Abstract
Here, we show that novel 2-aryl-3-(4-adamantyl-thiazol-21,3-thiazolidin-4-one derivatives have a mixed- or fully competitive mechanism of inhibition towards HIV-1 Reverse Transcriptase with respect to the substrates of the reaction. Thus, they are interesting starting points for the development of novel NNRTIs with an uncommon mechanism of action.
Keywords: HIV-1 RT, HAART, NNRTIs, AIDS, Antiretroviral therapy, Enzyme kinetics
Letters in Drug Design & Discovery
Title: Novel Thiazolidinone Derivatives with an Uncommon Mechanism of Inhibition Towards HIV-1 Reverse Transcriptase
Volume: 7 Issue: 4
Author(s): Eleni Pitta, Emmanuele Crespan, Athina Geronikaki, Giovanni Maga and Alberta Samuele
Affiliation:
Keywords: HIV-1 RT, HAART, NNRTIs, AIDS, Antiretroviral therapy, Enzyme kinetics
Abstract: Here, we show that novel 2-aryl-3-(4-adamantyl-thiazol-21,3-thiazolidin-4-one derivatives have a mixed- or fully competitive mechanism of inhibition towards HIV-1 Reverse Transcriptase with respect to the substrates of the reaction. Thus, they are interesting starting points for the development of novel NNRTIs with an uncommon mechanism of action.
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Cite this article as:
Pitta Eleni, Crespan Emmanuele, Geronikaki Athina, Maga Giovanni and Samuele Alberta, Novel Thiazolidinone Derivatives with an Uncommon Mechanism of Inhibition Towards HIV-1 Reverse Transcriptase, Letters in Drug Design & Discovery 2010; 7 (4) . https://dx.doi.org/10.2174/157018010790945869
DOI https://dx.doi.org/10.2174/157018010790945869 |
Print ISSN 1570-1808 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-628X |
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