Discovery of novel indoleamine 2,3-dioxygenase 1 (IDO1) inhibitors by virtual screening-Reference-Cited by-同舟云学术

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Discovery of novel indoleamine 2,3-dioxygenase 1 (IDO1) inhibitors by virtual screening

Published:2019-02 Issue: Volume:78 Page:306-316
ISSN:1476-9271
Container-title:Computational Biology and Chemistry
language:en
Short-container-title:Computational Biology and Chemistry

Author:

Zhou Yeheng,Peng Jiale,Li Penghua,Du Haibo,Li Yaping,Li Yingying,Zhang Li,Sun Wei,Liu Xingyong,Zuo Zhili

Funder

General Program of Applied Basic Research of Yunnan Province

Strategic Priority Research Program of the Chinese Academy of Sciences

Publisher

Elsevier BV

Subject

Computational Mathematics,Organic Chemistry,Biochemistry,Structural Biology

Reference44 articles.

1. Preparation of Cycloalkylaryl Amide Compounds As Indoleamine 2,3-Dioxygenase and Therapeutic Uses Thereof;Balog,2014

2. Consensus superiority of the pharmacophore-based alignment, over maximum common substructure (MCS): 3D-QSAR studies on carbamates as acetylcholinesterase inhibitors;Chaudhaery;J. Chem. Inf. Model.,2009

3. Discovery and structure-activity relationships of phenyl benzenesulfonylhydrazides as novel indoleamine 2,3-dioxygenase inhibitors;Cheng;Bioorg. Med. Chem. Lett.,2014

4. A patent review of IDO1 inhibitors for cancer;Cheong;Expert Opin. Ther. Pat.,2018

Cited by 12 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Mendelian randomization analysis to elucidate the causal relationship between small molecule metabolites and ovarian cancer risk;Frontiers in Oncology;2023-11-28

2. Virtual screening based on pharmacophore model for developing novel HPPD inhibitors;Pesticide Biochemistry and Physiology;2022-06

3. A theranostic probe of indoleamine 2,3-dioxygenase 1 (IDO1) for small molecule cancer immunotherapy;European Journal of Medicinal Chemistry;2021-03

4. Machine and deep learning approaches for cancer drug repurposing;Seminars in Cancer Biology;2021-01

5. Discovery and structure-activity relationship studies of 1-aryl-1H-naphtho[2,3-d][1,2,3]triazole-4,9-dione derivatives as potent dual inhibitors of indoleamine 2,3-dioxygenase 1 (IDO1) and trytophan 2,3-dioxygenase (TDO);European Journal of Medicinal Chemistry;2020-12

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