US20090163586A1 - Bis-(Sulfonylamino) Derivatives in Therapy 205 - Google Patents
Bis-(Sulfonylamino) Derivatives in Therapy 205 Download PDFInfo
- Publication number
- US20090163586A1 US20090163586A1 US12/337,125 US33712508A US2009163586A1 US 20090163586 A1 US20090163586 A1 US 20090163586A1 US 33712508 A US33712508 A US 33712508A US 2009163586 A1 US2009163586 A1 US 2009163586A1
- Authority
- US
- United States
- Prior art keywords
- benzenesulfonamide
- phenyl
- sulfonylamino
- fluoro
- ethenyl
- Prior art date
- Legal status (The legal status 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 status listed.)
- Abandoned
Links
- 238000002560 therapeutic procedure Methods 0.000 title abstract description 11
- 150000001875 compounds Chemical class 0.000 claims abstract description 370
- 238000000034 method Methods 0.000 claims abstract description 85
- 150000003839 salts Chemical class 0.000 claims abstract description 55
- 102100033076 Prostaglandin E synthase Human genes 0.000 claims abstract description 25
- 101710096361 Prostaglandin E synthase Proteins 0.000 claims abstract description 25
- 238000002360 preparation method Methods 0.000 claims abstract description 24
- 230000008569 process Effects 0.000 claims abstract description 16
- 239000008194 pharmaceutical composition Substances 0.000 claims abstract description 14
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 179
- -1 2,3-dihydro-indenyl Chemical group 0.000 claims description 109
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 claims description 99
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 91
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 65
- 229910052736 halogen Inorganic materials 0.000 claims description 59
- 150000002367 halogens Chemical class 0.000 claims description 59
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 55
- 229910052739 hydrogen Inorganic materials 0.000 claims description 50
- 239000001257 hydrogen Substances 0.000 claims description 49
- 125000004076 pyridyl group Chemical group 0.000 claims description 44
- 125000001153 fluoro group Chemical group F* 0.000 claims description 41
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims description 38
- 125000001424 substituent group Chemical group 0.000 claims description 38
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims description 37
- 125000000623 heterocyclic group Chemical group 0.000 claims description 37
- 125000001544 thienyl group Chemical group 0.000 claims description 31
- 125000001072 heteroaryl group Chemical group 0.000 claims description 30
- 125000004452 carbocyclyl group Chemical group 0.000 claims description 28
- 208000002193 Pain Diseases 0.000 claims description 26
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 23
- 206010028980 Neoplasm Diseases 0.000 claims description 18
- 230000000694 effects Effects 0.000 claims description 16
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 16
- 125000001041 indolyl group Chemical group 0.000 claims description 13
- 125000000335 thiazolyl group Chemical group 0.000 claims description 13
- 230000001154 acute effect Effects 0.000 claims description 12
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 12
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 12
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 12
