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Correction: Generation and Characterization of New Entrance Antiretroviral Drug 2-Indolinone: Results of a Classical R & D Study

Author

Listed:
  • Ramesh Paranjape

    (National AIDS Research Institute, India)

  • Rahul Hajare

    (Indian Council of Medical Research, Vinayaka Mission University, India)

Abstract

HIV has true evolutionary history of a homologous of sequences. It has mutations do not have appreciated. It has some other property and impact on the fitness of the HIV carrier indicates how these analyses can be useful in the drug discovery process. HIV has same organ under every variety of form and function. It has variety of forms this definition still holds secrete even today. HIV has been come homologous proteins can differ in their specificities, specific activities, level of expression or some other basic property. However homologous will have some residual similarity in their form and function. HIV from all of its hiding places within the body has difficult. The approach can be used in bioinformatics innovation in practices, including complex binding energy estimation in novel HIV-1 inhibitors. Here we showed how a space filling model-based approach used infection HIV-1 inhibitors and role of target compound located insight into the host cell machinery. Process technology by parallel synthesizer major has used for the purposes of synthesized 2- Indolinones potential derivatives. In vitro anti-HIV-1 activity of new entrance compound 8-methoxy-5-(morpholin-4-ylmethyl)-4,4a,5,9b-tetrahydro-1H-pyrazino[2,3-b]indole-2,3 dicarbonitrile (1b) and studies have suggested that above has a novel reservoir has very low cytotoxicity(CC50>1mM) and it has been displays 15.5μg/ml to cell lines, TZM-bl. Also it displayed potent anti-HIV-1 activity and found 3.96μg/ml against laboratory adapted strains UG070, 7th PID.

Suggested Citation

  • Ramesh Paranjape & Rahul Hajare, 2018. "Correction: Generation and Characterization of New Entrance Antiretroviral Drug 2-Indolinone: Results of a Classical R & D Study," Organic & Medicinal Chemistry International Journal, Juniper Publishers Inc., vol. 6(2), pages 46-49, April.
  • Handle: RePEc:adp:jomcij:v:6:y:2018:i:2:p:46-49
    DOI: 10.19080/OMCIJ.2018.06.555685
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