JP2008524244A - 水酸化ステロイド脱水素酵素阻害剤 - Google Patents
水酸化ステロイド脱水素酵素阻害剤 Download PDFInfo
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- JP2008524244A JP2008524244A JP2007546949A JP2007546949A JP2008524244A JP 2008524244 A JP2008524244 A JP 2008524244A JP 2007546949 A JP2007546949 A JP 2007546949A JP 2007546949 A JP2007546949 A JP 2007546949A JP 2008524244 A JP2008524244 A JP 2008524244A
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- alkyl
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- cycloalkyl
- bicycloaryl
- aryl
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- -1 Hydroxyl steroid Chemical class 0.000 title claims description 773
- 229940124186 Dehydrogenase inhibitor Drugs 0.000 title description 5
- 150000001875 compounds Chemical class 0.000 claims abstract description 141
- 238000000034 method Methods 0.000 claims abstract description 37
- 239000008194 pharmaceutical composition Substances 0.000 claims abstract description 11
- 125000000217 alkyl group Chemical group 0.000 claims description 1289
- 125000005842 heteroatom Chemical group 0.000 claims description 726
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 487
- 125000001072 heteroaryl group Chemical group 0.000 claims description 459
- 150000001602 bicycloalkyls Chemical group 0.000 claims description 433
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 claims description 413
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 369
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 claims description 362
- 125000003118 aryl group Chemical group 0.000 claims description 261
- 125000001841 imino group Chemical group [H]N=* 0.000 claims description 258
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims description 221
- 239000001257 hydrogen Substances 0.000 claims description 211
- 229910052739 hydrogen Inorganic materials 0.000 claims description 211
- 125000002813 thiocarbonyl group Chemical group *C(*)=S 0.000 claims description 207
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 164
- 125000003545 alkoxy group Chemical group 0.000 claims description 139
- 125000004104 aryloxy group Chemical group 0.000 claims description 139
- 125000005553 heteroaryloxy group Chemical group 0.000 claims description 139
- 125000003282 alkyl amino group Chemical group 0.000 claims description 138
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 136
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 117
- 229940124530 sulfonamide Drugs 0.000 claims description 104
- 150000003456 sulfonamides Chemical class 0.000 claims description 104
- 201000010099 disease Diseases 0.000 claims description 43
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 43
- 239000000203 mixture Substances 0.000 claims description 43
- 229910052760 oxygen Inorganic materials 0.000 claims description 26
- 229910052717 sulfur Inorganic materials 0.000 claims description 25
- 238000001727 in vivo Methods 0.000 claims description 18
