Please use this identifier to cite or link to this item: http://10.1.7.192:80/jspui/handle/123456789/8259
Title: Recent updates for designing CCR5 antagonists as anti-retroviral agents
Authors: Shah, Harshil R.
Savjani, Jignasa Ketan
Keywords: HIV
Anti-retroviral therapy
CCR5
Reverse transcriptase inhibitors
Protease inhibitors
CXCR4 antagonists
Issue Date: 2018
Publisher: Elsevier
Series/Report no.: IPFP0291;
Abstract: The healthcare system faces various challenges in human immunodeficiency virus (HIV) therapy due to resistance to Anti-Retroviral Therapy (ART) as a consequence of the evolutionary process. Despite the success of antiretroviral drugs like Zidovudine, Zalcitabine, Raltegravir WHO ranks HIV as one of the deadliest diseases with a mortality of one million lives in 2016. Thus, there emerges an urgency of developing a novel anti-retroviral agent that combat resistant HIV strains. The clinical development of ART from a single drug regimen to current triple drug combination is very slow. The progression in the structural biology of the viral envelope prompted the discovery of novel targets, which can be demonstrated a proficient approach for drug design of anti-retroviral agents. The current review enlightens the recent updates in the structural biology of the viral envelope and focuses on CCR5 as a validated target as well as ways to overcome CCR5 resistance. The article also throws light on the SAR studies and most prevalent mutations in the receptor for designing CCR5 antagonists that can combat HIV-1 infection. To conclude, the paper lists diversified scaffolds that are in pipeline by various pharmaceutical companies that could provide an aid for developing novel CCR5 antagonists
Description: European Journal of Medicinal Chemistry; 147 (2018): 115-129
URI: http://10.1.7.192:80/jspui/handle/123456789/8259
Appears in Collections:Faculty Papers

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