- 125000002541 furyl group Chemical group 0.000 claims description 12
- 125000003226 pyrazolyl group Chemical group 0.000 claims description 12
- 125000000714 pyrimidinyl group Chemical group 0.000 claims description 12
- 229910052717 sulfur Inorganic materials 0.000 claims description 12
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 claims description 12
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- 208000005298 acute pain Diseases 0.000 claims description 11
- 125000002433 cyclopentenyl group Chemical group C1(=CCCC1)* 0.000 claims description 11
- 201000010099 disease Diseases 0.000 claims description 11
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 11
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- 206010039073 rheumatoid arthritis Diseases 0.000 claims description 11
- ZMSIFDIKIXVLDF-UHFFFAOYSA-N 2-methyl-1,3,4-oxadiazole Chemical compound CC1=NN=CO1 ZMSIFDIKIXVLDF-UHFFFAOYSA-N 0.000 claims description 10
- 208000034972 Sudden Infant Death Diseases 0.000 claims description 10
- 206010042440 Sudden infant death syndrome Diseases 0.000 claims description 10
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 10
- 125000001624 naphthyl group Chemical group 0.000 claims description 10
- HCMJWOGOISXSDL-UHFFFAOYSA-N (2-isothiocyanato-1-phenylethyl)benzene Chemical compound C=1C=CC=CC=1C(CN=C=S)C1=CC=CC=C1 HCMJWOGOISXSDL-UHFFFAOYSA-N 0.000 claims description 9
- HWNKAJDTOOPJAM-CMDGGOBGSA-N 2-[[(e)-2-(4-bromophenyl)ethenyl]sulfonylamino]-5-methylbenzenesulfonamide Chemical compound NS(=O)(=O)C1=CC(C)=CC=C1NS(=O)(=O)\C=C\C1=CC=C(Br)C=C1 HWNKAJDTOOPJAM-CMDGGOBGSA-N 0.000 claims description 9
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- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 9
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- NDGUTZUJOOVPOQ-ACCUITESSA-N 2-[[(e)-2-[4-(furan-2-yl)phenyl]ethenyl]sulfonylamino]benzenesulfonamide Chemical compound NS(=O)(=O)C1=CC=CC=C1NS(=O)(=O)\C=C\C1=CC=C(C=2OC=CC=2)C=C1 NDGUTZUJOOVPOQ-ACCUITESSA-N 0.000 claims description 8
- KHBQMWCZKVMBLN-UHFFFAOYSA-N Benzenesulfonamide Chemical compound NS(=O)(=O)C1=CC=CC=C1 KHBQMWCZKVMBLN-UHFFFAOYSA-N 0.000 claims description 8
- 239000002671 adjuvant Substances 0.000 claims description 8
- 208000004296 neuralgia Diseases 0.000 claims description 8
- 208000021722 neuropathic pain Diseases 0.000 claims description 8
- DSRGLCZJLTWWFA-UHFFFAOYSA-N 2,3-dichloro-n-(4-methyl-2-sulfamoylphenyl)benzenesulfonamide Chemical compound NS(=O)(=O)C1=CC(C)=CC=C1NS(=O)(=O)C1=CC=CC(Cl)=C1Cl DSRGLCZJLTWWFA-UHFFFAOYSA-N 0.000 claims description 7
- LGEWRKDNMAFFRB-UHFFFAOYSA-N 2-[2-(4-bromophenyl)ethylsulfonylamino]-5-methylbenzenesulfonamide Chemical compound NS(=O)(=O)C1=CC(C)=CC=C1NS(=O)(=O)CCC1=CC=C(Br)C=C1 LGEWRKDNMAFFRB-UHFFFAOYSA-N 0.000 claims description 7
- MZYSHZXYUOUIBX-UHFFFAOYSA-N 2-[2-(4-chlorophenyl)ethylsulfonylamino]-5-methylbenzenesulfonamide Chemical compound NS(=O)(=O)C1=CC(C)=CC=C1NS(=O)(=O)CCC1=CC=C(Cl)C=C1 MZYSHZXYUOUIBX-UHFFFAOYSA-N 0.000 claims description 7
- RWIPRVONYAMWLE-UHFFFAOYSA-N 2-[[3-(3,4-dichlorophenyl)phenyl]sulfonylamino]-5-methylbenzenesulfonamide Chemical compound NS(=O)(=O)C1=CC(C)=CC=C1NS(=O)(=O)C1=CC=CC(C=2C=C(Cl)C(Cl)=CC=2)=C1 RWIPRVONYAMWLE-UHFFFAOYSA-N 0.000 claims description 7
- 208000024827 Alzheimer disease Diseases 0.000 claims description 7
