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: oligomer
Location inside paper: p. 153, column 2, paragraph 1, compound 4, compound 8, compound 9
Trivial name: quercetin 3-O-rutinoside, quercetin 3-O-glucoside, quercetin 3-O-β-(6''-galloylglucoside)
Compound class: glycoside
Contained glycoepitopes: IEDB_136105,IEDB_142488,IEDB_144144,IEDB_146664,IEDB_225177,IEDB_885823,IEDB_983931,SB_192
Methods: 13C NMR, 1H NMR, FAB-MS, acid hydrolysis, UV, extraction, CC
Related record ID(s): 63741, 63750, 63751, 63752, 63753
NCBI Taxonomy refs (TaxIDs): 2768810
Show glycosyltransferases
There is only one chemically distinct structure: