Structure-activity relationship studies on O-alkylamino-tethered salicylamide derivatives with various amino acid linkers as potent anticancer agents-Reference-Cited by-同舟云学术

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Structure-activity relationship studies on O-alkylamino-tethered salicylamide derivatives with various amino acid linkers as potent anticancer agents

Published:2022-04 Issue: Volume:234 Page:114229
ISSN:0223-5234
Container-title:European Journal of Medicinal Chemistry
language:en
Short-container-title:European Journal of Medicinal Chemistry

Author:

Xu Jimin,Kim Hyejin,Dong Jiabin,Chen Haiying,Xu Junhai,Ma Ruixia,Zhou Mingxiang,Wang Tianzhi,Shen Qiang,Zhou Jia

Funder

National Institutes of Health

University of Texas Medical Branch

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Pharmacology,General Medicine

Reference41 articles.

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3. Revisiting signal transducer and activator of transcription 3 (STAT3) as an anticancer target and its inhibitor discovery: where are we and where should we go?;Huang;Eur. J. Med. Chem.,2020

4. Central role of the threonine residue within the p+1 loop of receptor tyrosine kinase in STAT3 constitutive phosphorylation in metastatic cancer cells;Yuan;Mol. Cell Biol.,2004

5. STAT3 isoforms: alternative fates in cancer?;Aigner;Cytokine,2019

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1. Conformational and Chiroptical Properties of Salicylamide-Based Peptidomimetics;Symmetry;2024-01-24

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