Chevalierinoside B and C: Two new isoflavonoid glycosides from the stem bark of Antidesma laciniatum Muell. Arg (syn. Antidesma chevalieri Beille)

被引:6
作者
Djouossi, Marie Genevieve [1 ]
Mabou, Florence Declaire [1 ]
Tebou, Perrin Lanversin Foning [1 ]
Ngnokam, David [1 ]
Tapondjou, Leon A. [1 ]
Harakat, Dominique [2 ]
Voutquenne-Nazabadioko, Laurence [3 ]
机构
[1] Univ Dschang, Fac Sci, Dept Chem, Dschang, Cameroon
[2] Inst Chim Mol Reims, CNRS UMR 7312, Serv Commun Anal, F-51687 Reims 2, France
[3] Inst Chim Mol Reims, CNRS UMR 7312, Grp Isolement & Struct, F-51687 Reims 2, France
关键词
Antidesma laciniatum/Antidesma chevalieri; Phyllantaceae; Isoflavonoid glycosides; Chevalierinosides; Triterpene; Structure elucidation; ANTIINFLAMMATORY ISOFLAVONOIDS; PRENYLATED ISOFLAVONOIDS; ERYTHRINA;
D O I
10.1016/j.phytol.2014.05.013
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Chevalierinosides B (1) and C (2), two new isoflavonoid glycosides, characterized as biochanin A 7-O-[beta-D-apiofuranosyl-(1 -> 2)-beta-D-glucopyranoside] and genistein 7-O-[beta-D-apiofuranosyl-(1 -> 2)-beta-D-glucopyranoside], together with the known isoflavonoids, chevalierinoside A (3) and genistein 7-O-beta-D-glucopyranoside (4), kaempferol 3-O-beta-D-glucopyranoside (5) and triterpenes, friedelin (6), betulinic acid (7), 30-oxobetulinic acid (8), 30-hydroxybetulinic acid (9), were isolated from the stem bark of Antidesma laciniatum Muell. Arg. (syn. Antidesma chevalieri Beille). Their structures were established by direct interpretation of their spectral data, mainly HR-TOFESIMS, 1D-NMR (H-1, C-13 and DEPT) and 2D-NMR (COSY, NOESY, TOCSY, HSQC and HMBC), and by comparison with the literature. (C) 2014 Phytochemical Society of Europe. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:149 / 152
页数:4
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