- 125000003118 aryl group Chemical group 0.000 claims description 7
- 239000003085 diluting agent Substances 0.000 claims description 7
- 125000004972 1-butynyl group Chemical group [H]C([H])([H])C([H])([H])C#C* 0.000 claims description 6
- VQTKZMCTWPHJHD-UHFFFAOYSA-N 2-(1-phenylpropan-2-ylsulfonylamino)benzenesulfonamide Chemical compound C=1C=CC=C(S(N)(=O)=O)C=1NS(=O)(=O)C(C)CC1=CC=CC=C1 VQTKZMCTWPHJHD-UHFFFAOYSA-N 0.000 claims description 6
- BWRGXJUAIRMKBR-UHFFFAOYSA-N 2-[(2-nitrophenyl)sulfonylamino]benzenesulfonamide Chemical compound NS(=O)(=O)C1=CC=CC=C1NS(=O)(=O)C1=CC=CC=C1[N+]([O-])=O BWRGXJUAIRMKBR-UHFFFAOYSA-N 0.000 claims description 6
- MTYAYRDXCSXATC-UHFFFAOYSA-N 2-[(4-aminophenyl)sulfonylamino]benzenesulfonamide Chemical compound C1=CC(N)=CC=C1S(=O)(=O)NC1=CC=CC=C1S(N)(=O)=O MTYAYRDXCSXATC-UHFFFAOYSA-N 0.000 claims description 6
- PCWVGEPALSDKRK-UHFFFAOYSA-N 2-[(4-nitrophenyl)sulfonylamino]benzenesulfonamide Chemical compound NS(=O)(=O)C1=CC=CC=C1NS(=O)(=O)C1=CC=C([N+]([O-])=O)C=C1 PCWVGEPALSDKRK-UHFFFAOYSA-N 0.000 claims description 6
- OVELXBOBYSFKET-UHFFFAOYSA-N 2-[2-(4-chloro-2-methoxyphenyl)ethylsulfonylamino]-5-methylbenzenesulfonamide Chemical compound COC1=CC(Cl)=CC=C1CCS(=O)(=O)NC1=CC=C(C)C=C1S(N)(=O)=O OVELXBOBYSFKET-UHFFFAOYSA-N 0.000 claims description 6
- XJWAJGXHQJXRMR-UHFFFAOYSA-N 2-[2-(4-chlorophenyl)prop-2-enylsulfonylamino]benzenesulfonamide Chemical compound NS(=O)(=O)C1=CC=CC=C1NS(=O)(=O)CC(=C)C1=CC=C(Cl)C=C1 XJWAJGXHQJXRMR-UHFFFAOYSA-N 0.000 claims description 6
- TWKSLVDUWUDLGR-CSKARUKUSA-N 2-[[(e)-1-(4-chlorophenyl)prop-1-en-2-yl]sulfonylamino]-4-fluorobenzenesulfonamide Chemical compound C=1C(F)=CC=C(S(N)(=O)=O)C=1NS(=O)(=O)C(/C)=C/C1=CC=C(Cl)C=C1 TWKSLVDUWUDLGR-CSKARUKUSA-N 0.000 claims description 6
- RLJRHWYXJQHCIL-ZHACJKMWSA-N 2-[[(e)-1-(4-chlorophenyl)prop-1-en-2-yl]sulfonylamino]benzenesulfonamide Chemical compound C=1C=CC=C(S(N)(=O)=O)C=1NS(=O)(=O)C(/C)=C/C1=CC=C(Cl)C=C1 RLJRHWYXJQHCIL-ZHACJKMWSA-N 0.000 claims description 6
- APMRRWAAFOTXJP-VOTSOKGWSA-N 2-[[(e)-2-(3,4-dichlorophenyl)ethenyl]sulfonylamino]-4-methylbenzenesulfonamide Chemical compound CC1=CC=C(S(N)(=O)=O)C(NS(=O)(=O)\C=C\C=2C=C(Cl)C(Cl)=CC=2)=C1 APMRRWAAFOTXJP-VOTSOKGWSA-N 0.000 claims description 6
- TVWUTLDKFWRVKN-ZHACJKMWSA-N 2-[[(e)-2-(4-chlorophenyl)prop-1-enyl]sulfonylamino]benzenesulfonamide Chemical compound C=1C=C(Cl)C=CC=1C(/C)=C/S(=O)(=O)NC1=CC=CC=C1S(N)(=O)=O TVWUTLDKFWRVKN-ZHACJKMWSA-N 0.000 claims description 6
- SYRHWHGERYMDIA-CMDGGOBGSA-N 2-[[(e)-2-(4-cyanophenyl)ethenyl]sulfonylamino]-6-fluorobenzenesulfonamide Chemical compound NS(=O)(=O)C1=C(F)C=CC=C1NS(=O)(=O)\C=C\C1=CC=C(C#N)C=C1 SYRHWHGERYMDIA-CMDGGOBGSA-N 0.000 claims description 6
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- UYGDVXHADRKHEX-UHFFFAOYSA-N 2-amino-n-(2-sulfamoylphenyl)benzenesulfonamide Chemical compound NC1=CC=CC=C1S(=O)(=O)NC1=CC=CC=C1S(N)(=O)=O UYGDVXHADRKHEX-UHFFFAOYSA-N 0.000 claims description 6
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- 125000001246 bromo group Chemical group Br* 0.000 claims description 6
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- 208000027866 inflammatory disease Diseases 0.000 claims description 6
