Current Approaches and Strategies Applied in First-in-class Drug Discovery

被引:0
|
作者
Mohammed, Idrees [1 ]
Sagurthi, Someswar Rao [1 ,2 ]
机构
[1] Osmania Univ, Dept Genet & Biotechnol, Drug Design & Mol Med Lab, Hyderabad 500007, Telangana, India
[2] Jawaharlal Nehru Univ, Special Ctr Mol Med, New Delhi 110067, India
关键词
First-in-class drug discovery; current screening approaches; medicinal chemistry strategies; Functional genomics and structural biology; Artificial Intelligence; HIV-1 ATTACHMENT INHIBITOR; LEAD OPTIMIZATION; MEDICINAL CHEMISTRY; POTENT INHIBITORS; WEB TOOL; FRAGMENT; DESIGN; CELL; IDENTIFICATION; PRODRUGS;
D O I
10.1002/cmdc.202400639
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
First-in-class drug discovery (FICDD) offers novel therapies, new biological targets and mechanisms of action (MOAs) toward targeting various diseases and provides opportunities to understand unexplored biology and to target unmet diseases. Current screening approaches followed in FICDD for discovery of hit and lead molecules can be broadly categorized and discussed under phenotypic drug discovery (PDD) and target-based drug discovery (TBDD). Each category has been further classified and described with suitable examples from the literature outlining the current trends in screening approaches applied in small molecule drug discovery (SMDD). Similarly, recent applications of functional genomics, structural biology, artificial intelligence (AI), machine learning (ML), and other such advanced approaches in FICDD have also been highlighted in the article. Further, some of the current medicinal chemistry strategies applied during discovery of hits and optimization studies such as hit-to-lead (HTL) and lead optimization (LO) have been simultaneously overviewed in this article.
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页数:24
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