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公开(公告)号:US20100305174A1
公开(公告)日:2010-12-02
申请号:US11918235
申请日:2006-04-12
申请人: Surendrakumar Satyanarayan Pandey , Gadam Om Reddy , Shiv Kumar Agarwal , Gajendra Singh , Santhanagopalan Chithra , Debendranath Dey , Abhijeet Nag , Kadnur Venkatachalapathi Sanjay
发明人: Surendrakumar Satyanarayan Pandey , Gadam Om Reddy , Shiv Kumar Agarwal , Gajendra Singh , Santhanagopalan Chithra , Debendranath Dey , Abhijeet Nag , Kadnur Venkatachalapathi Sanjay
IPC分类号: A61K31/427 , C07D417/12 , C07D413/12 , A61K31/422 , A61P3/10 , A61P3/06 , A61P3/04 , A61P37/00 , A61P29/00 , A61P35/00
CPC分类号: C07D413/12 , C07D417/12
摘要: The present invention relates to novel heterocyclic derivatives of formula (I) and their pharmaceutically acceptable salts, their derivatives, their analogs, their tautomeric forms, their stereoisomers, their polymorphs, their hydrates, their solvates, their pharmaceutically acceptable salts, their pharmaceutical compositions, and their prodrugs thereof. The present invention more particularly provides novel compounds of the general formula (1).
摘要翻译: 本发明涉及式(I)的新型杂环衍生物及其药学上可接受的盐,其衍生物,其类似物,其互变异构形式,其立体异构体,它们的多晶型物,它们的水合物,它们的溶剂合物,其药学上可接受的盐,其药物组合物, 及其前药。 本发明更具体地提供了通式(1)的新型化合物。
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公开(公告)号:US20080319031A1
公开(公告)日:2008-12-25
申请号:US11886460
申请日:2006-03-10
申请人: Surendrakumar Satyanarayan Pandey , Shiv Kumar Agarwal , Gajendra Singh , Santhanagopalan Chithra , Sangmesh Badiger , Bishwajit Nag , Debendranath Dey , Abhijeet Nag , Partha Neogi
发明人: Surendrakumar Satyanarayan Pandey , Shiv Kumar Agarwal , Gajendra Singh , Santhanagopalan Chithra , Sangmesh Badiger , Bishwajit Nag , Debendranath Dey , Abhijeet Nag , Partha Neogi
IPC分类号: A61K31/428 , A61P3/00 , A61P29/00 , A61P37/00 , A61P35/00 , A61P3/04 , C07D209/32 , C07D277/68 , A61K31/404
CPC分类号: C07D209/34 , C07D277/68
摘要: The present invention relates to novel tyrosine derivatives of formula (I), their pharmaceutically acceptable salts and pharmaceutically acceptable compositions containing them. The present invention more particularly provides novel tyrosine derivatives of the general formula (I).
摘要翻译: 本发明涉及式(I)的新型酪氨酸衍生物,其药学上可接受的盐和含有它们的药学上可接受的组合物。 本发明更具体地提供了通式(I)的新型酪氨酸衍生物。
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公开(公告)号:US07521465B2
公开(公告)日:2009-04-21
申请号:US11096718
申请日:2005-03-31
申请人: Bishwajit Nag , Abhijeet Nag , Debendranath Dey , Shiv Kumar Agarwal , Partha Neogi , Gaddam Om Reddy , Sangamesh Badiger , Gajendra Singh , Surendra Kumar Pandey , Santhanagopalan Chithra
发明人: Bishwajit Nag , Abhijeet Nag , Debendranath Dey , Shiv Kumar Agarwal , Partha Neogi , Gaddam Om Reddy , Sangamesh Badiger , Gajendra Singh , Surendra Kumar Pandey , Santhanagopalan Chithra
IPC分类号: A61K31/426 , A61K31/421
CPC分类号: C07D277/20 , A61K31/4164 , A61K31/421 , A61K31/426 , C07D277/34 , C07D277/36
摘要: Novel diphenyl ether derivatives are provided that exhibit activity useful for reducing glucose, cholesterol, and/or triglyceride levels in plasma, and for treatment of obesity, inflammation, immunological diseases, autoimmune diseases, diabetes and disorders associated with insulin resistance.