- 125000001424 substituent group Chemical group 0.000 claims description 16
- 230000002401 inhibitory effect Effects 0.000 claims description 14
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 claims description 13
- 230000000694 effects Effects 0.000 claims description 12
- 230000007170 pathology Effects 0.000 claims description 12
- 150000003839 salts Chemical class 0.000 claims description 9
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims description 7
- 125000004103 aminoalkyl group Chemical group 0.000 claims description 6
- 239000005022 packaging material Substances 0.000 claims description 6
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims description 6
- 208000001145 Metabolic Syndrome Diseases 0.000 claims description 5
- 201000000690 abdominal obesity-metabolic syndrome Diseases 0.000 claims description 5
- 150000001408 amides Chemical class 0.000 claims description 5
- 239000002552 dosage form Substances 0.000 claims description 4
- 125000000623 heterocyclic group Chemical group 0.000 claims description 4
- 238000003860 storage Methods 0.000 claims description 4
- 206010020772 Hypertension Diseases 0.000 claims description 3
- 208000010067 Pituitary ACTH Hypersecretion Diseases 0.000 claims description 3
- 208000020627 Pituitary-dependent Cushing syndrome Diseases 0.000 claims description 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 3
- 230000003920 cognitive function Effects 0.000 claims description 3
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 3
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims description 3
- 230000004382 visual function Effects 0.000 claims description 3
- 239000004480 active ingredient Substances 0.000 claims description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 2
- 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 2
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
- 238000001361 intraarterial administration Methods 0.000 claims description 2
- 238000007918 intramuscular administration Methods 0.000 claims description 2
- 238000007912 intraperitoneal administration Methods 0.000 claims description 2
- 238000007913 intrathecal administration Methods 0.000 claims description 2
- 238000001990 intravenous administration Methods 0.000 claims description 2
- 239000002502 liposome Substances 0.000 claims description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 238000007920 subcutaneous administration Methods 0.000 claims description 2
- KXDAEFPNCMNJSK-UHFFFAOYSA-N Benzamide Chemical compound NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 claims 4
- 125000005059 halophenyl group Chemical group 0.000 claims 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 3
- KFPPCXCRXLVUSU-UHFFFAOYSA-N 3-chloro-n-[4-(1-hydroxy-2-pyrimidin-4-ylethyl)-1,3-thiazol-2-yl]-2-methylbenzenesulfonamide Chemical compound CC1=C(Cl)C=CC=C1S(=O)(=O)NC1=NC(C(O)CC=2N=CN=CC=2)=CS1 KFPPCXCRXLVUSU-UHFFFAOYSA-N 0.000 claims 2
