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公开(公告)号:US5565469A
公开(公告)日:1996-10-15
申请号:US402744
申请日:1995-03-13
申请人: Gerhard Mihm , Norbert Hauel , Uwe Ries , Jacobus C. Antonius van Meel , Wolfgang Wienen , Michael Entzeroth
发明人: Gerhard Mihm , Norbert Hauel , Uwe Ries , Jacobus C. Antonius van Meel , Wolfgang Wienen , Michael Entzeroth
IPC分类号: C07D235/20 , A61K31/415 , A61K31/4184 , A61K31/425 , A61K31/435 , A61P9/00 , A61P9/10 , A61P9/12 , A61P43/00 , C07D235/18 , C07D235/26 , C07D235/28 , C07D403/04 , C07D403/14 , C07D413/04 , C07D413/14 , C07D417/04 , C07D417/14 , C07D471/04
CPC分类号: C07D413/14 , C07D235/18 , C07D417/04 , C07D417/14 , C07D471/04
摘要: Angiotensin-II inhibiting benzimidazoles, useful for the treatment of hypertension. Exemplary compounds are:(a) 4'-[(2-n-propyl-4-methyl-6-(1-methylbenzimidazol-2-yl)-benzimidazol-1-yl)-methyl]-2-(1,3-thiazolidin-2,4-dione-5-methylidinyl)-biphenyl,(b) 4'-[(2-n-propyl-4-methyl-6-(1-methylbenzimidazol-2-yl)-benzimidazol-1-yl)-methyl]-2-sulpho-biphenyl,(c) 4'-[(2-ethyl-4-methyl-6-(5,6,7,8-tetrahydro-imidazo[1,2-a]pyridin-2-yl)-benzimidazol-1-yl)-methyl]-2-sulpho-biphenyl,(d) 4'-[(2-n-propyl-4-methyl-6-(1-methylbenzimidazol-2-yl)-benzimidazol-1-yl)-methyl]-2-trifluoroacetylamino-biphenyl,(e) 4'-[(2-ethyl-4-methyl-6-(5,6,7,8-tetrahydro-imidazo[1,2-a]pyridin-2-yl)-benzimidazol-1-yl)-methyl]-2-trifluoroacetylamino-biphenyl,(f) 4'-[(2-n-propyl-4-methyl-6-(1-methylbenzimidazol-2-yl)-benzimidazol-1-yl)-methyl]-2-(4-methoxy-benzylaminocarbonylaminosulphonyl)-biphenyl,(g) 4'-[(2-n-propyl-4-methyl-6-(1-methylbenzimidazol-2-yl)-benzimidazol-1-yl)-methyl]-2-(cyclohexylamino-carbonylaminosulphonyl)-biphenyl,(h) 4'-[(2-n-propyl-4-methyl-6-(1-methylbenzimidazol-2-yl)-benzimidazol-1-yl)-methyl]-2-(benzoylamino-sulphonyl)-biphenyl,(i) 4'-[(2-ethyl-4-methyl-6-(5,6,7,8-tetrahydro-imidazo[1,2-a]pyridin-2-yl)-benzimidazol-1-yl)-methyl]-2-(benzoylaminosulphfonyl)-biphenyl,(j) 4'-[(2-n-butyl-4-methyl-6-(propanesultam-1-yl)-benzimidazol-1-yl)-methyl]-2-(benzoylaminosulphonyl)-biphenyl and(k) 4'-[(2-ethyl-4-methyl-6-(5,6,7,8-tetrahydro-imidazo[1,2-a]pyridin-2-yl)-benzimidazol-1-yl)-methyl]-2-(cyclohexylaminocarbonylaminosulphonyl)-biphenyl.
