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May 3, 2010Journal of Medicinal Chemistry228 citations

Crystal Structures of HIV-1 Reverse Transcriptase with Etravirine (TMC125) and Rilpivirine (TMC278): Implications for Drug Design

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ELE.B. LansdonGilead Sciences (United Kingdom)KBKatherine M. BrendzaGilead Sciences (United States)MHMagdeleine HungGilead Sciences (United States)

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Abstract

Diarylpyrimidine (DAPY) non-nucleoside reverse transcriptase inhibitors (NNRTIs) have inherent flexibility, helping to maintain activity against a wide range of resistance mutations. Crystal structures were determined with wild-type and K103N HIV-1 reverse transcriptase with etravirine (TMC125) and rilpivirine (TMC278). These structures reveal a similar binding mode for TMC125 and TMC278, whether bound to wild-type or K103N RT. Comparison to previously published structures reveals differences in binding modes for TMC125 and differences in protein conformation for TMC278.

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Cite This Study

Lansdon et al. (2010) studied this question.

synapsesocial.com/papers/6a1fed367110a651dc04b77ehttps://doi.org/10.1021/jm1002233
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