- VPBQKCAXFSUGHX-UHFFFAOYSA-N 3-chloro-n-[4-[(2-chloropyridin-3-yl)-hydroxymethyl]-1,3-thiazol-2-yl]-2-methylbenzenesulfonamide Chemical compound CC1=C(Cl)C=CC=C1S(=O)(=O)NC1=NC(C(O)C=2C(=NC=CC=2)Cl)=CS1 VPBQKCAXFSUGHX-UHFFFAOYSA-N 0.000 claims 2
- 125000005036 alkoxyphenyl group Chemical group 0.000 claims 2
- 125000002431 aminoalkoxy group Chemical group 0.000 claims 2
- YDVJBLJCSLVMSY-UHFFFAOYSA-N carbamoyl cyanide Chemical class NC(=O)C#N YDVJBLJCSLVMSY-UHFFFAOYSA-N 0.000 claims 2
- 125000004802 cyanophenyl group Chemical group 0.000 claims 2
- 125000004786 difluoromethoxy group Chemical group [H]C(F)(F)O* 0.000 claims 2
- 239000012669 liquid formulation Substances 0.000 claims 2
- 125000004076 pyridyl group Chemical group 0.000 claims 2
- 125000003944 tolyl group Chemical group 0.000 claims 2
- MPDDTAJMJCESGV-CTUHWIOQSA-M (3r,5r)-7-[2-(4-fluorophenyl)-5-[methyl-[(1r)-1-phenylethyl]carbamoyl]-4-propan-2-ylpyrazol-3-yl]-3,5-dihydroxyheptanoate Chemical compound C1([C@@H](C)N(C)C(=O)C2=NN(C(CC[C@@H](O)C[C@@H](O)CC([O-])=O)=C2C(C)C)C=2C=CC(F)=CC=2)=CC=CC=C1 MPDDTAJMJCESGV-CTUHWIOQSA-M 0.000 claims 1
- PHKCXCSOILQNJY-UHFFFAOYSA-N 2-chloro-4-[3-(dimethylamino)propyl]-n-[4-(2-ethyl-2-hydroxybutyl)-1,3-thiazol-2-yl]benzenesulfonamide Chemical compound CCC(O)(CC)CC1=CSC(NS(=O)(=O)C=2C(=CC(CCCN(C)C)=CC=2)Cl)=N1 PHKCXCSOILQNJY-UHFFFAOYSA-N 0.000 claims 1
- LUCQCNONRGGAFF-UHFFFAOYSA-N 2-chloro-4-[4-(dimethylamino)butyl]-n-[4-(2-ethyl-2-hydroxybutyl)-1,3-thiazol-2-yl]benzenesulfonamide Chemical compound CCC(O)(CC)CC1=CSC(NS(=O)(=O)C=2C(=CC(CCCCN(C)C)=CC=2)Cl)=N1 LUCQCNONRGGAFF-UHFFFAOYSA-N 0.000 claims 1
- GNBJPDZEVGQCLW-UHFFFAOYSA-N 2-chloro-n-[4-(2-ethyl-2-hydroxybutyl)-1,3-thiazol-2-yl]-4-(3-morpholin-4-ylpropyl)benzenesulfonamide Chemical compound CCC(O)(CC)CC1=CSC(NS(=O)(=O)C=2C(=CC(CCCN3CCOCC3)=CC=2)Cl)=N1 GNBJPDZEVGQCLW-UHFFFAOYSA-N 0.000 claims 1
- LMCXALCBMPZMFT-UHFFFAOYSA-N 2-chloro-n-[4-(2-ethyl-2-hydroxybutyl)-1,3-thiazol-2-yl]-4-(4-morpholin-4-ylbutyl)benzenesulfonamide Chemical compound CCC(O)(CC)CC1=CSC(NS(=O)(=O)C=2C(=CC(CCCCN3CCOCC3)=CC=2)Cl)=N1 LMCXALCBMPZMFT-UHFFFAOYSA-N 0.000 claims 1
- JEHQGKQGBCZUKA-UHFFFAOYSA-N 2-fluoro-n-[4-(3-hydroxypentan-3-yl)-1,3-thiazol-2-yl]-5-methylbenzenesulfonamide Chemical compound CCC(O)(CC)C1=CSC(NS(=O)(=O)C=2C(=CC=C(C)C=2)F)=N1 JEHQGKQGBCZUKA-UHFFFAOYSA-N 0.000 claims 1
- BJDWYDVMERXVHB-UHFFFAOYSA-N 3-chloro-2-methyl-n-[4-[(2-methylphenyl)methyl]-1,3-thiazol-2-yl]benzenesulfonamide Chemical compound CC1=CC=CC=C1CC1=CSC(NS(=O)(=O)C=2C(=C(Cl)C=CC=2)C)=N1 BJDWYDVMERXVHB-UHFFFAOYSA-N 0.000 claims 1
- BYXFCRIHQDHIAK-UHFFFAOYSA-N 3-chloro-2-methyl-n-[4-[(3-methylphenyl)methyl]-1,3-thiazol-2-yl]benzenesulfonamide Chemical compound CC1=CC=CC(CC=2N=C(NS(=O)(=O)C=3C(=C(Cl)C=CC=3)C)SC=2)=C1 BYXFCRIHQDHIAK-UHFFFAOYSA-N 0.000 claims 1
