Taxonomic group: plant / Streptophyta
(Phylum: Streptophyta)
NCBI PubMed ID: 11142853Publication DOI: 10.1016/s0031-9422(00)00309-5Journal NLM ID: 0151434Publisher: Elsevier
Correspondence: y.lu
irl.cri.nz
Institutions: Industrial Research Limited, Lower Hutt, New Zealand
Two novel phenolic glycosides cis-p-coumaric acid 4-O-(2′-O-β-d-apiofuranosyl)-β-d-glucopyranoside and trans-p-coumaric acid 4-O-(2′-O-β-d-apiofuranosyl)-β-d-glucopyranoside were isolated and identified from Salvia officinalis together with 4-hydroxyacetophenone 4-O-(6′-O-β-d-apiofuranosyl)-β-d-glucopyranoside, luteolin 7-O-β-d-glucoside, 7- and 3′-O-β-d-glucuronide, 6-hydroxyluteolin 7-O-β-d-glucoside and 7-O-glucuronide, and 6,8-di-C-β-d-glucosylapigenin (vicenin-2). The luteolin glucuronides and vicenin-2 were identified as new sage constituents.
phenolic glycosides, flavonoids, Labiatae, Salvia offcinalis, cis- and trans-p-coumaric acid 4-O-(2'-O-apiosyl)glucoside
Structure type: monomer
Location inside paper: p. 264, structure 4
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, NMR-2D, TLC, ESI-MS, HPLC, extraction, HR-ESI-MS, evaporation, centrifugation
Related record ID(s): 66618, 66619, 66620, 66622, 66623, 66624, 66625, 66626
NCBI Taxonomy refs (TaxIDs): 38868Reference(s) to other database(s): CCSD:
50066, CBank-STR:939
Show glycosyltransferases
There is only one chemically distinct structure:
Found 
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