Suppr超能文献

关于强效κ阿片受体激动剂Salvinorin A药效基团的研究。

Studies toward the pharmacophore of salvinorin A, a potent kappa opioid receptor agonist.

作者信息

Munro Thomas A, Rizzacasa Mark A, Roth Bryan L, Toth Beth A, Yan Feng

机构信息

School of Chemistry, The University of Melbourne, Victoria, 3010, Australia.

出版信息

J Med Chem. 2005 Jan 27;48(2):345-8. doi: 10.1021/jm049438q.

Abstract

Salvinorin A (1), from the sage Salvia divinorum, is a potent and selective kappa opioid receptor (KOR) agonist. We screened other salvinorins and derivatives for binding affinity and functional activity at opioid receptors. Our results suggest that the methyl ester and furan ring are required for activity but that the lactone and ketone functionalities are not. Other salvinorins showed negligible binding affinity at the KOR. None of the compounds bound to mu or delta opioid receptors.

摘要

从鼠尾草中提取的Salvinorin A(1)是一种强效且具有选择性的κ阿片受体(KOR)激动剂。我们筛选了其他Salvinorins及其衍生物与阿片受体的结合亲和力和功能活性。我们的结果表明,甲酯和呋喃环是活性所必需的,但内酯和酮官能团并非如此。其他Salvinorins在KOR上的结合亲和力可忽略不计。这些化合物均未与μ或δ阿片受体结合。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验