

35 General protocol 3: Sulfonamide from sulfonyl chloride and carboxylic acid. This protocol is particularly suitable for the reaction of biphenylethylsulfonyl chloride with iminocarboxylic acids (see Example 6 and Example 7) or 5 similar, more hydrolysis-labile sulfonyl chlorides. 8 mmol of the imino acid were dissolved or suspended in 30 ml of acetonitrile. 2.3 g (9 mmol) of BSTFA (bis(trimethylsilyl)trifluoroacetamide) were added at RT and under an inert gas (N 2 ) and the mixture was heated 10 for 2 h under reflux. 2.84 g (9 mmol) of 4-chlorobiphenylethanesulfonyl chloride, dissolved in 30 ml of acetonitrile, were added to this solution and the whole was once again heated for 3 h under reflux conditions. After the reaction mixture had cooled down, aqueous 1 N HCI was added and the mixture was stirred for 1 h; the solvent was then removed under reduced 15 pressure on a rotary evaporator, after which ethyl acetate or chloroform was added; the organic phase was then separated off, extracted with a saturated solution of NaCI, dried over sodium sulfate and concentrated under reduced pressure. Depending on its purity, it was either possible to subject the reaction product directly to further reaction or necessary to 20 previously chromatograph it through silica gel. General protocol 4: Preparing the hydroxamic acid from carboxylic acid by way of chloroformate activation 25 The sulfonated carboxylic acid was dissolved in 10 ml of DMF after which 1.1 equivalents of ethyl chloroformate, 2.2 equivalents of N-ethylmorpholine and, after a preactivation time of from 30 min to 1 h, 3 equivalents of trimethylsilylhydroxylamine were added at 00C. After the mixture had been heated at 800C for at least 4 h, the solvent was removed under reduced 30 pressure and the crude product purified using chromatographic methods. General protocol 5: Preparing the hydroxamic acid by way of the corresponding carbonyl chloride 35 The sulfonated carboxylic acid was initially introduced in dry chloroform (ethanol-free) (about 5 ml for 0.5 mmol) and 3 equivalents of oxalyl chloride were added at RT. The mixture was then heated at 450C for about 30 min. In order to monitor the chloride formation, a small sample was removed from the reaction flask and treated with a little benzylamine in THF. It was 36 possible to ascertain when the reaction was complete by the quantitative formation of benzylamide; it was no longer possible to detect the carboxylic acid (monitoring by HPLC-MS). It may be necessary to heat for a longer period or to heat under reflux conditions. The solvent was then distilled off 5 under reduced pressure, after which the residue was taken up repeatedly in dry toluene and once again subjected to rotary evaporation. The acid chloride was now once again taken up in chloroform (10 ml per 0.5 mmol) and this mixture was treated, at RT, with 3 equivalents of O-trimethylsilylhydroxylamine. After a reaction period of at least 30 min 10 (reaction monitored by HPLC-MS), the reaction mixture was evaporated under reduced pressure and the residue was purified directly by chromatography. Special protocols 15 4-Chlorobiphenylethanesulfonyl chloride (intermediate for Example 7) Step 1: 1-(2-Bromoethenone)-4-(4-chlorophenyl)benzene 4-Chlorobiphenyl (23.6 g, 0.125 mol) was introduced, in portions and at 0°C, into a stirred suspension of AICI 3 (34.7 g, 0.26 mol) and bromoacetyl 20 bromide (25.2 g, 0.125 mol) in 400 ml of CS2 and the reaction mixture was then heated under reflux for 3 h. After that, it was slowly poured onto ice and subsequently extracted with ethyl acetate; the organic phase was then washed with an aqueous solution of NaHCO 3 and with water. It was then dried over anhydrous sodium sulfate and evaporated under reduced 25 pressure. The residue which remained was recrystallized from dichloromethane. Yield: 24.2 g (62% of theory). m.p.: 127 - 1280C 1 H-NMR: (300 MHz) 5.0 (s, 2H, CH 2 ); 7.5-8.1 (4 d, 8H, ar) MS: 311.1 (M+H) 30 Step 2: 4-Chlorobiphenylethane bromide tert-Butylamineborane (27.5 g, 0.31 mol) was added, at 0°C, to a stirred suspension of AICI 3 (20.0 g, 0.15 mol) in dichloromethane (500 ml). After the mixture had been stirred at 0OC for 15 min, a solution of the 35 bromoketone from step 1 (16.0 g, 50 mmol) in dichloromethane (150 ml) was added and the mixture was stirred at 00C for a further 4 h. Cold dilute HCI (1 N, 30 ml) was added dropwise, after which the mixture was extracted several times with ethyl acetate. The combined organic phases were washed first with dilute HCI and then with a saturated solution of sodium 37 chloride, after which they were evaporated. An oily compound, which was purified by flash chromatography on silica gel, was obtained. Yield: 15 g (quantitative), m.p.: 1420C 1 H-NMR: (300 MHz) 3.2; 3.78 (2t, 4H, OH 2 ); 7.4-7.7 (4 d, 8H, ar) 5 MS: 296.2 (M+H) Step 3: Sodium salt of the 4-chlorobiphenylethanesulfonic acid The compound from step 2 (14.8 g, 50 mmol) was dissolved in a mixture of 10 ethanol and water (1:1, 200 ml). Sodium sulfite (9.5 g, 75 mmol) and tetrabutylammonium iodide (1.8 g, 5 mmol) were added and the mixture was heated under reflux for 16 h. After that, the liquid reaction mixture was decanted off from a small quantity of a solid and the volume of this mixture was reduced by partially evaporating the mixture under reduced pressure. 15 Then the mixture was cooled, the product crystallized out and was subsequently filtered off and recrystallized from MeOH/H 2 0. It was then dried under reduced pressure. Yield: 13.9 g (94% of theory). 1 H-NMR: (300 MHz) 2.6; 2.95 (2 m, 4 H, OH 2 ); 7.3-7.7 (4 d, 8H, ar) 20 Step 4: 4-Chlorobiphenylethanesulfonyl chloride Phosphorus pentachloride (3.2 g, 15 mmol) was added to a suspension of the compound from step 3 (4.8 g, 15 mmol) in phosphorus oxychloride (50 ml). The mixture was heated at 600C for 6 h and was subsequently 25 poured onto ice after methylene chloride had been added. This mixture was neutralized with a saturated solution of sodium hydrogen carbonate and the organic phase was separated off, dried and evaporated under reduced pressure. Yield: 5 g (quantitative) 1 H-NMR: (300 MHz) 2.9 (m, 4H, CH 2 ); 7.3-7.7 30 (4 d, 8H, ar) Using chiral high pressure liquid chromatography (HPLC) to separate the enantiomers of preparation example 3: 35 Column employed: Chiralpak ADR, 250 x 4.6 mm, 300C, running time: 30 min, injection volume: 5 pl, flow rate: 1 ml/min, solvent MeOH/EtOH 1:1 isocratic, detection at 277 nm.

38 isomer 1 (example 14): running time (RT) 6.33 min, 50.48% and isomer 2 (example 15): RT 14.65 min, 49.52%. Two-dimensional NMR spectroscopy was used to determine the structure 5 of isomer I. The methodology only makes it possible to determine the relative stereochemistry, i.e. the positions of the chiral centers in relation to each other. This means that, when only one single enantiomer is present, as is to be expected after an enantiomer separation, this enantiomer can have either the absolute stereochemistry which is specified or else the 10 absolute stereochemistry which is the mirror image to it. The final structural proof can only be obtained by carrying out X-ray structural analyses. This was done both by means of cocrystallizing with MMP-13 and by means of a single-crystal structural analysis. Both methods showed unambiguously that the stereochemistry which is specified is in accordance with the actual 15 stereochemistry, Chiral HPLC can likewise be used to carry out chiral separations of the other compounds which represent such enantiomeric mixtures, i.e. which have been prepared from the same decahydroisoquinoline derivatives. 20 Table 1 shows the results: 16 1 6 17 CI 6 H 8 12 15 13 5 7 I 14 24 10. I :1 N N 3H S 3 H 18 0 0 HN 0 Molecular Weight =448.97 I Exact Mass =448 OH Molecular Formula =C22H25CIN204S Table 1: Chemical shift of isomer 1 at 300 K. 1H 13c 1 4.12 55.15 2 1.93 . 35.68 3 1.67/1.41 26.37 4 1.19 21.03 5 1.48/1.16 24.26 6 1.86/1.12 26.06 7 1.52 32.00 8 1.55/1.45 28.88 9 3.75/3.53 38.95 10 - 138.99 11 7.81 127.29 12 7.87 127.26 13 - 142.45 39 14 - 137.19 15 7.78 128.81 16 7.57 129.05 17 - 133.42 18 - 166.96 18-NH 10.86 18-NOH 8.88 Preparation example 2: N-(4-Chlorobiphenylsulfonyl)decahydroiso quinoline-1-carboxylic acid Decahydroisoquinolinecarboxylic acid was prepared and used as described in US 5,430,023. The resulting imino acid (2.0 g, 9.1 mmol) was dissolved 5 or suspended in THF (20 ml) and the pH was adjusted to 10.5 with 1 molar sodium hydroxide solution using an autotitrator. After that, 4-chlorobiphenylsulfonyl chloride (2.745 g, 9.6 mmol, 1.05 eq.), dissolved in 10 ml of THF, was added dropwise over a period of 2 hours while the pH was maintained constant. After a further 2 hours, it was not possible to 10 observe any further consumption of sodium hydroxide solution. LC-MS, which was carried out as a reaction control, confirmed this. The solution was then adjusted to a pH of from 3 to 4 with dilute hydrochloric acid; 100 ml of ethyl acetate were then added and the solution was extracted by being shaken. The aqueous phase was extracted a further 2 times with 15 small portions of ethyl acetate and the combined organic phases were dried over sodium sulfate. After the solvent had been removed, there then remained an oily residue which became solid under an oil pump vacuum. Yield: 2.31 g (58% of theory). Analytical data: see Table 1. 20 Preparation example 3: N-(4-Chlorobiphenylsulfonyl)decahydroiso quinoline-1 -(N-hydroxy)carboxamide The carboxylic acid from Example 2 (2.3 g, 5.3 mmol) was dissolved in 50 ml of chloroform. Oxalyl chloride (1.345 g, 10.6 mmol, 0.924 ml) was then added dropwise within the space of 10 min and the resulting reaction 25 mixture was heated at 450C for one hour. After this time, a small sample of the reaction mixture (0.1 ml) was removed, for monitoring the reaction by HPLC-MS, and treated with 0.05 ml of benzylamine. Subsequently, the solvent was distilled off under reduced pressure and the resulting oily residue was entrained with toluene for the purpose of removing any 30 possible oxalyl chloride residues or HCI and left under reduced pressure for 15 min. It was then once again taken up in chloroform (50 ml) after which O-trimethylsilylhydroxylamine (2.23 g, 21.2 mmol, 2.593 ml) was added at 40 RT. After 2 hours, the solvent was removed under reduced pressure and the residue was dissolved in a small quantity of a mixture of acetonitrile/water/0.01% trifluoroacetic acid for the purpose of direct preparative RP-HPLC. Product fractions were combined, acetonitrile was 5 removed under reduced pressure and the remaining aqueous phase was freeze-dried. Yield: 749 mg (32% of theory; 36 mg of another diastereomer of the same molar mass is obtained in addition). Unreacted acid chloride was reisolated in the form of the carboxylic acid. Analytical data: see Table 1. 10 The following examples were prepared in analogy with the previously mentioned protocols. Table 2 shows the results. 15 Table 2: Example Structure Molecular ES + 1H-NMR weight 1 459.52 460.2 1.1-2.0 (4 m, 12 H); . 461.2 3.5-3.9 (m, 2 H); 4.15 / a (d, 1 H); 7.88;8.0; 8.07; 8.35 (4 d, 8 H); H o 10.9 (s, 1 H) I OH 2 433.95 433.11 1.2-2.1 (4 m, 12 H); 3.4-3.6 (m, 2 H); 4.2 (d, 1 H); 7.60; 7.8; (2 N. d, 4 H); 7.9 (m, 4 H); o "0 12.8 (s, 1 H) O 3 c 448.97 449.15 1.1-2.0 (4 m, 12 H); 1 451.10 3.5-3.9 (m, 2 H); 4.15 (d, 1 H); 7.60; 7.7; o s 7.8; 7.9 (4 d, 8 H); HN o 10.9 (s, 1 H) OH

OH

41 4 530.52 415.16 o (ES-) ~s F OH F 5 545.54 ES- 1.1-2.0 (4 m, 12 H); o 430.17 3.4-3.8 (2m, 2 H); os o 4.08 (d, 1 H); 7.2 (m, H FF\ O 4 H); 7.45 (m, 2 H); IOHT OH F 8,1 (dd, 1 H); 8.45 (s, 1 H); 10.8 (s, 1 H) 6 462.01 461.14 1.15-2.05 (4 m, 12 a H); 2.9-3.5 (mm, CII SK 0 about 6 H, O overlapping with water); 3.85 (m, 1 H); 4.0 (d, 1 H); 7.48; 7.5; 7.61; 7.7 (4 d, 8 H) 7 477.03 477.7 1.15-2.05 (m m, 12 a H); 2.9-3.5 (mm, about 6 H, overlapping with O O water); 4.85 (m, 1 H); - 7.48; 7.5; 7.65; 7.72 (4d, 8H) 8 530.52 416.14 1.2-2.1 (4 m, 12 H); o 2.9-4.3 (mm, about 3 o H, overlapping with HO 2 o o water); 7.3; 7.45; F ,?- 7.95; 8.70 (4 m, 8 H); F OH 12.8 (s, 1H) F 9 545.54 431.15 1.1-2.0 (4 m, 12 H); o 3.55 (m, 1 H); 3.8 (m, h 1 H); 4.1 (d, 1 H); .,,4.- o / N -0 NO 7.35; 7.45; 7.9; 8.70 H F (4 d, 8 H); 10.8 (s, CH 1H) 10 445.54 446.1 0 447.1 -O -G_

O-&

42 11 460.55 461.2 1.1-1.95 (4m, 12 H); o 462.2 3.45 (m, 1 H); 3.7 (m, N1 H); 3.8 (s, 2 H); O 4.05 (d, 1 H); 7.0 (m, 4 H); 7.1 (m, 2 H); CH 7.7 (m, 2 H); 10.8 (s, 1 H). 12 513.54 514.15 0 515.2 0 F F 13 528.55 529.2 1.1-2.0 (4m, 12 H); o 530.2 3.45 (m, 1 H); 3.7 (m, O F 1 H); 4.07 (d, 1 H); o 7.0 (d, 2 H); 7.17 (s, I F 01 4 H); 7.7 (d, 2 H); 10.8 (s, 1 H). 14 Chemistry 16 448.9726 449.15,4 1.1-2.0 (4 m, 12 H); 3.5 H CHIRAL 51.10 3.8 (2m, 2 H); 4.15 (d, 1 0 H); 7.55-7.9 (3 m, 8 H) N H O \\8.9 (s, 1 H); 10.9 (s, 1 NH 0 0 H) HO 15 Chemistry 19 448.9726 449.15,4 1.1-2.0 (4 m, 12 H); 3.5 H HIRAL 51.10 3.8 (2m,2 H); 4.15 (d, 1 H); 7.55-7.9 (3 m, 8 H); - o " 8.9 (s, 1 H); 10.9 (s, 1 0 HO H) 16 Chemistry 35 500.6187 501.18 1.25 (d, 6 H); 1.2-1.7 (m, 11 H); 2.05 (m, 1 /so H); 3.44; 4.20; 4.90 (3 01 HO " 0 m, 3-4 H); 7.6; 7.7 (dd, o 4 H); 7.87 (m, 4 H); 9.8 (s, 1 H); 12.8 (s, 1 H) 43 17 Chemistry 36 515.6334 516.19 1.25 (d, 6 H); 1.1-1.95 (m, 12 H); 3.55; 3.75 o - 4.12; 4.91 (4 m, 4 H) N 01 H 0 0 7.6-7.88(2 dd, 8H) O H N N 0- 1H H 18 Chemistry 37 512.5524 513.13 1.1-2.0 (m, 12 H); 3.50 3.75, 4.11; 4.83 (4 m, 5 0 NAO& & F H); 7.2 (d, 2 H); 7.8 (m 01 + F 6 H); 8.9 (s, 1 H); 10.9 0 S(s, 1 H). Chemistry 38 498.5253 450.08 1.1-2.0 (m, 12 H); 3.50 19 3.75, 4.15 (3 m, 3 H) s 7.5 (d, 2 H); 7.9 (m, 6 -HS// o F H); 8.9 (s, 1 H); 10.9 (s, F

F

F 1 H). 20 Chemistry 39 448.5174 449.24 1.1-2.0 (m, 12 H); 3.50 2N 03.75, 4.10 (3 m, 3 H); 0 s 7.0-7.7 (4 m. 8 H); 8.E HN (s, 1 H); 10.9 (s, 1 H). OH F 21 Chemistry 44 448.5174 449.21 1.1-2.0 (m, 12 H); 3.50; H O CHIRAL 3.75, 4.10 (3 m, 3 H) 7.0-7.7 (4 m. 8 H); 8.9 H sO O (s, 1 H); 10.9 (s, 1 H) H 0 I OH 22 Chemistry 49 499.51 500.18 1.2-1.7 (m, 11 H); 2.05 S 0 F (m, 1 H); 3.5 (m, +/- 2 S0 F H); 4.2 (d, 1 H); 7.15 e" O 7.80 (4 m ("d"), 8 H) 0 12.7 (s, 1 H) 44 23 Chemistry48 514.5247 515.21 1.1-2.0 (m, 12 H); 3.50 0 3.75, 4.10 (3 m, 3 H) S !F 7.1-7.8 (4 m ("d"), 8 H) - F 8.9 (s, 1 H); 10.9 (s, 1 0 H) 24 Chemistry 53 399.5129 400.24 1.1-2.0 (4 m, 12 H); 3.5 1 H); 7.4-8.0 (m, 9 H) C2'o~ 0 0 25 Chemistry 52 14.5275 415.26 1.1-2.0 (4 m, 12 H); 3.5 3.8 (2 m, 2 H); 4.15 (d 1 H); 7.4-8.0 (m, 9 H) so 8.9 (s, 1 H); 10.9 (s, 1 O NH H) OH 26 Chemistry 55 455.5368 456.30 1.1-2.0 (m, 12 H); 3.50 3.75, 4.10 (3 m, 3 H); - 7.2 (m, 4 H); 7.8-8. SO N (dd, 4 H); 8.9 (s, 1 H) o 10.9 (s, 1 H) CH 27 O 413.4963 414.14 1.2-1.7 (m, 11 H); 2.05 N / \(m, 1 H); 3.5 (m, +/- 2 H); 4.3 (d, 1 H); 7.5-7.9 0 H O (6 m, 7 H); 8.7 (s, 1 H) 28 Chemistry 57 428.511 429.21 1.1-2.0 (m, 12 H); 3.60 o 3.75, 4.10 (3 m, 3 H) N/ 7.5-8.9 (7 m, 8 H); 10.9 H Co (s, 1 H)

