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pubmed-article:17950601pubmed:abstractTextThe previously discovered salicylhydrazide class of compounds displayed potent HIV-1 integrase (IN) inhibitory activity. The development of this class of compounds as antiretroviral agents was halted due to cytotoxicity in the nanomolar to sub-micromolar range. We identified a novel class of non-cytotoxic hydrazide IN inhibitors utilizing the minimally required salicylhydrazide substructure as a template in a small-molecule database search. The novel hydrazides displayed low micromolar IN inhibitory activity and are several hundred-fold less cytotoxic than previously disclosed salicylhydrazide IN inhibitors.lld:pubmed
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pubmed-article:17950601pubmed:year2007lld:pubmed
pubmed-article:17950601pubmed:articleTitleDiscovery of novel non-cytotoxic salicylhydrazide containing HIV-1 integrase inhibitors.lld:pubmed
pubmed-article:17950601pubmed:affiliationDepartment of Pharmacology and Pharmaceutical Sciences, School of Pharmacy, University of Southern California, Los Angeles, CA 90089, USA.lld:pubmed
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