Literature DB >> 24729281

Suffrutines A and B: a pair of Z/E isomeric indolizidine alkaloids from the roots of Flueggea suffruticosa.

Zhen-Long Wu1, Bing-Xin Zhao, Xiao-Jun Huang, Gen-Yun Tang, Lei Shi, Ren-Wang Jiang, Xin Liu, Ying Wang, Wen-Cai Ye.   

Abstract

Suffrutines A (1) and B (2), a pair of novel photochemical Z/E isomeric indolizidine alkaloids, with a unique and highly conjugated C20 skeleton, were isolated from the roots of Flueggea suffruticosa. The structures were elucidated by extensive analysis of NMR spectra and single-crystal X-ray diffraction. The light-induced isomerization and hypothetical biogenetic pathway to 1 and 2, as well as their activity for regulating the morphology of Neuro-2a cells are also discussed.
© 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  NMR spectroscopy; alkaloids; natural products; photochemistry; structure elucidation

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Year:  2014        PMID: 24729281     DOI: 10.1002/anie.201400048

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  2 in total

1.  Chemical Constituents from Flueggea virosa and the Structural Revision of Dehydrochebulic Acid Trimethyl Ester.

Authors:  Chih-Hua Chao; Ying-Ju Lin; Ju-Chien Cheng; Hui-Chi Huang; Yung-Ju Yeh; Tian-Shung Wu; Syh-Yuan Hwang; Yang-Chang Wu
Journal:  Molecules       Date:  2016-09-16       Impact factor: 4.411

Review 2.  Unique indolizidine alkaloid securinine is a promising scaffold for the development of neuroprotective and antitumor drugs.

Authors:  Sergey Klochkov; Margarita Neganova
Journal:  RSC Adv       Date:  2021-05-26       Impact factor: 4.036

  2 in total

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