OH

45 29 Chemistry 62 478.5438 479.22 1.0-1.95 (m) and 2.6 | 4.05 (m, together 14 H) 0 o 3.7 (s, 3 H); 6.7 - 7.8 (8 N, S'F m, 8 H); 8.9 (s, 1 H) e "0 10.9 (2 s, 1 H) H O I OH Pharmacological examples Determining the enzyme activity of the catalytic domain of human 5 collagenase-1 (MMP-1). This protein is obtained as an inactive proenzyme from Biocol, Potsdam (catalog No. MMP1). Activation of the proenzyme: 2 parts by volume of proenzyme are incubated, at 370C for 1 hour, with 1 part by volume of APMA solution. The APMA solution is prepared from a 10 10 mmol/I solution of p-aminophenylmercuric acetate in 0.1 mmol/I NaOH by diluting with 3 parts by volume of tris/HCI buffer, pH 7.5 (see below). The pH is adjusted to between 7.0 and 7.5 by adding 1 mmol/I HCI. After the enzyme has been activated, it is diluted with the tris/HCI buffer to a concentration of 2.5 pg/ml. 15 In order to measure the enzyme activity, 10 p 1 l of enzyme solution are incubated for 15 minutes with 10 pl of a 3% (v/v) buffered solution of dimethyl sulfoxide (reaction 1). In order to measure the enzyme inhibitor activity, 10 [d of enzyme solution are incubated with 10 RI of a 3% (v/v) buffered solution of dimethyl sulfoxide which contains the enzyme inhibitor 20 (reaction 2). Both in the case of reaction 1 and in the case of reaction 2, the enzyme reaction is monitored by fluorescence spectroscopy (328 nm (extinction)/ 393 nm (emission)) after adding 10 Rl of a 3% (v/v) aqueous solution of dimethyl sulfoxide which contains 0.3 mmol of the substrate/I. 25 The enzyme activity is presented as increase in extinction/minute. The inhibitory effect is calculated as percentage inhibition using the following formula: % inhibition = 100 - [(increase in extinction/minute in reaction 2) / (increase in extinction/minute in reaction 1) x 100]. 30 The IC50, i.e. the inhibitor concentration which is required for 50% inhibition of the enzyme activity, is determined graphically by plotting the percentage inhibitions at different inhibitor concentrations.

46 The buffer solution contains 0.05% Brij (Sigma, Deisenhofen, Germany) and also 0.1 mol of tris/HCI/I, 0.1 mol of NaCI/l, 0.01 mol of CaCI 2 /1 (pH=7.5). The enzyme solution contains 2.5 pg of the enzyme domain/mi. 5 The substrate solution contains 0.3 mmol of the fluorogenic substrate (7-methoxycoumarin-4-yl)acetyl-Pro-Leu-Gly-Leu-3-(2',4'-dinitrophenyl)-L 2,3-diaminopropionyl-Ala-Arg-NH 2 /1 (Bachem, Heidelberg, Germany). Preparation, and determination of the enzyme activity, of the catalytic 10 domain of human stromelysin (MMP-3) and neutrophilic collagenase (MMP-8). The two enzymes, i.e. stromelysin (MMP-3) and neutrophilic collagenase (MMP-8), were prepared as described by Ye et al. (Biochemistry; 31 (1992) pages 11231-11235). In order to measure the enzyme activity or the 15 inhibitory effect on the enzyme, 10 pl of enzyme solution were incubated, for 15 minutes, with 10 pl of a 3% (v/v) buffered solution of dimethyl sulfoxide which contained the enzyme inhibitor, where appropriate. After 10 pl of a 3% (v/v) aqueous solution of dimethyl sulfoxide which contained 1 mmol of substrate/I had been added, the enzyme reaction was monitored 20 by fluorescence spectroscopy (328 nm (ex)/393 nm(em)). The enzyme activity is presented as increase in extinction/minute. The IC 5 0 values listed in Table 2 were determined as the inhibitor concentrations which in each case resulted in the enzyme being inhibited by 50%. The buffer solution contained 0.05% Brij (Sigma, Deisenhofen, Germany) 25 as well as 0.1 mol of tris/HCI/I, 0.1 mol of NaCI/I, 0.01 mol of CaCI 2 /1 and 0.1 mol of piperazine-N,N'-bis[2-ethanesulfonic acid]/I (pH= 7.5). The MMP-3 enzyme solution contained 2.3 pg, and the MMP-8 enzyme solution contained 0.6 j.g, of one of the enzyme domains/ml prepared as described by Ye et al. The substrate solution contained 1 mmol of the 30 fluorogenic substrate (7-methoxycoumarin-4-yl)acetyl-Pro-Leu-Gly-Leu-3 (2',4'-dinitrophenyl)-L-2,3-diaminopropionyl-Ala-Arg-NH 2 /I (Bachem, Heidelberg, Germany). Determining the enzyme activity of the catalytic domain of human 35 collagenase-3 (MMP-13). This protein was obtained as an inactive proenzyme from INVITEK, Berlin (catalog No. 30 100 803). Activation of the proenzyme: 2 parts by volume of proenzyme were incubated, at 370C for 1.5 hours, with 1 part by volume of APMA solution. The APMA solution was prepared from 47 a 10 mmol/I solution of p-aminophenylmercuric acetate in 0.1 mmol/I NaOH by diluting the solution with 3 parts by volume of tris/HCI buffer, pH 7.5 (see below). The pH was adjusted to between 7.0 and 7.5 by adding 1 mmol/I HCI. After the enzyme had been activated, it was diluted with the tris/HCI 5 buffer to a concentration of 1.67 .g/ml. In order to measure the enzyme activity, 10 gl of enzyme solution were incubated for 15 minutes with 10 il of a 3% (v/v) buffered solution of dimethyl sulfoxide (reaction 1). In order to measure the enzyme inhibitor activity, 10 pl of enzyme solution were incubated with 10 gl of a 3% (v/v) 10 buffered solution of dimethyl sulfoxide which contained the enzyme inhibitor (reaction 2). Both in the case of reaction 1 and in the case of reaction 2, the enzyme reaction was monitored by fluorescence spectroscopy (328 nm (extinction)/ 393 nm (emission)) after 10 tl of a 3% (v/v) aqueous solution of dimethyl 15 sulfoxide which contained 0.075 mmol of the substrate/I had been added. The enzyme activity was presented as increase in extinction/minute. The effect of the inhibitor was calculated as a percentage inhibition in accordance with the following formula: % inhibition = 100 - [(increase in extinction/minute in reaction 2) / (increase 20 in extinction/minute in reaction 1) x 100]. The IC50, that is the concentration of inhibitor which is required for 50% inhibition of the enzyme activity, was determined graphically by plotting the percentage inhibitions at different inhibitor concentrations. 25 The buffer solution contained 0.05% Brij (Sigma, Deisenhofen, Germany) and also 0.1 mol of tris/HCI/I, 0.1 mol of NaCI/l, 0.01 mol of CaCI 2 /1 (pH=7.5). The enzyme solution contained 1.67 pg of the enzyme domain/ml. The substrate solution contained 0.075 mmol of the fluorogenic substrate (7-methoxycoumarin-4-yl)acetyl-Pro-Leu-Gly-Leu-3-(2',4' 30 dinitrophenyl)-L-2,3-diaminopropionyl-Ala-Arg-NH 2 /1 (Bachem, Heidelberg, Germany). Determining the enzyme activity of the catalytic domain of human gelatinase A (MMP-2). 35 This protein was obtained as an inactive proenzyme from INVITEK, Berlin (catalog No. 30 100 602). Activation of the proenzyme: 2 parts by volume of proenzyme were incubated, at 37°C for 0.5 hour, with 1 part by volume of APMA solution. The APMA solution was prepared from 48 a 10 mmol/I solution of p-aminophenylmercuric acetate in 0.1 mmol/I NaOH by diluting it with 3 parts by volume of tris/HCI buffer, pH 7.5 (see below). The pH was adjusted to between 7.0 and 7.5 by adding 1 mmol/I HCI. After the enzyme had been activated, it was diluted with the tris/HCI buffer to a 5 concentration of 0.83 gg/ml. In order to measure the enzyme activity, 10 il of enzyme solution were incubated for 15 minutes with 10 il of a 3% (v/v) buffered solution of dimethyl sulfoxide (reaction 1). In order to measure the enzyme inhibitor activity, 10 il of enzyme solution were incubated with 10 il of a 3% (v/v) 10 buffered solution of dimethyl sulfoxide which contained the enzyme inhibitor (reaction 2). Both in the case of reaction 1 and in the case of reaction 2, the enzyme reaction was monitored by fluorescence spectroscopy (328 nm (extinction)/ 393 nm (emission)) after 10 il of a 3% (v/v) aqueous solution of dimethyl 15 sulfoxide which contained 0.3 mmol of the substrate/I had been added. The enzyme activity was presented as increase in extinction/minute. The effect of the inhibitor was calculated as percentage inhibition in accordance with the following formula: % inhibition = 100 - [(increase in extinction/minute in reaction 2) / (increase 20 in extinction/minute in reaction 1) x 100]. The IC 50 , that is the concentration of inhibitor which is required for 50% inhibition of the enzyme activity, was determined graphically by plotting the percentage inhibitions at different inhibitor concentrations. The buffer solution contained 0.05% Brij (Sigma, Deisenhofen, Germany) 25 and also 0.1 mol of tris/HCI/I, 0.1 mol of NaCI/I, 0.01 mol of CaCI 2 /1 (pH=7.5). The enzyme solution contained 0.83 jg of the enzyme domain/mi. The substrate solution contained 0.3 mmol of the fluorogenic substrate (7-methoxycoumarin-4-yl)acetyl-Pro-Leu-Gly-Leu-3-(2',4' dinitrophenyl)-L-2,3-diaminopropionyl-Ala-Arg-NH 2 /1 (Bachem, Heidelberg, 30 Germany). Determining the enzyme activity of the catalytic domain of human gelatinase B (MMP-9). This protein was obtained as an inactive proenzyme from Roche, 35 Mannheim (catalog No. 1 758 896). Activation of the proenzyme: 2 parts by volume of proenzyme were incubated, at 370C for 4 hours, with 1 part by volume of APMA solution. The APMA solution was prepared from a 10 mmol/I solution of p-aminophenylmercuric acetate in 0.1 mmol/I NaOH by diluting it with 3 parts by volume of tris/HCI buffer, pH 7.5 (see below).

