[go: up one dir, main page]

TNSN97084A1 - BIARYL ACETYLENES AS INHIBITORS OF METALLOPROTEINASE MATRICES - Google Patents

BIARYL ACETYLENES AS INHIBITORS OF METALLOPROTEINASE MATRICES

Info

Publication number
TNSN97084A1
TNSN97084A1 TNTNSN97084A TNSN97084A TNSN97084A1 TN SN97084 A1 TNSN97084 A1 TN SN97084A1 TN TNSN97084 A TNTNSN97084 A TN TNSN97084A TN SN97084 A TNSN97084 A TN SN97084A TN SN97084 A1 TNSN97084 A1 TN SN97084A1
Authority
TN
Tunisia
Prior art keywords
disease
compounds
conditions
matrices
treating
Prior art date
Application number
TNTNSN97084A
Other languages
French (fr)
Inventor
r dixon Brian
Chen Jinshan
Original Assignee
Bayer Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Bayer Corp filed Critical Bayer Corp
Publication of TNSN97084A1 publication Critical patent/TNSN97084A1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/44Iso-indoles; Hydrogenated iso-indoles
    • C07D209/48Iso-indoles; Hydrogenated iso-indoles with oxygen atoms in positions 1 and 3, e.g. phthalimide
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/02Stomatological preparations, e.g. drugs for caries, aphtae, periodontitis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/02Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00Drugs for genital or sexual disorders; Contraceptives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • A61P27/02Ophthalmic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C229/00Compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C229/02Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton
    • C07C229/34Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton containing six-membered aromatic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C59/00Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
    • C07C59/40Unsaturated compounds
    • C07C59/76Unsaturated compounds containing keto groups
    • C07C59/90Unsaturated compounds containing keto groups containing singly bound oxygen-containing groups

Landscapes

  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Rheumatology (AREA)
  • Oncology (AREA)
  • Dermatology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Pain & Pain Management (AREA)
  • Cardiology (AREA)
  • Ophthalmology & Optometry (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Endocrinology (AREA)
  • Reproductive Health (AREA)
  • Hematology (AREA)
  • Urology & Nephrology (AREA)
  • Immunology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Enzymes And Modification Thereof (AREA)
  • Steroid Compounds (AREA)

Abstract

LA MATRICE METALLOPROTEASE INHIBITANT LES COMPOSES, LES COMPOSITIONS PHARMACEUTIQUES ET LA METHODE DE TRAITEMENT DE LA MALADIE EN UTILISANT CES COMPOSES SONT PRESENTES. LES COMPOSES DE CETTE INVENTION ONT LES FORMULES GENERALISEES : R45 EST SELECTIONNE DU GROUPE COMPRENANT : HOCH2, M2OCH2, (n-Pr)2NCH2, CH3,CH2CG2, ETOCO2 CH2, HO (CH2), CH3 (CH2) 2, HO2C(CH2)2, OHC(CH2)3, HO(CH2)4, Ph, 3-HO-Ph and PhCH2OCH2 ; and R 16 is. CES COMPOSES SONT UTILES POUR INHIBITANT LES MATRICES METALLOPROTEASES ET COMBATTANT LES CONDITIONS OU MMP’s : ALLEGER LES EFFETS D’OSTEOARTHRITIS. RHEUMATOID ARTHRISTIS, ARTHRITIS SEPTIQUE, MALADIE PERIODONTALE, ULCERATION DE LA CORNEE, PROTEINURIA. MALADIE ANEURYSMAL AORTIQUE. EPIDERMLYSIS DISTROPHOBIQUE, BULLOSA, DES CONDITIONS MENANT A DES REACTIONS INFLAMMATOIRES, OSTEOPENIAS EN MEDIATION PAR L’ACTIVITE MMP. MALADIE TEMPERO MANDIBULAIRE DES JOINTS, DES MALADIES DEMYELANTE DU SYSTEME NERVEUX : RETARDER LA TUMEUR METASTASIS ET LA PERTE DEGENERATIVE DU CARTILAGE SUIVANT UNE BLESSURE TRAUMATIQUE DES JOINTS : REDUIT LA THROMBOSIS CORONAIRE DE LA RUPTURE DE LA PLAQUE ATHROSCLEROTIQUE : OU CETTE PRESENTE INVENTION DONNE AUSSI DES COMPOSITIONS ET METHODES PHARMACEUTIQUES POUR TRAITER CES CONDITIONS.THE METALLOPROTEASE MATRIX INHIBITING COMPOUNDS, PHARMACEUTICAL COMPOSITIONS AND THE METHOD OF TREATING DISEASE USING THESE COMPOUNDS ARE PRESENT. THE COMPOUNDS OF THIS INVENTION HAVE THE GENERALIZED FORMULAS: R45 IS SELECTED FROM THE GROUP INCLUDING: HOCH2, M2OCH2, (n-Pr) 2NCH2, CH3, CH2CG2, ETOCO2 CH2, HO (CH2), CH3 (CH2) 2, HO2C (CH2) 2, OHC (CH2) 3, HO (CH2) 4, Ph, 3-HO-Ph and PhCH2OCH2; and R 16 is. THESE COMPOUNDS ARE USEFUL FOR INHIBITING METALLOPROTEASE MATRICES AND COMBATTING CONDITIONS OR MMP’s: ALLEVIATING THE EFFECTS OF OSTEOARTHRITIS. RHEUMATOID ARTHRISTIS, SEPTIC ARTHRITIS, PERIODONTAL DISEASE, ULCERATION OF THE CORNEA, PROTEINURIA. AORTIC ANEURYSMAL DISEASE. DISTROPHOBIC EPIDERMLYSIS, BULLOSA, CONDITIONS LEADING TO INFLAMMATORY REACTIONS, OSTEOPENIAS MEDIATED BY MMP ACTIVITY. TEMPERO-MANDIBULAR DISEASE OF JOINTS, DEMYELANT DISEASE OF THE NERVOUS SYSTEM: DELAYING METASTASIS TUMOR AND DEGENERATIVE LOSS OF CARTILAGE FOLLOWING TRAUMATIC JOINT INJURY: REDUCES THE CORONARY THROMBOSIS OF THE RUPTURE OF PLAQUE INHIBITION PHARMACEUTICAL METHODS AND METHODS FOR TREATING THESE CONDITIONS.