摘要翻译: 血管紧张素II抑制苯并咪唑,可用于治疗高血压。 示例性化合物是:(a)4' - [(2-正丙基-4-甲基-6-(1-甲基苯并咪唑-2-基) - 苯并咪唑-1-基) - 甲基] -2-(1,3 - 联苯并联,(b)4' - [(2-正丙基-4-甲基-6-(1-甲基苯并咪唑-2-基) - 苯并咪唑-1-基] (c)4' - [(2-乙基-4-甲基-6-(5,6,7,8-四氢 - 咪唑并[1,2-a]吡啶 -2-基) - 苯并咪唑-1-基) - 甲基] -2-磺基 - 联苯,(d)4' - [(2-正丙基-4-甲基-6-(1-甲基苯并咪唑-2-基) ) - 苯并咪唑-1-基) - 甲基] -2-三氟乙酰基氨基 - 联苯,(e)4' - [(2-乙基-4-甲基-6-(5,6,7,8-四氢 - 咪唑并[1 ,2-a]吡啶-2-基) - 苯并咪唑-1-基) - 甲基] -2-三氟乙酰基氨基 - 联苯,(f)4' - [(2-正丙基-4-甲基-6- - 甲基苯并咪唑-2-基) - 苯并咪唑-1-基) - 甲基] -2-(4-甲氧基 - 苄基氨基羰基氨基磺酰基) - 联苯,(g)4' - [(2-正丙基-4-甲基-6- (1-甲基苯并咪唑-2-基) - 苯并咪唑-1-基) - 甲基] -2-(环己基氨基 - 羰基氨基磺酰基) - 联苯,(h)4' - [(2-正丙基-4-甲基-6- (1-甲基苯并咪唑-2-基) - 苯并咪唑 (甲基)-2-(苯甲酰氨基磺酰基) - 联苯,(i)4' - [(2-乙基-4-甲基-6-(5,6,7,8-四氢 - 咪唑并[ [1,2-a]吡啶-2-基) - 苯并咪唑-1-基) - 甲基] -2-(苯甲酰氨基磺酰基) - 联苯,(j)4' - [(2-正丁基-4-甲基 - 6-(丙磺酰基-1-基) - 苯并咪唑-1-基) - 甲基] -2-(苯甲酰基氨基磺酰基) - 联苯和(k)4' - [(2-乙基-4-甲基-6- ,7,8-四氢 - 咪唑并[1,2-a]吡啶-2-基) - 苯并咪唑-1-基) - 甲基] -2-(环己基氨基羰基氨基磺酰基) - 联苯。
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公开(公告)号:US5541229A
公开(公告)日:1996-07-30
申请号:US227291
申请日:1994-04-13
申请人: Berthold Narr , Andreas Bomhard , Norbert Hauel , Jacques Van Meel , Wolfgang Wienen , Michael Entzeroth
发明人: Berthold Narr , Andreas Bomhard , Norbert Hauel , Jacques Van Meel , Wolfgang Wienen , Michael Entzeroth
IPC分类号: A61K31/415 , A61K31/4184 , A61K31/425 , A61K31/496 , A61K31/505 , A61K31/535 , A61K31/5355 , A61P1/00 , A61P3/10 , A61P9/00 , A61P9/08 , A61P9/10 , A61P9/12 , A61P13/02 , A61P13/10 , A61P15/00 , A61P27/02 , A61P27/06 , C07D235/02 , C07D235/04 , C07D235/06 , C07D235/08 , C07D235/12 , C07D235/16 , C07D235/18 , C07D235/24 , C07D235/26 , C07D235/28 , C07D235/30 , C07D401/04 , C07D403/04 , C07D403/10 , C07D403/12 , C07D405/04 , C07D405/12 , C07D409/04 , C07D417/04 , C07D417/12 , C07D487/04 , C07D495/14 , C07D513/04 , C07D521/00 , A61K31/41
CPC分类号: C07D235/02 , C07D231/12 , C07D233/56 , C07D235/06 , C07D235/08 , C07D235/12 , C07D235/18 , C07D235/24 , C07D235/26 , C07D235/28 , C07D235/30 , C07D249/08 , C07D401/04 , C07D403/04 , C07D403/10 , C07D405/04 , C07D405/12 , C07D417/04 , C07D417/12 , C07D487/04 , C07D513/04
摘要: The invention relates to benzimidazoles of the formula ##STR1## in which R.sub.1 to R.sub.2 are as defined in claim 1,1 and 3 isomer mixtures thereof and addition salts thereof which have valuable properties.In particular, the novel compounds are angiotensin II antagonists.