49 The pH was adjusted to between 7.0 and 7.5 by adding 1 mmol/I HCI. After the enzyme had been activated, it was diluted with the tris/HCI buffer to a concentration of 4.2 mU/ml. In order to measure the activity of the enzyme, 10 ipl of enzyme solution 5 were incubated for 15 minutes with 10 pl of a 3% (v/v) buffered solution of dimethyl sulfoxide (reaction 1). In order to measure the enzyme inhibitor activity, 10 ~l of enzyme solution were incubated with 10 fl of a 3% (v/v) buffered solution of dimethyl sulfoxide which contained the enzyme inhibitor (reaction 2). 10 Both in the case of reaction 1 and in the case of reaction 2, the enzyme reaction was monitored by fluorescence spectroscopy (328 nm (extinction)/393 nm (emission)) after 10 pl of a 3% (v/v) aqueous solution of dimethyl sulfoxide, which contained 0.15 mmol of the substrate/I, had been added. 15 The enzyme activity was presented as increase in extinction/minute. The inhibitory effect was calculated as percentage inhibition in accordance with the following formula: % inhibition = 100 - [(increase in extinction/minute in reaction 2)/(increase in extinction/minute in reaction 1) x 100]. 20 The IC50, that is the concentration of inhibitor which is required for 50% inhibition of the enzyme activity, was determined graphically by plotting the percentage inhibitions at different inhibitor concentrations. The buffer solution contained 0.05% Brij (Sigma, Deisenhofen, Germany) and also 0.1 mol of tris/HCI/I, 0.1 mol of NaCI/I, 0.01 mol of CaCI 2 /1 25 (pH=7.5). The enzyme solution contained 4.2 mU of the enzyme domain/mi. The substrate solution contained 0.15 mmol of the fluorogenic substrate (7-methoxycoumarin-4-yl)acetyl-Pro-Leu-Gly-Leu-3-(2',4' dinitrophenyl)-L-2,3-diaminopropionyl-Ala-Arg-NH 2 /1 (Bachem, Heidelberg, Germany). 30 Table 3 below shows the results. Table 3: Example MMP-1 IC50 MMP-2 IC 5 0 MMP-3 IC 50 MMP-8 IC50 MMP-9 IC50 MMP-13 ICx [nM) [nM] [nM] [nM] [nM] [nM] 3 400 30 40 3 100 3 5 70 2 28 2.5 1.2 1.8 7 600 4 65 13 3 7 50 9 1000 20 160 22 12 21 11 220 2 25 2.5 2 1.5 13 180 2.6 30 4 2 2 14 400 2 25 2.2 3.5 2 15 6000 2300 10000 2000 4000 2300 19 2100 3 59 10 5 3 20 41 2 26 3 2 2 21 21 1.5 23 2.3 0.45 1.3 23 290 2 50 9 2 2.1 26 450 3 41 16 3 3

Claims

1. A compound of the formula I n2 n1 O "R2 I N 0 R1 5 R3 X 5 0 and/or all the stereoisomeric forms of the compound of the formula I and/or mixtures of these forms in any ratio, and/or a physiologically tolerated salt of the compound of the formula I, wherein 10 A is -(Co-C4)-alkylene, B, D and E are identical or different and are, independently of each other, -(Co-C 4 )-alkylene or the radical -B1-B2-B3- in which B1 is -(CH 2 )n-, in which n is the integer zero, 1 or 2, B3 is -(CH 2 )m-, in which m is the integer zero, 1 or 2, 15 with the proviso that the sum of n and m amounts to zero, 1 or 2, and B2 is 1) -C(0) 2) -(C 2 -C4)-alkenylene, 20 3) -S(0)o-, where o is the integers zero, 1 or 2, 4) -N(R6)-, in which R6 is hydrogen atom, methyl or ethyl, 5) -N(R6)-C(Y)-, in which Y is oxygen atom or sulfur atom and R6 is defined as above, 6) -C(Y)-N(R6)-, in which Y is oxygen atom or sulfur atom and 25 R6 is defined as above, 7) -N(R6)-SO 2 -, in which R6 is defined as above, 8) -SO 2 -N(R6)-, in which R6 is defined as above, 9) -N(R6)-SO 2 -N(R6)-, in which R6 is defined as above, 10) -N(R6)-C(Y)-N(R6)-, in which Y is oxygen atom or sulfur atom 30 and R6 is defined as above, 11) -O-C(0)-N(R6)-, 12) -NH-C(0)-O-, 13) -0-, 52 14) -C(O)-O-, 15) -O-C(0)-, 16) -O-C(0)-O-, 17) -O-CH 2 -C(0)-, 5 18) -O-CH 2 -C(0)-O-, 19) -O-CH 2 -C(0)-N(R6)-, in which R6 is defined as above, 20) -C(0)-CH 2 -O-, 21) -O-C(0)-CH 2 -O-, 22) -N(R6)-C(0)-CH 2 -O-, in which R6 is defined as above, 10 23) -O-(CH 2 )n-O-, in which n is the integer 2 or 3, or 24) -O-(CH 2 )m-N(R6)-, in which m is the integer 2 or 3 and R6 is defined as above, 25) -N(R6)-(CH 2 )m-O-, in which m is the integer 2 or 3 and R6 is defined as above, 15 26) -N(R6)-N(R6)-, in which R6 is defined as above, 27) -N=N-, 28) -N(R6)-CH=N-, in which R6 is defined as above, 29) -N=CH-N(R6)-, in which R6 is defined as above, 30) -N(R6)-C(R7)=N-, in which R6 is defined as above and R7 is 20 -NH-R6, 31) -N=C(R7)-N(R6)-, in which R6 is defined as above and R7 is -NH-R6, or 32) -(C 2 -C 6 )-alkynylene, ring, ring2 and ring3 are identical or different and are, 25 independently of each other, 1) covalent bond, 2) -(C 6 -C 14 )-aryl, in which aryl is unsubstituted or substituted, independently of each other, once, twice or three times, by G, or 30 3) 4- to 15-membered Het ring, in which Het ring is unsubstituted or substituted, independently of each other, once, twice or three times, by G, ring4 is 1) -(C 6 -C 14 )-aryl, in which aryl is unsubstituted or substituted, 35 independently of each other, once, twice or three times, by G, 2) 4- to 15-membered Het ring, in which the Het ring is unsubstituted or substituted, independently of each other, once, twice or three times, by G, or 3) is one of the following radicals 53 H H and these radicals are unsubstituted or substituted once by 5 G, G is 1) hydrogen atom, 2) halogen, 3) =O, 4) -(C 1 -C 6 )-alkyl, in which alkyl is unsubstituted or 10 substituted, once, twice or three times, by halogen, -(C 3 -C 6 )-cycloalkyl, -(C 2 -C 6 )-alkynyl, -(C 6 -C 14 )-aryl or Het ring, 5) -(C 6 -C 14 )-aryl, 6) Het ring, 15 7) -C(0)-O-R10, in which R10 is a) -(C-C 6 )-alkyl, in which alkyl is unsubstituted or substituted, once or twice, by -(C 3 -C 6 )-cycloalkyl, -(C 2 -C 6 )-alkynyl, -(C 6 -0 14 )-aryl or Het ring, or b) -(C 6 -C 1 4 )-aryl or Het ring, 20 8) -C(S)-O-R10, in which R10 is defined as above, 9) -C(0)-NH-R1 1, in which R11 is a) -(C -C 6 )-alkyl, in which alkyl is unsubstituted or substituted, once or twice, by -(C 3 -C 6 )-cycloalkyl, -(C 6 -C 1 4)-aryl or Het ring, or 25 b) -(C 6 -C1 4 )-aryl or Het ring, 10) -C(S)-NH-R1 1, in which R11 is defined as above, 11) -O-R12, in which R12 is a) hydrogen atom, b) -(C -C 6 )-alkyl, in which alkyl is unsubstituted or 30 substituted, once, twice or three times, by halogen, -(C 3 -C 6 )-cycloalkyl, -(C 2 -C 6 )-alkynyl, -(C 6 -C 1 4)-aryl or Het ring, c) -(C 6 -0 1 4)-aryl, d) Het ring, 35 e) -C(0)-O-R13, in which R13 is 54 e)1) -(CO-C 6 )-alkyl, in which alkyl is unsubstituted or substituted, once or twice, by -(C 3 -C6)-cycloalkyl, -(C2-C6) alkynyl, -(C 6 -C14)-aryl, or Het ring, or 5 e)2) -(C 6 -C 14 )-aryl or Het ring, f) -C(S)-O-R13, in which R13 is defined as above, g) -C(O)-NH-R14, in which R14 is g)1) -(C 1 -C 6 )-alkyl, in which alkyl is unsubstituted or substituted, once or 10 twice, by -(C 3 -C 6 )-cycloalkyl, -(C 2 -C 6 ) alkynyl, -(C 6 -0 14 )-aryl or Het ring, or g)2) -(C 6 -C 14 )-aryl or Het ring, or h) -C(S)-NH-R14, in which R14 is defined as above, 12) -C(O)-R10, in which R10 is defined as above, 15 13) -S(O)p-R12, in which R12 is defined as above and p is the integers zero, 1 or 2, 14) -NO 2 , 15) -CN, 16) -N(R15)-R12, in which R15 is 20 16)1) hydrogen atom, 16)2) -(C 1 -C 6 )-alkyl, or 16)3) -SO 2 -(C 1 -C 6 )-alkyl, in which alkyl is unsubstituted or substituted, once or twice, by -(C3-C6) cycloalkyl, -(C 2 -C 6 )-alkynyl, -(C 6 -0 14 )-aryl or Het 25 ring, and R12 is defined as above, or 17) -SO 2 -N(R12)-R1, in which R12 is defined as above and R1 is defined as below, X is -OH or -NH-OH, n1 is the integer zero, 1, 2 or 3, 30 n2 is the integer zero, 1, 2, 3 or 4, with the proviso that the sum of n1 and n2 amounts to 1, 2, 3, 4, 5, 6 or 7, R1, R2, R3, R4 and R5 are identical or different and are, independently of each other, 1) hydrogen atom, 35 2) -(Cl-C 6 )-alkyl, in which alkyl is unsubstituted or substituted, once or twice, by -(C 3 -C 6 )-cycloalkyl, -(C 2 -C 6 )-alkynyl, -(C6 0 14 )-aryl or Het ring, 3) -C(O)-O-R8, in which R8 is 3)1) hydrogen atom, 55 3)2) -(C-C 6 )-alkyl, in which alkyl is unsubstituted or substituted, once or twice, by -(C 3 -C 6 )-cycloalkyl, -(C 2 -C 6 )-alkynyl, -(C 6 -C 14 )-aryl or Het ring, or substituted once to five times, by fluorine, or 5 3)3) -(C 6 -C 1 4)-aryl or Het ring, 4) -O-R8, in which R8 has the abovementioned meaning, or 5) -(C 3 -C 6 )-cycloalkyl.