- YDPAQELDBKPASA-UHFFFAOYSA-N 3-chloro-2-methyl-n-[4-[(4-methyloxan-4-yl)methyl]-1,3-thiazol-2-yl]benzenesulfonamide Chemical compound CC1=C(Cl)C=CC=C1S(=O)(=O)NC1=NC(CC2(C)CCOCC2)=CS1 YDPAQELDBKPASA-UHFFFAOYSA-N 0.000 claims 1
- AWKIRIFWOJWVBO-UHFFFAOYSA-N 3-chloro-2-methyl-n-[4-[[3-(trifluoromethyl)phenyl]methyl]-1,3-thiazol-2-yl]benzenesulfonamide Chemical compound CC1=C(Cl)C=CC=C1S(=O)(=O)NC1=NC(CC=2C=C(C=CC=2)C(F)(F)F)=CS1 AWKIRIFWOJWVBO-UHFFFAOYSA-N 0.000 claims 1
- CPIHTKBKMBJTNQ-UHFFFAOYSA-N 3-chloro-4-[2-(dimethylamino)ethoxy]-n-[4-(2-ethyl-2-hydroxybutyl)-1,3-thiazol-2-yl]benzenesulfonamide Chemical compound CCC(O)(CC)CC1=CSC(NS(=O)(=O)C=2C=C(Cl)C(OCCN(C)C)=CC=2)=N1 CPIHTKBKMBJTNQ-UHFFFAOYSA-N 0.000 claims 1
- AVFXATVCYLCYFE-UHFFFAOYSA-N 3-chloro-4-[2-(dimethylamino)ethoxy]-n-[4-[(1-hydroxycyclohexyl)methyl]-1,3-thiazol-2-yl]benzenesulfonamide Chemical compound C1=C(Cl)C(OCCN(C)C)=CC=C1S(=O)(=O)NC1=NC(CC2(O)CCCCC2)=CS1 AVFXATVCYLCYFE-UHFFFAOYSA-N 0.000 claims 1
- QHIXYOXOJBMSTB-UHFFFAOYSA-N 3-chloro-4-[2-(dimethylamino)ethoxy]-n-[4-[(1-hydroxycyclopentyl)methyl]-1,3-thiazol-2-yl]benzenesulfonamide Chemical compound C1=C(Cl)C(OCCN(C)C)=CC=C1S(=O)(=O)NC1=NC(CC2(O)CCCC2)=CS1 QHIXYOXOJBMSTB-UHFFFAOYSA-N 0.000 claims 1
- JXTLNGMJRGZROG-UHFFFAOYSA-N 3-chloro-4-[3-(dimethylamino)propoxy]-n-[4-(2-ethyl-2-hydroxybutyl)-1,3-thiazol-2-yl]benzenesulfonamide Chemical compound CCC(O)(CC)CC1=CSC(NS(=O)(=O)C=2C=C(Cl)C(OCCCN(C)C)=CC=2)=N1 JXTLNGMJRGZROG-UHFFFAOYSA-N 0.000 claims 1
- ZPHQEQHBZRFYRL-UHFFFAOYSA-N 3-chloro-5-[2-(dimethylamino)ethoxy]-n-[4-(2-ethyl-2-hydroxybutyl)-1,3-thiazol-2-yl]benzenesulfonamide Chemical compound CCC(O)(CC)CC1=CSC(NS(=O)(=O)C=2C=C(OCCN(C)C)C=C(Cl)C=2)=N1 ZPHQEQHBZRFYRL-UHFFFAOYSA-N 0.000 claims 1
- VORJWBYARBJIJW-UHFFFAOYSA-N 3-chloro-5-[3-(dimethylamino)propoxy]-n-[4-(2-ethyl-2-hydroxybutyl)-1,3-thiazol-2-yl]benzenesulfonamide Chemical compound CCC(O)(CC)CC1=CSC(NS(=O)(=O)C=2C=C(OCCCN(C)C)C=C(Cl)C=2)=N1 VORJWBYARBJIJW-UHFFFAOYSA-N 0.000 claims 1
- LWWBYWVWSIFAPY-UHFFFAOYSA-N 3-chloro-N-[4-[1-hydroxy-2-(1H-pyrazol-5-yl)ethyl]-1,3-thiazol-2-yl]-2-methylbenzenesulfonamide Chemical compound CC1=C(Cl)C=CC=C1S(=O)(=O)NC1=NC(C(O)CC=2NN=CC=2)=CS1 LWWBYWVWSIFAPY-UHFFFAOYSA-N 0.000 claims 1
- WXYKPGAUQXEQRE-UHFFFAOYSA-N 3-chloro-n-[4-(1-hydroxy-2-methylpropyl)-1,3-thiazol-2-yl]-2-methylbenzenesulfonamide Chemical compound CC(C)C(O)C1=CSC(NS(=O)(=O)C=2C(=C(Cl)C=CC=2)C)=N1 WXYKPGAUQXEQRE-UHFFFAOYSA-N 0.000 claims 1
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- LFZDLJDTBDTGGX-UHFFFAOYSA-N 3-chloro-n-[4-(1-hydroxy-3-phenylpropyl)-1,3-thiazol-2-yl]-2-methylbenzenesulfonamide Chemical compound CC1=C(Cl)C=CC=C1S(=O)(=O)NC1=NC(C(O)CCC=2C=CC=CC=2)=CS1 LFZDLJDTBDTGGX-UHFFFAOYSA-N 0.000 claims 1
- WGEUQASJGZRSSF-UHFFFAOYSA-N 3-chloro-n-[4-(1-hydroxybutyl)-1,3-thiazol-2-yl]-2-methylbenzenesulfonamide Chemical compound CCCC(O)C1=CSC(NS(=O)(=O)C=2C(=C(Cl)C=CC=2)C)=N1 WGEUQASJGZRSSF-UHFFFAOYSA-N 0.000 claims 1
