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1.
公开(公告)号:US20060111406A1
公开(公告)日:2006-05-25
申请号:US10517581
申请日:2003-06-11
申请人: Rafael Ferritto Crespo , Jose Martin , Maria Martinortega Finger , Isabel Rojo Garcia , Quanrong Shen , Alan Warshawsky , Yanping Xu
发明人: Rafael Ferritto Crespo , Jose Martin , Maria Martinortega Finger , Isabel Rojo Garcia , Quanrong Shen , Alan Warshawsky , Yanping Xu
IPC分类号: A61K31/44 , A61K31/433 , A61K31/428 , A61K31/42 , A61K31/195 , A61K31/381
CPC分类号: C07C235/06 , C07C69/734 , C07C233/18 , C07C235/08 , C07C235/14 , C07C235/20 , C07C235/22 , C07C235/24 , C07C235/26 , C07C235/34 , C07C323/41 , C07C2601/04 , C07C2601/14 , C07D211/32 , C07D213/40 , C07D217/06 , C07D277/46 , C07D277/82 , C07D285/12 , C07D285/135 , C07D295/18 , C07D295/185 , C07D317/58 , C07D317/60 , C07D333/20
摘要: The present invention is directed to compounds, compositions, and use of compounds the structural Formula (I).
摘要翻译: 本发明涉及结构式(I)的化合物,组合物和化合物的用途。
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2.
公开(公告)号:US07220880B2
公开(公告)日:2007-05-22
申请号:US10517581
申请日:2003-06-11
申请人: Rafael Ferritto Crespo , Jose Alfredo Martin , Maria Dolores Martin-Ortega Finger , Isabel Rojo Garcia , Quanrong Shen , Alan M Warshawsky , Yanping Xu
发明人: Rafael Ferritto Crespo , Jose Alfredo Martin , Maria Dolores Martin-Ortega Finger , Isabel Rojo Garcia , Quanrong Shen , Alan M Warshawsky , Yanping Xu
IPC分类号: C07C229/28 , A61K31/195
CPC分类号: C07C235/06 , C07C69/734 , C07C233/18 , C07C235/08 , C07C235/14 , C07C235/20 , C07C235/22 , C07C235/24 , C07C235/26 , C07C235/34 , C07C323/41 , C07C2601/04 , C07C2601/14 , C07D211/32 , C07D213/40 , C07D217/06 , C07D277/46 , C07D277/82 , C07D285/12 , C07D285/135 , C07D295/18 , C07D295/185 , C07D317/58 , C07D317/60 , C07D333/20
摘要: The present invention is directed to compounds, compositions, and use of compounds the structural Formula (I)
摘要翻译: 本发明涉及化合物,组合物和化合物的用途,结构式(I)
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公开(公告)号:US20050107449A1
公开(公告)日:2005-05-19
申请号:US10505089
申请日:2003-02-13
申请人: Scott Conner , James Knobelsdorf , Nathan Mantlo , Jeffrey Schkeryantz , Quanrong Shen , Alan Warshawsky , Guoxin Zhu
发明人: Scott Conner , James Knobelsdorf , Nathan Mantlo , Jeffrey Schkeryantz , Quanrong Shen , Alan Warshawsky , Guoxin Zhu
IPC分类号: A61K31/421 , A61K31/422 , A61K31/426 , A61K31/429 , A61K31/4439 , A61K31/444 , A61K31/454 , A61K31/497 , A61K31/506 , A61K31/5377 , A61P3/10 , A61P9/10 , A61P43/00 , C07D263/02 , C07D263/32 , C07D277/20 , C07D277/24 , C07D277/26 , C07D277/28 , C07D277/30 , C07D403/10 , C07D413/04 , C07D413/10 , C07D413/12 , C07D417/04 , C07D417/10 , C07D417/14 , C07D513/04
CPC分类号: C07D263/32 , C07D277/24 , C07D277/26 , C07D277/28 , C07D277/30 , C07D403/10 , C07D413/04 , C07D413/10 , C07D417/04 , C07D417/10 , C07D417/14