- URCXBBNYLDJMDK-UHFFFAOYSA-N n-(2-sulfamoylphenyl)quinoline-8-sulfonamide Chemical compound NS(=O)(=O)C1=CC=CC=C1NS(=O)(=O)C1=CC=CC2=CC=CN=C12 URCXBBNYLDJMDK-UHFFFAOYSA-N 0.000 claims description 6
- MPRDETHCLKAVEA-UHFFFAOYSA-N n-[2-(dimethylsulfamoyl)phenyl]-5,7-dimethyl-[1,2,4]triazolo[1,5-a]pyrimidine-2-sulfonamide Chemical compound CN(C)S(=O)(=O)C1=CC=CC=C1NS(=O)(=O)C1=NN2C(C)=CC(C)=NC2=N1 MPRDETHCLKAVEA-UHFFFAOYSA-N 0.000 claims description 6
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- UGOMMVLRQDMAQQ-UHFFFAOYSA-N xphos Chemical compound CC(C)C1=CC(C(C)C)=CC(C(C)C)=C1C1=CC=CC=C1P(C1CCCCC1)C1CCCCC1 UGOMMVLRQDMAQQ-UHFFFAOYSA-N 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 229960001360 zolmitriptan Drugs 0.000 description 1
- ULSDMUVEXKOYBU-ZDUSSCGKSA-N zolmitriptan Chemical compound C1=C2C(CCN(C)C)=CNC2=CC=C1C[C@H]1COC(=O)N1 ULSDMUVEXKOYBU-ZDUSSCGKSA-N 0.000 description 1
Classifications
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- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/78—Benzo [b] furans; Hydrogenated benzo [b] furans
- C07D307/79—Benzo [b] furans; Hydrogenated benzo [b] furans with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the hetero ring
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- C07C311/30—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/37—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
- C07C311/38—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring having sulfur atoms of sulfonamide groups and amino groups bound to carbon atoms of six-membered rings of the same carbon skeleton
- C07C311/39—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring having sulfur atoms of sulfonamide groups and amino groups bound to carbon atoms of six-membered rings of the same carbon skeleton having the nitrogen atom of at least one of the sulfonamide groups bound to hydrogen atoms or to an acyclic carbon atom
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- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
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- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/32—One oxygen, sulfur or nitrogen atom
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- C07D265/28—1,4-Oxazines; Hydrogenated 1,4-oxazines
- C07D265/34—1,4-Oxazines; Hydrogenated 1,4-oxazines condensed with carbocyclic rings
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- C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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Definitions
- the present invention relates to bis-(sulfonylamino) derivatives, processes for their preparation, pharmaceutical compositions containing them and their use in therapy.
- G 3 is phenyl, pyridyl or 2-methyl-1,3,4-oxadiazole
- G 2 represents H, phenyl or 5- or 6-membered heteroaryl; optionally fused to one further ring independently selected from phenyl, a 5- or 6-membered heteroaryl, C 5-6 carbocyclyl or C 5-6 heterocyclyl ring; and any phenyl or heteroaryl moieties in G 1 and G 2 are optionally substituted by one or more substituents independently selected from halogen, C 1-6 alkyl and C 1-6 alkoxy; said C 1-6 alkyl being optionally substituted by OH or by one or more F atoms.
- n an integer 0, 1, 2, 3 or 4;
- neuropathic pain therapies including for example gabapentin, lidoderm, pregablin and equivalents and pharmaceutically active isomer(s) and metabolite(s) thereof.
