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N-sulfonylanthranilic acid derivatives as allosteric inhibitors of dengue viral RNA-dependent RNA polymerase.

Journal of medicinal chemistry (2009-12-18)
Zheng Yin, Yen-Liang Chen, Ravinder Reddy Kondreddi, Wai Ling Chan, Gang Wang, Ru Hui Ng, Joanne Y H Lim, Wan Yen Lee, Duraiswamy A Jeyaraj, Pornwaratt Niyomrattanakit, Daying Wen, Alex Chao, J Fraser Glickman, Hans Voshol, Dieter Mueller, Carsten Spanka, Sigmar Dressler, Shahul Nilar, Subhash G Vasudevan, Pei-Yong Shi, Thomas H Keller
RESUMEN

A novel class of compounds containing N-sulfonylanthranilic acid was found to specifically inhibit dengue viral polymerase. The structural requirements for inhibition and a preliminary structure-activity relationship are described. A UV cross-linking experiment was used to map the allosteric binding site of the compound on the viral polymerase.

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Sigma-Aldrich
4-Pyrazoleboronic acid pinacol ester, 97%
Sigma-Aldrich
3-Bromobenzenesulfonyl chloride, 96%