| Literature DB >> 30634084 |
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.Entities:
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