Taxonomic group: plant / Streptophyta
(Phylum: Streptophyta)
Organ / tissue: root
Publication DOI: 10.4314/bcse.v11i1.21013Journal NLM ID: 101549991Publisher: Addis Ababa
Institutions: Department of Chemistry, Department of Physiology, College of Medical Science, University of Maiduguri, P.M.B. 1069, Maiduguri, Nigeria
Chemical investigations on the roots of ricinus communis resulted in the isolation and characterization of a novel flavonol glycoside, kaempferol 3-O-β-D-[6'''-O-acetylglucopyranosyl [1→3)-β-D-galactopyranoside] for which the trivial name ricinitin is proposed. The structure of ricinitin was established on the basis of chemical and spectroscopic techniques. Other flavonoids that have been identified include: quercetin 3-O-glucoside and quercetin 3-O-rhamnosylglucoside (rutin).
Structure type: monomer
Location inside paper: p.52, 2
Trivial name: isoquercitrin
Compound class: saponin glycoside, glycoside, flavonoid glycoside, flavonol glycoside, flavone glycoside
Contained glycoepitopes: IEDB_142488,IEDB_146664,IEDB_983931,SB_192
Methods: 13C NMR, 1H NMR, FAB-MS, TLC, ESI-MS, acid hydrolysis, chemical methods, extraction
Related record ID(s): 60202, 60204
NCBI Taxonomy refs (TaxIDs): 3988Reference(s) to other database(s): CCSD:
49965, CBank-STR:953
Show glycosyltransferases
There is only one chemically distinct structure:
Found 
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