中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Abietane derived diterpenoids as Cav3.1 antagonists from Salvia digitaloides

文献类型:期刊论文

作者Zhao,Jianjun; Du,Shuzong; Hu,Kun; Hu,Yali; Xia,Fan; Ye,Yansong; Yang,Jian; Nian,Yin; Xu,Gang
刊名CHINESE CHEMICAL LETTERS
出版日期2023
卷号34期号:4页码:107737
关键词10-Methylated 6 7 6 carbon ring system Icetexane Diterpenoid Salvia digitaloides Ca v 3 1 low voltage -gated Ca 2+channel (LVGCC) ROOTS TANSHINLACTONE CONSTITUENTS ELUCIDATION INHIBITORS CHANNELS SKELETON SYSTEM
ISSN号1878-5964
DOI10.1016/j.cclet.2022.08.017
英文摘要Nineteen diterpenoids, including saldigitin A ( 1 ) bearing an unprecedented 10-methylated 6/7/6 carbon ring system, two new icetexanes ( 2 , 3 ), and two new nor-abietanes ( 5 , 6 ) were characterized from the roots of Salvia digitaloides. Their structures were elucidated by the analysis of the spectroscopic data, X-ray crystallography, and TDDFT calculations of ECD spectra. The novel architecture of 1 should be biogenetically derived through the cleavage and re-cyclization of the B/C rings from the normal abi-etane skeleton. Biologically, 1 -5 exhibited noticeable inhibitions on Cav 3.1 low voltage-gated Ca2 + channel (LVGCC), with IC50 values in the range of 3.43-11.70 mu mol/L. They are the first example of diterpenoids with 6/7/6 carbon rings system as Cav 3.1 antagonists. (c) 2023 Published by Elsevier B.V. on behalf of Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences.
学科主题Chemistry
WOS记录号WOS:000961376200001
源URL[http://ir.kib.ac.cn/handle/151853/75456]  
专题中国科学院昆明植物研究所
推荐引用方式
GB/T 7714
Zhao,Jianjun,Du,Shuzong,Hu,Kun,et al. Abietane derived diterpenoids as Cav3.1 antagonists from Salvia digitaloides[J]. CHINESE CHEMICAL LETTERS,2023,34(4):107737.
APA Zhao,Jianjun.,Du,Shuzong.,Hu,Kun.,Hu,Yali.,Xia,Fan.,...&Xu,Gang.(2023).Abietane derived diterpenoids as Cav3.1 antagonists from Salvia digitaloides.CHINESE CHEMICAL LETTERS,34(4),107737.
MLA Zhao,Jianjun,et al."Abietane derived diterpenoids as Cav3.1 antagonists from Salvia digitaloides".CHINESE CHEMICAL LETTERS 34.4(2023):107737.

入库方式: OAI收割

来源:昆明植物研究所

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