2. A compound of the formula I as claimed in claim 1, 10 A is -(Co-C 4 )-alkylene, B, D and E are identical or different and are, independently of each other, -(Co-C 4 )-alkylene or the radical -B1-B2-B3- in which B1 is -(CH 2 )n-, in which n is the integer zero, 1 or 2, B3 is -(CH 2 )m-, in which m is the integer zero, 1 or 2, 15 with the proviso that the sum of n and m amounts to zero, 1 or 2, and B2 is 1) -C(0) 2) -(C2-C 4 )-alkenylene, 3) -S(0)o-, where o is the integers zero, 1 or 2, 20 4) -N(R6)-, in which R6 is hydrogen atom, methyl or ethyl, 5) -N(R6)-C(Y)-, in which Y is oxygen atom or sulfur atom and R6 is defined as above, 6) -C(Y)-N(R6)-, in which Y is oxygen atom or sulfur atom and R6 is defined as above, 25 7) -N(R6)-SO 2 -, in which R6 is defined as above, 8) -SO 2 -N(R6)-, in which R6 is defined as above, 9) -N(R6)-SO 2 -N(R6)-, in which R6 is defined as above, 10) -N(R6)-C(Y)-N(R6)-, in which Y is oxygen atom or sulfur atom and R6 is defined as above, 30 11) -O-C(O)-N(R6)-, 12) -NH-C(0)-O-, 13) -0-, 14) -C(O)-O-, 15) -o-C(o)-, 35 16) -O-C(O)-O-, 17) -O-CH 2 -C(0)-, 18) -O-CH 2 -C(0)-O-, 19) -O-CH 2 -C(0)-N(R6)-, in which R6 is defined as above, 20) -C(0)-CH 2 -O-, 56 21) -O-C(O)-CH 2 -O-, 22) -N(R6)-C(O)-CH 2 -O-, in which R6 is defined as above, 23) -O-(CH 2 )n-O-, in which n is the integer 2 or 3, or 24) -O-(CH 2 )m-N(R6)-, in which m is the integer 2 or 3 and R6 is 5 defined as above, 25) -N(R6)-(CH 2 )m-O-, in which m is the integer 2 or 3 and R6 is defined as above, 26) -N(R6)-N(R6)-, in which R6 is defined as above, 27) -N=N-, 10 28) -N(R6)-CH=N-, in which R6 is defined as above, 29) -N=CH-N(R6)-, in which R6 is defined as above, 30) -N(R6)-C(R7)=N-, in which R6 is defined as above and R7 is -NH-R6, 31) -N=C(R7)-N(R6)-, in which R6 is defined as above and R7 is 15 -NH-R6, or 32) -(C 2 -C 6 )-alkynylene, ring, ring2 and ring3 are identical or different and are, independently of each other, 1) covalent bond, 20 2) phenyl or naphthyl and are unsubstituted or substituted, independently of each other, once, twice or three times, by G, or 3) 4- to 15-membered Het ring, in which the Het ring is a radical from the series acridinyl, azepinyl, azetidinyl, aziridinyl, 25 benzimidazalinyl, benzimidazolyl, benzofuranyl, benzothiofuranyl, benzothiophenyl, benzoxazolyl, benzothiazolyl, benzotriazolyl, benzotetrazolyl, benzisoxazolyl, benzisothiazolyl, carbazolyl, 4aH-carbazolyl, carbolinyl, quinazolinyl, quinolinyl, 4H-quinolizinyl, 30 quinoxalinyl, quinuclidinyl, chromanyl, chromenyl, cinnolinyl, deca-hydroquinolinyl, dibenzofuranyl, dibenzothiophenyl, dihydrofuran[2,3-b]tetrahydrofuranyl, dihydrofuranyl, dioxolyl, dioxanyl, 2H,6H-1,5,2-dithiazinyl, furanyl, furazanyl, imidazolidinyl, imidazolinyl, imidazolyl, 1H-indazolyl, indolinyl, 35 indolizinyl, indolyl, 3H-indolyl, isobenzofuranyl, isochromanyl, isoindazolyl, isoindolinyl, isoindolyl, isoquinolinyl (benzimidazolyl), isothiazolidinyl, 2-isothiazolinyl, isothiazolyl, isoxazolyl, isoxazolidinyl, 2-isoxazolinyl, morpholinyl, naphthyridinyl, octahydroisoquinolinyl, oxadiazolyl, 1,2,3- 57 oxadiazolyl, 1,2,4-oxadiazolyl, 1,2,5-oxadiazolyl, 1,3,4 oxadiazolyl, oxazolidinyl, oxazolyl, oxothiolanyl, pyrimidinyl, phenanthridinyl, phenanthrolinyl, phenazinyl, phenothiazinyl, phenoxathiinyl, phenoxazinyl, phthalazinyl, piperazinyl, 5 piperidinyl, pteridinyl, purinyl, pyranyl, pyrazinyl, pyroazolidinyl, pyrazolinyl, pyrazolyl, pyridazinyl, pyridooxazolyl, pyridoimidazolyl, pyridothiazolyl, pyridothiophenyl, pyridinyl, pyridyl, pyrimidinyl, pyrrolidinyl, pyrrolinyl, 2H-pyrrolyl, pyrrolyl, tetrahydrofuranyl, 10 tetrahydroisoquinolinyl, tetrahydroquinolinyl, tetrahydro pyridinyl, 6H-1,2,5-thiadazinyl, 1,2,3-thiadiazolyl, 1,2,4-thia diazolyl, 1,2,5-thiadiazolyl, 1,3,4-thiadiazolyl, thianthrenyl, thiazolyl, thienyl, thienothiazolyl, thienooxazolyl, thienoimidazolyl, thiomorpholinyl, thiophenyl, triazinyl, 1,2,3 15 triazolyl, 1,2,4-triazolyl, 1,2,5-triazolyl, 1,3,4-triazolyl and xanthenyl, and these radicals are unsubstituted or substituted, independently of each other, once, twice or three times, by G, ring4 is 20 1) -(C 6 -C1 4 )-aryl, in which aryl is a radical from the series phenyl, naphthyl, 1-naphthyl, 2-naphthyl, anthryl and fluorenyl, and these radicals are unsubstituted or substituted, independently of each other, once, twice or three times, by G, 2) 4- to 15-membered Het ring, in which the Het ring is a radical 25 from the series acridinyl, azepinyl, azetidinyl, aziridinyl, benzimidazalinyl, benzimidazolyl, benzofuranyl, benzothiofuranyl, benzothiophenyl, benzoxazolyl, benzothiazolyl, benzotriazolyl, benzotetrazolyl, benzisoxazolyl, benzisothiazolyl, carbazolyl, 4aH-carbazolyl, 30 carbolinyl, quinazolinyl, quinolinyl, 4H-quinolizinyl, quinoxalinyl, quinuclidinyl, chromanyl, chromenyl, cinnolinyl, deca-hydroquinolinyl, dibenzofuranyl, dibenzothiophenyl, dihydrofuran[2,3-b]tetrahydrofuranyl, dihydrofuranyl, dioxolyl, dioxanyl, 2H,6H-1,5,2-dithiazinyl, furanyl, furazanyl, 35 imidazolidinyl, imidazolinyl, imidazolyl, 1H-indazolyl, indolinyl, indolizinyl, indolyl, 3H-indolyl, isobenzofuranyl, isochromanyl, isoindazolyl, isoindolinyl, isoindolyl, isoquinolinyl (benzimidazolyl), isothiazolidinyl, 2-isothiazolinyl, isothiazolyl, isoxazolyl, isoxazolidinyl, 2-isoxazolinyl, 2'-methylbiphenyl-2- 58 ol, morpholinyl, naphthyridinyl, octahydroisoquinolinyl, oxadiazolyl, 1,2,3-oxadiazolyl, 1,2,4-oxadiazolyl, 1,2,5 oxadiazolyl, 1,3,4-oxadiazolyl, oxazolidinyl, oxazolyl, oxothiolanyl, pyrimidinyl, phenanthridinyl, phenanthrolinyl, 5 phenazinyl, phenothiazinyl, phenoxathiinyl, phenoxazinyl, phthalazinyl, piperazinyl, piperidinyl, pteridinyl, purinyl, pyranyl, pyrazinyl, pyroazolidinyl, pyrazolinyl, pyrazolyl, pyridazinyl, pyridooxazolyl, pyridoimidazolyl, pyridothiazolyl, pyridothiophenyl, pyridinyl, pyridyl, pyrimidinyl, pyrrolidinyl, 10 pyrrolinyl, 2H-pyrrolyl, pyrrolyl, tetrahydrofuranyl, tetrahydroisoquinolinyl, tetrahydroquinolinyl, tetrahydro pyridinyl, 6H-1,2,5-thiadazinyl, 1,2,3-thiadiazolyl, 1,2,4-thia diazolyl, 1,2,5-thiadiazolyl, 1,3,4-thiadiazolyl, thianthrenyl, thiazolyl, thienyl, thienothiazolyl, thienooxazolyl, 15 thienoimidazolyl, thiomorpholinyl, thiophenyl, triazinyl, 1,2,3 triazolyl, 1,2,4-triazolyl, 1,2,5-triazolyl, 1,3,4-triazolyl and xanthenyl, and are unsubstituted or substituted, independently of each other, once, twice or three times, by G, or 20 3) is one of the following radicals 0 N 00 N H H and these radicals are unsubstituted or substituted once by 25 G, G is 1) hydrogen atom, 2) halogen, 3) =O, 4) -(C 1 -C 6 )-alkyl, in which alkyl is unsubstituted or 30 substituted, once, twice or three times, by halogen, -(C