TNTNSN97084A 1996-05-15 1997-05-09 BIARYL ACETYLENES AS INHIBITORS OF METALLOPROTEINASE MATRICES TNSN97084A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US64502896A 1996-05-15 1996-05-15

Publications (1)

Publication Number Publication Date
TNSN97084A1 true TNSN97084A1 (en) 2005-03-15

Family

ID=24587368

Family Applications (1)

Application Number Title Priority Date Filing Date
TNTNSN97084A TNSN97084A1 (en) 1996-05-15 1997-05-09 BIARYL ACETYLENES AS INHIBITORS OF METALLOPROTEINASE MATRICES

Country Status (18)

Country Link
EP (1) EP0912496A1 (en)
JP (1) JP3090957B2 (en)
CN (1) CN1139570C (en)
AR (1) AR007097A1 (en)
AU (1) AU710759B2 (en)
BR (1) BR9709077A (en)
CA (1) CA2253796C (en)
CO (1) CO5080759A1 (en)
HN (1) HN1997000088A (en)
HR (1) HRP970245B1 (en)
ID (1) ID16910A (en)
PA (1) PA8429301A1 (en)
SV (1) SV1997000035A (en)
TN (1) TNSN97084A1 (en)
TW (1) TW381079B (en)
WO (1) WO1997043245A1 (en)
YU (1) YU18697A (en)
ZA (1) ZA974031B (en)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6288063B1 (en) 1998-05-27 2001-09-11 Bayer Corporation Substituted 4-biarylbutyric and 5-biarylpentanoic acid derivatives as matrix metalloprotease inhibitors
AR035478A1 (en) * 1999-01-27 2004-06-02 Wyeth Corp AMIDA-HYDROXAMIC ACID, ACETYLLENE, BETA-SULPHONAMIDE AND PHOSPHINIC ACID AS INHIBITORS OF TACE, USE OF THE SAME FOR THE MANUFACTURE OF A MEDICINAL PRODUCT AND PHARMACEUTICAL COMPOSITION CONTAINING THEM
US6326516B1 (en) 1999-01-27 2001-12-04 American Cyanamid Company Acetylenic β-sulfonamido and phosphinic acid amide hydroxamic acid TACE inhibitors
EP1031349A1 (en) * 1999-02-25 2000-08-30 Bayer Aktiengesellschaft Use of substituted 4-biarylbutyric and 5-biarylpentanoic acid derivatives for the treatment of cerebral diseases
US7141607B1 (en) 2000-03-10 2006-11-28 Insite Vision Incorporated Methods and compositions for treating and inhibiting retinal neovascularization
EP2597084B1 (en) * 2010-07-08 2016-06-29 Kaken Pharmaceutical Co., Ltd. N-hydroxyformamide derivative and pharmaceutical containing same
EP3126358A1 (en) 2014-04-03 2017-02-08 Bayer Pharma Aktiengesellschaft 2,5-disubstituted cyclopentane carboxylic acids for the treatment of respiratoy tract diseases
WO2015150363A1 (en) 2014-04-03 2015-10-08 Bayer Pharma Aktiengesellschaft 2,5-disubstituted cyclopentane carboxylic acids and use thereof
CA2944617A1 (en) 2014-04-03 2015-10-08 Bayer Pharma Aktiengesellschaft Chiral 2,5-disubstituted cyclopentanecarboxylic acid derivatives and use thereof

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3784701A (en) * 1970-09-21 1974-01-08 American Cyanamid Co Compositions containing substituted benzoylpropionic acids and method of use to treat inflammation and pain
DE2112716A1 (en) * 1971-03-17 1972-10-05 Thomae Gmbh Dr K Biphenylyl-butyric acid derivs. - anti phlogistics
FR2378741A1 (en) 1977-02-01 1978-08-25 Fabre Sa Pierre GARYL GOXO ISOVALERIC ACIDS WITH ANTIPHLOGISTIC AND ANTALGIC PROPERTIES
US5789434A (en) 1994-11-15 1998-08-04 Bayer Corporation Derivatives of substituted 4-biarylbutyric acid as matrix metalloprotease inhibitors
ZA974033B (en) 1996-05-15 1998-02-19 Bayer Ag Substituted 4-arylbutyric acid derivatives as matrix metalloprotease inhibitors.

