Abstract
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.
Original language | English (US) |
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Pages (from-to) | 7934-7937 |
Number of pages | 4 |
Journal | Journal of medicinal chemistry |
Volume | 52 |
Issue number | 24 |
DOIs | |
State | Published - Dec 24 2009 |
Externally published | Yes |
ASJC Scopus subject areas
- Molecular Medicine
- Drug Discovery