3 -C 6 )-cycloalkyl, -(C 2 -C 6 )-alkynyl, -(C 6 -C 14 )-aryl or Het ring, where aryl and Het ring are defined as above, 5) -(C 6 -C 14 )-aryl, where aryl is defined as above, 6) Het ring, where Het ring is defined as above, 35 7) -C(0)-O-R10, in which R10 is a) -(C 1 -C 6 )-alkyl, in which alkyl is unsubstituted or substituted, once or twice, by -(C 3 -C 6 )-cycloalkyl, 59 -(C 2 -C 6 )-alkynyl, -(C 6 -C 1 4)-aryl or Het ring, where aryl and Het ring are defined as above, or b) -(C 6 -C 14 )-aryl or Het ring, where aryl and Het ring are defined as above, 5 8) -C(S)-O-R10, where R10 is defined as above, 9) -C(O)-NH-Rl1, in which R1 1 is a) -(C 1 -C 6 )-alkyl, in which alkyl is unsubstituted or substituted, once or twice, by -(C 3 -C 6 )-cycloalkyl, -(C 2 -C 6 )-alkynyl, -(C 6 -C 14 )-aryl or Het ring, where 10 aryl and Het ring are defined as above, or b) -(C 6 -C 14 )-aryl or Het ring, where aryl and Het ring are defined as above, 10) -C(S)-NH-R 11, in which R 1 is defined as above, 11) -O-R12, in which R12 is 15 a) hydrogen atom, b) -(Ci-C 6 )-alkyl, in which alkyl is unsubstituted or substituted, once, twice or three times, by halogen, -(C 3 -C 6 )-cycloalkyl, -(C 2 -C 6 )-alkynyl, (C 6 -C14)-aryl or Het ring, where aryl and Het ring 20 are defined as above, c) -(C 6 -C1 4 )-aryl, where aryl is defined as above, d) Het ring, where Het ring is defined as above, e) -C(O)-O-R13, in which R13 is e)1) -(C 1 -C 6 )-alkyl, in which alkyl is 25 unsubstituted or substituted, once or twice, by -(C 3 -0 6 )-cycloalkyl, -(C2-C6) alkynyl, -(C 6 -C1 4 )-aryl, or Het ring, where aryl and Het ring are defined as above, or e)2) -(C 6 -C 1 4)-aryl or Het ring, where aryl and 30 Het ring are defined as above, f) -C(S)-O-R13, in which R13 is defined as above, g) -C(O)-NH-R14, in which R14 is g)1) -(C 1 -C 6 )-alkyl, in which alkyl is unsubstituted or substituted, once or 35 twice, by -(C 3 -C 6 )-cycloalkyl, -(C2-06) alkynyl, -(C6-C14)-aryl or Het ring, where aryl and Het ring are defined as above, or g)2) -(C6-014)-aryl or Het ring, where aryl and Het ring are defined as above, or 60 h) -C(S)-NH-R14, in which R14 is defined as above, 12) -C(O)-RO10, in which R10 is defined as above, 13) -S(O)p-R12, in which R12 is defined as above and p is the integers zero, 1 or 2, 5 14) -NO 2 , 15) -CN, or 16) -N(R15)-R12, in which R15 is 16)1) hydrogen atom, 16)2) -(C1-C 6 )-alkyl or 10 16)3) -SO 2 -(C 1 -C 6 )-alkyl, in which alkyl is unsubstituted or substituted, once or twice, by -(C 3 -C 6 )-cycloalkyl, (C 2 -C 6 )-alkynyl, -(C 6 -01 4 )-aryl or Het ring, and R12 is defined as above, 17) -SO 2 -N(R12)-R1, in which R12 is defined as above and R1 is 15 defined as below, X is -OH or -NH-OH, nl is the integer 1 or 2, n2 is the integer 2 or 3, R1, R2, R3, R4 and R5 are identical or different and are, 20 independently of each other, 1 ) hydrogen atom, 2) -(C 1 -C 6 )-alkyl, in which alkyl is unsubstituted or substituted, once or twice, by -(C 3 -C 6 )-cycloalkyl, -(C 2 -C 6 )-alkynyl, -(C6 C 1 4 )-aryl or Het ring, 25 3) -C(O)-O-R8, in which R8 is 3)1) hydrogen atom, 3)2) -( 1 -C 6 )-alkyl, in which alkyl is unsubstituted or substituted, once or twice, by -(C 3 -C 6 )-cycloalkyl, -(C 2 -C6)-alkynyl, -(C 6 -C14)-aryl or Het ring, or is 30 substituted once to five times by fluorine, or 3)3) -(C 6 -C 1 4)-aryl or Het ring, 4) -O-R8, in which R8 has the abovementioned meaning, or 5) -(C 3 -C 6 )-cycloalkyl. 35 3. A compound of the formula I as claimed in claim 1 or 2, wherein A is -(Co-C4)-alkylene, B, D and E are identical or different and are, independently of each other, -(Co-C 4 )-alkylene or the radical -B1-B2-B3- in which B1 is -(CH 2 )n-, in which n is the integer zero, 1 or 2, 61 B3 is -(CH 2 )m-, in which m is the integer zero, 1 or 2, with the proviso that the sum of n and m amounts to zero, 1 or 2, and B2 is 5 1) -(Co-C 2 )-alkylene, 2) ethenylene, 3) ethynylene, 4) -C(0) 5) -N(R6)-C(0)-, in which R6 is hydrogen atom, methyl or ethyl, 10 6) -C(O)-N(R6)-, in which R6 is defined as above, 7) -0-, or 8) -S-, ring1, ring2 and ring3 are identical or different and are, independently of each other, 15 1) covalent bond, 2) phenyl or naphthyl and are unsubstituted or substituted, independently of each other, once or twice, by G, or 3) Het ring, in which the Het ring is a radical from the series dihydrofuranyl, furanyl, pyridinyl, pyrimidinyl, pyrrolyl, 20 thiadiazolyl, thiazolyl or thiophenyl, and the radicals are unsubstituted or substituted, independently of each other, once or twice, by G, ring4 is 1) phenyl or naphthyl and is unsubstituted or substituted, 25 independently of each other, once or twice, by G, 2) Het ring, in which the Het ring is a radical from the series benzofuranyl, dihydrofuranyl, dibenzofuranyl, dibenzothiophenyl, furanyl, 2'-methylbiphenyl-2-ol, morpholinyl, piperazinyl, piperidinyl, pyridinyl, pyrimidinyl, 30 pyridothiophenyl, pyrrolyl, pyrrolidinyl, thiazolyl or thiophenyl and is unsubstituted or substituted, independently of each other, once or twice, by G, or 3) the following radical 35 N i O and this radical is unsubstituted or substituted once by G, 62 G is 1) hydrogen atom, 2) Br, CI or F, 3) -(C 1 -C4)-alkyl, in which alkyl is unsubstituted or substituted once or twice by F, phenyl, -C 3 -cycloalkyl 5 or Het ring, where Het ring is defined as above, 4) phenyl, 5) Het ring, where Het ring is defined as above, 6) -C(O)-O-R10, in which R10 is a) -(C1-C 6 )-alkyl, in which alkyl is unsubstituted or 10 substituted, once or twice, by cyclopropyl, phenyl or Het ring, where Het ring is defined as above, b) phenyl, or c) Het ring, where Het ring is defined as above, 7) -C(O)-NH-R1 1, in which R11 is 15 a) -(C1-C 6 )-alkyl, in which alkyl is unsubstituted or substituted, once or twice, by cyclopropyl, phenyl or Het ring, where Het ring is defined as above, b) phenyl, or c) Het ring, where Het ring is defined as above, 20 8) -O-R12, in which R12 is a) hydrogen atom, b) -(Cl-C 6 )-alkyl, in which alkyl is unsubstituted or substituted, once, twice or three times, by halogen, cyclopropyl, phenyl or Het ring, where 25 Het ring is defined as above, c) phenyl, d) Het ring, where Het ring is defined as above, e) -C(O)-O-R13, in which R13 is e)1) -(C 1 -C 6 )-alkyl, in which alkyl is 30 unsubstituted or substituted, once or twice, by cyclopropyl, phenyl or Het ring, where Het ring is defined as above, or e)2) phenyl or Het ring, where Het ring is defined as above, 35 f) -C(S)-O-R13, in which R13 is defined as above, or g) -C(O)-NH-R14, in which R14 is g)1) -(C 1 -C 6 )-alkyl, in which alkyl is unsubstituted or substituted, once or 63 twice, by phenyl or Het ring, where Het ring is defined as above, or g)2) phenyl or Het ring, where Het ring is defined as above, 5 9) -C(O)-R10, in which R10 is defined as above, 10) -S(O)p-R12, in which R12 is defined as above and p is the integers 1 or 2, 11) -NO 2 , 12) -CN, or 10 13) -N(R15)-R12, in which R15 is 13)1) hydrogen atom, or 13)2) -(C 1 -C 6 )-alkyl and R12 is defined as above, X is -OH or -NH-OH, n1 is the integer 1 or 2, 15 n2 is the integer 2 or 3, R1, R2 and R3 are in each case hydrogen atom, R4 and R5 are identical or different and are, independently of each other, 1) hydrogen atom, 20 2) methyl, 3) ethyl, or 4) -OH.

