MEDICINAL FOODSTUFFS .5. MOROHEIYA .1. ABSOLUTE STEREOSTRUCTURES OF CORCHOIONOSIDE-A, CORCHOIONOSIDE-B, AND CORCHOIONOSIDE-C, HISTAMINE-RELEASE INHIBITORS FROM THE LEAVES OF VIETNAMESE CORCHORUS-OLITORIUS L (TILIACEAE)
M. Yoshikawa et al., MEDICINAL FOODSTUFFS .5. MOROHEIYA .1. ABSOLUTE STEREOSTRUCTURES OF CORCHOIONOSIDE-A, CORCHOIONOSIDE-B, AND CORCHOIONOSIDE-C, HISTAMINE-RELEASE INHIBITORS FROM THE LEAVES OF VIETNAMESE CORCHORUS-OLITORIUS L (TILIACEAE), Chemical and Pharmaceutical Bulletin, 45(3), 1997, pp. 464-469
Three new ionone glucosides named corchoionosides A, B, and C were iso
lated from the leaves of Corchorus olitorius, commonly called ''morohe
iya'' in Japanese, together with seven known compounds, an ionone gluc
oside (6S,9R)-roseoside, a monoterpene glucoside betulalbuside A, two
flavonol glucosides astragalin and isoquercitrin, two coumarin glucosi
des scopolin and cichoriine, and chlorogenic acid. The absolute stereo
structures of corchoionosides A, B, and C mere determined by chemical
and physicochemical evidence, which included the result of application
of a modified Mosher's method, the CD helicity rule, and chemical cor
relation with (6S,9R)-roseoside. Corchoionosides A and B and (6S,9R)-r
oseoside were found to inhibit the histamine release from rat peritone
al exudate cells induced by antigen-antibody reaction.