| Literature DB >> 32551023 |
Ting-Rong Chern1, Liu Liu1, Elyse Petrunak1, Jeanne A Stuckey1, Mi Wang1, Denzil Bernard1, Haibin Zhou1, Shirley Lee1, Yali Dou1, Shaomeng Wang1.
Abstract
The mixed-lineage leukemia (MLL) protein, also known as MLL1, is a lysine methyltransferase specifically responsible for methylation of histone 3 lysine 4. MLL has been pursued as an attractive therapeutic target for the treatment of acute leukemia carrying the MLL fusion gene or MLL leukemia. Herein, we report the design, synthesis, and evaluation of an S-adenosylmethionine-based focused chemical library which led to the discovery of potent small-molecule inhibitors directly targeting the MLL SET domain. Determination of cocrystal structures for a number of these MLL inhibitors reveals that they adopt a unique binding mode that locks the MLL SET domain in an open, inactive conformation.Entities:
Year: 2020 PMID: 32551023 PMCID: PMC7294728 DOI: 10.1021/acsmedchemlett.0c00229
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345