4. A compound of the formula I as claimed in one or more of claims I 25 to 3, wherein A is -(Co-C 4 )-alkylene, B, D and E are identical or different and are, independently of each other, -(Co-C 4 )-alkylene or the radical -BI-B2-B3- in which BI is -(CH 2 )n-, in which n is the integer zero, 1 or 2, 30 B3 is -(CH 2 )m-, in which m is the integer zero, 1 or 2, with the proviso that the sum of n and m amounts to zero, I or 2, and B2 is I ) -(Co-C 2 )-alkylene, 35 2) ethenylene, or 3) ethynylene, ringl1, ring2 and ring3 are identical or different and are, independently of each other, 1) covalent bond, 64 2) phenyl, and are unsubstituted or substituted, independently of each other, once or twice, by G, or 3) Het ring, in which the Het ring is a radical from the series dihydrofuranyl, furanyl, morpholinyl, piperazinyl, piperidinyl, 5 pyridinyl, pyrimidinyl, pyrrolyl, thiazolyl or thiophenyl, and are unsubstituted or substituted, independently of each other, once or twice, by G, ring4 is 1) phenyl, and is unsubstituted or substituted, independently of 10 each other, once or twice, by G, 2) Het ring, in which the Het ring is a radical from the series benzofuranyl, dihydrofuranyl, dibenzofuranyl, dibenzothiophenyl, furanyl, 2'-methylbiphenyl-2-ol, morpholinyl, piperazinyl, piperidinyl, pyridinyl, pyrimidinyl, 15 pyridothiophenyl, pyrrolyl, pyrrolidinyl, thiazolyl or thiophenyl and is unsubstituted or substituted, independently of each other, once or twice, by G, or 3) the following radical 20 0 0 20 N and this radical is unsubstituted or substituted once by G, G is 1) hydrogen atom, 2) Br, Cl or F, 25 3) -(C1-C 4 )-alkyl, in which alkyl is unsubstituted or substituted once, twice or three times, by Br, CI, F, -C 3 cycloalkyl, phenyl or Het ring, where Het ring is defined as above, 4) phenyl, 30 5) Het ring, where Het ring is defined as above, 6) -C(O)-O-R10, in which R10 is a) -(C-C 6 )-alkyl, in which alkyl is unsubstituted or substituted, once or twice, by cyclopropyl, phenyl or Het ring, where Het ring is defined as above, 35 b) phenyl, or c) Het ring, where Het ring is defined as above, 7) -C(O)-NH-R1 1, in which R1 1 is 65 a) -(C 1 -C 6 )-alkyl, in which alkyl is unsubstituted or substituted, once or twice, by cyclopropyl, phenyl or Het ring, where Het ring is defined as above, b) phenyl or naphthyl, or 5 c) Het ring, where Het ring is defined as above, 8) -O-R12, in which R12 is a) hydrogen atom, b) -(C 1 -C 6 )-alkyl, in which alkyl is unsubstituted or substituted, once, twice or three times, by 10 halogen, cyclopropyl, phenyl or Het ring, where Het ring is defined as above, c) phenyl, d) Het ring, where Het ring is defined as above, e) -C(O)-O-R13, in which R13 is 15 e)1) -(C 1 -C 6 )-alkyl, in which alkyl is unsubstituted or substituted, once or twice, by cyclopropyl, phenyl, naphthyl, or Het ring, where Het ring is defined as above, or 20 e)2) phenyl or Het ring, where Het ring is defined as above, f) -C(S)-O-R13, in which R13 is defined as above, or g) -C(O)-NH-R14, in which R14 is 25 g)1) -(C 1 -C 6 )-alkyl, in which alkyl is unsubstituted or substituted, once or twice, by phenyl or Het ring, where Het ring is defined as above, or g)2) phenyl or Het ring, where Het ring is 30 defined as above, 9) -C(O)-R10, in which R10 is defined as above, 10) -S(O)p-R12, in which R12 is defined as above and p is the integers 1 or 2, 11) -NO 2 , 35 12) -CN, or 13) -N(R15)-R12, in which R15 is 13)1) hydrogen atom, or . 13)2) -(C1-C 6 )-alkyl and R12 is defined as above, X is -OH or -NH-OH, 66 n1 is the integer 2, n2 is the integer 3, R1, R2, R3, R4 and R5 are in each case hydrogen atom.

5 5. A compound of the formula I as claimed in one or more of claims 1 to 4, wherein A is a covalent bond or -CH 2 -CH 2 -, B, D and E are identical or different and are, independently of each other, -(Co-C 4 )-alkylene or the radical -B1-B2-B3- in which 10 B1 is -(CH 2 )n-, in which n is the integer zero, 1 or 2, B3 is -(CH 2 )m-, in which m is the integer zero, 1 or 2, with the proviso that the sum of n and m amounts to zero, 1 or 2, and B2 is 1) -C(0) 15 2) -(C 2 -C 4 )-alkynylene, 3) -S(0)o-, where o is the integers zero or 1, 4) -N(R6)-C(Y)-, in which Y is oxygen atom and R6 is hydrogen atom, 5) -C(Y)-N(R6)-, in which Y is oxygen atom and R6 is hydrogen 20 atom, or 6) -0-, ring, ring2 and ring3 are identical or different and are, independently of each other, 1) covalent bond, 25 2) phenyl and are unsubstituted or substituted, independently of each other, once or twice, by G, or 3) Het ring, in which the Het ring is a radical from the series furanyl, pyridinyl, pyrimidinyl or thiophenyl, and are unsubstituted or substituted, independently of each other, 30 once or twice, by G, ring4 is 1) phenyl and is unsubstituted or substituted, independently of each other, once or twice, by G, 2) Het ring, in which the Het ring is a radical from the series 35 benzofuranyl, dibenzofuranyl, furanyl, 2'-methylbiphenyl-2-ol, morpholinyl, piperazinyl, piperidinyl, pyridinyl, pyrimidinyl, pyridothiophenyl, pyrrolyl, pyrrolidinyl, thiazolyl or thiophenyl and is unsubstituted or substituted, independently of each other, once or twice, by G, or 67 3) the following radical o O and this radical is unsubstituted or substituted once by G, 5 G is 1) hydrogen atom, 2) Br, CI or F, 3) -(C 1 -C 4 )-alkyl, in which alkyl is unsubstituted or substituted once, twice or three times, by Br, Cl, F, -C3 cycloalkyl, phenyl or Het ring, where Het ring is defined 10 as above, 4) phenyl, 5) Het ring, where Het ring is defined as above, 6) -C(O)-O-R1 0, in which R10 is a) -(Cl-C 6 )-alkyl, in which alkyl is unsubstituted or 15 substituted, once or twice, by cyclopropyl, phenyl or Het ring, where Het ring is defined as above, b) phenyl, or c) Het ring, where Het ring is defined as above, 7) -C(O)-NH-R1 1, in which R11 is 20 a) -(C-C 6 )-alkyl, in which alkyl is unsubstituted or substituted, once or twice, by cyclopropyl, phenyl or Het ring, where Het ring is defined as above, b) phenyl, or c) Het ring, where Het ring is defined as above, 25 8) -O-R12, in which R12 is a) hydrogen atom, b) -(C -C 6 )-alkyl, in which alkyl is unsubstituted or substituted, once, twice or three times, by halogen, cyclopropyl, phenyl or Het ring, where 30 Het ring is defined as above, c) phenyl, d) Het ring, where Het ring is defined as above, e) -C(O)-O-R13, in which R13 is e)1) -(C 1 -C 6 )-alkyl, in which alkyl is 35 unsubstituted or substituted, once or twice, by cyclopropyl, phenyl or Het ring, where Het ring is defined as above, or 68 e)2) phenyl or Het ring, where Het ring is defined as above, f) -C(S)-O-R13, in which R13 is defined as above, or 5 g) -C(O)-NH-R14, in which R14 is g)1) -(C 1 -C 6 )-alkyl, in which alkyl is unsubstituted or substituted, once or twice, by phenyl or Het ring, where Het ring is defined as above, or 10 g)2) phenyl or Het ring, where Het ring is defined as above, 9) -C(O)-RO10, in which R10 is defined as above, 10) -S(O)p-R12, in which R12 is defined as above and p is the integers zero, 1 or 2, 15 11) -NO 2 , 12) -CN, or 13) -N(R15)-R12, in which R15 is 13)1) hydrogen atom, or 13)2) -(C 1 -C 6 )-alkyl and R12 is defined as above, 20 X is -NH-OH, n1 is the integer 2, n2 is the integer 3, and R1, R2, R3, R4 and R5 are in each case hydrogen atom. 25

