Taxonomic group: plant / Streptophyta
(Phylum: Streptophyta)
Organ / tissue: leaf
Publication DOI: 10.1248/cpb.40.249Journal NLM ID: 0377775Publisher: Pharmaceutical Society Of Japan
Institutions: College of Pharmacy, Nihon University, 7-7 Narashinodai, Funabashi-shi, Chiba 274, Japan
Two new flavone glycosides were isolated along with diosmetin, luteolin, and luteolin 7-O-glucoside, from the leaves of Cassia torosa CAV., and their structures were established as diosmetin 3'-O-β-D-glucopyranoside (1) and torosaflavone B 3'-O-β-D-glucopyranoside (2) (diosmetin 6-C-β-D-oliopyranosyl-3'-O-β-D-glucopyranoside) on the basis of spectroscopic and chemical evidence.
2, flavone glycoside, Leguminosae, Cassia torosa, oliose, 6-dideoxyglycoside, torosaflavone B 3'-O-β-D-glucopyranoside, diosmetin 3'-O-β-D-glucopyranoside
Structure type: monomer
Location inside paper: luteolin 7-O-glucoside
Trivial name: glucoluteolin, luteolin 7-glucoside
Compound class: saponin glycoside, glycoside, flavonoid glycoside, flavonol glycoside, flavone glycoside, flavone glucoside
Contained glycoepitopes: IEDB_142488,IEDB_146664,IEDB_613439,IEDB_983931,SB_192
Methods: 13C NMR, 1H NMR, IR, TLC, enzymatic hydrolysis, UV, optical rotation measurement, CD, FD-MS, HCl hydrolysis
Comments, role: structure of luteolin 7-O-glucoside was determined by means of spectral and chemical evidence
Related record ID(s): 62912, 62913, 62914
NCBI Taxonomy refs (TaxIDs): 53851Reference(s) to other database(s): CCSD:
50066, CBank-STR:939
Show glycosyltransferases
There is only one chemically distinct structure:
Found 
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