| Literature DB >> 31938461 |
Ying Wu1, Lei Wang1, Yahui Huang1, Shuqiang Chen1, Shanchao Wu1, Guoqiang Dong1, Chunquan Sheng1,2.
Abstract
Chidamide is a histone deacetylase (HDAC) inhibitor that is currently used to treat cutaneous T-cell lymphoma in clinic. Herein nicotinamide phosphoribosyltransferase (NAMPT) was identified to be a new target of chidamide on the basis of the pharmacophore analysis, molecular docking, biological assays, inhibitor design, and structure-activity relationship study. The polypharmacology of chidamide will provide important information for better understanding its antitumor mechanism. Also, design of dual NAMPT/HDAC inhibitors may serve as an effective strategy to develop novel antitumor agents.Entities:
Year: 2019 PMID: 31938461 PMCID: PMC6956351 DOI: 10.1021/acsmedchemlett.9b00407
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345