摘要: The present invention is directed to compounds represented by the following structural formula, and pharmaceutically acceptable salts thereof, Formula I. (Formula I); wherein: (a) R5 is selected from the group consisting of (C1-C6) alkyl, (C1-C6) alkenyl, aryl (C0-C4) alkyl, aryloxy (C0-C4) alkyl, arylthio (C0-C4) alkyl, and further wherein when R5 is alkyl, R5 can optionally combine with W to form a 6 membered cycloheteroalkyl ring that is fused with the oxazole or thiazole ring to which the R5 group is attached; (b) R9 is selected from the group consisting of C1-C5 alkyl, C1-C5 alkenyl, and arylC0-C3alkyl. (c) T1 is selected from the group consisting of C and N, (d) W is selected from the group consisting of CH2, C(O)N(R21), N(R21), N(R21)CH2, O, OCH2, S, and SO2; and (e) X is selected from the group consisting of C, CH2C, and CCH2
摘要翻译: 本发明涉及由以下结构式表示的化合物及其药学上可接受的盐,式I(式I); 其中:(a)R 5选自(C 1 -C 6 -C 6)烷基,(C 1 -C 6 - C 烷基,芳基(C 0 -C 4 -C 4)烷基,芳氧基(C 1 -C 4)烷基, 烷基,芳硫基(C 0 -C 4 -C 4)烷基,并且其中当R 5为烷基时,R 5可任意地与W结合形成6元 与R5基团连接的恶唑或噻唑环稠合的环杂烷基环; (b)R 9选自C 1 -C 5烷基,C 1 -C 5烷基,C 1 -C 5 - 烯基和芳基C 0 -C 3烷基。 (c)T 1选自C和N,(d)W选自CH 2,C(O)N( R 21),N(R 21),N(R 21)CH 2,O,OCH 2,S和SO 2; 和(e)X选自C,CH 2 C和CCH 2,
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4.
公开(公告)号:US20050075378A1
公开(公告)日:2005-04-07
申请号:US10477405
申请日:2002-05-24
申请人: Lynn Gossett , Jonathan Green , James Henry , Winton Jones , Donald Matthews , Quanrong Shen , Daryl Smith , Jennifer Vance , Alan Warshawsky , Maria Gonzalez-Garcia
发明人: Lynn Gossett , Jonathan Green , James Henry , Winton Jones , Donald Matthews , Quanrong Shen , Daryl Smith , Jennifer Vance , Alan Warshawsky , Maria Gonzalez-Garcia
IPC分类号: C07D233/64 , A61K31/195 , A61K31/27 , A61K31/277 , A61K31/343 , A61K31/381 , A61K31/4035 , A61K31/415 , A61K31/4164 , A61K31/421 , A61K31/422 , A61K31/426 , A61K31/427 , A61K31/428 , A61K31/4402 , A61K31/443 , A61K31/4439 , A61K31/454 , A61K31/455 , A61K31/4709 , A61K31/496 , A61K31/497 , A61K31/506 , A61K31/5377 , A61K45/00 , A61P3/02 , A61P3/04 , A61P3/06 , A61P3/10 , A61P9/00 , A61P9/04 , A61P9/10 , A61P9/12 , A61P25/00 , A61P43/00 , C07C233/63 , C07C233/84 , C07C233/87 , C07C255/57 , C07C271/22 , C07C271/24 , C07D209/48 , C07D213/81 , C07D231/12 , C07D233/58 , C07D239/28 , C07D263/32 , C07D277/20 , C07D277/24 , C07D277/28 , C07D277/42 , C07D307/79 , C07D333/28 , C07D333/38 , C07D401/06 , C07D401/12 , C07D405/12 , C07D409/12 , C07D413/04 , C07D413/06 , C07D413/10 , C07D413/12 , C07D413/14 , C07D417/04 , C07D417/12 , C07D417/14 , C07D495/04 , C07D277/18 , C07D263/52
CPC分类号: C07D209/48 , C07C233/63 , C07C233/87 , C07C255/57 , C07C271/22 , C07C271/24 , C07C2601/04 , C07C2601/14 , C07D213/81 , C07D231/12 , C07D239/28 , C07D263/32 , C07D277/28 , C07D277/42 , C07D307/79 , C07D333/28 , C07D401/06 , C07D409/12 , C07D413/04 , C07D413/06 , C07D413/12 , C07D413/14 , C07D417/04 , C07D417/12 , C07D417/14 , C07D495/04
摘要: The present invention is directed to a compound of formula I, and pharmaceutically acceptable salts, solvates, hydrates or stereoisomer thereof, which are useful in treating Syndrome X, Type II diabetes, hyperglycemia, hyperlipidemia, obesity, coagaulopathy, hypertension, arteriosclerosis, and other disorders related to Syndrome X as well as cardiovascular diseases.