摘要翻译: 本发明涉及式(I)的苯并咪唑,其中R1至R2如权利要求1,1,3和3所述的异构体混合物及其加成盐具有有价值的性质。 特别地,新化合物是血管紧张素II拮抗剂。
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63.Benzimidazoles, pharmaceutical compositions containing these compounds and processes for preparing them 失效
标题翻译: 苯并咪唑,含有这些化合物的药物组合物及其制备方法公开(公告)号:US5521177A
公开(公告)日:1996-05-28
申请号:US132065
申请日:1993-10-04
IPC分类号: A61K31/415 , A61K31/4184 , A61P1/00 , A61P9/00 , A61P9/10 , A61P9/12 , A61P11/00 , A61P13/02 , A61P15/00 , A61P27/02 , A61P27/06 , A61P43/00 , C07D235/06 , C07D235/08 , C07D235/26 , C07D235/28 , C07D403/10 , A61K31/535 , C07D413/14
CPC分类号: C07D403/10 , C07D235/08
摘要: The invention relates to benzimidazoles of general formula ##STR1## Exemplary compounds are: (a) 4'-[[2-Ethyl-4-methyl-6-[(2-dimethylamino-3,4-dioxo-1-cyclobuten-1-yl)amino]-1H-benzimidazol-1-yl]-methyl]-2-(1H-tetrazol-5-yl)-biphenyl,(b) 4'-[[2-n-Propyl-4-methyl-6-(2-cyano-3,3-dimethyl-guanidino)-1H-benzimidazol-1-yl]-methyl]-2-(1H-tetrazol-5-yl)-biphenyl,(c) 4'-[[2-n-Propyl-4-methyl-6-(2,2-dicyano-1-dimethylamino-etheneamino)-1H-benzimidazol -1-yl]-methyl]-2-(1H-tetrazol-5-yl)-biphenyl,(d) 4'-[[2-n-Propyl-4-methyl-6-(1-morpholino-2-nitro-etheneamino)-1H-benzimidazol -1 -yl]-methyl]-2-(1H-tetrazol-5-yl)-biphenyl, and(e) 4'-[[2-n-Propyl-4-methyl-6-(1,1-dimethylamino-2-nitro-etheneamino)-1H-benzimidazol -1-yl]-methyl]-2-(1H-tetrazol-5-yl)-biphenyl.The new compounds are angiotensin-antagonists.
摘要翻译: 本发明涉及通式(I)的苯并咪唑:(I)示例性化合物是:(a)4' - [[2-乙基-4-甲基-6 - [(2-二甲基氨基-3,4-二氧代-1- 环丁烯-1-基)氨基] -1H-苯并咪唑-1-基] - 甲基] -2-(1H-四唑-5-基) - 联苯,(b)4' - [[2-正丙基-4- (2-氰基-3,3-二甲基 - 胍基)-1H-苯并咪唑-1-基] - 甲基] -2-(1H-四唑-5-基) - 联苯,(c)4 ' - [[2-正丙基-4-甲基-6-(2,2-二氰基-1-二甲基氨基 - 乙烯基氨基)-1H-苯并咪唑-1-基] - 甲基] -2-(1H-四唑 - (d)4' - [[2-正丙基-4-甲基-6-(1-吗啉代-2-硝基 - 乙烯基氨基)-1H-苯并咪唑-1-基]甲基 ] -2-(1H-四唑-5-基) - 联苯,和(e)4' - [[2-正丙基-4-甲基-6-(1,1-二甲基氨基-2-硝基 - 乙烯基氨基) -1H-苯并咪唑-1-基] - 甲基] -2-(1H-四唑-5-基) - 联苯。 新化合物是血管紧张素拮抗剂。
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64.Substituted N- [1-cyano-2- (phenyl) ethyl] -2-azabicyclo [2.2.1] heptane-3-carboxamide inhibitors of cathepsin C 有权
标题翻译: 取代的组织蛋白酶C的N- [1-氰基-2-(苯基)乙基] -2-氮杂双环[2.2.1]庚烷-3-甲酰胺抑制剂公开(公告)号:US08999975B2
公开(公告)日:2015-04-07
申请号:US13615781
申请日:2012-09-14
申请人: Marc Grundl , Thorsten Oost , Alexander Pautsch , Stefan Peters , Doris Riether , Wolfgang Wienen
发明人: Marc Grundl , Thorsten Oost , Alexander Pautsch , Stefan Peters , Doris Riether , Wolfgang Wienen