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- NDCAZJSKDRJZGP-UHFFFAOYSA-N 3-chloro-n-[4-(2-cyclopropyl-2-hydroxyethyl)-1,3-thiazol-2-yl]-2-methylbenzenesulfonamide Chemical compound CC1=C(Cl)C=CC=C1S(=O)(=O)NC1=NC(CC(O)C2CC2)=CS1 NDCAZJSKDRJZGP-UHFFFAOYSA-N 0.000 claims 1
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- JCKGOHNDNXKVHW-UHFFFAOYSA-N 3-chloro-n-[4-(2-ethyl-2-hydroxybutyl)-1,3-thiazol-2-yl]-4-(3-morpholin-4-ylpropoxy)benzenesulfonamide Chemical compound CCC(O)(CC)CC1=CSC(NS(=O)(=O)C=2C=C(Cl)C(OCCCN3CCOCC3)=CC=2)=N1 JCKGOHNDNXKVHW-UHFFFAOYSA-N 0.000 claims 1
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Images
Classifications
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- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D277/38—Nitrogen atoms
- C07D277/50—Nitrogen atoms bound to hetero atoms
- C07D277/52—Nitrogen atoms bound to hetero atoms to sulfur atoms, e.g. sulfonamides
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- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- Urology & Nephrology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US63733504P | 2004-12-17 | 2004-12-17 | |
| PCT/US2005/045704 WO2006066109A2 (en) | 2004-12-17 | 2005-12-16 | Hydroxysteroid dehydrogenase inhibitors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2008524244A true JP2008524244A (ja) | 2008-07-10 |
| JP2008524244A5 JP2008524244A5 (enExample) | 2009-01-15 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007546949A Withdrawn JP2008524244A (ja) | 2004-12-17 | 2005-12-16 | 水酸化ステロイド脱水素酵素阻害剤 |
Country Status (3)
| Country | Link |
|---|---|
| EP (1) | EP1888544A2 (enExample) |
| JP (1) | JP2008524244A (enExample) |
| WO (1) | WO2006066109A2 (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2008540539A (ja) * | 2005-05-10 | 2008-11-20 | バーテックス ファーマシューティカルズ インコーポレイテッド | イオンチャンネルの調節因子としての二環系誘導体 |
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|---|---|---|---|---|
| US7880001B2 (en) | 2004-04-29 | 2011-02-01 | Abbott Laboratories | Inhibitors of the 11-beta-hydroxysteroid dehydrogenase Type 1 enzyme |
| US20100222316A1 (en) | 2004-04-29 | 2010-09-02 | Abbott Laboratories | Inhibitors of the 11-beta-hydroxysteroid dehydrogenase type 1 enzyme |
| US8415354B2 (en) | 2004-04-29 | 2013-04-09 | Abbott Laboratories | Methods of use of inhibitors of the 11-beta-hydroxysteroid dehydrogenase type 1 enzyme |
| KR101496206B1 (ko) | 2005-01-05 | 2015-02-27 | 애브비 인코포레이티드 | 11-베타-하이드록시스테로이드 데하이드로게나제 타입 1 효소의 억제제로서의 아다만틸 유도체 |
| EP1846362A2 (en) | 2005-01-05 | 2007-10-24 | Abbott Laboratories | Inhibitors of the 11-beta-hydroxysteroid dehydrogenase type 1 enzyme |
| US8198331B2 (en) | 2005-01-05 | 2012-06-12 | Abbott Laboratories | Inhibitors of the 11-beta-hydroxysteroid dehydrogenase type 1 enzyme |
| US20090192198A1 (en) | 2005-01-05 | 2009-07-30 | Abbott Laboratories | Inhibitors of the 11-beta-hydroxysteroid dehydrogenase type 1 enzyme |
