A NEW APPROACH TO ANTI-HIV CHEMOTHERAPY DEVISED BY LINKING THE VITAL FRAGMENTS OF ACTIVE RT INHIBITORS SUCH AS ETRAVIRINE TO THE MOLECULAR FRAMEWORK OF ANTI-HIV PRONE PRIVILEGED NUCLEUS OF 1,4-BENZODIAZEPINE AS POSSIBLE SUBSTITUTE TO 'HAART'

Authors

  • NAVJEET KAUR Department of Chemistry, Banasthali University, Banasthali-304022 (Rajasthan), India

Keywords:

AIDS, etravirine, FDA, HAART, privileged heterocyclic scaffolds (1,4-benzodiazepine, pyrimidine), RT inhibitors.

Abstract

In the anticipation of finding potential substitutes of highly active antiretroviral therapy [HAART], several molecular probes (9-12) have been developed by incorporating the vital fragments of RT inhibitor ‘etravirine’ to the anti-HIV prone privileged template of 1,4-benzodiazepine (2), on the premise that their presence in tandem in the same molecular framework could produce a positive impact in overcoming the problem arising due to the emergence of the multidrug resistant mutants of the virus.

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Published

30.06.2013

How to Cite

NAVJEET KAUR. (2013). A NEW APPROACH TO ANTI-HIV CHEMOTHERAPY DEVISED BY LINKING THE VITAL FRAGMENTS OF ACTIVE RT INHIBITORS SUCH AS ETRAVIRINE TO THE MOLECULAR FRAMEWORK OF ANTI-HIV PRONE PRIVILEGED NUCLEUS OF 1,4-BENZODIAZEPINE AS POSSIBLE SUBSTITUTE TO ’HAART’. International Journal of Pharma and Bio Sciences, 4(2), 309–317. Retrieved from https://ijpbs.net/index.php/journal/article/view/2174

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Research Articles

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