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Acylated Triterpene Saponins from Atroxima liberica Stapf
Authors:Turibio Kuiate Tabopda  Anne‐Claire Mitaine‐Offer  Tomofumi Miyamoto  Chiaki Tanaka  Jean‐François Mirjolet  Olivier Duchamp  Bonaventure Tchaleu Ngadjui  Marie‐Aleth Lacaille‐Dubois
Affiliation:1. Laboratoire de Pharmacognosie, Unité de Molécules d'Intérêt Biologique, UMIB, UPRES‐EA 3660, Faculté de Pharmacie, Université de Bourgogne, 7, Bd. Jeanne d'Arc, BP 87900, F‐21079 Dijon Cedex, (phone: +33‐3‐80393229;2. fax: +33‐3‐80393300);3. Département de Chimie Organique, Université de Yaoundé 1, BP 812, Yaoundé, Cameroon;4. Graduate School of Pharmaceutical Sciences, Kyushu University, Fukuoka 812‐8582, Japan;5. Oncodesign, 20 rue Jean Mazen, BP 27627, F‐21076 Dijon Cedex
Abstract:The four new acylated triterpene saponins 1 – 4 , isolated as two pairs of isomers and named libericosides A1/A2 and B1/B2, one pair of isomers 5 / 6 , the (Z)‐isomer libericoside C2 ( 5 ) being new, one new sucrose ester, atroximoside ( 7 ), and eight known compounds were isolated from the roots of Atroxima liberica by repeated MPLC and VLC on normal and reversed‐phase silica gel. Their structures were elucidated on the basis of extensive 1D‐ and 2D‐NMR studies (1H‐ and 13C‐NMR, DEPT, COSY, TOCSY, NOESY, HSQC, and HMBC) and mass spectrometry as 3‐Oβ‐D ‐glucopyranosylpresenegenin 28‐{Oα‐L ‐arabinopyranosyl‐(1→3)‐Oβ‐D ‐xylopyranosyl‐(1→4)‐Oα‐L ‐rhamnopyranosyl‐(1→2)‐4‐O‐[(E)‐3,4‐dimethoxycinnamoyl]‐β‐D ‐fucopyranosyl} ester ( 1 ) and its (Z)‐isomer 2 , 3‐Oβ‐D ‐glucopyranosylpresenegenin 28‐{Oα‐L ‐arabinopyranosyl‐(1→4)‐Oβ‐D ‐xylopyranosyl‐(1→4)‐Oα‐L ‐rhamnopyranosyl‐(1→2)‐O‐[O‐β‐D ‐xylopyranosyl‐(1→3)‐β‐D ‐glucopyranosyl‐(1→3)]‐4‐O‐[(E)‐3,4‐dimethoxycinnamoyl]‐β‐D ‐fucopyranosyl} ester ( 3 ) and its (Z)‐isomer 4 , 3‐Oβ‐D ‐glucopyranosylpresenegenin 28‐{Oβ‐D ‐xylopyranosyl‐(1→4)‐Oα‐L ‐rhamnopyranosyl‐(1→2)‐O‐[6‐O‐acetyl‐β‐D ‐glucopyranosyl‐(1→3)]‐4‐O‐[(Z)‐3,4‐dimethoxycinnamoyl]‐β‐D ‐fucopyranosyl} ester ( 5 ), and 3‐O‐[(Z)‐feruloyl]‐β‐D ‐fructofuranosyl α‐D ‐glucopyranoside ( 7 ). Compounds 1 – 6 and the known saponins 8 / 9 were evaluated against the human colon cancer cells HCT 116 and HT‐29 and showed moderate to weak cytotoxicity.
Keywords:Atroxima liberica  Triterpene saponins  Saponins  Libericosides A1/A2, B1/B2, and C2  Cytotoxic activity
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