Design, synthesis and biological activity evaluation of novel covalent S-acylation inhibitors-Reference-Cited by-同舟云学术

Design, synthesis and biological activity evaluation of novel covalent S-acylation inhibitors

Published:2023-04-24 Issue: Volume: Page:
ISSN:1381-1991
Container-title:Molecular Diversity
language:en
Short-container-title:Mol Divers

Author:

Yu Wei,Yang Kan,Zhao Mengmiao,Liu Han,You Zhihao,Liu Zhenming,Qiao Xiaoqiang,Song Yali^ORCID

Funder

National Natural Science Foundation of China

Natural Science Foundation of Hebei Province

Science and Technology Project of Hebei Education Department

Hebei youth talent project; the Innovation Capacity Improvement Plan of Hebei Province

Natural Science Interdisciplinary Research Program of Hebei University

Post-graduate’s Innovation Found Project of Hebei University

Publisher

Springer Science and Business Media LLC

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Drug Discovery,Molecular Biology,General Medicine,Information Systems,Catalysis

Link

https://link.springer.com/content/pdf/10.1007/s11030-023-10633-7.pdf

Reference32 articles.

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3. Qiu N, Abegg D, Guidi M, Gilmore K et al (2022) Artemisinin inhibits NRas palmitoylation by targeting the protein acyltransferase ZDHHC6. Cell Chem Biol 29:530–537. https://doi.org/10.1016/j.chembiol.2021.07.012

4. Li Y, Martin BR, Cravatt BF, Hofmann SL (2012) DHHC5 protein palmitoylates flotillin-2 and is rapidly degraded on induction of neuronal differentiation in cultured cells. J Biol Chem 287:523–530. https://doi.org/10.1074/jbc.m111.306183

5. Zhang Y, Li F, Fu K, Liu X et al (2021) Potential role of s-palmitoylation in cancer stem cells of lung adenocarcinoma. Front Cell Dev Biol 9:734897. https://doi.org/10.3389/fcell.2021.734897

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