摘要翻译: 本发明涉及式I化合物及其药学上可接受的盐,溶剂化物,水合物或立体异构体,它们可用于治疗综合征X,II型糖尿病,高血糖症,高脂血症,肥胖症,凝血病,高血压,动脉硬化等 与综合征X相关的疾病以及心血管疾病。
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公开(公告)号:US20070149810A1
公开(公告)日:2007-06-28
申请号:US10579564
申请日:2004-11-16
申请人: Jianliang Lu , Tainwei Ma , Sunil Nagpal , Quanrong Shen , Alan Warshawsky , Ying Yee , Michael Rupp
发明人: Jianliang Lu , Tainwei Ma , Sunil Nagpal , Quanrong Shen , Alan Warshawsky , Ying Yee , Michael Rupp
IPC分类号: C07C303/00
CPC分类号: C07D333/68 , C07D333/70
摘要: The present invention relates to novel, non-secosteroidal, phenyl-benzothiophene compounds with vitamin D receptor (VDR) modulating activity that are less hypercalcemic than 1α,25 dihydroxy vitamin D3. These compounds are useful for treating bone disease and psoriasis.
摘要翻译: 本发明涉及具有维生素D受体(VDR)调节活性的新型非异构体苯基 - 苯并噻吩化合物,其比1α,25二羟基维生素D3低钙高。 这些化合物可用于治疗骨病和牛皮癣。
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公开(公告)号:US20070106095A1
公开(公告)日:2007-05-10
申请号:US10579563
申请日:2004-11-16
申请人: Jianliang Lu , Tianwei Ma , Sunil Nagpal , Quanrong Shen , Alan Warshawsky , Jason Ochoada , Ying Yee
发明人: Jianliang Lu , Tianwei Ma , Sunil Nagpal , Quanrong Shen , Alan Warshawsky , Jason Ochoada , Ying Yee
IPC分类号: C07C303/00
CPC分类号: C07D405/12 , C07D307/80 , C07D407/12
摘要: The present invention relates to novel, non-secosteroidal, phenyl-benzofuran compounds with vitamin D receptor (VDR) modulating activity that are less hypercalcemic than 1α,25 dihydroxy vitamin D3. These compounds are useful for treating bone disease and psoriasis.