IPC分类号: C07D209/52 , A61K31/416 , A61K31/4178 , A61K31/437 , C07D519/00 , A61K31/538 , A61K31/4709 , C07D495/04 , A61K31/4725 , A61K31/536 , C07D401/14 , A61K31/551 , A61K31/501 , A61K31/4439 , A61K31/4365 , A61K31/404 , A61K45/06 , A61K31/506 , A61K31/4184 , A61K31/454 , C07D401/12 , C07D471/04 , A61K31/4155 , A61K31/4192 , C07D413/12 , A61K31/4035 , A61K31/428 , A61K31/423 , A61K31/403 , C07D405/12 , C07D471/08 , C07D487/04 , A61K31/496 , A61K31/497 , C07D403/12 , C07D417/12 , A61K31/4985 , A61K31/4245 , A61K31/517
CPC分类号: C07D209/52 , A61K31/403 , A61K31/4035 , A61K31/404 , A61K31/4155 , A61K31/416 , A61K31/4178 , A61K31/4184 , A61K31/4192 , A61K31/423 , A61K31/4245 , A61K31/428 , A61K31/4365 , A61K31/437 , A61K31/4439 , A61K31/454 , A61K31/4709 , A61K31/4725 , A61K31/496 , A61K31/497 , A61K31/4985 , A61K31/501 , A61K31/506 , A61K31/517 , A61K31/536 , A61K31/538 , A61K31/551 , A61K45/06 , C07D401/12 , C07D401/14 , C07D403/12 , C07D405/12 , C07D413/12 , C07D417/12 , C07D471/04 , C07D471/08 , C07D487/04 , C07D495/04 , C07D519/00
摘要: The present invention is directed to compounds of Formula I: wherein R1, R2 and n are described herein. These compounds and their pharmaceutically acceptable salts thereof are inhibitors of Cathepsin C.
摘要翻译: 本发明涉及式I化合物:其中R1,R2和n在本文中描述。 这些化合物及其药学上可接受的盐是组织蛋白酶C的抑制剂
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65.(Alkanesultam-1-yl)-benzimidazol-1-yl)-1yl)-methyl-biphenyls useful as angiotensin-II antagonists 失效
标题翻译: (烷基磺酰基-1-基) - 苯并咪唑-1-基)-1-基) - 甲基 - 联苯作为血管紧张素II拮抗剂公开(公告)号:US5602127A
公开(公告)日:1997-02-11
申请号:US456978
申请日:1995-06-01
申请人: Norbert Hauel , Berthold Narr, deceased , Uwe Ries , Jacobus C. A. van Meel , Wolfgang Wienen , Michael Entzeroth
发明人: Norbert Hauel , Berthold Narr, deceased , Uwe Ries , Jacobus C. A. van Meel , Wolfgang Wienen , Michael Entzeroth
IPC分类号: A61K31/415 , A61K31/42 , C07D235/08 , C07D235/24 , C07D401/04 , C07D401/14 , C07D403/04 , C07D403/10 , C07D403/14 , C07D413/04 , C07D413/14 , C07D417/04 , C07D417/14 , C07D471/04 , C07D487/04 , C07D513/04 , C07D521/00 , A61K31/54 , C07D279/02
CPC分类号: A61K31/415 , A61K31/42 , C07D231/12 , C07D233/56 , C07D235/08 , C07D235/24 , C07D249/08 , C07D401/04 , C07D401/14 , C07D403/04 , C07D403/10 , C07D403/14 , C07D413/04 , C07D413/14 , C07D417/04 , C07D417/14 , C07D471/04 , C07D487/04 , C07D513/04
摘要: Angiotensin-II antagonists of the formula ##STR1## wherein R.sub.1 is, other than hydrogen and, inter alia, halogen, lower alkyl or cycloalkyl; R.sub.2 is, inter alia, optionally substituted benzimidazol-2-yl, 5,6,7,8-tetrahydro-imidazo [1,2-a]pyridin-2-yl, butanesultam-1-yl, imidazol-4-yl, and tetrahydobenzimidazol-2-yl; R.sub.3 is, inter alia, lower alkyl; and, R.sub.4 is an acidic group, such as carboxyl or tetrazolyl. An exemplary compound is: 4'-[(2-n-propyl-4-methyl-6-(butanesultam-1-yl)benzimidazol-1-yl)-methyl]-biphenyl-2-carboxylic acid.
