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Fragment-based drug discovery supports drugging ‘undruggable’ protein–protein interactions

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成果类型:
期刊论文
作者:
Wang, Zhi-Zheng;Shi, Xing-Xing;Huang, Guang-Yi;Hao, Ge-Fei*;Yang, Guang-Fu
通讯作者:
Hao, Ge-Fei;Yang, GF;Hao, GF
作者机构:
[Yang, Guang-Fu; Wang, Zhi-Zheng; Yang, GF; Shi, Xing-Xing; Huang, Guang-Yi; Hao, Ge-Fei] Cent China Normal Univ, Natl Key Lab Green Pesticide, Key Lab Pesticide & Chem Biol, Minist Educ, Wuhan 430079, Peoples R China.
[Hao, Ge-Fei] Guizhou Univ, Ctr R&D Fine Chem, Natl Key Lab Green Pesticide, Key Lab Green Pesticide & Agr BioEngn,Minist Educ, Guiyang 550025, Peoples R China.
通讯机构:
[Hao, GF ] G
[Yang, GF ; Hao, GF] C
Cent China Normal Univ, Natl Key Lab Green Pesticide, Key Lab Pesticide & Chem Biol, Minist Educ, Wuhan 430079, Peoples R China.
Guizhou Univ, Ctr R&D Fine Chem, Natl Key Lab Green Pesticide, Key Lab Green Pesticide & Agr BioEngn,Minist Educ, Guiyang 550025, Peoples R China.
语种:
英文
关键词:
PPI modulator;fragment evolution;fragment screening;hot spot;structure-based drug design
期刊:
Trends in Biochemical Sciences
ISSN:
0968-0004
年:
2023
卷:
48
期:
6
页码:
539-552
基金类别:
National Natural Science Foundation of China#&#&#32125033
机构署名:
本校为第一且通讯机构
院系归属:
化学学院
摘要:
Protein-protein interactions (PPIs) have important roles in various cellular processes, but are commonly described as 'undruggable' therapeutic targets due to their large, flat, featureless interfaces. Fragment-based drug discovery (FBDD) has achieved great success in modulating PPIs, with more than ten compounds in clinical trials. Here, we highlight the progress of FBDD in modulating PPIs for therapeutic development. Targeting hot spots that have essential roles in both fragment binding and PPIs provides a shortcut for the development of PPI modulators via FBDD. We highlight successful cases...

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