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题名: Diterpene Alkaloids with an Aza-ent-kaurane Skeleton from Isodon rubescens
作者: Liu, Xu1, 2; Yang, Jing1, 3; Wang, Wei-Guang1; null(李艳)1; Wu, Ji-Zhou2; Pu, Jian-Xin1; null(孙汉董)1
刊名: JOURNAL OF NATURAL PRODUCTS
出版日期: 2015-02-01
卷号: 78, 期号:2, 页码:196-201
学科分类: Plant Sciences; Chemistry, Medicinal; Pharmacology & Pharmacy
DOI: 10.1021/np5006136
通讯作者: Pu,JX (reprint author),Chinese Acad Sci,Kunming Inst Bot,State Key Lab Phytochem & Plant Resources West Ch,Kunming 650201,Yunnan,Peoples R China. ; pujianxin@mail.kib.ac.cn ; hdsun@mail.kib.ac.cn
文章类型: Article
英文摘要: Two compounds belonging to a new group of diterpene alkaloids, kaurines A and B (1 and 2), and an alkaloid bearing a succinimide moiety (3) were obtained from Isodon rubescens. Their structures and absolute configurations were determined by spectroscopy and quantum-chemical computational C-13 NMR and ECD data analysis. These alkaloids differ from known diterpene alkaloids and diterpenoids and are presumably biosynthesized from ent-kaurane diterpenoids.
类目[WOS]: Plant Sciences ; Chemistry, Medicinal ; Pharmacology & Pharmacy
研究领域[WOS]: Plant Sciences ; Pharmacology & Pharmacy
关键词[WOS]: ROOTS
收录类别: SCI
项目资助者: NSFC-Joint Foundation of Yunnan Province [U1302223] ; National Natural Science Foundation of China [21322204, 81172939] ; Reservation-Talent Project of Yunnan Province [2011CI043] ; West Light Foundation of the Chinese Academy of Sciences
语种: 英语
WOS记录号: WOS:000350328600004
Citation statistics:
内容类型: 期刊论文
URI标识: http://ir.kib.ac.cn/handle/151853/20592
Appears in Collections:植物化学与西部植物资源持续利用国家重点实验室_期刊论文

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作者单位: 1.Chinese Acad Sci, Kunming Inst Bot, State Key Lab Phytochem & Plant Resources West Ch, Kunming 650201, Yunnan, Peoples R China
2.Huazhong Univ Sci & Technol, Tongji Sch Pharm, Hubei Key Lab Nat Med Chem & Resource Evaluat, Wuhan 430030, Hunan, Peoples R China
3.Chinese Acad Sci, Shanghai Inst Mat Med, State Key Lab Drug Res, Ctr Drug Discovery & Design, Shanghai 201203, Peoples R China
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