Synthesis, structure–activity relationship and molecular docking of cyclohexenone based analogous as potent non-nucleoside reverse-transcriptase inhibitors-Reference-Cited by-同舟云学术

Synthesis, structure–activity relationship and molecular docking of cyclohexenone based analogous as potent non-nucleoside reverse-transcriptase inhibitors

Published:2015-04 Issue: Volume:1086 Page:8-16
ISSN:0022-2860
Container-title:Journal of Molecular Structure
language:en
Short-container-title:Journal of Molecular Structure

Author:

Nazar Muhammad Faizan,Abdullah Muhammad Imran,Badshah Amir,Mahmood Asif,Rana Usman Ali,Khan Salah Ud-Din

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Spectroscopy,Analytical Chemistry

Reference47 articles.

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2. Antiviral Drug Resistance: Mechanisms and Clinical Implications

3. Design, Synthesis, and Biological Evaluation of 1-[(2-Benzyloxyl/alkoxyl)methyl]-5-halo-6-aryluracils as Potent HIV-1 Non-nucleoside Reverse Transcriptase Inhibitors with an Improved Drug Resistance Profile

4. Inhibitors of HIV- I reverse transcriptase

5. Potent Inhibition of HIV-1 Reverse Transcriptase and Replication by Nonpseudoknot, “UCAA-motif” RNA Aptamers

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