软骨发育不全
突变
生物信息学
医学
计算生物学
计算机科学
遗传学
生物
儿科
基因
作者
Ding-Wei Fu,Tian Han,Zimo Yang,Yuanfeng Xia,Zhilong Hu,Fanglong Yang,Siqi Wang,Lei Jin
标识
DOI:10.1021/acsmedchemlett.5c00294
摘要
Achondroplasia (ACH), the most prevalent form of human dwarfism, is caused by the G380R mutation in FGFR3 in approximately 99% of cases. Through structural hybridization of Tyra-300 and LY2874455, we developed compound 23, a new dual-target FGFR2/3 inhibitor demonstrating potent activity against both wild-type and mutant FGFR3. In preclinical ACH mouse models, compound 23 showed a dose-dependent improvement in growth rate, with significantly enhanced efficacy versus infigratinib at equivalent doses. This work presents a new structural scaffold for developing FGFR3 kinase inhibitors to target pathogenic FGFR3 mutations and treat ACH.
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