| Literature DB >> 34055214 |
Zirui Lü1, Xiaona Li1, Kebin Li1, Cong Wang1, Tingting Du2, Wei Huang2, Ming Ji2, Changhong Li3, Fengrong Xu1, Ping Xu1, Yan Niu1.
Abstract
We identified nitazoxanide (NTZ) as a moderate STAT3 pathway inhibitor through immunoblot analysis and a cell-based IL-6/JAK/STAT3 pathway activation assay. A series of thiazolide derivatives were designed and synthesized to further validate the thiazolide scaffold as STAT3 inhibitors. Eight out of 25 derivatives displayed potencies greater than that of NTZ, and their STAT3 pathway inhibitory activities were found to be significantly correlated with their antiproliferative activities in HeLa cells. Derivatives 15 and 24 were observed to be more potent than the positive control WP1066, which is under phase I clinical trials. Compared with NTZ, 15 also exhibited much improved in vivo pharmacokinetic parameters in rats and efficacies against proliferations in multiple cancer cell lines, indicating a broad-spectrum effect of these thiazolides as antitumor agents targeted on STAT3.Entities:
Year: 2021 PMID: 34055214 PMCID: PMC8155281 DOI: 10.1021/acsmedchemlett.0c00544
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345