Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12779/6110
Title: Synthesis, biological activity, and ADME properties of novel S-DABOs/N-DABOs as HIV reverse transcriptase inhibitors.
Authors: Botta, Maurizio 
Pagano, M
Franchi, L
Castagnolo, D
Schenone, S
Casaluce, G
Zamperini, Claudio
Dreassi, Elena 
Maga, G
Samuele, A
Gonzalo, E
Clotet, B
Esté, Ja
Botta, Maurizio 
Issue Date: 2012
Project: None 
Journal: CHEMMEDCHEM
Abstract: 
Previous studies aimed at exploring the SAR of C2-functionalized S-DABOs demonstrated that the substituent at this position plays a key role in the inhibition of both wild-type RT and drug-resistant enzymes, particularly the K103N mutant form. The introduction of a cyclopropyl group led us to the discovery of a potent inhibitor with picomolar activity against wild-type RT and nanomolar activity against many key mutant forms such as K103N. Despite its excellent antiviral profile, this compound suffers from a suboptimal ADME profile typical of many S-DABO analogues, but it could, however, represent a promising candidate as an anti-HIV microbicide. In the present work, a new series of S-DABO/N-DABO derivatives were synthesized to obtain additional SAR information on the C2-position and in particular to improve ADME properties while maintaining a good activity profile against HIV-1 RT. In vitro ADME properties (PAMPA permeation, water solubility, and metabolic stability) were also experimentally evaluated for the most interesting compounds to obtain a reliable indication of their plasma levels after oral administration.
Description: 
43816
URI: http://hdl.handle.net/20.500.12779/6110
ISSN: 1860-7187
DOI: 10.1002/cmdc.201200056
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