Discovery of diarylpyrimidine derivatives bearing piperazine sulfonyl as potent HIV-1 nonnucleoside reverse transcriptase inhibitors

HIV-1 reverse transcriptase is one of the most attractive targets for the treatment of AIDS. However, the rapid emergence of drug-resistant strains and unsatisfactory drug-like properties seriously limit the clinical application of HIV-1 non-nucleoside reverse transcriptase inhibitors (NNRTIs). Here we show that a series of piperazine sulfonyl-bearing diarylpyrimidine-based NNRTIs were designed to improve the potency against wild-type and NNRTI-resistant strains by enhancing backbone-binding interactions. Among them, compound 18b1 demonstrates single-digit nanomolar potency against the wild-type and five mutant HIV-1 strains, which is significantly better than the approved drug etravirine. The co-crystal structure analysis and molecular dynamics simulation studies were conducted to explain the broad-spectrum inhibitory activity of 18b1 against reverse transcriptase variants. Besides, compound 18b1 demonstrates improved water solubility, cytochrome P450 liability, and other pharmacokinetic properties compared to the currently approved diarylpyrimidine (DAPY) NNRTIs. Therefore, we consider compound 18b1 a potential lead compound worthy of further study. Non-nucleoside reverse transcriptase inhibitors (NNRTIs) exhibit promising anti-HIV-1 activities, however, their effectiveness is limited by drug resistant mutations, low solubility, and drug-drug interactions. Here, the authors develop a series of piperazine sulfonyl-bearing diarylpyrimidine based NNRTIs which show improved potency against HIV-1 by enhancing backbone-binding interactions.

Automated summary

The authors developed a series of piperazine sulfonyl-bearing diarylpyrimidine-based non-nucleoside reverse transcriptase inhibitors (NNRTIs) that have improved potency against HIV-1 by enhancing backbone-binding interactions. Compound 18b1 demonstrated high potency against multiple strains of HIV-1, including drug-resistant strains, and showed better pharmacokinetic properties compared to currently approved NNRTIs. This compound is considered a potential lead compound for further study.