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1.1-aryl-2-acylamino-ethane compounds and their use as neurokinin especially neurokinin 1 antagonists 失效
标题翻译: 1-芳基-2-酰基氨基 - 乙烷化合物及其作为神经激肽,特别是神经激肽1拮抗剂的用途公开(公告)号:US5929067A
公开(公告)日:1999-07-27
申请号:US913352
申请日:1997-08-21
申请人: Marc Gerspacher , Andreas Von Sprecher , Silvio Roggo , Robert Mah , Silvio Ofner , Siem Jacob Veenstra , Claudia Betschart , Yves Auberson , Walter Schilling
发明人: Marc Gerspacher , Andreas Von Sprecher , Silvio Roggo , Robert Mah , Silvio Ofner , Siem Jacob Veenstra , Claudia Betschart , Yves Auberson , Walter Schilling
IPC分类号: C07D249/08 , A61K31/16 , A61K31/165 , A61K31/40 , A61K31/4015 , A61K31/403 , A61K31/404 , A61K31/405 , A61K31/41 , A61K31/415 , A61K31/4184 , A61K31/425 , A61K31/44 , A61K31/4427 , A61K31/443 , A61K31/445 , A61K31/4468 , A61K31/451 , A61K31/454 , A61K31/47 , A61K31/495 , A61K31/496 , A61K31/505 , A61K31/535 , A61K31/5355 , A61K31/5375 , A61K31/55 , A61P1/00 , A61P9/00 , A61P11/00 , A61P11/06 , A61P25/00 , A61P29/00 , A61P37/08 , A61P43/00 , C07C231/02 , C07C231/12 , C07C237/22 , C07C255/29 , C07C311/51 , C07D207/27 , C07D209/08 , C07D209/12 , C07D209/18 , C07D209/20 , C07D211/16 , C07D211/22 , C07D211/44 , C07D211/48 , C07D211/58 , C07D211/62 , C07D213/40 , C07D213/70 , C07D213/81 , C07D215/46 , C07D223/12 , C07D223/16 , C07D231/38 , C07D233/60 , C07D235/16 , C07D235/28 , C07D239/28 , C07D239/42 , C07D241/14 , C07D241/20 , C07D295/13 , C07D295/135 , C07D295/14 , C07D295/18 , C07D295/185 , C07D401/12 , C07D403/12 , C07D405/12 , C07D417/12 , C07D471/10 , C07D521/00 , C07D223/10
CPC分类号: C07D213/40 , C07C237/22 , C07C255/29 , C07C311/51 , C07D209/08 , C07D209/12 , C07D209/20 , C07D211/22 , C07D211/44 , C07D211/48 , C07D211/58 , C07D213/70 , C07D215/46 , C07D223/12 , C07D231/12 , C07D231/38 , C07D233/56 , C07D235/16 , C07D235/28 , C07D239/42 , C07D241/20 , C07D249/08 , C07D295/13 , C07D295/135 , C07D295/185 , C07D401/12 , C07D403/12 , C07D417/12 , C07D471/10 , C07C2101/02 , C07C2101/04 , C07C2101/08 , C07C2101/14 , C07C2101/18
摘要: 1-Aryl-2-acylaminoethane compounds of formula I ##STR1## wherein R.sub.1 -R.sub.4, X and Am are as defined in the description, have valuable pharmaceutical properties and are especially effective as NK-1 antagonists.
摘要翻译: PCT No.PCT / EP96 / 00555 Sec。 371日期1997年8月21日 102(e)日期1997年8月21日PCT 1996年2月9日PCT公布。 WO96 / 26183 PCT出版物 日期1961年8月29日 - 式I的芳基-2-酰基氨基乙烷化合物,其中R 1 -R 4,X和Am如说明书中所定义,具有有价值的药物性质,并且作为NK-1拮抗剂特别有效。
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公开(公告)号:US5604247A
公开(公告)日:1997-02-18
申请号:US632971
申请日:1996-04-16
申请人: Andreas Von Sprecher , Marc Gerspacher , Robert Mah , Silvio Roggo , Walter Schilling , Silvio Ofner , Siem J. Veenstra
发明人: Andreas Von Sprecher , Marc Gerspacher , Robert Mah , Silvio Roggo , Walter Schilling , Silvio Ofner , Siem J. Veenstra
IPC分类号: A61K31/352 , A61K31/4402 , A61K31/443 , A61K31/445 , A61K31/4468 , A61P1/00 , A61P1/08 , A61P1/12 , A61P3/12 , A61P9/00 , A61P9/08 , A61P9/12 , A61P11/00 , A61P11/06 , A61P11/08 , A61P25/00 , A61P25/04 , A61P25/08 , A61P25/20 , A61P25/24 , A61P25/26 , A61P29/00 , A61P35/00 , A61P37/00 , A61P37/08 , A61P43/00 , C07D405/12 , G07D405/12
CPC分类号: C07D405/12
摘要: Compounds of formula I ##STR1## wherein rings A and B are as defined in the specification, have valuable pharmacological properties and are particularly effective as NK1 antagonists and substance P antagonists. Said compounds are prepared in a manner known per se.
摘要翻译: 其中环A和B如说明书中所定义的式I的化合物具有有价值的药理学性质,并且作为NK1拮抗剂和P物质拮抗剂是特别有效的。 所述化合物以本身已知的方式制备。
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3.
