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. 2005 Apr;12(4):439-44.
doi: 10.1016/j.chembiol.2005.02.004.

Switching between allosteric and dimerization inhibition of HIV-1 protease

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Switching between allosteric and dimerization inhibition of HIV-1 protease

Michael J Bowman et al. Chem Biol. 2005 Apr.

Abstract

Refining the functional groups on a phenethylamine moiety within an inhibitor of HIV-1 protease led to a switch in the mechanism of inhibition from competitive and allosteric to dimerization inhibition. Phenylether extensions to the phenethylamine group led to agents that target the dimerization interface of HIV-1 protease with high potency.

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