摘要翻译: 提供新的二苯醚衍生物,其显示可用于降低血浆中的葡萄糖,胆固醇和/或甘油三酯水平的活性,以及用于治疗肥胖,炎症,免疫疾病,自身免疫性疾病,糖尿病和与胰岛素抵抗相关的疾病。
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公开(公告)号:US20080267888A1
公开(公告)日:2008-10-30
申请号:US11920719
申请日:2006-05-25
申请人: Surendrakumar Satyanarayan Pandey , Gaddam Om Reddy , Gajendra Singh , Chitra Santhanagopalan , Sanjay Venkatachalapathi Kadnur , Debendranath Dey , Abhijeet Nag
发明人: Surendrakumar Satyanarayan Pandey , Gaddam Om Reddy , Gajendra Singh , Chitra Santhanagopalan , Sanjay Venkatachalapathi Kadnur , Debendranath Dey , Abhijeet Nag
IPC分类号: A61K9/12 , C07D417/12 , A61K31/5377 , A61P29/00 , C07D413/12
CPC分类号: C07D417/12 , C07D413/12
摘要: The present invention relates to novel heterocyclic derivatives of the general formula (I), their pharmaceutically acceptable salts and compositions, their analogs, their tautomeric forms, and their stereoisomers. The present invention more particularly provides novel compounds of the general formula (I).
摘要翻译: 本发明涉及通式(I)的新型杂环衍生物,其药学上可接受的盐和组合物,它们的类似物,它们的互变异构形式及其立体异构体。 本发明更具体地提供了通式(I)的新型化合物。
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公开(公告)号:US20050288341A1
公开(公告)日:2005-12-29
申请号:US11096718
申请日:2005-03-31
申请人: Bishwajit Nag , Abhijeet Nag , Debendranath Dey , Shiv Agarwal , Partha Neogi , Gaddam Reddy , Sangamesh Badiger , Gajendra Singh , Surendra Pandey , Santhanagopalan Chithra
发明人: Bishwajit Nag , Abhijeet Nag , Debendranath Dey , Shiv Agarwal , Partha Neogi , Gaddam Reddy , Sangamesh Badiger , Gajendra Singh , Surendra Pandey , Santhanagopalan Chithra
IPC分类号: A61K31/4164 , A61K31/421 , A61K31/426
CPC分类号: C07D277/20 , A61K31/4164 , A61K31/421 , A61K31/426 , C07D277/34 , C07D277/36
摘要: Novel diphenyl ether derivatives are provided that exhibit activity useful for reducing glucose, cholesterol, and/or triglyceride levels in plasma, and for treatment of obesity, inflammation, immunological diseases, autoimmune diseases, diabetes and disorders associated with insulin resistance.
摘要翻译: 提供新的二苯醚衍生物,其显示可用于降低血浆中的葡萄糖,胆固醇和/或甘油三酯水平的活性,以及用于治疗肥胖,炎症,免疫疾病,自身免疫性疾病,糖尿病和与胰岛素抵抗相关的疾病。
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公开(公告)号:US20090082408A1
公开(公告)日:2009-03-26
申请号:US11914484
申请日:2006-05-18
申请人: Surendrakumar Satyanarayan Pandey , Gajendra Singh , Kadnur Venkatachalapathi Sanjay , Bishwajit Nag
发明人: Surendrakumar Satyanarayan Pandey , Gajendra Singh , Kadnur Venkatachalapathi Sanjay , Bishwajit Nag
IPC分类号: A61K31/4402 , C07D211/72 , A61P35/00
CPC分类号: C07D213/74 , C07D213/85
摘要: The present invention relates to novel heterocyclic derivatives of the general formula (I), their pharmaceutically acceptable salts, and their pharmaceutical compositions. The present invention more particularly provides novel compounds of the general formula (I).
摘要翻译: 本发明涉及通式(I)的新型杂环衍生物,其药学上可接受的盐及其药物组合物。 本发明更具体地提供了通式(I)的新型化合物。
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公开(公告)号:US20090131420A1
公开(公告)日:2009-05-21
申请号:US11992951
申请日:2006-09-27
申请人: Surendrakumar S. Pandey , Gajendra Singh , Santhanagopalan Chithra , Gaddam O. Reddy , Somasundaram Sangeetha , Debendranath Dey
发明人: Surendrakumar S. Pandey , Gajendra Singh , Santhanagopalan Chithra , Gaddam O. Reddy , Somasundaram Sangeetha , Debendranath Dey
IPC分类号: A61K31/5377 , C07D413/10 , A61P37/02 , A61P3/10
CPC分类号: C07D413/12
摘要: The present invention relates to novel compounds of formula (I) and their pharmaceutically acceptable salts and compositions. The present invention more particularly provides novel heterocyclic analogs of biphenyl ethers of the general formula (I).
