Prenylated chalcones, flavone and other constituents of the twigs of Dorstenia angusticornis and Dorstenia barteri var. subtriangularis

被引:23
作者
Ngadjui, BT
Watchueng, J
Keumedjio, F
Ngameni, B
Simo, IK
Abegaz, BM
机构
[1] Univ Yaounde, Fac Sci, Dept Organ Chem, Yaounde, Cameroon
[2] Univ Botswana, Fac Sci, Dept Chem, Gaborone, Botswana
关键词
Dorstenia angusticornis; Dorstenia barteri var. subtriangularis; Moraceae; twigs; isolation; prenylated chalcones; bartericins; A-D; an-guticornins A and B;
D O I
10.1016/j.phytochem.2004.10.016
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The twigs of Dorstenia angusticornis and Dorstenia barteri var. subtriangularis yielded 16 compounds. Two novel diprenylated chalcones: 3,5'-di-(2-hydroxy-3-methylbut-3-enyl)-4,2',4'-trihydroxychalcone, 3, 4-(2,2-dimethylpyrano)-3'-(2-hydroxy-3-methylbut-3-enyl)-2',4'-dihydroxychalcone and the known stipulin were isolated from both species. 3-(2-Hydroxy-3-methylbut-3-enyl)-5'-(3,3-dimethylallyl)-4,2',4'-trihydroxychalcone and the known compounds: 4-hydroxylonchocarpin, kanzonol B, bartericins A, B, C and 3'-(2-hydroxy -3-methylbut-3-enyl)-4,2',4'-trihydroxychalcone were isolated from D. barteri while the known compounds: gancaonin Q, paratocarpins C, F, and lupeol were obtained from Dorstenia angusticornis. beta-Sitosterol and its beta-D-glucopyranoside were isolated from both species. Structures of these secondary metabolites were established using spectroscopic analysis, especially, NMR spectra in conjunction with 2D experiments, COSY, HMQC and HMBC. (c) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:687 / 692
页数:6
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