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Optimization of pyrimidinyl- and triazinyl-amines as non-nucleoside inhibitors of HIV-1 reverse transcriptase. 2006
Vinay V Thakur, and
Joseph T Kim, and
Andrew D Hamilton, and
Christopher M Bailey, and
Robert A Domaoal, and
Ligong Wang, and
Karen S Anderson, and
William L Jorgensen
Department of Chemistry, Yale University, New Haven, CT 06520-8107, USA.
Non-nucleoside inhibitors of HIV-1 reverse transcriptase are being pursued through synthesis and assaying for anti-viral activity. Following computational analyses, the focus has been on the motif Het-NH-Ph-U, where Het is an aromatic heterocycle and U is an unsaturated, hydrophobic group. Previous investigations with Het=2-thiazoyl and 2-pyrimidinyl are extended here to triazinyl derivatives. The result is several NNRTIs in the 2-20 nM range with negligible cytotoxicity and auspicious predicted pharmacological properties.
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