Rational design of dually active inhibitors against human immunodeficiency virus (HIV) reverse transcriptase (RT) and integrase (IN) has proved viable with 1-[(2-hydroxyethoxy) methyl]-6-(phenylthio) thymine (HEPT) type of non-nucleoside RT inhibitors (NNRTIs). To establish the pharmacophore and study the structure–activity relationships (SAR) of integrase inhibition within a previously disclosed RT/IN dual inhibitor scaffold, new ...
[Pieck, J. Carsten; Kuch, David; Grolle, Friederike; Linne, Uwe; Haas, Clemens; Carell, Thomas Journal of the American Chemical Society, 2006 , vol. 128, # 5 p. 1404 - 1405]