Taxonomic group: plant / Streptophyta
(Phylum: Streptophyta)
Organ / tissue: leaf
The structure was elucidated in this paperJournal NLM ID: 9714997Publisher: Seoul, Korea: Korean Society of Pharmacognosy
Institutions: National Research Centre, Dokki, Cairo, Egypt
The aqueous ethanolic leaf extract of Ailanthus altissima was found to contain the new natural product, luteolin 7-O-β-(6'- galloylglucopyranoside), 13, along with fourteen known phenotic metabolites (1-12, 14 and 15). Structures of all compounds (1-15) were established by conventional methods of analysis and confirmed by FAB-MS, 1H- and 13C-NMR spectral analysis.
13C-NMR, FAB-MS, phenolics, Simaroubaceae, Ailanthus altissima, luteolin 7-O-β-(6'- galloylglucopyranoside)
Structure type: monomer
C
21H
20O
11Location inside paper: p. 153, column 2, paragraph 1, compound 7
Trivial name: quercitrin, baohuoside-II, quercetin 3-rhamnoside, quercetin 3-O-rhamnoside
Compound class: saponin glycoside, glycoside, flavonoid glycoside, flavonol glycoside
Contained glycoepitopes: IEDB_136105,IEDB_225177,IEDB_885823
Methods: 13C NMR, 1H NMR, FAB-MS, acid hydrolysis, UV, extraction, CC
Related record ID(s): 63523, 63750, 63751, 63752, 63753
NCBI Taxonomy refs (TaxIDs): 2768810Reference(s) to other database(s): CCSD:
49971, CBank-STR:599
Show glycosyltransferases
There is only one chemically distinct structure: