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- W1994834807 abstract "HIV is the most significant risk factor for many opportunistic infections like tuberculosis. In this study, we designed an isatinimino lead compound as a novel non-nucleoside reverse transcriptase inhibitor with antimycobacterial properties for the effective treatment of AIDS and AIDS-related tuberculosis. Among the compounds sythesized, 1-cyclopropyl-6-fluoro-8-methoxy-1,4-dihydro-4-oxo-7[[N4-[3'-[(4,6-dimethylpyrimidin-2-yl)benzenesulfonamido-4-yl]imino-1'-(5-fluoroisatinyl)]methyl]-3-methyl N1-piperazinyl]-3-quinoline carboxylic acid (9) emerged as the most potent broad-spectrum chemotherapeutic agent active against HIV (EC50: 12.1 microg/ml), and Mycobacterium tuberculosis (MIC: 1.22 microg/ml)." @default.
- W1994834807 created "2016-06-24" @default.
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- W1994834807 date "2006-07-18" @default.
- W1994834807 modified "2023-09-26" @default.
- W1994834807 title "Synthesis, anti-HIV and Antitubercular Activities of Isatin Derivatives." @default.
- W1994834807 doi "https://doi.org/10.1002/chin.200629154" @default.
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