Journal of Medicinal Chemistry p. 6992 - 7014 (2019)
Update date:2022-08-28
Topics:
Zhang, Kehui
Lai, Fangfang
Lin, Songwen
Ji, Ming
Zhang, Jingbo
Zhang, Yan
Jin, Jing
Fu, Rong
Wu, Deyu
Tian, Hua
Xue, Nina
Sheng, Li
Zou, Xiaowen
Li, Yan
Chen, Xiaoguang
Xu, Heng
Polypharmacology is a promising paradigm in modern drug discovery. Herein, we have discovered a series of novel PI3K and HDAC dual inhibitors in which the hydroxamic acid moiety as the zinc binding functional group was introduced to a quinazoline-based PI3K pharmacophore through an appropriate linker. Systematic structure-activity relationship studies resulted in lead compounds 23 and 36 that simultaneously inhibited PI3K and HDAC with nanomolar potencies and demonstrated favorable antiproliferative activities. Compounds 23 and 36 efficiently modulated the expression of p-AKT and Ac-H3, arrested the cell cycle, and induced apoptosis in HCT116 cancer cells. Following pharmacokinetic studies, 23 was further evaluated in HCT116 and HGC-27 xenograft models to show significant in vivo anticancer efficacies with tumor growth inhibitions of 45.8% (po, 150 mg/kg) and 62.6% (ip, 30 mg/kg), respectively. Overall, this work shows promise in discovering new anticancer therapeutics by the approach of simultaneously targeting PI3K and HDAC pathways with a single molecule.
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