Taxonomic group: plant / Streptophyta
(Phylum: Streptophyta)
Organ / tissue: aerial part
Journal NLM ID: 9441222WWW link: https://cir.nii.ac.jp/crid/1520853834365277184Publisher: Kyoto: Nihon Shōyaku Gakkai
Institutions: Osaka University of Pharmaceutical Sciences, Osaka, Japan, Ain shams Uhiversity, Faculty of Pharmacy, Department of Pharmacognosy, Cairo, Egypt
Two new flavonol glycosides were isolated from Morettia philaena (Cruciferae) growing in Egypt together with four known compounds (kaempferol, quercetin, kaempferol 3-O-β-D-glucopyranoside, quercetin 3-O-β-D- glucopyranoside). Their structures were determined as quercetin 3-O-{2''- (6'''-p-cumaroyl-β-D-glucopyranosyl)- α-L-arabinopyranosyl}7''-O-β-D- glucopyranoside; kaempferol 3-O-{2''(6'''p-cumaroyl-β-D-glucopyranosyl)-α- L-arabinopyranosyl}7-O-β -D-glucopyranoside by spectroscopy and chemical methods.
flavonol glycoside, kaempferol glycoside, Cruciferae, quercetin glycoside, Morettia philaeana
Structure type: monomer
Location inside paper: abstract
Trivial name: isoquercitrin
Compound class: saponin glycoside, glycoside, flavonoid glycoside, flavonol glycoside, flavone glycoside
Contained glycoepitopes: IEDB_142488,IEDB_146664,IEDB_983931,SB_192
Methods: 13C NMR, 1H NMR, NMR-2D, FAB-MS, TLC, ESI-MS, HPLC, extraction, column chromatography
Related record ID(s): 67923, 67924, 67925
NCBI Taxonomy refs (TaxIDs): 369026Reference(s) to other database(s): CCSD:
49965, CBank-STR:953
Show glycosyltransferases
There is only one chemically distinct structure:
Found 
report error