Also Published As

Publication number Publication date
HRP970245A2 (en) 1998-04-30
WO1997043245A1 (en) 1997-11-20
JPH11511179A (en) 1999-09-28
SV1997000035A (en) 1999-01-14
CA2253796C (en) 2003-10-28
AU710759B2 (en) 1999-09-30
BR9709077A (en) 1999-08-03
JP3090957B2 (en) 2000-09-25
AR007097A1 (en) 1999-10-13
AU2938697A (en) 1997-12-05
CN1225623A (en) 1999-08-11
HN1997000088A (en) 1997-06-18
HRP970245B1 (en) 2002-06-30
TW381079B (en) 2000-02-01
ID16910A (en) 1997-11-20
CN1139570C (en) 2004-02-25
CO5080759A1 (en) 2001-09-25
YU18697A (en) 1999-11-22
CA2253796A1 (en) 1997-11-20
PA8429301A1 (en) 2000-05-24
ZA974031B (en) 1998-02-19
EP0912496A1 (en) 1999-05-06

Similar Documents

Publication Publication Date Title
TNSN97083A1 (en) INHIBITION OF METALLOPROTEASE MATRICES BY SUBSTITUTION OF OXOBUTYRIC BIARYL ACID
TNSN97084A1 (en) BIARYL ACETYLENES AS INHIBITORS OF METALLOPROTEINASE MATRICES
MA26697A1 (en) NOVEL GSK-3 INHIBITOR COMPOUNDS AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
EA200101085A1 (en) HYDROXAMIC ACIDS, DERIVATIVES OF AROMATIC SULPHONES, - METALLOPROTEASIS INHIBITORS
BG102510A (en) Inhibitors of metalloproteinase, pharmaceutical compositions containing them, their pharmaceutical application and methods and intermediate compounds for their preparation
BE900481A (en) COMPOSITION AND METHOD FOR PREVENTING OR INHIBITING RESORPTION OF ALVELOLAR BONES.
ES2101358T3 (en) INHIBITION OF TNF PRODUCTION.
MA26720A1 (en) NOVEL MONOAMINE REABSORPTION INHIBITORS, PROCESSES FOR THEIR PREPARATION, AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM.
TNSN98127A1 (en) AZETIDINYLPROPYLPIPERIDINE DERIVATIVES, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM.
BR0008491A (en) Aromatic sulfone hydroxamic acid metalloprotease inhibitors
NO991674L (en) Interleukin-1 <beta> converting enzyme inhibitor sulfonamides
ATE203409T1 (en) PHOSPHONOCARBOXYLATE COMPOUNDS FOR TREATING ABNORMAL CALCIUM AND PHOSPHATE METABOLISM
CA2254750A1 (en) Inhibition of matrix metalloproteases by 2-(.omega.-aroylalkyl)-4-biaryl-oxobutyric acids
JPH11504646A (en) Peptide compounds inhibiting the release of metalloproteases and TNF and their therapeutic use
DE69811360D1 (en) DIAZEPINOINDOLONE AS A PHOPHODIESTERASE 4 INHIBITORS
TNSN97082A1 (en) INHIBITION OF METALLOPROTEASE MATRICES BY SUBSTITUTION OF PHENETYLE COMPOUNDS
CA2266759A1 (en) 3-mercaptoacetylamino-1,5-substituted-2-oxo-azepan derivatives useful as inhibitors of matrix metalloproteinase
DE69735230D1 (en) SULPHONAMIDE-SUBSTITUTED ASPARAGINIC ACIDS AS INHIBITORS OF INTERLEUKIN-1BETA CONVERTING ENZYMES
TNSN97085A1 (en) OXYBUTERIC SUBSTITUTION OF ACIDS AS METALLOPROTEASE MATRIX INHIBITORS
US5627173A (en) Phosphonoacetic acid derivatives and their use for treating degenerative joint disorders
TH12333B (en) Inhibition of matrix methalloprotein by substitutedphenethyl compounds.
TH35864A (en) Inhibition of matrix methalloprotein by substitutedphenethyl compounds.
ECSP972114A (en) BIARYLACETYLENE AS INHIBITORS OF MATRIX METALOPROTEASE
ECSP972112A (en) INHIBITION OF MATRIX METALOPROTEASES BY SUBSTITUTED FENETILE COMPOUNDS
ECSP972113A (en) INHIBITION OF MATRIX METALOPROTEASES BY SUBSTITUTED BIARILOXOBUTIRIC ACIDS