FEP-Guided Selection of Bicyclic Heterocycles in Lead Optimization for Non-Nucleoside Inhibitors of HIV-1 Reverse Transcriptase
Journal of the American Chemical Society2006Vol. 128(48), pp. 15372–15373
Citations Over TimeTop 13% of 2006 papers
Joseph T. Kim, Andrew D. Hamilton, Christopher M. Bailey, Robert A. Domoal, Ligong Wang, Karen S. Anderson, William L. Jorgensen
Abstract
Monte Carlo simulations using free energy perturbation theory have been used to guide the selection of bicyclic heterocycles in the lead optimization of non-nucleoside inhibitors of HIV-1 reverse transcriptase (NNRTIs). Good correlation is found between predicted and observed activities. Six compounds are reported with EC50 values below 20 nM for protection of human MT-2 cells against the cytopathogenicity of HIV-1. Striking variation in activity is found and analyzed for an isomeric pyrrolopyrimidine and pyrrolopyrazine pair.
Related Papers
- → Lipodystrophy and metabolic changes in HIV-infected children on non-nucleoside reverse transcriptase inhibitor-based antiretroviral therapy(2007)70 cited
- → Comparison of the induction of P-glycoprotein activity by nucleotide, nucleoside, and non-nucleoside reverse transcriptase inhibitors(2007)57 cited
- → Time to discontinuation of the first highly active antiretroviral therapy regimen: a comparison between protease inhibitor- and non-nucleoside reverse transcriptase inhibitor-containing regimens(2001)41 cited
- → Etravirine: Clinical review of a treatment option for HIV type-1-infected patients with non-nucleoside reverse transcriptase inhibitor resistance(2010)8 cited
- [Antiretroviral therapy. NNRTI (non-nucleoside reverse transcriptase inhibitor)].(2000)