6. A compound of the formula I as claimed in one or more of claims 1 to 5, which is a compound from the series 2-(4'-nitrobiphenyl-4-sulfonyl)decahydroisoquinoline-1 -(N hydroxy)carboxamide, 2-(4'-chlorobiphenyl-4-sulfonyl)decahydroisoquinoline-1 -carboxylic 30 acid, 2-(4'-chlorobiphenyl-4-sulfonyl)decahydroisoquinoline-1 -(N hydroxy)carboxamide, 2-(6-phenoxypyridine-3-sulfonyl)decahydroisoquinoline-1 -carboxylic acid; trifluoroacetate, 35 2-(6-phenoxypyridine-3-sulfonyl)decahydroisoquinoline-1 -(N hydroxy)carboxamide; trifluoroacetate, 2-[2-(4'-chlorobiphenyl-4-yl)ethanesulfonyl]decahydroisoquinoline-1 carboxylic acid, 69 2-[2-(4'-chlorobiphenyl-4-yI)ethanesulfonyl]decahydroisoquinoline-1 (N-hydroxy)carboxamide, 2-[4-(pyridin-4-yloxy)benzenesulfonyl]decahydroisoquinoline-1 carboxylic acid; trifluoroacetate, 5 2-[4-(pyridin-4-yloxy)benzenesulfonyl]decahydroisoqu inoline-1 -(N hydroxy)carboxamide; trifluoroacetate, 2-[4-(4-methoxyphenoxy)benzenesulfonyl]decahydroisoquinoline-1 carboxylic acid, 2-[4-(4-methoxyphenoxy)benzenesulfonyl]decahydroisoquinoline-1 10 (N-hydroxy)carboxamide, 2-{4-[4-(2 ,2 ,2-trifluoroethoxy)phenoxy]benzenesu Ifonyl~decahydro isoquinoline-1 -carboxylic acid, 2-{4-[4-(2 ,2 ,2-trifluoroethoxy)phenoxy]benzenesulfonyl~decahydro isoquinoline-1 -(N-hydroxy)carboxamide, 15 2-[4'-(2 ,2,2-trifluoroethoxy)biphenyl-4-sulfonyljdecahydroiso quinoline-1 -carboxylic acid, 2-(4'-isopropoxycarbonylaminobiphenyl-4-sulfonyl)decahydroiso quinoline-1 - carboxylic acid, [4'-(l1 -hydroxycarbamoyloctahydroisoquinoline-2-sulfonyl)biphenyl-4 20 yI]carboxamide isopropyl ester, 2-[4'-(2 ,2 ,2-trifluoroethoxy)biphenyl-4-sulfonyl]decahydroiso quinoline-1 -(N-hydroxy)carboxamide, 2-(4'-trifluoromethoxybi phenyl-4-sulfonyl)decahydroisoquinoline-1 (N-hydroxy)carboxamide, 25 2-[4-(4-fluorophenoxy)benzenesulfonyl]decahydroisoquinoline-1 -(N hydroxy)carboxamide, 2-[4-(4-trifluoromethoxyphenoxy)benzenesulfonyl]decahydroiso quinoline-1 -(N-hydroxy)carboxamide, 2-[4-(4-trifluoromethoxyphenoxy)benzenesulfonyl]decahydroiso 30 quinoline-1 - carboxylic acid, 2-(biphenyl-4-sulfonyl)decahydroisoquinoline-1 -(N-hydroxy)car boxamide, 2-(biphenyl-4-sulfonyl)decahydroisoquinoline-1-carboxylic acid, 2-[4-(4-cya nophenoxy)benzenesulfonyl]decahydroisoquinoline-1 -(N 35 hydroxy)carboxamide, 2-(dibenzofuran-2-sulfonyl)decahydroisoquinoline-1 -carboxylic acid, 2-(dibenzofuran-2-sulfonyl)decahydroisoquinoline-1 -(N-hydroxy)car boxamide, or 70 2-[4-(4-fluorophenoxy)benzenesulfonyl]-6-methoxydecahydroiso quinrioline-1-(N-hydroxy)carboxamide, and also all the isomeric forms of the abovementioned compounds. 5

7. A process for preparing the compound of the formula I as claimed in one or more of claims 1 to 6, which comprises a) reacting a compound of the formula IV, O n2, R2 ,Re R4 t NH (v) R5 R3 10 in which Re is a hydrogen atom or an ester-protecting group, with a compound of the formula V, O II Rz-S- A -ring,- B-ring2-D-ring3-E-ring 4 (V) II O 15 in which A, B, D, E and ring1, ring2, ring3 and ring4 are defined as in formula I, and in which Rz is chlorine atom, imidazoyl or OH, in the presence of a base or following silylation with a suitable 20 silylating agent, or using a suitable dehydrating agent when Rz = OH, to give a compound of the formula VI, n2 O R2 ,Re 0 R4 R" ~ N ,O . ' , / \ 0nD ri i NNO R5R3 S- A-ring, -B-ring 7 -D ring3- E-ring 4 O 25 in which A, B, D, E, Re and ring, ring2, ring3 and ring4 are defined as above, or 71 b) when Re = ester reacting a compound of the formula VI prepared as described in a) with a solution of alkali such as NaOH or LiOH, and then treating the product with acid, to give the carboxylic acid according to the invention of the formula I, in which X = OH 5 (corresponding to VII), with modifications in one of the side chains of the rings ringl-ring4 also having previously been made, where appropriate; or converting said ester, by treating it with a mineral acid, such as hydrochloric acid, into the free carboxylic acid VII 10 n2 O R2 OH R4 NO R5R3 S- A-ring,-B-ring2-D-ring3-E-ring4 and then converting this into the hydroxamic acid according to the 15 invention, in which X = NH-OH, of the formula I, or c) using salt formation with enantiomerically pure acids or bases, chromatography on chiral stationary phases, or derivatization with chiral, enantiomerically pure compounds such as amino acids, 20 separation of the resulting diastereomers and elimination of the chiral auxiliary groups, to separate a compound of formula I prepared as described in procedure a), or a suitable precursor of the formula I, which arises in enantiomeric forms due to its chemical structure, into the pure enantiomers, or 25 d) either isolating the compound of the formula I prepared as described in procedures b) or c) in free form, or, when acid or basic groups are present, converting it into physiologically tolerated salts. 30

8. A pharmaceutical, which comprises an effective content of at least one compound of the formula I as claimed in one or more of claims 1 to 6 together with a pharmaceutically suitable and physiologically tolerated carrier substance, additive and/or other active compounds and auxiliary substances. 72

9. The use of the compound of formula I as claimed in one or more of claims 1 to 6 for producing a pharmaceutical for the prophylaxis and therapy of degenerative joint diseases such as osteoarthroses, 5 spondyloses and chondrolysis following joint trauma or a relatively long period of joint immobilization following meniscus injuries or patella injuries or ligament ruptures, diseases of the connective tissue such as collagenoses, periodontal diseases, wound healing disturbances and chronic diseases of the locomotory apparatus such 10 as inflammatory, immunologically determined or metabolism determined acute and chronic arthritides, arthropathies, myalgias and disturbances of bone metabolism, for the treatment of ulceration, atherosclerosis and stenoses, for the treatment of inflammations, cancer diseases, tumor metastases formation, 15 cachexia, anorexia, heart failure and septic shock, or for the prophylaxis of myocardial and cerebral infarctions.