Abstract
In the present study, authors want to encourage the research exertions through structureactivity relationship for the identification of effective molecules for the treatment of Human immunodeficiency virus because nowadays AIDS is considered as one of the main causes of death in human beings. A diversity of biological resources has been searched and developed for the treatment of HIV but unfortunately, until now, no medicine is found to be fully effective and safe for the cure of patients. Human immunodeficiency virus is a type of lentivirus which causes the infection of HIV and once it enters the human body, it stays for a longer period of time triggering immunodeficiency syndrome. For searching and developing new potent and effective anti-HIV molecules, medicinal chemists have engaged in countless targets with the structure-activity relationship (SAR) of molecules and on this basis, many antiretroviral therapies have been developed to cure HIV infection. Most of these new searched molecules have been found to be clinically active against various types of AIDS patient and auxiliary research in this area may lead to better treatment in the near future. This article encompasses and highlights the recent advancement of innumerable inhibitors laterally through synthetic, semi-synthetic and structure-activity relationship approaches.
Keywords: SAR, protease inhibitor, integrase inhibitor, chemokine receptor, fusion inhibitors, NNRTIs.
Mini-Reviews in Medicinal Chemistry
Title:Recent Advances Towards Treatment of HIV: Synthesis and SAR Studies
Volume: 21 Issue: 4
Author(s): Neelima Shrivastava, Asif Husain*, Mohammad Rashid*, Nimer Fehaid Alsabeelah, Shahid Karim and Nasir Ali Siddiqui
Affiliation:
- Department of Pharmaceutical Chemistry, School of Pharmaceutical Education and Research, Jamia Hamdard (Hamdard University), New Delhi 110062,India
- College of Pharmacy and Dentistry, Buraydah Colleges, Buraydah, Al-Qassim 31717,Saudi Arabia
Keywords: SAR, protease inhibitor, integrase inhibitor, chemokine receptor, fusion inhibitors, NNRTIs.
Abstract: In the present study, authors want to encourage the research exertions through structureactivity relationship for the identification of effective molecules for the treatment of Human immunodeficiency virus because nowadays AIDS is considered as one of the main causes of death in human beings. A diversity of biological resources has been searched and developed for the treatment of HIV but unfortunately, until now, no medicine is found to be fully effective and safe for the cure of patients. Human immunodeficiency virus is a type of lentivirus which causes the infection of HIV and once it enters the human body, it stays for a longer period of time triggering immunodeficiency syndrome. For searching and developing new potent and effective anti-HIV molecules, medicinal chemists have engaged in countless targets with the structure-activity relationship (SAR) of molecules and on this basis, many antiretroviral therapies have been developed to cure HIV infection. Most of these new searched molecules have been found to be clinically active against various types of AIDS patient and auxiliary research in this area may lead to better treatment in the near future. This article encompasses and highlights the recent advancement of innumerable inhibitors laterally through synthetic, semi-synthetic and structure-activity relationship approaches.
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Cite this article as:
Shrivastava Neelima , Husain Asif *, Rashid Mohammad *, Alsabeelah Fehaid Nimer , Karim Shahid and Siddiqui Ali Nasir , Recent Advances Towards Treatment of HIV: Synthesis and SAR Studies, Mini-Reviews in Medicinal Chemistry 2021; 21 (4) . https://dx.doi.org/10.2174/1389557519666190312170158
DOI https://dx.doi.org/10.2174/1389557519666190312170158 |
Print ISSN 1389-5575 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-5607 |
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