| PE20110235A1 (es) | 2006-05-04 | 2011-04-14 | Boehringer Ingelheim Int | Combinaciones farmaceuticas que comprenden linagliptina y metmorfina |
| BRPI0715160A2 (pt) | 2006-08-08 | 2013-06-11 | Sanofi Aventis | imidazolidina-2,4-dionas substituÍdas por arilamimoaril-alquil-, processo para preparÁ-las, medicamentos compeendendo estes compostos, e seu uso |
| JP5223864B2 (ja) | 2007-06-27 | 2013-06-26 | 大正製薬株式会社 | 11β−HSD1阻害活性を有する化合物 |
| EP2025674A1 (de) | 2007-08-15 | 2009-02-18 | sanofi-aventis | Substituierte Tetrahydronaphthaline, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel |
| JP5736098B2 (ja) | 2007-08-21 | 2015-06-17 | アッヴィ・インコーポレイテッド | 中枢神経系障害を治療するための医薬組成物 |
| WO2010003624A2 (en) | 2008-07-09 | 2010-01-14 | Sanofi-Aventis | Heterocyclic compounds, processes for their preparation, medicaments comprising these compounds, and the use thereof |
| WO2010068601A1 (en) | 2008-12-08 | 2010-06-17 | Sanofi-Aventis | A crystalline heteroaromatic fluoroglycoside hydrate, processes for making, methods of use and pharmaceutical compositions thereof |
| ES2443016T3 (es) | 2009-08-26 | 2014-02-17 | Sanofi | Nuevos hidratos cristalinos de fluoroglicósidos heteroaromáticos, productos farmacéuticos que comprenden estos compuestos, y su empleo |
| WO2011107494A1 (de) | 2010-03-03 | 2011-09-09 | Sanofi | Neue aromatische glykosidderivate, diese verbindungen enthaltende arzneimittel und deren verwendung |
| EP2563786B1 (de) | 2010-04-28 | 2016-11-02 | Bayer Intellectual Property GmbH | Ketoheteroarylpiperidin und -piperazin Derivate als Fungizide |
| US8933024B2 (en) | 2010-06-18 | 2015-01-13 | Sanofi | Azolopyridin-3-one derivatives as inhibitors of lipases and phospholipases |
| US8530413B2 (en) | 2010-06-21 | 2013-09-10 | Sanofi | Heterocyclically substituted methoxyphenyl derivatives with an oxo group, processes for preparation thereof and use thereof as medicaments |
| TW201221505A (en) | 2010-07-05 | 2012-06-01 | Sanofi Sa | Aryloxyalkylene-substituted hydroxyphenylhexynoic acids, process for preparation thereof and use thereof as a medicament |
| TW201215388A (en) | 2010-07-05 | 2012-04-16 | Sanofi Sa | (2-aryloxyacetylamino)phenylpropionic acid derivatives, processes for preparation thereof and use thereof as medicaments |
| TW201215387A (en) | 2010-07-05 | 2012-04-16 | Sanofi Aventis | Spirocyclically substituted 1,3-propane dioxide derivatives, processes for preparation thereof and use thereof as a medicament |
| EP2683701B1 (de) | 2011-03-08 | 2014-12-24 | Sanofi | Mit benzyl- oder heteromethylengruppen substituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
| US8828994B2 (en) | 2011-03-08 | 2014-09-09 | Sanofi | Di- and tri-substituted oxathiazine derivatives, method for the production thereof, use thereof as medicine and drug containing said derivatives and use thereof |
| US8895547B2 (en) | 2011-03-08 | 2014-11-25 | Sanofi | Substituted phenyl-oxathiazine derivatives, method for producing them, drugs containing said compounds and the use thereof |
