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• W1990789059 abstract "With the U.S. Food and Drug Administration approval of raltegravir (RAL; MK-0518; Merck & Co.), HIV-1 integrase (IN) is the newest therapeutic target for AIDS and HIV infections. Recent structural analyses show that IN strand transfer inhibitors (INSTIs) share a common binding mode in the enzyme active site. While RAL represents a therapeutic breakthrough, the emergence of IN resistance mutations imposes the development of new INSTIs. We report here the biochemical and antiviral activities of MK-0536, a new IN inhibitor. We demonstrate that, like RAL, MK-0536 is highly potent against recombinant IN and viral replication. It is also effective against INs that carry the three main RAL resistance mutations (Y143R, N155H, and to a lesser extent G140S-Q148H) and against the G118R mutant. Modeling of IN developed from recent prototype foamy virus structures is presented to account for the differences in the drug activities of MK-0536 and RAL against the IN mutants." @default.
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• W1990789059 date "2011-11-01" @default.
• W1990789059 modified "2023-10-14" @default.
• W1990789059 title "MK-0536 Inhibits HIV-1 Integrases Resistant to Raltegravir" @default.
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• W1990789059 doi "https://doi.org/10.1128/aac.05288-11" @default.
• W1990789059 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3195008" @default.
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