公开(公告)号:US06319917B1
公开(公告)日:2001-11-20
申请号:US09655170
申请日:2000-09-05
IPC分类号: A61K3155
CPC分类号: C07D403/12 , C07C237/22 , C07D209/20 , C07D209/24 , C07D223/12
摘要: Compounds of formula I wherein R1, R1-R3, R4′, R4″ and R5 are as defined in the description, have valuable pharmaceutical properties and are effective especially as NK1 and NK2 antagonists. They are prepared in a manner known per se.
摘要翻译: 在R1,R1-R3,R4',R4“和R5中的式I化合物如说明书中所定义,具有有价值的药物性质,特别是作为NK1和NK2拮抗剂是有效的。 它们是以本身已知的方式准备的。
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公开(公告)号:US20110243923A1
公开(公告)日:2011-10-06
申请号:US13133464
申请日:2009-07-12
申请人: Birgit Baumgarten , Francois Gessier , Andreas Katopodis , Richard Knochenmuss , Rocco Falchetto , Silvio Roggo , Andreas Sailer , Klaus Seuwen , Carsten Spanka , Juan Zhang , Sebastien Hannedouche , Sophie Noel , Marie-Odile Roy , Yu Chen , Charles Y. Cho , Wei Li , Weijun Shen
发明人: Birgit Baumgarten , Francois Gessier , Andreas Katopodis , Richard Knochenmuss , Rocco Falchetto , Silvio Roggo , Andreas Sailer , Klaus Seuwen , Carsten Spanka , Juan Zhang , Sebastien Hannedouche , Sophie Noel , Marie-Odile Roy , Yu Chen , Charles Y. Cho , Wei Li , Weijun Shen
IPC分类号: A61K39/395 , C07H21/00 , C07K16/00 , C07K14/00 , C07H21/02 , C07K2/00 , C07K16/18 , C07K16/28 , A61K38/16 , A61K31/7088 , A61P9/10 , A61P9/04 , A61P3/04 , A61P9/12 , A61P29/00 , A61P11/06 , A61P31/12 , A61P31/18 , A61P31/14 , A61P35/00 , A61P3/10 , A61P13/12 , A61P11/00 , A61P1/16 , A61P9/00 , A61P3/06 , A61P37/06 , A61P37/08 , G01N33/566
CPC分类号: C07K14/705 , C12N15/1138 , C12N2310/14 , G01N33/56994 , G01N33/92 , G01N2800/044 , G01N2800/2871 , G01N2800/321
摘要: The present invention relates to modulators of the interaction between Epstein-Barr Virus induced receptor-2 (EBi2) and cholest-5-ene-3b,7b,25-triol (7, 25-dihydroxycholesterol) (“7,25DHC”) and/or cholest-5-ene-3b, 7b-diol (7-hydroxycholesterol) (“7HC”). The modulator maybe a small chemical molecule, antibody or other therapeutic protein. Methods of medical treatment and methods of identifying modulators are also described.
摘要翻译: 本发明涉及爱泼斯坦 - 巴尔病毒诱导的受体-2(EBi2)和胆甾烯-5-烯-3b,7b,25-三醇(7,25-二羟基胆固醇)(“7,25DHC”)和 /或胆甾烯-5-烯-3b,7b-二醇(7-羟基胆固醇)(“7HC”)。 调节剂可能是一种小的化学分子,抗体或其他治疗性蛋白质。 还描述了治疗方法和识别调节剂的方法。
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5.Methods of identifying a modulator that inhibits the binding between Epstein-Barr virus induced receptor 2 and cholesterol derived ligands 有权
标题翻译: 鉴定抑制爱泼斯坦 - 巴尔病毒诱导受体2与胆固醇衍生配体结合的调节剂的方法公开(公告)号:US08497075B2
公开(公告)日:2013-07-30
申请号:US13133464
申请日:2009-07-12
申请人: Birgit Baumgarten , Francois Gessier , Andreas Katopodis , Richard Knochenmuss , Rocco Falchetto , Silvio Roggo , Andreas Sailer , Klaus Seuwen , Carsten Spanka , Juan Zhang , Sebastien Hannedouche , Sophie Noel , Marie-Odile Roy , Yu Chen , Charles Y. Cho , Wei Li , Weijun Shen
发明人: Birgit Baumgarten , Francois Gessier , Andreas Katopodis , Richard Knochenmuss , Rocco Falchetto , Silvio Roggo , Andreas Sailer , Klaus Seuwen , Carsten Spanka , Juan Zhang , Sebastien Hannedouche , Sophie Noel , Marie-Odile Roy , Yu Chen , Charles Y. Cho , Wei Li , Weijun Shen
IPC分类号: G01N33/53 , C07K14/435
CPC分类号: C07K14/705 , C12N15/1138 , C12N2310/14 , G01N33/56994 , G01N33/92 , G01N2800/044 , G01N2800/2871 , G01N2800/321
摘要: The present invention relates to modulators of the interaction between Epstein-Barr Virus induced receptor-2 (EBi2) and cholest-5-ene-3b,7b,25-triol (7,25-dihydroxycholesterol) (“7,25DHC”) and/or cholest-5-ene-3b, 7b-diol (7-hydroxycholesterol) (“7HC”). The modulator maybe a small chemical molecule, antibody or other therapeutic protein. Methods of medical treatment and methods of identifying modulators are also described.
摘要翻译: 本发明涉及爱泼斯坦 - 巴尔病毒诱导的受体-2(EBi2)和胆甾烯-5-烯-3b,7b,25-三醇(7,25-二羟基胆固醇)(“7,25DHC”)和 /或胆甾烯-5-烯-3b,7b-二醇(7-羟基胆固醇)(“7HC”)。 调节剂可能是一种小的化学分子,抗体或其他治疗性蛋白质。 还描述了治疗方法和识别调节剂的方法。
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