摘要翻译: 其中R1不是氢,尤其是卤素,低级烷基或环烷基;式 R2尤其是任选取代的苯并咪唑-2-基,5,6,7,8-四氢 - 咪唑并[1,2-a]吡啶-2-基,丁磺酰-1-基,咪唑-4-基, 和四氢苯并咪唑-2-基; R3尤其是低级烷基; R4是酸性基团,例如羧基或四唑基。 示例性的化合物是4' - [(2-正丙基-4-甲基-6-(丁内酰胺-1-基)苯并咪唑-1-基) - 甲基] - 联苯-2-羧酸。
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66.
公开(公告)号:US5587393A
公开(公告)日:1996-12-24
申请号:US299693
申请日:1994-09-01
申请人: Berthold Narr , Norbert Hauel , Jacques Van Meel , Wolfgang Wienen , Michael Entzeroth , Uwe Ries
发明人: Berthold Narr , Norbert Hauel , Jacques Van Meel , Wolfgang Wienen , Michael Entzeroth , Uwe Ries
IPC分类号: C07D235/08 , C07D403/04 , C07D403/10 , C07D403/14 , A61K31/42 , C07D235/06 , C07D257/04
CPC分类号: C07D403/04 , C07D235/08 , C07D403/10 , C07D403/14
摘要: The invention relates to benzimidazoles of general formula ##STR1## wherein R.sub.1 to R.sub.4 are as defined herein, the 1-, 3-isomer mixtures thereof and the addition salts thereof. The new compounds are useful, in particular, as angiotensin antagonists.
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67.Amino acid derivatives, pharmaceutical compositions containing these compounds and processes for preparing them 失效
标题翻译: 氨基酸衍生物,含有这些化合物的药物组合物及其制备方法公开(公告)号:US6114390A
公开(公告)日:2000-09-05
申请号:US950113
申请日:1997-10-14
申请人: Wolfhard Engel , Wolfgang Eberlein , Klaus Rudolf , Henri Doods , Heike-Andrea Wieland , Klaus-Dieter Willim , Michael Entzeroth , Wolfgang Wienen
发明人: Wolfhard Engel , Wolfgang Eberlein , Klaus Rudolf , Henri Doods , Heike-Andrea Wieland , Klaus-Dieter Willim , Michael Entzeroth , Wolfgang Wienen
IPC分类号: A61K38/00 , C07C257/18 , C07C275/24 , C07C275/56 , C07C279/14 , C07C279/24 , C07C279/36 , C07C307/06 , C07C311/35 , C07D209/08 , C07D209/18 , C07D209/24 , C07D209/42 , C07D209/44 , C07D223/20 , C07D233/26 , C07D233/36 , C07D233/72 , C07D233/88 , C07D235/06 , C07D235/08 , C07D239/46 , C07D249/14 , C07D271/06 , C07D307/85 , C07K5/078 , A61K31/17 , C07C275/14
CPC分类号: C07D235/06 , C07C257/18 , C07C275/24 , C07C275/56 , C07C279/14 , C07C279/24 , C07C279/36 , C07C307/06 , C07C311/35 , C07D209/08 , C07D209/18 , C07D209/24 , C07D209/42 , C07D209/44 , C07D223/20 , C07D233/26 , C07D233/36 , C07D233/72 , C07D233/88 , C07D235/08 , C07D239/47 , C07D249/14 , C07D271/06 , C07D307/85 , C07K5/06139 , A61K38/00
摘要: NPY-antagonistic compounds of the formula ##STR1## Exemplary are: (A) (R)-N-[[4-(Aminocarbonylaminomethyl)phenyl]methyl]-N.sup.2 -bis(4-hydroxyphenyl)acetyl]-argininamide-trifluoracetate;(B) (R)-N-[[4-(Aminocarbonylaminomethyl)phenyl]methyl]-N.sup.2 -[bis(4-chlorphenyl)acetyl]-argininamide-trifluoracetate;(C) (R)-N-[[4-Aminocarbonylaminomethyl)phenyl]methyl]-N.sup.2 -(diphenylacetyl)-argininamide-trifluoracetate;(D) (R)-N.sup.2 -(Diphenylacetyl)-N-[[4-(ethoxycarbonylmethylamino-carbonylaminomethyl)phenyl]methyl]-argininamide-trifluoroacetate;(E) (R,S)-N.sup.5 -(Aminoiminomethyl)-N.sup.2 -(diphenylacetyl)-N-[(4-hy-droxyphenyl)methyl]-N.sup.5 -methyl-ornithinamide-hydrochloride;(F) (R)-N-[[4-(Aminocarbonylmethyl)phenyl]methyl]-N.sup.2 -(diphenyl-acetyl)-argininamide-diacetate;(G) (R)-N.sup.2 -(Diphenylacetyl)-N-[[4-(ethylaminocarbonylamino-methyl)-phenyl]methyl]-argininamide-bis-(trifluoroacetate); and,(H) (R)-N.sup.2 -(Diphenylacetyl)-N-[[4-(ethoxycarbonylamino-carbonylaminomethyl)phenyl]methyl]-argininamide-trifluoroacetate.
