Taxonomic group: plant / Streptophyta
(Phylum: Streptophyta)
Organ / tissue: leaf
Publication DOI: 10.1002/jccs.200000030Journal NLM ID: 16210600RPublisher: Taipei: Chinese Chemical Society
Institutions: National Research Institute of Chinese Medicine, Taipei, Taiwan, China, Department of Chemistry, National Taiwan University, Taipei, Taiwan, China, Department of Medical Research and Education, Veterans General Hospital, Taipei, Taiwan, China
Under the inhibition of Cu+2-induced LDL oxidation-guided fractionation, two new flavone glycosides with galloyl substitution were isolated from the dried fallen leaves of Terminalia catappa L. Their structures were established as apigenin 6-C-(2″-O-galloyl)-β-D-glucopyranoside (1) and apigenin 8-C-(2″-O-galloyl)-β-D-glucopyranoside (2), together with four known flavone glycosides, isovitexin, vitexin, isoorientin, and rutin, on the basis of spectroscopic method. Compounds 1 and 2 showed significant antioxidative effects. Their IC50 were 2.1 and 4.5 μM, respectively.
Antioxidant, Combretaceae, Terminalia catappa L., dried fallen leaves, flavone glucopyranosides
Structure type: oligomer
C
27H
30O
16Location inside paper: p. 254, structure 6
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: biological assays, extraction, evaporation, centrifugation
Related record ID(s): 66565, 66566, 66567, 66568, 66569
NCBI Taxonomy refs (TaxIDs): 39993Reference(s) to other database(s): CCSD:
50720, CBank-STR:3399
Show glycosyltransferases
There is only one chemically distinct structure:
Found 
report error