Four new cassane diterpenoid amides from Erythrophleum suaveolens [(Guill. et Perr.), Brenan]

被引：12
|
作者：
Kablan, Landry A. [1 ,4 ]
Dade, Joel M. E. [1 ]
Say, Martial [1 ]
Okpekon, Timothee A. [1 ]
Yapo, Kicho D. [1 ]
Ouffoue, Sebastian K. [1 ]
Koffi, Armand P. [2 ]
Retailleau, Pascal [3 ]
Champy, Pierre [4 ]
机构：
[1] Univ Felix Houphouet Boigny, Dept Sci Struct Matter & Technol, Lab Organ & Biochem, Felix Houphouet Boigny, Cote Ivoire
[2] Felix Houphouet Boigny Univ, Dept Pharmaceut Sci, Lab Galen, Abidjan, Cote Ivoire
[3] ICSN CNRS, Crystallog Lab, F-91198 Gif Sur Yvette, France
[4] Univ Paris 11, Lab Pharmacognosia, CNRS UMR BioCIS 8076, LabEX LERMIT,Fac Pharm, Orsay, France
来源：
PHYTOCHEMISTRY LETTERS | 2014年 / 10卷
关键词：
Fabaceae; Erythrophleum; Erythrophleum suaveolens; Cassane diterpenoid amide; CHLOROSTACHYS LEGUMINOSAE; ALKALOIDS; FORDII; BARK;
D O I：
10.1016/j.phytol.2014.08.005
中图分类号：
Q94 [植物学];
学科分类号：
071001 ;
摘要：
Four new cassane diterpenoid amides, 1-4 and six known cassane diterpenoid amides have been isolated from the stem bark of Erythrophleum suaveolens. The isolated compounds were subjected to phytochemical investigation. The structures of those compounds were elucidated on the basis of one-and two-dimensional NMR, HRMS and ESIMS analyses. Nor-cassamide was obtained as crystal and characterized by X-ray method. This was the first crystallographic description of cassane diterpenoid and it allowed to confirm the absolute configuration of the stereogenic centers and the stereochemistry of the double exocyclic bond. (C) 2014 Phytochemical Society of Europe. Published by Elsevier B.V. All rights reserved.
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收藏
页码：60 / 64
页数：5
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