摘要翻译: 式(A)(R)-N - [[4-(氨基羰基氨基甲基)苯基]甲基] -N2-双(4-羟基苯基)乙酰基] - 炔丙酰胺 - 三氟乙酸盐; (B)(R)-N - [[4-(氨基羰基氨基甲基)苯基]甲基] -N 2 - [双(4-氯苯基)乙酰基] - 炔丙酰胺 - 三氟乙酸盐; (C)(R)-N - [[4-氨基羰基氨基甲基)苯基]甲基] -N2-(二苯基乙酰基) - 炔丙酰胺 - 三氟乙酸盐; (D)(R)-N2-(二苯基乙酰基)-N - [[4-(乙氧基羰基甲基氨基 - 羰基氨基甲基)苯基]甲基] - 炔丙酰胺 - 三氟乙酸盐; (E)(R,S)-N5-(氨基亚氨基甲基)-N2-(二苯基乙酰基)-N - [(4-羟基苯基)甲基] -N5-甲基 - 鸟氨酰胺 - 盐酸盐; (F)(R)-N - [[4-(氨基羰基甲基)苯基]甲基] -N2-(二苯基 - 乙酰基) - 鸟氨酰胺 - 二乙酸酯; (G)(R)-N2-(二苯基乙酰基)-N - [[4-(乙基氨基羰基氨基 - 甲基) - 苯基]甲基] - 炔丙酰胺 - 双 - (三氟乙酸盐) 和(H)(R)-N2-(二苯基乙酰基)-N - [[4-(乙氧基羰基氨基 - 羰基氨基甲基)苯基]甲基] - 炔丙酰胺 - 三氟乙酸盐。
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68.Amino acid derivatives, pharmaceutical compositions containing these compounds and their use in the treatment of obesity 失效
标题翻译: 氨基酸衍生物,含有这些化合物的药物组合物及其在治疗肥胖症中的应用公开(公告)号:US5616620A
公开(公告)日:1997-04-01
申请号:US458093
申请日:1995-06-01
申请人: Klaus Rudolf , Wolfgang Eberlein , Wolfhard Engel , Gerhard Mihm , Henri Doods , Heike A. Wieland , Klaus-Dieter Willim , Jurgen Krause , Horst Dollinger , Franz Esser , Gerd Schnorrenberg , Michael Entzeroth , Wolfgang Wienen
发明人: Klaus Rudolf , Wolfgang Eberlein , Wolfhard Engel , Gerhard Mihm , Henri Doods , Heike A. Wieland , Klaus-Dieter Willim , Jurgen Krause , Horst Dollinger , Franz Esser , Gerd Schnorrenberg , Michael Entzeroth , Wolfgang Wienen
IPC分类号: A61K31/155 , A61K31/165 , A61K31/195 , A61K31/198 , A61K31/38 , A61K31/381 , A61K31/40 , A61K31/403 , A61K31/404 , A61K31/41 , A61K31/415 , A61K31/4184 , A61K31/4245 , A61K31/44 , A61K31/4409 , A61K31/4418 , A61K31/4427 , A61K31/445 , A61K31/4465 , A61K31/4468 , A61K31/454 , A61K31/47 , A61K38/00 , A61P9/12 , A61P43/00 , C07C237/22 , C07C237/42 , C07C255/60 , C07C257/12 , C07C257/14 , C07C257/18 , C07C259/10 , C07C259/18 , C07C261/04 , C07C275/40 , C07C279/10 , C07C279/12 , C07C279/14 , C07C279/18 , C07C279/36 , C07C307/02 , C07C307/10 , C07C311/08 , C07C311/15 , C07C311/19 , C07C311/39 , C07C311/42 , C07D209/14 , C07D209/16 , C07D209/42 , C07D209/44 , C07D211/28 , C07D213/38 , C07D213/55 , C07D215/12 , C07D215/38 , C07D223/20 , C07D233/24 , C07D233/48 , C07D233/54 , C07D233/64 , C07D233/66 , C07D233/72 , C07D233/88 , C07D235/06 , C07D235/08 , C07D249/08 , C07D249/10 , C07D249/12 , C07D249/14 , C07D271/06 , C07D271/07 , C07D295/15 , C07D333/20 , C07D333/36 , C07D401/12 , C07D471/04 , C07K5/072 , C07C273/00 , C07C275/00
