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 |
Files in This Item:
File | Description | Size | Format | |
---|---|---|---|---|
IPFP0291.pdf | IPFP0291 | 1.9 MB | Adobe PDF | ![]() View/Open |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.