Scaffold Hopping in Discovery of HIV-1 Non-Nucleoside Reverse Transcriptase Inhibitors: From CH(CN)-DABOs to CH(CN)-DAPYs.

ABSTRACT: Scaffold hopping is a frequently-used strategy in the development of non-nucleoside reverse transcriptase inhibitors. Herein, CH(CN)-DAPYs were designed by hopping the cyano-methylene linker of our previous published CH(CN)-DABOs onto the etravirine (ETR). Eighteen CH(CN)-DAPYs were synthesized and evaluated for their anti-HIV activity. Most compounds exhibited promising activity against wild-type (WT) HIV-1. Compounds B4 (EC₅₀ = 6 nM) and B6 (EC₅₀ = 8 nM) showed single-digit nanomolar potency against WT HIV-1. Moreover, these two compounds had EC₅₀ values of 0.06 and 0.08 μM toward the K103N mutant, respectively, which were comparable to the reference efavirenz (EFV) (EC₅₀ = 0.08 μM). The preliminary structure-activity relationship

SUBMITTER: Li TT 

PROVIDER: S-EPMC7180830 | biostudies-literature | 2020 Mar

REPOSITORIES: biostudies-literature