Rational design, synthesis and biological evaluation of ubiquinone derivatives as IDO1 inhibitors-Reference-Cited by-同舟云学术

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Rational design, synthesis and biological evaluation of ubiquinone derivatives as IDO1 inhibitors

Published:2019-08 Issue: Volume:89 Page:102870
ISSN:0045-2068
Container-title:Bioorganic Chemistry
language:en
Short-container-title:Bioorganic Chemistry

Author:

Ding Yuyang,Tang Fei,Xue Xiaoqian,Luo Jinfeng,Hussain Muzammal,Huang Yanhui,Wang Zhen,Jiang Hao,Tu Zhengchao,Zhang Jiancun

Funder

Key Laboratory of Respiratory Disease

“Personalized Medicines – Novel Target-based Antitumor Drug Discovery and Development”

Strategic Priority Research Program of the Chinese Academy of Sciences

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Molecular Biology,Biochemistry

Reference53 articles.

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3. The combined effects of tryptophan starvation and tryptophan catabolites down-regulate T cell receptor z-chain and induce a regulatory phenotype in naive T cells;Fallarino;J. Immunol.,2006

4. GCN2 kinase in T cells mediates proliferative arrest and anergy induction in response to indoleamine 2,3-dioxygenase;Munn;Immun.,2005

5. IDO expression by dendritic cells: Tolerance and tryptophan catabolism;Mellor;Nat. Rev. Immunol.,2004

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1. Small-molecule modulators of tumor immune microenvironment;Bioorganic Chemistry;2024-04

2. Indoleamine 2, 3-dioxygenase 1 inhibitory compounds from natural sources;Frontiers in Pharmacology;2022-11-04

3. An updated patent review of IDO1 inhibitors for cancer (2018–2022);Expert Opinion on Therapeutic Patents;2022-11-02

4. Indoleamine and tryptophan 2,3-dioxygenases as important future therapeutic targets;Pharmacology & Therapeutics;2021-05

5. Diverse chemical space of indoleamine-2,3-dioxygenase 1 (Ido1) inhibitors;European Journal of Medicinal Chemistry;2021-02

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