An Analysis of Successful Hit-to-Clinical Candidate Pairs

被引:22
|
作者
Brown, Dean G. [1 ]
机构
[1] Jnana Therapeut, Boston, MA 02210 USA
关键词
TYROSINE KINASE INHIBITOR; SELECTIVE INHIBITOR; RECEPTOR ANTAGONIST; TOPICAL TREATMENT; HORMONE RECEPTOR; CYSTIC-FIBROSIS; DISCOVERY; POTENT; DESIGN; IDENTIFICATION;
D O I
10.1021/acs.jmedchem.3c00521
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
An analysis of 156 published clinical candidates fromthe Journal of Medicinal Chemistry between 2018 and2021 wasconducted to identify lead generation strategies most frequently employedleading to drug candidates. As in a previous publication, the mostfrequent lead generation strategies resulting in clinical candidateswere from known compounds (59%) followed by random screening approaches(21%). The remainder of the approaches included directed screening,fragment screening, DNA-encoded library screening (DEL), and virtualscreening. An analysis of similarity was also conducted based on Tanimoto-MCSand revealed most clinical candidates were distant from their originalhits; however, most shared a key pharmacophore that translated fromhit-to-clinical candidate. An examination of frequency of oxygen,nitrogen, fluorine, chlorine, and sulfur incorporation in clinicalcandidates was also conducted. The three most similar and least similarhit-to-clinical pairs from random screening were examined to provideperspective on changes that occur that lead to successful clinicalcandidates.
引用
收藏
页码:7101 / 7139
页数:39
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