T-type calcium channel blockers: spiro-piperidine azetidines and azetidinones—optimization, design and synthesis
作者:Elizabeth M. Smith、Steve Sorota、Hyunjin M. Kim、Brian A. McKittrick、Terry L. Nechuta、Chad Bennett、Chad Knutson、Duane A. Burnett、Jane Kieselgof、Zheng Tan、Diane Rindgen、Terry Bridal、Xiaoping Zhou、Yu-Ping Jia、Zoe Dong、Debbie Mullins、Xiaoping Zhang、Tony Priestley、Craig C. Correll、Deen Tulshian、Michael Czarniecki、William J. Greenlee
DOI:10.1016/j.bmcl.2010.06.012
日期:2010.8
A series of spiro-azetidines and azetidinones has been evaluated as novel blockers of the T-type calcium channel (CaV3.2) which is a new therapeutic target for the potential treatment of both inflammatory and neuropathic pain. Confirmation and optimization of the potency, selectivity and DMPK properties of leads will be described.
已经评估了一系列螺氮杂环丁烷和氮杂环丁酮作为T型钙通道(Ca V 3.2)的新型阻滞剂,它是潜在治疗炎性和神经性疼痛的新治疗靶标。将描述和验证潜在性,选择性和DMPK特性的优化。