A novel mechanism for inhibition of HIV-1 reverse transcriptase

The human immunodeficiency virus (HIV) epidemic is an important medical problem. Although combination drug regimens have produced dramatic decreases in viral load, current therapies do not provide a cure for HIV infection. We have used structure- based design and combinatorial medicinal chemistry to identify potent and selective HIV-1 reverse transcriptase (RT) inhibitors that may work by a mechanism distinct from that of current HIV drugs. The most potent of these compounds (compound 4, 2-naphthalenesulfonic acid, 4-hydroxy-7-[[[[5-hydroxy-6-[(4- cinnamylphenyl)-azo]-7-sulfo-2- naphthalenyl]amino]carbonyl]amino]-3-[(4-cinnamylphenyl)- azo], disodium salt) has an IC50 of 90 nM for inhibition of polymerase chain extension, a K-d of 40 nM for inhibition of DNA-RT binding, and an IC50 of 25-100 nM for inhibition of RNaseH cleavage. The parent compound (1) was as effective against 10 nucleoside and non-nucleoside resistant HIV-1 RT mutants as it was against the wild-type enzyme. Compound 4 inhibited HIV-1 RT and murine leukemia virus (MLV) RT, but it did not inhibit T-4 DNA polymerase, T-7 DNA polymerase, or the Klenow fragment at concentrations up to 200 nM. Finally, compound 4 protected cells from HIV-1 infection at a concentration more than 40 times lower than the concentration at which it caused cellular toxicity. (C) 2002 Elsevier Science (USA). All rights reserved.

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