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公开(公告)号:US20080090865A1
公开(公告)日:2008-04-17
申请号:US11794591
申请日:2006-01-24
申请人: Min Ge , Lihu Yang , Changyou Zhou , Songnian Lin , Eric Cline
发明人: Min Ge , Lihu Yang , Changyou Zhou , Songnian Lin , Eric Cline
IPC分类号: A61K31/47 , A61K31/435 , A61P3/10 , C07D215/00 , C07D221/02
CPC分类号: C07D413/12 , C07D215/20 , C07D413/04 , C07D417/04 , C07D417/12
摘要: Bicyclic compounds containing a fused pyridine ring, including pharmaceutically acceptable salts and prodrugs thereof, are agonists of G-protein coupled receptor 40 (GPR40) and are useful as therapeutic compounds, particularly in the treatment of Type 2 diabetes mellitus, and of conditions that are often associated with this disease, including obesity and lipid disorders, such as mixed or diabetic dyslipidemia, hyperlipidemia, hypercholesterolemia, and hypertriglyceridemia.
摘要翻译: 含有稠合吡啶环的双环化合物,包括其药学上可接受的盐和前体药物,是G蛋白偶联受体40(GPR40)的激动剂,可用作治疗性化合物,特别是治疗2型糖尿病, 通常与该疾病有关,包括肥胖症和脂质疾病,例如混合或糖尿病性血脂异常,高脂血症,高胆固醇血症和高甘油三酯血症。
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32.Tetrahydropyranyl cyclopentyl tetrahydropyridopyridine modulators of chemokine receptor activity 有权
标题翻译: 趋化因子受体活性的四氢吡喃基环戊基四氢吡啶并吡啶调节剂公开(公告)号:US20050101628A1
公开(公告)日:2005-05-12
申请号:US10856012
申请日:2004-05-28
申请人: Richard Jiao , Gregori Morriello , Lihu Yang , Christopher Moyes , Changyou Zhou , Shankaran Kothandaraman
发明人: Richard Jiao , Gregori Morriello , Lihu Yang , Christopher Moyes , Changyou Zhou , Shankaran Kothandaraman
IPC分类号: C07D471/04 , A61P29/00 , C07D20060101 , A61K31/4745 , A61K31/195 , A61K31/325 , A61K31/35 , A61K31/40
CPC分类号: C07D471/04
摘要: The present invention is directed to compounds of the formula I: (wherein R1, R2, R3, R4, R5, R6, R7, R8, R9, R10, X, n and the dashed line are defined herein) which are useful as modulators of chemokine receptor activity. In particular, these compounds are useful as modulators of the chemokine receptor CCR-2. The present invention is also directed to intermediates useful in the preparation of formula I compounds.
摘要翻译: 本发明涉及式I化合物:其中R 1,R 2,R 3,R 4, R 5,R 6,R 7,R 8,R 9,R 9, / SUP>,R 10,X,n,虚线在本文中定义),其可用作趋化因子受体活性的调节剂。 特别地,这些化合物可用作趋化因子受体CCR-2的调节剂。 本发明还涉及可用于制备式I化合物的中间体。
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33.FUSED TETRA OR PENTA-CYCLIC PYRIDOPHTHALAZINONES AS PARP INHIBITORS 有权
标题翻译: 作为PARP抑制剂的FUSED TETRA或PENTA-CYCLIC PYRIDOPHTHALAZINONES公开(公告)号:US20150018356A1
公开(公告)日:2015-01-15
申请号:US14369388
申请日:2011-12-31
申请人: Changyou Zhou , Bo Ren , Hexiang Wang
发明人: Changyou Zhou , Bo Ren , Hexiang Wang
IPC分类号: C07D471/14 , C07D471/04
CPC分类号: C07D471/14 , C07D471/04 , C07D471/06 , C07D471/16
摘要: Provided are certain fused tetra or penta-cyclic compounds and salts thereof, compositions thereof, and methods of use thereof.
摘要翻译: 提供一些稠合的四或五环化合物及其盐,其组合物及其使用方法。
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34.Fused tetra or penta-cyclic dihydrodiazepinocarbazolones as PARP inhibitors 有权
标题翻译: 熔融的四环或五环二氢二氮杂咔唑酮作为PARP抑制剂公开(公告)号:US09260440B2
公开(公告)日:2016-02-16
申请号:US14369374
申请日:2011-12-31
申请人: Changyou Zhou , Bo Ren , Hexiang Wang
发明人: Changyou Zhou , Bo Ren , Hexiang Wang
IPC分类号: C07D487/06 , C07D487/14 , C07D487/04 , C07D471/16 , C07D471/22
CPC分类号: C07D487/06 , A61K31/551 , A61P29/00 , A61P35/00 , A61P37/00 , C07D471/16 , C07D471/22 , C07D487/04 , C07D487/14
摘要: Provided are certain fused tetra or penta-cyclic compounds and salts thereof, compositions thereof, and methods of use thereof.
