Taxonomic group: plant / Streptophyta
(Phylum: Streptophyta)
Organ / tissue: flower
Journal NLM ID: 2985167RWWW link: https://ptfarm.pl/pub/File/Acta_Poloniae/1999/1/069.pdfPublisher: Polski Towarzystwo Farmaceutyczne
Institutions: Department of Pharmacognosy, Karol Marcinkowski University of Medical Sciences in Poznań 10 Sieroca Str., 61-771 Poznań, Poland
The following flavonoid compounds have been isolated and identified from flowers of Urena lobata L.: kaempferol 3-O-(6-O-trans-p-coumaroyl)-β-glucoside (tiliroside), dihydrokaempferol 4'-O-β-glucopyranoside, kaempferol and quercetin 3-O-β-glucosides and 3-O-β-rutinosides also luteolin 4'-O-β-glucopyranoside. Their structures were established by conventional (acid, enzymatic and alkaline hydrolysis) and spectral analysis (UV, 1H NMR, 13C NMR). Chromatographical investigations indicated the presence of quercetin, kaempferol and kaempferol 7-O-glucoside.
flavonoid, quercetin, kaempferol, luteolin, Malvaceae, Urena lobata L., dihydrokaempferol glycosides, tiliroside
Structure type: oligomer
C
27H
30O
16Location inside paper: compound IX, p. 70 (compound IX)
Trivial name: rutin, rutoside, rutin, quercetin rutinoside, rutoside, quercetin 3-O-rutinose, quercetin-3-O-rutinoside, quercetin 3-O-rutinoside
Compound class: saponin glycoside, glycoside, flavonoid glycoside, flavonol glycoside, flavone glycoside
Contained glycoepitopes: IEDB_136105,IEDB_142488,IEDB_144144,IEDB_146664,IEDB_225177,IEDB_885823,IEDB_983931,SB_192
Methods: 13C NMR, 1H NMR, TLC, enzymatic hydrolysis, alkaline hydrolysis, UV, PC, HCl hydrolysis
Comments, role: compound VIII was identified by UV, PC and acid hydrolysis data
Related record ID(s): 60082, 60204, 60258, 60341, 62228, 62229, 62230, 62231, 62232, 62234, 64156, 146810, 149316
NCBI Taxonomy refs (TaxIDs): 263848Reference(s) to other database(s): CCSD:
50720, CBank-STR:3399
Show glycosyltransferases
There is only one chemically distinct structure:
Found 
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