| Literature DB >> 25921402 |
Bian Zhang1, Bernard T Golding, Ian R Hardcastle.
Abstract
Potent and selective small-molecule inhibitors of the p53-MDM2 interaction intended for the treatment of p53 wild-type tumors have been designed and optimized in a number of chemical series. This review details recent disclosures of compounds in advanced optimization and features key series that have given rise to clinical trial candidates. The structure-activity relationships for inhibitor classes are discussed with reference to x-ray structures, and common structural features are identified.Entities:
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Year: 2015 PMID: 25921402 DOI: 10.4155/fmc.15.13
Source DB: PubMed Journal: Future Med Chem ISSN: 1756-8919 Impact factor: 3.808