CPC分类号: C07D233/64 , C07C237/22 , C07C237/42 , C07C255/60 , C07C257/12 , C07C257/14 , C07C257/18 , C07C259/10 , C07C259/18 , C07C261/04 , C07C275/40 , C07C279/14 , C07C279/18 , C07C279/36 , C07C307/02 , C07C307/10 , C07C311/08 , C07C311/19 , C07C311/39 , C07C311/42 , C07D209/16 , C07D209/42 , C07D209/44 , C07D213/38 , C07D215/38 , C07D223/20 , C07D233/24 , C07D233/48 , C07D233/72 , C07D233/88 , C07D235/06 , C07D249/12 , C07D249/14 , C07D271/07 , C07D295/15 , C07D333/20 , C07D471/04 , C07K5/06095 , A61K38/00 , C07C2101/08 , C07C2101/14 , C07C2103/18 , C07C2103/74
摘要: Amino acid derivatives, suitable for the treatment of obesity. The following compound is exemplary of the class: (R)-N2-(diphenylacetyl)-N-[(4-hydroxyphenyl) methyl]-argininamide-acetate.
摘要翻译: 氨基酸衍生物,适用于治疗肥胖症。 以下化合物是以下类别的示例:(R)-N 2 - (二苯基乙酰基)-N - [(4-羟基苯基)甲基] - 炔丙酰胺 - 乙酸酯。
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69.Tetrahydroimidazo[1,2-a]pyridin-2-yl-(benzimidazol-1-yl)-methyl-biph enyls useful as angiotensin-II antagonists 失效
标题翻译: 用作血管紧张素II拮抗剂的四氢咪唑并[1,2-a]吡啶-2-基 - (苯并咪唑-1-基) - 甲基 - 联苯公开(公告)号:US5594003A
公开(公告)日:1997-01-14
申请号:US456337
申请日:1995-06-01
申请人: Norbert Hauel , Berthold Narr, deceased , Uwe Ries , Jacobus C. A. van Meel , Wolfgang Wienen , Michael Entzeroth
发明人: Norbert Hauel , Berthold Narr, deceased , Uwe Ries , Jacobus C. A. van Meel , Wolfgang Wienen , Michael Entzeroth
IPC分类号: A61K31/415 , A61K31/42 , C07D235/08 , C07D235/24 , C07D401/04 , C07D401/14 , C07D403/04 , C07D403/10 , C07D403/14 , C07D413/04 , C07D413/14 , C07D417/04 , C07D417/14 , C07D471/04 , C07D487/04 , C07D513/04 , C07D521/00 , A61K31/44 , C07D471/02
CPC分类号: C07D235/24 , A61K31/415 , A61K31/42 , C07D231/12 , C07D233/56 , C07D235/08 , C07D249/08 , C07D401/04 , C07D401/14 , C07D403/04 , C07D403/10 , C07D403/14 , C07D413/04 , C07D413/14 , C07D417/04 , C07D417/14 , C07D471/04 , C07D487/04 , C07D513/04
摘要: Angiotensin-II antagonists of the formula ##STR1## wherein R.sub.1 is, other than hydrogen and, inter alia, halogen, lower alkyl or cycloalkyl; R.sub.2 is, inter alia, optionally substituted benzimidazol-2-yl, 5,6,7,8-tetrahydro-imidazo[1,2-a]pyridin-2-yl, butanesultam-1-yl, imidazol-4-yl, and tetrahydobenzimidazol-2-yl; R.sub.3 is, inter alia, lower alkyl; and, R.sub.4 is an acidic group, such as carboxyl or tetrazolyl. An compound is:4'-[(2-Ethyl-4-methyl-6-(5,6,7,8-tetrahydro-imidazo[1,2-a]pyridin-2-yl)-benzimidazol-1-yl)-methyl]-biphenyl-2-carboxylic acid.
