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紫堇属生物碱和尖刺碱生物碱。

The Hasubanan and Acutumine Alkaloids.

作者信息

King Sandra M, Herzon Seth B

机构信息

Department of Chemistry, Yale University, New Haven, Connecticut, USA.

Department of Chemistry, Yale University, New Haven, Connecticut, USA.

出版信息

Alkaloids Chem Biol. 2014;73:161-222. doi: 10.1016/B978-0-12-411565-1.00003-2. Epub 2013 Dec 25.

Abstract

Research in the hasubanan and acutumine alkaloid fields up to 1970 was discussed under "morphine alkaloids" in Volume 13 of this chapter. Advances in the field of hasubanan alkaloids from 1971 to 1975 were reviewed in Volume 16 and from 1976 to 1986 in Volume 33. This chapter extends the information in the three preceding reviews to hasubanan alkaloid literature published from 1987 to June 2013. This chapter covers acutumine alkaloid literature since (-)-acutumine (3) was isolated in 1929. This chapter includes occurrence and physical constants, new alkaloids, synthesis, biosynthesis, and pharmacology. Section 1 introduces the foremost alkaloids, (-)-hasubanonine (1) and (-)-acutumine (3), and the numbering systems of the hasubanan (2) and acutumine (4) skeletons. Section 2 details the occurrence and physical constants of 29 new hasubanan and 15 acutumine alkaloids. The isolation and structural determination of these new alkaloids are described in Section 3. Section 4 summarizes total syntheses and synthetic studies toward hasubanan and acutumine alkaloids. Completed syntheses of the hasubanan alkaloids (+)-cepharamine (ent-71), (-)-hasubanonine (1), (-)-runanine (8), (-)-delavayine (6), (+)-periglaucine B (19), and (-)-8-demethoxyrunanine (12) are reviewed. Completed syntheses of (-)-acutumine (3) and (-)-dechloroacutumine (52) are also described. Section 5 details biosyntheses of (-)-acutumine (3) advanced by Barton, Wipf, and Sugimoto. Section 6 summarizes pharmacological studies of hasubanan and acutumine alkaloids. Opioid receptor affinity, anti-HBV activity, and antimicrobial activity of hasubanan alkaloids are reported. Antiamnesic properties, cytotoxicity, and anti-HBV activity of acutumine alkaloids are described.

摘要

本章第13卷“吗啡生物碱”部分讨论了截至1970年关于青藤碱和尖刺碱领域的研究。第16卷综述了1971年至1975年青藤碱生物碱领域的进展,第33卷综述了1976年至1986年的进展。本章将前三次综述中的信息扩展至1987年至2013年6月发表的青藤碱生物碱文献。本章涵盖了自1929年分离出(-)-尖刺碱(3)以来的尖刺碱生物碱文献。本章包括存在情况和物理常数、新生物碱、合成、生物合成及药理学。第1节介绍了最重要的生物碱,即(-)-青藤碱宁(1)和(-)-尖刺碱(3),以及青藤碱(2)和尖刺碱(4)骨架的编号系统。第2节详细介绍了29种新的青藤碱生物碱和15种尖刺碱生物碱的存在情况和物理常数。第3节描述了这些新生物碱的分离和结构测定。第4节总结了青藤碱和尖刺碱生物碱的全合成及合成研究。综述了青藤碱生物碱(+)-千金藤胺(对映体-71)、(-)-青藤碱宁(1)、(-)-鲁南碱(8)、(-)-滇西青藤碱(6)、(+)-异千金藤碱B(19)和(-)-8-去甲氧基鲁南碱(12)的完成合成。还描述了(-)-尖刺碱(3)和(-)-去氯尖刺碱(52)的完成合成。第5节详细介绍了巴顿、维普夫和杉本等人推进的(-)-尖刺碱(3)的生物合成。第6节总结了青藤碱和尖刺碱生物碱的药理学研究。报道了青藤碱生物碱的阿片受体亲和力、抗乙肝病毒活性和抗菌活性。描述了尖刺碱生物碱的抗遗忘特性、细胞毒性和抗乙肝病毒活性。

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