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寻找人类免疫缺陷病毒/获得性免疫缺陷综合征(HIV/AIDS)的治疗候选药物:合理方法、设计策略、构效关系及作用机制见解

In search of therapeutic candidates for HIV/AIDS: rational approaches, design strategies, structure-activity relationship and mechanistic insights.

作者信息

Kumar Dinesh, Sharma Pooja, Kaur Ramandeep, Lobe Maloba M M, Gupta Girish K, Ntie-Kang Fidele

机构信息

Sri Sai College of Pharmacy Manawala Amritsar-143001 Punjab India

Department of Pharmaceutical Sciences and Drug Research, Punjabi University Patiala India.

出版信息

RSC Adv. 2021 May 18;11(29):17936-17964. doi: 10.1039/d0ra10655k. eCollection 2021 May 13.

Abstract

The HIV/AIDS pandemic is a serious threat to the health and development of mankind, which has affected about 37.9 million people worldwide. The increasing negative health, economic and social impacts of this disease have led to the search for new therapeutic candidates for the mitigation of AIDS/HIV. However, to date, there is still no treatment that can cure this disease. Furthermore, the clinically available drugs have numerous severe side effects. Hence, the synthesis of novel agents from natural leads is one of the rational approaches to obtain new drugs in modern medicinal chemistry. This review article is an effort to summarize recent developments with regards to the discovery of novel analogs with promising biological potential against HIV/AIDS. Herein, we also aim to discuss prospective directions on the progress of more credible and specific analogues. Besides presenting design strategies, the present communication also highlights the structure-activity relationship together with the structural features of the most promising molecules, their IC values, mechanistic insights and some interesting key findings revealed during their biological evaluation. The interactions with the amino acid residues of the enzymes responsible for HIV-1 inhibition are also discussed. This collection will be of great interest for researchers working in this area.

摘要

艾滋病毒/艾滋病大流行对人类健康和发展构成严重威胁,全球约有3790万人受到影响。这种疾病对健康、经济和社会的负面影响日益增加,促使人们寻找减轻艾滋病/艾滋病毒影响的新治疗候选药物。然而,迄今为止,仍没有能够治愈这种疾病的疗法。此外,临床上可用的药物有许多严重的副作用。因此,从天然先导化合物合成新型药物是现代药物化学中获取新药的合理方法之一。这篇综述文章旨在总结近期在发现具有抗艾滋病毒/艾滋病潜力的新型类似物方面的进展。在此,我们还旨在讨论更可靠和特异类似物进展的未来方向。除了介绍设计策略外,本交流还突出了构效关系以及最有前景分子的结构特征、它们的半数抑制浓度值、作用机制见解以及在生物学评估过程中揭示的一些有趣的关键发现。还讨论了与负责抑制HIV-1的酶的氨基酸残基的相互作用。该文集将引起该领域研究人员的极大兴趣。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b954/9033207/765841cd96be/d0ra10655k-f1.jpg

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