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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: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: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:US07217726B2
公开(公告)日:2007-05-15
申请号:US10469648
申请日:2003-08-21
申请人: Shiv Kumar Agarwal , Mrinal Kanti Guha , Surendrakumar Satyanarayan Pandey , Matte Marianna Samuel
发明人: Shiv Kumar Agarwal , Mrinal Kanti Guha , Surendrakumar Satyanarayan Pandey , Matte Marianna Samuel
IPC分类号: C07D413/10 , A61K31/422
CPC分类号: C07D263/20 , C07D413/12
摘要: The present invention provides novel compounds of the general formula (I), their derivatives, their analogs, their tautomeric forms, their stereoisomers, their polymorphs, their hydrates, their solvates, their pharmaceutically acceptable salts and pharmaceutically acceptable compositions containing them. 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,它们的衍生物,它们的类似物,它们的互变异构形式,它们的立体异构体,它们的多晶型物,它们的水合物,它们的溶剂合物,它们的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)的新的恶唑烷酮衍生物,
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