Insights into drug discovery from natural products through structural modification

被引:100
|
作者
Chen, Jichao
Li, Wenlong
Yao, Hequan
Xu, Jinyi
机构
[1] China Pharmaceut Univ, State Key Lab Nat Med, Nanjing 210009, Peoples R China
[2] China Pharmaceut Univ, Dept Med Chem, Nanjing 210009, Peoples R China
关键词
Natural products; Druggability; Structural modification; GAMMA-SECRETASE MODULATORS; HUMAN SERUM-ALBUMIN; POTENT IMMUNOSUPPRESSIVE ACTIVITY; METASTATIC BREAST-CANCER; HALICHONDRIN-B ANALOG; CHEMICAL SPACE; IN-VIVO; COMBRETASTATIN A-4; BIOLOGICAL EVALUATION; ANTIMALARIAL ACTIVITY;
D O I
10.1016/j.fitote.2015.04.012
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Natural products (NPs) have played a key role in drug discovery and are still a prolific source of novel lead compounds or pharmacophores for medicinal chemistry. Pharmacological activity and druggability are two indispensable components advancing NPs from leads to drugs. Although naturally active substances are usually good lead compounds, most of them can hardly satisfy the demands for druggability. Hence, these structural phenotypes have to be modified and optimized to overcome existing deficiencies and shortcomings. This review illustrates druggability optimization of NPs through structural modification with some successful examples. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:231 / 241
页数:11
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