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)

Citation
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
Citations number
40
Categorie Soggetti
Pharmacology & Pharmacy",Chemistry
ISSN journal
00092363
Volume
45
Issue
3
Year of publication
1997
Pages
464 - 469
Database
ISI
SICI code
0009-2363(1997)45:3<464:MF.M.A>2.0.ZU;2-2
Abstract
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.