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[EN] SUBSTITUTED HETEROCYCLIC-PYRIDINONES AS HIV-1 NEF-HCK INHIBITORS<br/>[FR] PYRIDINONES HÉTÉROCYCLIQUES SUBSTITUÉES EN TANT QU'INHIBITEURS DE NEF-HCK DE VIH-1
申请人:SOUTHERN RES INST
公开号:WO2019126567A1
公开(公告)日:2019-06-27
Disclosed are heterocyclic-pyridinone analogs that are capable of inhibiting Nef-Hck and methods of treating viral infections such as, for example, HIV-1. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.
本发明揭示了一种杂环吡啶酮类似物,能够抑制Nef-Hck并治疗病毒感染,例如HIV-1。本摘要旨在作为特定领域搜索的扫描工具,不旨在限制本发明。
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Regioselectivity and stereoselectivity of electrophilic quaternization of substituted 2-allyl(2-cyclohexen-1-yl)thionicotinic acids to thiazolo[3,2-a]pyridinium salts
作者:A. M. Shestopalov、L. A. Rodinovskaya、Yu. A. Sharanin、V. P. Litvinov
DOI:10.1007/bf00499421
日期:1990.2
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作者:SHESTOPALOV, A. M.、RODINOVSKAYA, L. A.、SHARANIN, YU. A.、LITVINOV, V. P.
DOI:——
日期:——
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作者:ZAWISZA, T.、MALINKA, W.、JOKOBIEC, T.
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日期:——
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作者:ZAWISZA, T.、MALINKA, W.
DOI:——
日期:——