| Literature DB >> 11425562 |
M L Barreca1, A Chimirri, L De Luca, A M Monforte, P Monforte, A Rao, M Zappalà, J Balzarini, E De Clercq, C Pannecouque, M Witvrouw.
Abstract
Design, synthesis and anti-HIV activity of a series of 2,3-diaryl-1,3-thiazolidin-4-ones are reported. Some derivatives proved to be highly effective in inhibiting HIV-1 replication at nanomolar concentrations thereby acting as non-nucleoside HIV-1 RT inhibitors (NNRTIs). SAR studies evidenced that the nature of the substituents at the 2 and 3 positions of the thiazolidinone nucleus largely influenced the in vitro anti-HIV activity of this new class of potent antiviral agents.Entities:
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Year: 2001 PMID: 11425562 DOI: 10.1016/s0960-894x(01)00304-3
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823