Discovery of a benzimidazole series as the first highly potent and selective ACSL1 inhibitors-Reference-Cited by-同舟云学术

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Discovery of a benzimidazole series as the first highly potent and selective ACSL1 inhibitors

Published:2021-02 Issue: Volume:33 Page:127722
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Hayashi Kyohei,Kondo Noriyasu,Omori Naoki,Yoshimoto Ryo,Hato Megumi,Shigaki Shuhei,Nagasawa Ayumi,Ito Mana,Okuno Takayuki

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference19 articles.

1. Structural Basis of the Substrate-specific Two-step Catalysis of Long Chain Fatty Acyl-CoA Synthetase Dimer

2. Structure and regulation of rat long-chain acyl-CoA synthetase.

3. Mammalian Long-Chain Acyl-CoA Synthetases

4. Liver-specific Loss of Long Chain Acyl-CoA Synthetase-1 Decreases Triacylglycerol Synthesis and β-Oxidation and Alters Phospholipid Fatty Acid Composition

5. Overexpression of Rat Long Chain Acyl-CoA Synthetase 1 Alters Fatty Acid Metabolism in Rat Primary Hepatocytes

Cited by 3 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. Anti-apoptotic MCL-1 promotes long-chain fatty acid oxidation through interaction with ACSL1;Molecular Cell;2024-04

2. Inhibiting ACSL1-Related Ferroptosis Restrains Murine Coronavirus Infection;Viruses;2021-11-28

3. Inhibiting ACSL1 related ferroptosis restrains MHV-A59 infection;2021-10-14

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