- R 3 , R 5 , R 6 and R 10 represents hydrogen
- G 3 represents phenyl or 5- or 6-membered heteroaryl
- n-Butyllithium (59.0 mL, 1.6M solution in hexanes) was added dropwise during 25 min to a solution of ethylmethanesulfonate (9.1 mL, 86 mmol) in THF (200 mL) at ⁇ 78° C.
- the reaction mixture was stirred for 15 min then diethyl chlorophosphate (7.2 ml, 50 mmol) was added dropwise.
- the solution was stirred at ⁇ 78° C. for 30 min, allowed to warm to 0° C. and then cooled to ⁇ 78° C. again.
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- Organic Chemistry (AREA)
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- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Neurology (AREA)
- Physical Education & Sports Medicine (AREA)
- Neurosurgery (AREA)
- Diabetes (AREA)
- Biomedical Technology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Rheumatology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Pain & Pain Management (AREA)
- Urology & Nephrology (AREA)
- Pulmonology (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
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- Emergency Medicine (AREA)
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- 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)
- Thiazole And Isothizaole Compounds (AREA)
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Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US12/337,125 US20090163586A1 (en) | 2007-12-20 | 2008-12-17 | Bis-(Sulfonylamino) Derivatives in Therapy 205 |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US1528707P | 2007-12-20 | 2007-12-20 | |
| US12/337,125 US20090163586A1 (en) | 2007-12-20 | 2008-12-17 | Bis-(Sulfonylamino) Derivatives in Therapy 205 |
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| US12/337,125 Abandoned US20090163586A1 (en) | 2007-12-20 | 2008-12-17 | Bis-(Sulfonylamino) Derivatives in Therapy 205 |
| US12/747,049 Expired - Fee Related US9145380B2 (en) | 2007-12-20 | 2008-12-18 | Bis-(sulfonylamino) derivatives for use in therapy |
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| US12/747,049 Expired - Fee Related US9145380B2 (en) | 2007-12-20 | 2008-12-18 | Bis-(sulfonylamino) derivatives for use in therapy |
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| Country | Link |
|---|---|
| US (2) | US20090163586A1 (es) |
| EP (1) | EP2234993B1 (es) |
| JP (1) | JP5555175B2 (es) |
| KR (1) | KR20100098711A (es) |
| CN (1) | CN101945859B (es) |
| AR (1) | AR069919A1 (es) |
| AU (1) | AU2008341173B2 (es) |
| BR (1) | BRPI0821299A2 (es) |
| CA (1) | CA2709510A1 (es) |
| CL (1) | CL2008003848A1 (es) |
| CO (1) | CO6270307A2 (es) |
| CR (1) | CR11517A (es) |
| DO (1) | DOP2010000191A (es) |
| EA (1) | EA017940B1 (es) |
| EC (1) | ECSP10010272A (es) |
| ES (1) | ES2397502T3 (es) |
| IL (1) | IL205758A0 (es) |
| NI (1) | NI201000109A (es) |
| PE (1) | PE20091175A1 (es) |
| TW (1) | TW200932210A (es) |
| UY (1) | UY31546A1 (es) |
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Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
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- 2008-12-18 US US12/747,049 patent/US9145380B2/en not_active Expired - Fee Related
- 2008-12-18 UY UY31546A patent/UY31546A1/es unknown
- 2008-12-18 WO PCT/SE2008/051500 patent/WO2009082347A1/en not_active Ceased
- 2008-12-18 EA EA201001013A patent/EA017940B1/ru not_active IP Right Cessation
- 2008-12-18 BR BRPI0821299-6A patent/BRPI0821299A2/pt not_active IP Right Cessation
