首页> 外文期刊>Bioorganic and Medicinal Chemistry Letters >T-type calcium channel blockers: spiro-piperidine azetidines and azetidinones-optimization, design and synthesis.
【24h】

T-type calcium channel blockers: spiro-piperidine azetidines and azetidinones-optimization, design and synthesis.

机译:T型钙通道阻滞剂:螺哌啶氮杂环丁烷和氮杂环丁烷酮的优化,设计和合成。

获取原文
获取原文并翻译 | 示例
           

摘要

A series of spiro-azetidines and azetidinones has been evaluated as novel blockers of the T-type calcium channel (Ca(V)3.2) 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.
机译:一系列螺-氮杂环丁烷和氮杂环丁酮已被评估为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。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号