Current Computational Approaches for the Development of Anti-HIV Inhibitors: An Overview

被引:12
|
作者
Panwar, Umesh [1 ]
Chandra, Ishwar [1 ]
Selvaraj, Chandrabose [2 ]
Singh, Sanjeev K. [1 ]
机构
[1] Alagappa Univ, Dept Bioinformat, Comp Aided Drug Design & Mol Modelling Lab, Karaikkudi 630004, Tamil Nadu, India
[2] Masaryk Univ, CEITEC Cent European Inst Technol, Kamenice, Czech Republic
关键词
AIDS; anti-HIV; biological targets; computational drug discovery; drugs; HIV-1 life cycle; virtual screening; LINKED-IMMUNOSORBENT-ASSAY; STRAND TRANSFER INHIBITORS; DRUG DESIGN; ANTIRETROVIRAL THERAPY; PROTEASE INHIBITORS; DISOPROXIL FUMARATE; MOLECULAR-DYNAMICS; INFECTION; DISCOVERY; EMTRICITABINE;
D O I
10.2174/1381612825666190911160244
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: Today, HIV-1 infection has become an extensive problem to public health and a greater challenge to all working researchers throughout the world. Since the beginning of HIV-1 virus, several antiviral therapeutic agents have been developed at various stages to combat HIV-1 infection. But, the many of antiviral drugs are on the platform of drug resistance and toxicology issues, needs an urgent constructive investigation for the development of productive and protective therapeutics to make an improvement of individual life suffering with viral infection. As developing a novel agent is very costly, challenging and time taking route in the recent times. Methods: The review summarized about the modern approaches of computational aided drug discovery to developing a novel inhibitor within a short period of time and less cost. Results: The outcome suggests on the premise of reported information that the computational drug discovery is a powerful technology to design a defensive and fruitful therapeutic agents to combat HIV-1 infection and recover the lifespan of suffering one. Conclusion: Based on survey of the reported information, we concluded that the current computational approaches is highly supportive in the progress of drug discovery and controlling the viral infection.
引用
收藏
页码:3390 / 3405
页数:16
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