摘要翻译: 提供一些稠合的四或五环化合物及其盐,其组合物及其使用方法。
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公开(公告)号:US09006433B2
公开(公告)日:2015-04-14
申请号:US13635275
申请日:2011-04-18
申请人: Changyou Zhou , Wuxin Zou , Yuxia Hua , Qun Dang
发明人: Changyou Zhou , Wuxin Zou , Yuxia Hua , Qun Dang
IPC分类号: A61K31/506 , C07D403/04 , C07D401/14 , C07D403/14 , C07D405/14
CPC分类号: C07D403/04 , C07D401/14 , C07D403/14 , C07D405/14
摘要: The present invention relates to substituted pyrimidines useful as HIF prolyl hydroxylase inhibitors to treat anemia and like conditions.
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公开(公告)号:US20160159820A1
公开(公告)日:2016-06-09
申请号:US14901556
申请日:2014-06-27
申请人: Changyou ZHOU , Guoliang ZHANG
发明人: Changyou Zhou , Gouliang Zhang
IPC分类号: C07D519/00 , C07D498/04 , C07D405/12 , C07D471/04
CPC分类号: C07D519/00 , C07D405/12 , C07D471/04 , C07D498/04
摘要: Provided are fused tricyclic amide compounds, pharmaceutical compositions comprising at least one such fused tricyclic compound, processes for the preparation thereof, and the use thereof in therapy. Disclosed herein are certain tricyclic amide compounds that can be useful for inhibiting multiple (specifically BRAF and/or EGFR-T790M) kinases and for treating disorders mediated thereby.
摘要翻译: 提供稠合三环酰胺化合物,包含至少一种这样的稠合三环化合物的药物组合物,其制备方法及其在治疗中的用途。 本文公开了可用于抑制多种(特别是BRAF和/或EGFR-T790M)激酶和用于治疗由此介导的病症的某些三环酰胺化合物。
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公开(公告)号:US09273046B2
公开(公告)日:2016-03-01
申请号:US14369379
申请日:2011-12-31
申请人: Changyou Zhou , Shaohui Wang , Guoliang Zhang
发明人: Changyou Zhou , Shaohui Wang , Guoliang Zhang
IPC分类号: C07D471/04 , C07D405/14 , C07D473/30 , C07D498/04 , C07D519/00
CPC分类号: A61K31/5365 , A61K31/437 , A61K31/4375 , A61K31/4439 , A61K31/506 , A61K31/52 , C07D405/14 , C07D471/04 , C07D473/30 , C07D498/04 , C07D519/00
摘要: Provided are certain fused tricyclic compounds and salts thereof, compositions thereof, and methods of use therefor.
摘要翻译: 提供某些稠合的三环化合物及其盐,其组合物及其用途。
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38.Substituted cycloocta[5,6]pyrido[4,3,2-de]phthalazines as PARP inhibitors 有权
标题翻译: 取代的环辛[5,6]吡啶并[4,3,2-de]酞嗪作为PARP抑制剂公开(公告)号:US09328111B2
公开(公告)日:2016-05-03
申请号:US14369388
申请日:2011-12-31
申请人: Changyou Zhou , Bo Ren , Hexiang Wang
发明人: Changyou Zhou , Bo Ren , Hexiang Wang
IPC分类号: A61K31/5025 , C07D237/26 , C07D471/14 , C07D471/06 , C07D471/16 , C07D471/04
CPC分类号: C07D471/14 , C07D471/04 , C07D471/06 , C07D471/16
摘要: The present invention provides a compound of Formula (I): wherein the variables Z, n, Y and p are as defined herein, and pharmaceutically acceptable salts thereof, which can inhibit the activity of poly (ADP-ribose)polymerases, and pharmaceutical compositions comprising the same.
摘要翻译: 本发明提供式(I)的化合物:其中变量Z,n,Y和p如本文所定义,及其药学上可接受的盐,其可以抑制聚(ADP-核糖)聚合酶的活性,以及药物组合物 包括它们。
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公开(公告)号:US20130018053A1
公开(公告)日:2013-01-17
申请号:US13635275
申请日:2011-04-18
申请人: Changyou Zhou , Wuxin Zou , Yuxia Hua , Qun Dang
发明人: Changyou Zhou , Wuxin Zou , Yuxia Hua , Qun Dang
IPC分类号: C07D403/04 , A61P7/06 , A61K31/506
CPC分类号: C07D403/04 , C07D401/14 , C07D403/14 , C07D405/14
摘要: The present invention relates to substituted pyrimidines useful as HIF prolyl hydroxylase inhibitors to treat anemia and like conditions.
摘要翻译: 本发明涉及用作HIF脯氨酰羟化酶抑制剂治疗贫血和类似病症的取代嘧啶。
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