| Literature DB >> 35450372 |
Xin Li1, Ping Dong1, Ting Zhang1, Guodong Cai1, Yang Chen1, Huaide Dong1, Fang Yang1, Lei Zhang1, Yuchang Mao1, Jun Feng1, Chang Bai1, Feng He1, Weikang Tao1.
Abstract
ERK1/2 kinase is a key downstream node of the RAS-RAF-MEK-ERK signaling pathway. A highly potent and selective ERK1/2 inhibitor is a promising option for cancer treatment that will provide a potential solution for overcoming drug resistance. Herein we designed and synthesized a novel scaffold featuring a pyrrole-fused urea template. The lead compound, SHR2415, was shown to be a highly potent ERK1/2 inhibitor that exhibited high cell potency based on the Colo205 assay. In addition, SHR2415 displayed favorable PK profiles across species as well as robust in vivo efficacy in a mouse Colo205 xenograft model.Entities:
Year: 2022 PMID: 35450372 PMCID: PMC9014502 DOI: 10.1021/acsmedchemlett.2c00029
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.632