Literature DB >> 30634084

Design, synthesis and biological evaluation of tetrazole-containing RXRα ligands as anticancer agents.

Zhiqiang Yan1, Shuyi Chong1, Huiyun Lin1, Qian Yang1, Xin Wang1, Weidong Zhang1, Xiaokun Zhang2, Zhiping Zeng3, Ying Su4.   

Abstract

Nuclear receptor RXRα plays an important role in many biological and pathological processes. The nongenomic action of RXRα is implicated in many cancers. K-8008, a non-canonical RXRα ligand derived from sulindac, inhibits the TNFα-activated PI3K/AKT pathway by mediating the interaction between a truncated form of RXRα (tRXRα) and the p85α regulatory subunit of PI3K and exerts potent anticancer activity in animal model. Herein we report our studies of a novel series of K-8008 analogs as potential anticancer agents targeting RXRα. Two compounds 8b and 18a were identified to have slightly stronger binding to RXRα and improved apoptotic activities in breast cancer cells.
Copyright © 2018 Elsevier Masson SAS. All rights reserved.

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Keywords:  Anticancer activity; Bioisostere; PI3K/AKT pathway; RXRα; RXRα modulator

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Year:  2018        PMID: 30634084     DOI: 10.1016/j.ejmech.2018.12.036

Source DB:  PubMed          Journal:  Eur J Med Chem        ISSN: 0223-5234            Impact factor:   6.514


  1 in total

1.  Practical scale up synthesis of carboxylic acids and their bioisosteres 5-substituted-1H-tetrazoles catalyzed by a graphene oxide-based solid acid carbocatalyst.

Authors:  Rupali Mittal; Amit Kumar; Satish Kumar Awasthi
Journal:  RSC Adv       Date:  2021-03-17       Impact factor: 3.361

  1 in total

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