摘要翻译: 本发明涉及新的式(I)化合物及其药学上可接受的盐和组合物。 本发明更具体地提供了通式(I)的联苯醚的新型杂环类似物。
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公开(公告)号:US20090203744A1
公开(公告)日:2009-08-13
申请号:US11997064
申请日:2006-07-28
申请人: Surendrakumar Satyanarayan Pande y , Gaddam Om Reddy , Gajendra Singh , Santhanagopalan Chithra , Jeganath Sivakumar , Venkatachalapathi Sanjay Kadnur , Debendranath Dey
发明人: Surendrakumar Satyanarayan Pande y , Gaddam Om Reddy , Gajendra Singh , Santhanagopalan Chithra , Jeganath Sivakumar , Venkatachalapathi Sanjay Kadnur , Debendranath Dey
IPC分类号: A61K31/4439 , C07D413/12
CPC分类号: C07D413/12
摘要: The present invention relates to novel pyridine derivatives of the formula (I), their stereoisomers, and their pharmaceutically acceptable salts, and compositions. The present invention more particularly provides novel pyridine derivatives of the general formula (I).
摘要翻译: 本发明涉及式(I)的新型吡啶衍生物,其立体异构体及其药学上可接受的盐和组合物。 本发明更具体地提供了通式(I)的新型吡啶衍生物。
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公开(公告)号:US20050203102A1
公开(公告)日:2005-09-15
申请号:US11074637
申请日:2005-03-09
IPC分类号: A61K31/496 , C07D263/20 , C07D413/12 , C07D413/14 , C07D417/12 , C07D417/14
CPC分类号: C07D263/20 , C07D413/12 , C07D417/12
摘要: The present invention provides novel compounds of the general formula (I) and their pharmaceutically acceptable salts. The present invention more particularly provides novel oxazolidinone derivatives of the general formula (I).
摘要翻译: 本发明提供了通式(I)的新化合物及其药学上可接受的盐。 本发明更具体地提供了通式(I)的新的恶唑烷酮衍生物。
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公开(公告)号:US20090069313A1
公开(公告)日:2009-03-12
申请号:US11896902
申请日:2007-09-06
IPC分类号: A61K31/5377 , C07D277/16 , A61K31/426 , C07D209/34 , A61P25/24 , A61P25/32 , A61P25/08 , A61P25/00 , A61P25/34 , A61P25/28 , A61K31/404 , C07D413/12 , A61K31/422
CPC分类号: C07D277/36 , C07D209/34 , C07D277/34 , C07D413/12 , C07D417/12
摘要: The present invention provides a new medical use for the compounds of the formula (I), their derivatives, analogs, tautomeric forms, stereoisomers, polymorphs, hydrates, solvates, pharmaceutically acceptable salts and compositions, metabolites and prodrugs thereof, as MAO-A inhibitors. Also included is a method for prophylaxis and treatment of mental disorders such as depression, in a mammal, comprising administering an effective amount of a compound of formula (I). These compounds are also effective in treating a disease, condition or disorder such as weight loss, obesity, bulimia, depression, bipolar disorders, psychoses, schizophrenia, behaviors, alcoholism, tobacco abuse, memory loss, Alzheimer's disease, dementia of aging, seizure disorders, epilepsy, attention deficit disorder, and Parkinson's disease, which is modulated by a cannabinoid receptor antagonist.
摘要翻译: 本发明提供了作为MAO-A抑制剂的式(I)化合物,其衍生物,类似物,互变异构形式,立体异构体,多晶型物,水合物,溶剂合物,药学上可接受的盐和组合物,其代谢物和前药的新医学用途 。 还包括在哺乳动物中预防和治疗精神障碍如抑郁症的方法,包括施用有效量的式(I)化合物。 这些化合物在治疗疾病,病症或病症如体重减轻,肥胖,贪食症,抑郁症,双相性精神障碍,精神病,精神分裂症,行为,酒精中毒,吸烟,记忆丧失,阿尔茨海默病,老年痴呆,癫痫发作障碍 ,癫痫,注意力缺陷障碍和由大麻素受体拮抗剂调节的帕金森病。
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