| EP2683698B1 (de) | 2011-03-08 | 2017-10-04 | Sanofi | Mit adamantan- oder noradamantan substituierte benzyl-oxathiazinderivate, diese verbindungen enthaltende arzneimittel und deren verwendung |
| EP2766349B1 (de) | 2011-03-08 | 2016-06-01 | Sanofi | Mit carbozyklen oder heterozyklen substituierte oxathiazinderivate, verfahren zu deren herstellung, diese verbindungen enthaltende arzneimittel und deren verwendung |
| US8871758B2 (en) | 2011-03-08 | 2014-10-28 | Sanofi | Tetrasubstituted oxathiazine derivatives, method for producing them, their use as medicine and drug containing said derivatives and the use thereof |
| WO2012120053A1 (de) | 2011-03-08 | 2012-09-13 | Sanofi | Verzweigte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
| WO2012120055A1 (de) | 2011-03-08 | 2012-09-13 | Sanofi | Di- und trisubstituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
| EP2683702B1 (de) | 2011-03-08 | 2014-12-24 | Sanofi | Neue substituierte phenyl-oxathiazinderivate, verfahren zu deren herstellung, diese verbindungen enthaltende arzneimittel und deren verwendung |
| WO2013037390A1 (en) | 2011-09-12 | 2013-03-21 | Sanofi | 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
| WO2013045413A1 (en) | 2011-09-27 | 2013-04-04 | Sanofi | 6-(4-hydroxy-phenyl)-3-alkyl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
| TW201512171A (zh) | 2013-04-19 | 2015-04-01 | Pfizer Ltd | 化學化合物 |
| AU2017268006B2 (en) | 2016-05-20 | 2021-03-11 | Xenon Pharmaceuticals Inc. | Benzenesulfonamide compounds and their use as therapeutic agents |
| RU2760303C2 (ru) | 2016-12-09 | 2021-11-23 | Ксенон Фармасьютикалз Инк. | Соединения бензолсульфонамидов и их использование в качестве терапевтических средств |
| JP7371029B2 (ja) | 2018-06-13 | 2023-10-30 | ゼノン・ファーマシューティカルズ・インコーポレイテッド | ベンゼンスルホンアミド化合物および治療剤としてのその使用 |
| EA202190395A1 (ru) | 2018-08-31 | 2021-06-15 | Ксенон Фармасьютикалз Инк. | Замещенные гетероарилом сульфонамидные соединения и их применение в качестве терапевтических средств |
| JP7383012B2 (ja) | 2018-08-31 | 2023-11-17 | ゼノン・ファーマシューティカルズ・インコーポレイテッド | ヘテロアリール置換スルホンアミド化合物、およびナトリウムチャネル阻害剤としてのその使用 |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SE0001899D0 (sv) * | 2000-05-22 | 2000-05-22 | Pharmacia & Upjohn Ab | New compounds |
-
2005
- 2005-12-16 WO PCT/US2005/045704 patent/WO2006066109A2/en not_active Ceased
- 2005-12-16 EP EP05854426A patent/EP1888544A2/en not_active Withdrawn
- 2005-12-16 JP JP2007546949A patent/JP2008524244A/ja not_active Withdrawn
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2008540539A (ja) * | 2005-05-10 | 2008-11-20 | バーテックス ファーマシューティカルズ インコーポレイテッド | イオンチャンネルの調節因子としての二環系誘導体 |
Also Published As
| Publication number | Publication date |
|---|---|
| EP1888544A2 (en) | 2008-02-20 |
| WO2006066109A2 (en) | 2006-06-22 |
| WO2006066109A3 (en) | 2009-04-23 |
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