摘要翻译: 本发明涉及具有维生素D受体(VDR)调节活性的新颖非壬基苯基 - 苯并呋喃化合物,其比1α,25二羟基维生素D3低高钙血症。 这些化合物可用于治疗骨病和牛皮癣。
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7.2,6-Substituted chroman derivatives useful as beta-3 adrenoreceptor agonists 失效
标题翻译: 用作β-3肾上腺素受体激动剂的2,6-取代的苯并二氢吡喃衍生物公开(公告)号:US06660752B2
公开(公告)日:2003-12-09
申请号:US10131448
申请日:2002-04-22
申请人: Stephen J. O'Connor , Gaetan H. Ladouceur , William H. Bullock , Ann-Marie Campbell , Miao Dai , Robert Dally , Jacques Dumas , Holia N. Hatoum-Mokdad , Uday Khire , Wendy Lee , Qingjie Liu , Derek B. Lowe , Steven R. Magnuson , Ning Qi , Tatiana E. Shelekhin , Quanrong Shen , Roger A. Smith , Ming Wang
发明人: Stephen J. O'Connor , Gaetan H. Ladouceur , William H. Bullock , Ann-Marie Campbell , Miao Dai , Robert Dally , Jacques Dumas , Holia N. Hatoum-Mokdad , Uday Khire , Wendy Lee , Qingjie Liu , Derek B. Lowe , Steven R. Magnuson , Ning Qi , Tatiana E. Shelekhin , Quanrong Shen , Roger A. Smith , Ming Wang
IPC分类号: A61K3144
CPC分类号: C07D405/12 , C07D311/58 , C07D405/14 , C07D407/12 , C07D409/12 , C07D413/12 , C07D417/14
摘要: This invention relates to novel 2,6-substituted chroman derivatives which are useful in the treatment of beta-3 adrenoreceptor-mediated conditions.
摘要翻译: 本发明涉及可用于治疗β-3肾上腺素受体介导的病症的新的2,6-取代的苯并二氢吡喃衍生物。
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公开(公告)号:US20120322841A1
公开(公告)日:2012-12-20
申请号:US13490530
申请日:2012-06-07
申请人: Michael Gregory Bell , Paul J. Hoogestraat , Thomas Edward Mabry , Quanrong Shen , Ana Maria Escribano
发明人: Michael Gregory Bell , Paul J. Hoogestraat , Thomas Edward Mabry , Quanrong Shen , Ana Maria Escribano
IPC分类号: A61K31/416 , C07D231/56 , A61P13/12 , C07D231/54
CPC分类号: C07D231/54 , C07D231/56
摘要: The present invention provides aldosterone synthase inhibitors of the formula: intermediates, methods for their preparation, pharmaceutical preparations, and methods for their use.
摘要翻译: 本发明提供下式的醛固酮合成酶抑制剂:中间体,其制备方法,药物制剂及其使用方法。
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公开(公告)号:US07579488B2
公开(公告)日:2009-08-25
申请号:US10579563
申请日:2004-11-16
申请人: Jianliang Lu , Tianwei Ma , Sunil Nagpal , Quanrong Shen , Alan M. Warshawsky , Jason Matthew Ochoada , Ying Kwong Yee
发明人: Jianliang Lu , Tianwei Ma , Sunil Nagpal , Quanrong Shen , Alan M. Warshawsky , Jason Matthew Ochoada , Ying Kwong Yee
IPC分类号: C07D307/87 , C07D307/00
CPC分类号: C07D405/12 , C07D307/80 , C07D407/12
摘要: The present invention relates to novel, non-secosteroidal, phenyl-benzofuran compounds with vitamin D receptor (VDR) modulating activity that are less hypercalcemic than 1α,25 dihydroxy vitamin D3. These compounds are useful for treating bone disease and psoriasis.
摘要翻译: 本发明涉及具有维生素D受体(VDR)调节活性的新颖非壬基苯基 - 苯并呋喃化合物,其比1α,25二羟基维生素D3低高钙血症。 这些化合物可用于治疗骨病和牛皮癣。
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公开(公告)号:US07659296B2
公开(公告)日:2010-02-09
申请号:US11721676
申请日:2005-12-19
IPC分类号: A61K31/423 , C07D417/02 , C07D498/04 , C07D263/08
CPC分类号: C07D263/56
摘要: The present invention relates to novel, non-secosteroidal, phenyl-benzoxazole compounds of Formula (I) wherein the variables R, R′, RP, RP3, LP1, LP2, ZP, RB, RB′, LXB and ZXB are as hereinafter defined, their preparation, pharmaceutical compositions, and methods of use.
摘要翻译: 本发明涉及式(I)的新型非异构体苯基 - 苯并恶唑化合物,其中变量R,R',RP,RP3,LP1,LP2,ZP,RB,RB',LXB和ZXB如下文所定义 ,它们的制备,药物组合物和使用方法。
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