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公开(公告)号:EP0482797A1
公开(公告)日:1992-04-29
申请号:EP91309304.3
申请日:1991-10-09
申请人: MERCK & CO. INC.
发明人: Balani, Suresh Kuman , Schwartz, Michael S. , Pitzenberger, Steven M. , Lu, Anthony Y.H. , Ramjit, Harri G.
IPC分类号: C07D295/08 , C07K1/06 , C07K5/02 , A61K37/64
CPC分类号: C07D295/088 , C07C2602/08
摘要: Novel dipeptide isosteres are the biotransformed products after incubation with rat liver slices. They inhibit HIV protease, and are useful in the prevention or treatment of infection by HIV and the treatment of AIDS, either as compounds, pharmaceutically acceptable salts (when appropriate), pharmaceutical composition ingredients, whether or not in combination with other antivirals, anti-infectives, immunomodulators, antibiotics or vaccines. Methods of treating AIDS and methods of preventing or treating infection by HIV are also described.
摘要翻译: 新型二肽等位基因是与大鼠肝切片孵育后的生物转化产物。 它们抑制HIV蛋白酶,可用于预防或治疗艾滋病毒和艾滋病感染,作为化合物,药学上可接受的盐(如适用),药物组合物成分,无论是否与其他抗病毒药物组合, 感染性,免疫调节剂,抗生素或疫苗。 还描述了治疗AIDS的方法和预防或治疗HIV感染的方法。
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公开(公告)号:EP0481802A1
公开(公告)日:1992-04-22
申请号:EP91309618.6
申请日:1991-10-17
申请人: MERCK & CO. INC.
发明人: Chen, Shieh-Shung Tom , Hsu, Annjia , Doss, George A. , Goldman, Mark E. , Balani, Suresh K. , Theoharides, Anthony D. , Hoffman, Jacob M., Jr. , Pitzenberger, Steven M. , Ramjit, Harri G. , Kauffman, Laura R. , Arison, Byron H. , Saari, Walfred S. , Rooney, Clarence S. , Wai, John S.
IPC分类号: C07D413/12 , C07D413/06 , C07D213/64 , C07D213/70 , C07D213/73 , A61K31/44
CPC分类号: C07D213/74 , C07D401/12 , C07D413/10 , C12P17/12 , C12P17/16
摘要: Novel biotransformed or synthetic hydroxy pyridinones inhibit HIV reverse transcriptase, and are useful in the prevention or treatment of infection by HIV and the treatment of AIDS, either as compounds, pharmaceutically acceptable salts (where appropriate), pharmaceutical composition ingredients, whether or not in combination with other antivirals, anti-infectives, immunomodulators, antibiotics or vaccines. Methods of treating AIDS and methods of preventing or treating infection by HIV are also described.
摘要翻译: 新型生物转化或合成的羟基吡啶酮抑制HIV逆转录酶,可用于预防或治疗艾滋病毒和艾滋病感染,作为化合物,药学上可接受的盐(如适用),药物组合物成分,无论是否组合 与其他抗病毒药,抗感染药,免疫调节剂,抗生素或疫苗。 还描述了治疗AIDS的方法和预防或治疗HIV感染的方法。
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