Concise synthesis and biological activity evaluation of novel pyrazinyl–aryl urea derivatives against several cancer cell lines, which can especially induce T24 apoptotic and necroptotic cell death

Author:

Chen Jia-Nian1ORCID,Chen Chu-Ting1,He Yue-Zhen1,Qin Tai-Sheng1,Cheng Li1,Sun Ye-Xiang1,Yang Kang-Jian1,Chen Qi1,Yang Chao1,Wei Ying1

Affiliation:

1. State Key Laboratory for Chemistry and Molecular Engineering of Medicinal Resources, Collaborative Innovation Center for Guangxi Ethnic Medicine, School of Chemistry and Pharmaceutical Sciences, Guangxi Normal University, Yucai Road 15, Guilin 541004, Guangxi, P.R. China

Abstract

Based on structural modification of regorafenib, 28 pyrazinyl–aryl urea derivatives were synthesized and the in vitro anti-cancer effects were evaluated. Compound 5-23 possessed the strongest inhibitory activity against bladder cancer T24 cell line.

Funder

National Natural Science Foundation of China

Middle-aged and Young Teachers' Basic Ability Promotion Project of Guangxi

Natural Science Foundation of Guangxi Province

State Key Laboratory for Chemistry and Molecular Engineering of Medicinal Resources

Guangxi Normal University

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Drug Discovery,Pharmaceutical Science,Pharmacology,Molecular Medicine,Biochemistry

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