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Privileged heterocycles for DNA-encoded library design and hit-to-lead optimization
被引:12
|作者:
Wen, Xin
[1
]
Wu, Xinyuan
[1
,2
]
Jin, Rui
[1
]
Lu, Xiaojie
[1
,2
]
机构:
[1] Chinese Acad Sci, Shanghai Inst Mat Med, State Key Lab Drug Res, 501 Haike Rd,Zhang Jiang Hitech Pk, Shanghai 201203, Peoples R China
[2] Univ Chinese Acad Sci, 19A Yuquan Rd, Beijing 100049, Peoples R China
关键词:
DNA Encoded library;
Drug discovery;
Heterocycles;
Hit identification;
Lead generation;
ACTIVITY-RELATIONSHIP SAR;
HIGHLY POTENT;
IN-VITRO;
BIOLOGICAL-ACTIVITIES;
BINDING MODE;
DISCOVERY;
INHIBITORS;
TECHNOLOGY;
IDENTIFICATION;
CHEMISTRY;
D O I:
10.1016/j.ejmech.2022.115079
中图分类号:
R914 [药物化学];
学科分类号:
100701 ;
摘要:
It is well known that heterocyclic compounds play a key role in improving drug activity, target selectivity, physicochemical properties as well as reducing toxicity. In this review, we summarized the representative het-erocyclic structures involved in hit compounds which were obtained from DNA-encoded library from 2013 to 2021. In some examples, the state of the art in heterocycle-based DEL synthesis and hit-to-lead optimization are highlighted. We hope that more and more novel heterocycle-based DEL toolboxes and in-depth pharmaceutical research on these lead compounds can be developed to accelerate the discovery of new drugs.
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页数:26
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