公开(公告)号：US20080045546A1

公开(公告)日：2008-02-21

申请号：US10575027

申请日：2004-10-02

申请人： Axel Bouchon ,  Nicole Diedrichs ,  Achim Hermann ,  Klemens Lustig ,  Heinrich Meier ,  Josef Pemerstorfer ,  Elke Reissmuller ,  Muneto Mogi ,  Takeshi Yura ,  Hiroshi Fujishima ,  Masanori Seki ,  Yuji Koriyama ,  Kayo Yasoshima ,  Keiko Misawa ,  Masaomi Tajimi ,  Noriyuki Yammoto ,  Klaus Urbahns ,  Fumihiko Hayashi ,  Yasuhiro Tsukimi ,  Jang Gupta

发明人： Axel Bouchon ,  Nicole Diedrichs ,  Achim Hermann ,  Klemens Lustig ,  Heinrich Meier ,  Josef Pemerstorfer ,  Elke Reissmuller ,  Muneto Mogi ,  Takeshi Yura ,  Hiroshi Fujishima ,  Masanori Seki ,  Yuji Koriyama ,  Kayo Yasoshima ,  Keiko Misawa ,  Masaomi Tajimi ,  Noriyuki Yammoto ,  Klaus Urbahns ,  Fumihiko Hayashi ,  Yasuhiro Tsukimi ,  Jang Gupta

IPC分类号： A61K31/519 ,  A61K31/44 ,  C07D211/68 ,  C07D213/06

CPC分类号： C07C275/32 ,  A61K31/167 ,  A61K31/17 ,  A61K31/357 ,  A61K31/42 ,  A61K31/433 ,  A61K31/4406 ,  A61K31/4409 ,  A61K31/4412 ,  A61K31/455 ,  A61K31/4706 ,  A61K31/472 ,  A61K31/517 ,  A61K47/54 ,  C07C233/29 ,  C07C233/75 ,  C07C235/24 ,  C07C235/38 ,  C07C235/56 ,  C07C235/64 ,  C07C237/04 ,  C07C275/30 ,  C07C275/38 ,  C07C2602/08 ,  C07C2602/10 ,  C07D209/18 ,  C07D213/40 ,  C07D213/56 ,  C07D213/89 ,  C07D215/46 ,  C07D217/22 ,  C07D239/94 ,  C07D261/14 ,  C07D285/06 ,  C07D317/66

摘要： This invention relates to tetrahydro-naphthalene and urea derivatives and salts thereof which are useful as active ingredients of pharmaceutical preparations. The tetrahydro-naphthalene and urea derivatives of the present invention have vanilloid receptor (VR1) antagonistic activity, and can be used for the prophylaxis and treatment of diseases associated with VR1 activity, in particular for the treatment of urological diseases or disorders, such as detrusor overactivity (overactive bladder), urinary incontinence, neurogenic detrusor overactivity (detrusor hyperflexia), idiopathic detrusor overactivity (detrusor instability), benign prostatic hyperplasia, and lower urinary tract symptoms; chronic pain, neuropathic pain, postoperative pain, rheumatoid arthritic pain, neuralgia, neuropathies, algesia, nerve injury, ischaemia, neurodegeneration, stroke, and inflammatory disorders such as asthma and chronic obstructive pulmonary (or airways) disease (COPD).

摘要翻译： 本发明涉及四氢萘和脲衍生物及其盐，其可用作药物制剂的活性成分。 本发明的四氢萘和脲衍生物具有香草素受体（VR1）拮抗活性，可用于预防和治疗与VR1活性相关的疾病，特别是用于治疗泌尿系统疾病或病症，如逼尿肌 过度活动（膀胱过度活动），尿失禁，神经源性逼尿肌过度活动（逼尿肌hyperflexia），特发性逼尿肌过度活动（逼尿肌不稳定），良性前列腺增生和下尿路症状; 慢性疼痛，神经性疼痛，术后疼痛，类风湿性关节炎疼痛，神经痛，神经病，痛觉，神经损伤，局部缺血，神经变性，中风和炎性疾病如哮喘和慢性阻塞性肺（或气道）疾病（COPD）。

公开(公告)号：US20070254938A1

公开(公告)日：2007-11-01

申请号：US11630874

申请日：2005-06-29

申请人： Kiyoshi Ichikawa ,  Keiko Misawa ,  Shuichiro Hamano

发明人： Kiyoshi Ichikawa ,  Keiko Misawa ,  Shuichiro Hamano

IPC分类号： A61K31/40 ,  A61P7/00

CPC分类号： C07D209/44 ,  A61K31/403 ,  A61K45/06

摘要： The present invention provides pharmaceutical compositions for the prevention or treatment of diseases associated with intimal hyperproliferation of a blood vessel such as restenosis after percutaneous coronary intervention or the like. Moreover, a pharmaceutical composition for the prevention or treatment of diseases associated with intimal hyperproliferation of a blood vessel such as restenosis after percutaneous coronary intervention or the like, which comprises as an active ingredient (2S)-2-benzyl-3-(cis-hexahydro-2-isoindolinylcarbonyl)propionic acid (the generic name: mitiglinide) represented by the following formula or a pharmaceutically acceptable salt thereof, or a hydrate thereof is provided.

摘要翻译： 本发明提供了用于预防或治疗与血管内膜过度增生有关的疾病的药物组合物，例如经皮冠状动脉介入治疗后的再狭窄等。 另外，作为活性成分（2S）-2-苄基-3-（顺式 - （3-甲氧基苯基）-3-甲氧基苯甲酰基 - 六氢-2-异吲哚啉基羰基）丙酸（通用名：米格列奈）或其药学上可接受的盐或其水合物。