Synthesis and Mechanism of p53‐MDM2 Inhibitors with Heterocyclic Structures: A Focused Review

Author:

Ji Li‐Tao1ORCID,Zhang Wenjing1,Zhang Yi1,Zhao Su1,Long Hai‐Tao1,Qin Li‐Qing1,Tian Jia‐Cheng1,Li Hong‐Zhang1,Zhu Dan‐Xue1,Zhou Yan1,Lu Yi‐Duo1,Wang Zhen‐Chao123ORCID,Li Cheng‐Peng123

Affiliation:

1. College of Pharmacy Guizhou University 550025 Guiyang Guizhou China

2. State Key Laboratory Breeding Base of Green Pesticide and Agricultural Bioengineering Key Laboratory of Green Pesticide and Agricultural Bioengineering Ministry of Education 550025 Guiyang China

3. Guizhou Engineering Laboratory for Synthetic Drugs Guizhou University 550025 Guiyang China

Abstract

AbstractP53 gene mutation is one of the important causes in tumors. p53‐MDM2 (murine double minute 2) inhibitors can interrupt p53‐dependent gene transcription activity, and inhibit p53‐mediated apoptosis, block p53‐MDM2/MDMx interaction, and significantly reduce DNA formation. In this article, we focused on the synthesis methods about nutlins and other p53 small molecule inhibitors, in order to find potential new structure for novel p53 small molecule inhibitor synthesizing.

Funder

Natural Science Foundation of Guizhou Province

Publisher

Wiley

Subject

General Chemistry

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