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公开(公告)号:US09353101B2
公开(公告)日:2016-05-31
申请号:US14398165
申请日:2013-04-26
发明人: John J. Acton, III , Feng Ye , Petr Vachal , Deyou Sha , James F. Dropinski , Lin Chu , Debra Ondeyka , Alexander J. Kim , Vincent J. Colandrea , Yi Zang , Fengqi Zhang , Guizhen Dong
IPC分类号: C07D417/14 , C07D413/14 , A61K31/506 , A61K31/5377 , A61K31/444 , A61K45/06
CPC分类号: C07D417/14 , A61K31/444 , A61K31/506 , A61K31/5377 , A61K45/06 , C07D413/14
摘要: Compounds having the structure of Formula I, including pharmaceutically acceptable salts of the compounds, are CETP inhibitors and may be useful for raising HDL-cholesterol and reducing LDL-cholesterol in human patients and for treating or preventing atherosclerosis.
摘要翻译: 具有式I结构的化合物,包括化合物的药学上可接受的盐,是CETP抑制剂,可用于提高人类患者的HDL-胆固醇和降低LDL-胆固醇,并用于治疗或预防动脉粥样硬化。
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公开(公告)号:US20150111866A1
公开(公告)日:2015-04-23
申请号:US14398165
申请日:2013-04-26
发明人: John J. Acton, III , Feng Ye , Petr Vachal , Deyou Sha , James F. Dropinski , Lin Chu , Debra Ondeyka , Alexander J. Kim , Vincent J. Colandrea , Yi Zang , Fengqi Zhang , Guizhen Dong
IPC分类号: C07D417/14 , A61K45/06 , A61K31/5377 , A61K31/444 , C07D413/14 , A61K31/506
CPC分类号: C07D417/14 , A61K31/444 , A61K31/506 , A61K31/5377 , A61K45/06 , C07D413/14
摘要: Compounds having the structure of Formula I, including pharmaceutically acceptable salts of the compounds, are CETP inhibitors and may be useful for raising HDL-cholesterol and reducing LDL-cholesterol in human patients and for treating or preventing atherosclerosis.
摘要翻译: 具有式I结构的化合物,包括化合物的药学上可接受的盐,是CETP抑制剂,可用于提高人类患者的HDL-胆固醇和降低LDL-胆固醇,并用于治疗或预防动脉粥样硬化。
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公开(公告)号:US10214554B2
公开(公告)日:2019-02-26
申请号:US15427674
申请日:2017-02-08
发明人: John Y. L. Chung , Amude Kassim , John Limanto , Michael Shevlin , Peter E. Maligres , Daniel A. DiRocco , James F. Dropinski , Rose Mathew , Yi Ning Ji Chen , Edward C. Sherer , Mikhail Reibarkh , Artis Klapars , Alan Hyde , Susan L. Zultanski , Aaron Moment , Bryon Simmons , Tyler A. Davis , Timothy James Wright , Ralph Calabria , Louis charles Campeau
IPC分类号: C07H19/00 , C07H19/048 , C07H19/10 , C07H19/06 , C07H19/24 , C07D487/04
摘要: The present invention is directed to a process for making Chloro-Substituted Nucleoside Phosphoramidate Compounds of formula (I): which are useful for the treatment and prophylaxis of HCV infection. The present invention is also directed to compounds that are useful as synthetic intermediates for making the compounds of formula (I).
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