广告
驱动蛋白
计算生物学
有丝分裂
Atom(片上系统)
药物发现
计算机科学
纳米技术
DNA
生物物理学
化学
抗癌药
微管蛋白
鉴定(生物学)
癌细胞系
生物信息学
染色体分离
细胞器
立体化学
生物
细胞生物学
微管
作者
Brian A. Sparling,Hyelee Lee,Mary-Margaret Zablocki,Maureen M. Lynes,Simina Grigoriu,Livia Shehaj,G.J. Lockbaum,Sanjoy Khan,Taylor Hotz,Young‐Tae Lee,Shane M. Buker,Deepali Gotur,Chuang Lu,Scott Ribich,Stephen J. Blakemore,P. Ann Boriack‐Sjodin,Serena J. Silver,Robert A. Copeland,Kenneth W. Duncan
标识
DOI:10.1021/acsmedchemlett.5c00512
摘要
KIF18A is an ATP-dependent, plus end-directed mitotic kinesin that facilitates chromosome alignment and spindle microtubule dynamics during mitosis. Certain cancer types may be particularly vulnerable to KIF18A inhibition, specifically cancer cells with high levels of chromosomal instability (CIN). As part of efforts to identify KIF18A inhibitors, silicon atom replacement was explored to improve ligand-KIF18A interactions and ADME parameters. This tactic resulted in the discovery of a series of silapiperidine-containing KIF18A inhibitors and culminated in the identification and characterization of ATX020. ATX020 is a potent KIF18A inhibitor with a high degree of kinesin selectivity, favorable in vitro and in vivo ADME properties, and robust efficacy in the OVCAR-3 cell-derived xenograft (CDX) model. A high-resolution crystal structure of the KIF18A-tubulin complex and an experimentally guided model of ATX020 bound to the complex are provided, supporting future structure-based drug design of KIF18A inhibitors.
科研通智能强力驱动
Strongly Powered by AbleSci AI