摘要翻译: 其中R1不是氢,尤其是卤素,低级烷基或环烷基;式 R2尤其是任选取代的苯并咪唑-2-基,5,6,7,8-四氢 - 咪唑并[1,2-a]吡啶-2-基,丁磺酰-1-基,咪唑-4-基, 和四氢苯并咪唑-2-基; R3尤其是低级烷基; R4是酸性基团,例如羧基或四唑基。 化合物是4' - [(2-乙基-4-甲基-6-(5,6,7,8-四氢 - 咪唑并[1,2-a]吡啶-2-基) - 苯并咪唑-1-基 ) - 甲基] - 联苯-2-羧酸。
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公开(公告)号:US5591762A
公开(公告)日:1997-01-07
申请号:US457204
申请日:1995-06-01
申请人: Norbert Hauel , Berthold Narr, deceased , Uwe Ries , Jacobus C. A. van Meel , Wolfgang Wienen , Michael Entzeroth
发明人: Norbert Hauel , Berthold Narr, deceased , Uwe Ries , Jacobus C. A. van Meel , Wolfgang Wienen , Michael Entzeroth
IPC分类号: A61K31/415 , A61K31/42 , C07D235/08 , C07D235/24 , C07D401/04 , C07D401/14 , C07D403/04 , C07D403/10 , C07D403/14 , C07D413/04 , C07D413/14 , C07D417/04 , C07D417/14 , C07D471/04 , C07D487/04 , C07D513/04 , C07D521/00
CPC分类号: A61K31/415 , A61K31/42 , C07D231/12 , C07D233/56 , C07D235/08 , C07D235/24 , C07D249/08 , C07D401/04 , C07D401/14 , C07D403/04 , C07D403/10 , C07D403/14 , C07D413/04 , C07D413/14 , C07D417/04 , C07D417/14 , C07D471/04 , C07D487/04 , C07D513/04
摘要: Disclosed herein are angiotensin-II antagonists of the formula ##STR1## wherein R.sub.1 is, other than hydrogen and, inter alia, halogen, lower alkyl or cycloalkyl; R.sub.2 is, inter alia, optionally substituted benzimidazol-2-yl, 5,6,7,8-tetrahydro-imidazo[1,2-a]pyridin-2-yl, butanesultam-1-yl, imidazol-4-yl, and tetrahydobenzimidazol-2-yl; R.sub.3 is, inter alia, lower alkyl; and, R.sub.4 is an acidic group, such as carboxyl or tetrazolyl.An exemplary compound is:(a) 4'-[[2-n-propyl-4-methyl-6-(1-methylbenzimidazole-2-yl)-benzimidazol-1-yl]methyl]-biphenyl-2-carboxylic acid.
摘要翻译: 本文公开了式IMAMA的血管紧张素-II拮抗剂,其中R 1除氢以外,特别是卤素,低级烷基或环烷基; R2尤其是任选取代的苯并咪唑-2-基,5,6,7,8-四氢 - 咪唑并[1,2-a]吡啶-2-基,丁磺酰-1-基,咪唑-4-基, 和四氢苯并咪唑-2-基; R3尤其是低级烷基; R4是酸性基团,例如羧基或四唑基。 示例性化合物是:(a)4' - [[2-正丙基-4-甲基-6-(1-甲基苯并咪唑-2-基) - 苯并咪唑-1-基]甲基]联苯-2-甲酸 。
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