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1.DERIVATIVES OF TRIAZINES AND URACILS, THEIR PREPARATION AND THEIR APPLICATION IN HUMAN THERAPEUTICS 有权
标题翻译: TRIAZIN- UND URACILDERIVATE,IHRE HERSTELLUNG UNDEREREUTISCHE ANWENDUNG BEIM MENSCHEN公开(公告)号:EP2328886B1
公开(公告)日:2016-12-28
申请号:EP09797466.1
申请日:2009-07-07
发明人: LEROY, Isabelle , DUPONT-PASSELAIGUE, Elisabeth , VALEILLE, Karine , RIVAL, Yves , JUNQUERO, Didier
IPC分类号: C07D401/04 , C07D401/14 , C07D403/04 , C07D403/14 , C07D409/14 , A61K31/506 , A61K31/53 , A61P3/00 , A61P17/00
CPC分类号: C07D403/04 , C07D401/04 , C07D401/14 , C07D403/14 , C07D409/14
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2.UTILISATION D'ANTAGONISTES PAR-1 POUR LA PREVENTION ET/OU LE TRAITEMENT DES PATHOLOGIES FONCTIONNELLES PELVI-PERINEALES 审中-公开
标题翻译: PAR-1拮抗剂用于预防和/或治疗肾盂会阴FUNCTIONAL病理病症的公开(公告)号:EP3082818A1
公开(公告)日:2016-10-26
申请号:EP14793086.1
申请日:2014-10-31
IPC分类号: A61K31/4965 , A61P13/00 , A61P13/10
CPC分类号: A61K31/5377 , A61K31/443 , A61K31/495
摘要: The present invention relates to the use of PAR1 antagonists, in particular of vorapaxar, of atopaxar and of 3‑(2-chlorophenyl)-1-[4-(4-fluorobenzyl)piperazin-1-yl]propenone, or a pharmaceutically acceptable salt thereof, for preventing and/or treating pelvi-perineal functional pathological conditions, and more particularly painful bladder syndrome.
摘要翻译: 本发明涉及利用PAR1拮抗剂,特别vorapaxar的,atopaxar的和3-(2-氯苯基)-1- [4-(4-氟苄基)哌嗪-1-基] propenones,或其药学上可接受 盐,其用于预防和/或治疗肾盂会阴官能病理条件下,并且更具体地膀胱疼痛综合征。
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3.ANILIDES-ALKYLTHIOÉTHERS COMME INHIBITEURS DE L'ACAT POUR LE TRAITEMENT DE MALADIES DERMATOLOGIQUES 有权
标题翻译: 苯胺硫醚AS ACAT抑制剂皮肤病学疾病的治疗公开(公告)号:EP2694477B1
公开(公告)日:2015-03-25
申请号:EP12711677.0
申请日:2012-04-04
IPC分类号: C07D211/60 , C07D207/16 , C07D277/06 , C07D333/24 , A61K31/445 , A61K31/40 , A61K31/426 , A61K31/381 , A61P17/00
CPC分类号: C07D211/60 , A61K31/381 , A61K31/40 , A61K31/426 , A61K31/445 , A61K45/06 , C07D207/16 , C07D277/06 , C07D333/24 , A61K2300/00
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4.DERIVES DE PYRAZINES EN TANT QU'INHIBITEURS DE L'ENZYME SCD-1 POUR LE TRAITEMENT DES MALADIES DE CANCER OU DU DIABETE 有权
标题翻译: 吡嗪衍生物作为酶SCD-1癌症和糖尿病的治疗的抑制剂。公开(公告)号:EP2560963B1
公开(公告)日:2016-10-05
申请号:EP11714629.0
申请日:2011-04-15
发明人: LEROY, Isabelle , DUPONT-PASSELAIGUE, Elisabeth , MIALHE, Samuel , JUNQUERO, Didier , VALEILLE, Karine
IPC分类号: C07D401/04 , A61K31/53 , A61P3/06
CPC分类号: C07D241/18 , C07D253/07 , C07D401/04
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5.DERIVATIVES OF BENZOTHIAZINES, PREPARATION THEREOF AND APPLICATION THEREOF AS DRUGS 有权
标题翻译: 衍生物的苯并噻嗪,其制备及其作为药物公开(公告)号:EP2403840B1
公开(公告)日:2014-05-14
申请号:EP10706624.3
申请日:2010-03-02
发明人: PEREZ, Michel , LAMOTHE, Marie , JUNQUERO, Didier , RIVAL, Yves
IPC分类号: C07D275/06 , A61K31/5415
CPC分类号: C07D275/06
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6.ANILIDES-ALKYLTHIOETHERS COMME INHIBITEURS DE L' ACAT POUR LE TRAITEMENT MALADIES DERMATOLOGIQUES 有权
标题翻译: 苯胺硫醚AS ACAT抑制剂皮肤病学疾病的治疗公开(公告)号:EP2694477A1
公开(公告)日:2014-02-12
申请号:EP12711677.0
申请日:2012-04-04
IPC分类号: C07D211/60 , C07D207/16 , C07D277/06 , C07D333/24 , A61K31/445 , A61K31/40 , A61K31/426 , A61K31/381 , A61P17/00
CPC分类号: C07D211/60 , A61K31/381 , A61K31/40 , A61K31/426 , A61K31/445 , A61K45/06 , C07D207/16 , C07D277/06 , C07D333/24 , A61K2300/00
摘要: The present invention relates to novel alkyl thioethers for the preparation of a medicament intended to prevent or to treat a disorder due to a dysfunction of the sebaceous glands in humans or animals. The compounds according to the present invention exert a strong inhibition of acyl CoA: cholesterol O-acyl transferase (ACAT): (I) in which - R
1 represents a hydroxyl or amino group, - R
2 represents a hydrogen or a methyl radical, - A represents a group chosen from: (II) - n represents an integer from 5 to 13.-
公开(公告)号:EP3285774B1
公开(公告)日:2020-01-08
申请号:EP16717911.8
申请日:2016-04-20
IPC分类号: A61K31/5415 , A61P1/16
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8.DERIVATIVES OF 2H PYRIDAZIN-3-ONES, THEIR PREPARATION AND THEIR USE AS SCD-1 INHIBITORS 有权
标题翻译: 2H-哒嗪3个-ON衍生物,制造方法及其作为SCD-1抑制剂公开(公告)号:EP2462121B1
公开(公告)日:2015-02-18
申请号:EP10742811.2
申请日:2010-08-05
发明人: DUPONT-PASSELAIGUE, Elisabeth , MIALHE, Samuel , RIEU, Jean-Pierre , JUNQUERO, Didier , VALEILLE, Karine
IPC分类号: C07D237/22 , C07D401/12 , C07D403/12 , A61K31/497 , A61K31/501 , A61P3/00 , A61P9/00 , A61P17/00
CPC分类号: C07D237/22 , C07D401/12 , C07D403/12
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