- 2008-12-18 JP JP2010539383A patent/JP5555175B2/ja not_active Expired - Fee Related
- 2008-12-18 AU AU2008341173A patent/AU2008341173B2/en not_active Ceased
- 2008-12-18 KR KR1020107016075A patent/KR20100098711A/ko not_active Ceased
- 2008-12-18 EP EP08863493A patent/EP2234993B1/en active Active
- 2008-12-18 PE PE2008002126A patent/PE20091175A1/es not_active Application Discontinuation
- 2008-12-18 CA CA2709510A patent/CA2709510A1/en not_active Abandoned
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- 2008-12-18 TW TW097149496A patent/TW200932210A/zh unknown
- 2008-12-19 AR ARP080105595A patent/AR069919A1/es unknown
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2010
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- 2010-05-13 IL IL205758A patent/IL205758A0/en unknown
- 2010-06-14 ZA ZA2010/04226A patent/ZA201004226B/en unknown
- 2010-06-18 DO DO2010000191A patent/DOP2010000191A/es unknown
- 2010-06-18 EC EC2010010272A patent/ECSP10010272A/es unknown
- 2010-06-18 NI NI201000109A patent/NI201000109A/es unknown
- 2010-06-18 CR CR11517A patent/CR11517A/es not_active Application Discontinuation
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20110021540A1 (en) * | 2007-11-15 | 2011-01-27 | Astrazeneca Ab | Bis-(Sulfonylamino) Derivatives in Therapy 066 |
| US20100292279A1 (en) * | 2009-05-14 | 2010-11-18 | Astrazeneca Ab | Bis-(Sulfonylamino) Derivatives in Therapy |
| WO2014062044A1 (en) | 2012-10-15 | 2014-04-24 | Vilnius University | Fluorinated benzenesulfonamides as inhibitors of carbonic anhydrase |
| US9725467B2 (en) | 2012-10-15 | 2017-08-08 | Vilnius University | Fluorinated benzenesulfonamides as inhibitors of carbonic anhydrase |
| WO2016085392A1 (en) * | 2014-11-27 | 2016-06-02 | Acturum Life Science AB | Bis(sulfonamide) derivatives and their use as mpges inhibitors |
| WO2016085391A1 (en) * | 2014-11-27 | 2016-06-02 | Acturum Life Science AB | Bis(sulfonamide) derivatives and their use as mpges inhibitors |
| US10081614B2 (en) | 2014-11-27 | 2018-09-25 | Acturum Real Estate Ab | Bis(sulfonamide) derivatives and their use as mPGES inhibitors |
| US10227296B2 (en) | 2014-11-27 | 2019-03-12 | Arcturum Real Estate AB | Bis(sulfonamide) derivatives and their use as mPGES inhibitors |
Also Published As
| Publication number | Publication date |
|---|---|
| BRPI0821299A2 (pt) | 2015-06-16 |
| US9145380B2 (en) | 2015-09-29 |
| EA017940B1 (ru) | 2013-04-30 |
| UY31546A1 (es) | 2009-08-03 |
| IL205758A0 (en) | 2010-11-30 |
| ZA201004226B (en) | 2011-04-28 |
| JP5555175B2 (ja) | 2014-07-23 |
| ECSP10010272A (es) | 2010-08-31 |
| CL2008003848A1 (es) | 2010-02-05 |
| AU2008341173A1 (en) | 2009-07-02 |
| EP2234993A1 (en) | 2010-10-06 |
| PE20091175A1 (es) | 2009-09-03 |
| HK1149259A1 (en) | 2011-09-30 |
| EP2234993A4 (en) | 2012-02-08 |
| AR069919A1 (es) | 2010-03-03 |
| EA201001013A1 (ru) | 2010-12-30 |
| CN101945859B (zh) | 2014-04-09 |
| EP2234993B1 (en) | 2012-11-07 |
| CR11517A (es) | 2010-08-05 |
| CA2709510A1 (en) | 2009-07-02 |
| ES2397502T3 (es) | 2013-03-07 |
| DOP2010000191A (es) | 2010-08-31 |
| KR20100098711A (ko) | 2010-09-08 |
| TW200932210A (en) | 2009-08-01 |
| WO2009082347A1 (en) | 2009-07-02 |
| JP2011507837A (ja) | 2011-03-10 |
| CO6270307A2 (es) | 2011-04-20 |
| CN101945859A (zh) | 2011-01-12 |
| AU2008341173B2 (en) | 2011-12-15 |
| US20100331321A1 (en) | 2010-12-30 |
| NI201000109A (es) | 2012-05-14 |
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