Taxonomic group: plant / Streptophyta
(Phylum: Streptophyta)
Organ / tissue: leaf
NCBI PubMed ID: 10683879Journal NLM ID: 9800766Publisher: Eschborn: Govi-Verlag Pharmazautischer Verlag
Correspondence: Pieroni A <experiences

netcologne.de>
Institutions: Pharmaceutical Institute, University of Bonn, Bonn, Germany
A new flavone, apigenin-7-O-β-(2",6"-di-α-rhamnopyranosyl)-glucopyranoside , named ligustroflavone, was isolated from the leaves of common privet (Ligustrum vulgare L., Oleaceae), whose popular use was well known in the Mediterranean historical medicine and ethnomedicine as anti-inflammatory. The structures of other five apigenin and luteolin derivates, isolated from the polar fractions of the methanolic leaf extracts, were elucidated.
Structure type: monomer
Location inside paper: p. 78, Fig. 1, compound 1
Trivial name: cosmosiin, apigenin 7-O-glucoside, rhoifolin, apigenin 7-glucoside, apigetrin
Compound class: glycoside, flavonoid glycoside, flavonol glycoside
Contained glycoepitopes: IEDB_142488,IEDB_146664,IEDB_613414,IEDB_983931,SB_192
Methods: 13C NMR, 1H NMR, NMR-2D, TLC, enzymatic hydrolysis, acid hydrolysis, HPLC, optical rotation measurement, HR-FAB-MS
Related record ID(s): 68913, 68914, 68915, 68916
NCBI Taxonomy refs (TaxIDs): 13597Reference(s) to other database(s): CCSD:
50502, CBank-STR:1305
Show glycosyltransferases
There is only one chemically distinct structure: