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#10;GOYASAPONIN-II;28-O-BETA-D-XYLOPYRANOSYL-(1->3)-BETA-D-XYLOPYRANOSYL-(1->4)-ALPHA-L-RHAMNOPYRANOSYL-(1->2)-[ALPHA-L-RHAMNOPYRANOSYL-(1->3)]-BETA-D-FUCOPYRA

Compound with spectra: 1 NMR

#10;GOYASAPONIN-II;28-O-BETA-D-XYLOPYRANOSYL-(1->3)-BETA-D-XYLOPYRANOSYL-(1->4)-ALPHA-L-RHAMNOPYRANOSYL-(1->2)-[ALPHA-L-RHAMNOPYRANOSYL-(1->3)]-BETA-D-FUCOPYRA
SpectraBase Compound ID DgJIwnybwp6
InChI InChI=1S/C70H110O35/c1-25-36(75)40(79)46(85)59(94-25)101-52-37(76)26(2)95-63(55(52)104-60-48(87)44(83)50(27(3)96-60)99-58-49(88)51(31(74)23-93-58)100-57-45(84)38(77)30(73)22-92-57)105-64(91)70-18-16-65(4,5)20-29(70)28-10-11-34-66(6)14-13-35(67(7,24-72)33(66)12-15-69(34,9)68(28,8)17-19-70)98-62-54(43(82)42(81)53(102-62)56(89)90)103-61-47(86)41(80)39(78)32(21-71)97-61/h10,24-27,29-55,57-63,71,73-88H,11-23H2,1-9H3,(H,89,90)/t25-,26-,27+,29+,30+,31+,32-,33-,34-,35+,36-,37+,38-,39+,40+,41+,42+,43+,44+,45+,46+,47-,48-,49+,50+,51-,52+,53+,54-,55-,57-,58-,59-,60+,61+,62-,63+,66+,67+,68-,69-,70+/m1/s1
InChIKey IVYQSEVUVAENJB-PMPVRRDOSA-N
Mol Weight 1511.6 g/mol
Molecular Formula C70H110O35
Exact Mass 1510.682765 g/mol
Enantiomer InChIKey IVYQSEVUVAENJB-NNIAKSBTSA-N

View Spectrum of #10;GOYASAPONIN-II;28-O-BETA-D-XYLOPYRANOSYL-(1->3)-BETA-D-XYLOPYRANOSYL-(1->4)-ALPHA-L-RHAMNOPYRANOSYL-(1->2)-[ALPHA-L-RHAMNOPYRANOSYL-(1->3)]-BETA-D-FUCOPYRA

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent C5D5N
#1;28-O-BETA-D-XYLOPYRANOSYL-(1->3)-BETA-D-XYLOPYRANOSYL-(1->4)-ALPHA-L-RHAMNOPYRANOSYL-(1->2)-[ALPHA-L-RHAMNOPYRANOSYL-(1->3)]-BETA-D-FUCOPYRANOSYL-GYPSOGENIN
Title Journal or Book Year
Medicinal Foodstuffs. XXI. Structures of New Cucurbitane-Type Triterpene Glycosides, Goyaglycosides-a, -b, -c, -d, -e, -f, -g, and -h, and New Oleanane-Type Triterpene Saponins, Goyasaponins I, II, and III, from the Fresh Fruit of Japanese Momordica charantia L. Chemical and Pharmaceutical Bulletin 2001
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