TY - JOUR
T1 - New acylated triterpene saponins from Polygala arenaria
AU - Mitaine-Offer, Anne Claire
AU - Miyamoto, Tomofumi
AU - Laurens, Véronique
AU - Delaude, Clément
AU - Lacaille-Dubois, Marie Aleth
PY - 2003/8/29
Y1 - 2003/8/29
N2 - Eight new acylated triterpene saponins 1-8 were isolated from the roots of Polygala arenaria as four inseparable (E)/(Z) mixtures of the 4-methoxycinnamoyl and 3,4-dimethoxycinnamoyl derivatives by repeated MPLC over silica gel. Their structures were established mainly by 600-MHz 2D-NMR techniques (1H,1H-COSY, TOCSY, NOESY, HSQC, HMBC) as 3-O-(β-D-glucopyranosyl)presenegenin 28-(O-β-D-galactopyranosyl-(1→4)-O-[β-D-glucopyranosyl-(1→3) ]-O-β-D-xylopyranosyl-(1→4)-O-α-L-rhamnopyranosyl-(1→2) {4-O-[(E)-4-methoxycinnamoyl]}-β-D-fucopyranosyl) ester and its (Z)-isomer (1/2), 3-O-(β-D-glucopyranosyl)presenegenin 28-(O-β-D-galactopyranosyl-(1→4)-O-[β-D-glucopyranosyl-(1→3) ]-O-β-D-xylopyranosyl-(1→4)-O-α-L-rhamnopyranosyl-(1→2) -{4-O-[(E)-3,4-dimethoxycinnamoyl]}-β-D-fucopyranosyl) ester and its (Z)-isomer (3/4), 3-O-(β-D-glucopyranosyl)presenegenin 28-(O-β-D-glucopyranosyl-(1→3)-O-α-L-arabinopyranosyl-(1→4) -O-α-L-rhamnopyranosyl-(1→2)-{4-O-[(E)-4-methoxycinnamoyl]} -β-D-fucopyranosyl) ester and its (Z)-isomer (5/6), and 3-O-(β-D-glucopyranosyl)presenegenin 28-(O-β-D-glucopyranosyl-(1→3)-O-α-L-arabinopyranosyl-(1→4) -O-α-L-rhamnopyranosyl-(1→2)-{4-O-[(E)-3,4-dimethoxycinnamoyl]} -β-D-fucopyranosyl) ester and its (Z)-isomer (7/8) (presenegenin= (2β,3β)-2,3,27-trihydroxyolean-12-ene-23,28-dioic acid). In our in vitro lymphocyte proliferation assay (Jurkat T-leukemia cells), a fraction containing 1-4 showed a concentration-dependent immunomodulatory effect. This effect was not found for the prosapogenin (tenuifolin=3-O-(β-D-glucopyranosyl)presenegenin), underlining the importance of the acyl-oligosaccharidic moiety.
AB - Eight new acylated triterpene saponins 1-8 were isolated from the roots of Polygala arenaria as four inseparable (E)/(Z) mixtures of the 4-methoxycinnamoyl and 3,4-dimethoxycinnamoyl derivatives by repeated MPLC over silica gel. Their structures were established mainly by 600-MHz 2D-NMR techniques (1H,1H-COSY, TOCSY, NOESY, HSQC, HMBC) as 3-O-(β-D-glucopyranosyl)presenegenin 28-(O-β-D-galactopyranosyl-(1→4)-O-[β-D-glucopyranosyl-(1→3) ]-O-β-D-xylopyranosyl-(1→4)-O-α-L-rhamnopyranosyl-(1→2) {4-O-[(E)-4-methoxycinnamoyl]}-β-D-fucopyranosyl) ester and its (Z)-isomer (1/2), 3-O-(β-D-glucopyranosyl)presenegenin 28-(O-β-D-galactopyranosyl-(1→4)-O-[β-D-glucopyranosyl-(1→3) ]-O-β-D-xylopyranosyl-(1→4)-O-α-L-rhamnopyranosyl-(1→2) -{4-O-[(E)-3,4-dimethoxycinnamoyl]}-β-D-fucopyranosyl) ester and its (Z)-isomer (3/4), 3-O-(β-D-glucopyranosyl)presenegenin 28-(O-β-D-glucopyranosyl-(1→3)-O-α-L-arabinopyranosyl-(1→4) -O-α-L-rhamnopyranosyl-(1→2)-{4-O-[(E)-4-methoxycinnamoyl]} -β-D-fucopyranosyl) ester and its (Z)-isomer (5/6), and 3-O-(β-D-glucopyranosyl)presenegenin 28-(O-β-D-glucopyranosyl-(1→3)-O-α-L-arabinopyranosyl-(1→4) -O-α-L-rhamnopyranosyl-(1→2)-{4-O-[(E)-3,4-dimethoxycinnamoyl]} -β-D-fucopyranosyl) ester and its (Z)-isomer (7/8) (presenegenin= (2β,3β)-2,3,27-trihydroxyolean-12-ene-23,28-dioic acid). In our in vitro lymphocyte proliferation assay (Jurkat T-leukemia cells), a fraction containing 1-4 showed a concentration-dependent immunomodulatory effect. This effect was not found for the prosapogenin (tenuifolin=3-O-(β-D-glucopyranosyl)presenegenin), underlining the importance of the acyl-oligosaccharidic moiety.
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U2 - 10.1002/hlca.200390193
DO - 10.1002/hlca.200390193
M3 - Article
AN - SCOPUS:0043016250
SN - 0018-019X
VL - 86
SP - 2404
EP - 2413
JO - Helvetica Chimica Acta
JF - Helvetica Chimica Acta
IS - 7
ER -