Taxonomic group: plant / Streptophyta
(Phylum: Streptophyta)
Organ / tissue: leaf
The structure was elucidated in this paperJournal NLM ID: 0377775WWW link: http://ci.nii.ac.jp/naid/110003629361Publisher: Pharmaceutical Society Of Japan
Institutions: School of Pharmaceutical Sciences, Showa University, Japan
Steroid sponins and flavonoids of leaves of Phoenix rupicola T. ANDERSON, P. loureirii KUNTH, P. reclinata N. J. JACQUIN, and Arecastrum romanzoffianum BECCARI have been investigated. Tricin 7-O, β-D-glucopyranoside (I), vitexin (II), methyl proto-Pb (VII), methyl proto-taccaoside (26- O, β-D-glucopyranosyl (25R)-22-O-methyl-furost-5-en-3β,26-diol 3-O-[α-L-rhamnopyranosyl-(1→2)][α-L-rhamnopyranosyl-(1→3)]-β-D-glucopyranoside, VI), and methyl proto-rupicolaside (26-O, β-D-glucopyranosyl (25R)-22-O-methy-furost-5-en-3β,26-diol 3-O-[β-D-glucopyranosyl-(1→2)-α-L-rhamnopyranosyl-(1→4)-α-L-rhamnopyranosyl-(1→4)][α-L-rhamnopyranosyl-(1→2)]-β-D-glucopyranoside, VIII) from P. rupicola, II, glucoluteolin (III), orientin (IV), isoorientin (V), VII, VIII, and methyl proto-loureiroside (26-O-β-D-glucopyranosyl (25R)-22-O-methyl-furost-5-en-3β,26-diol 3-O-[β-D-glucopyranosyl-(1→5)-α-L-arabinofuranosyl-(1→4)][α-L-rhamnopyranosyl-(1→2)]-β-D-glucopyranoside, IX) from P.loureirii, VII, VIII and methyl proto-reclinatoside (26-O-β-D-glucopyranosyl (25R)-22-O-methyl-furost-5-en-3β,26-diol 3-O-[α-L-rhamnopyranosyl-(1→5)-α-L-arabinofuranosyl-(1→4)][α-L-rhamnopyranosyl(1→2)]-β-D-glucopyranoside, X) from P. reclinata, III and VII from A. romanzoffianum were isolated are identified. VI, VIII, IX and X were the first isolated and characterized from natural sources.
flavonoid, diosgenin, furostanol oligoside, Palmae, proto-diosgenin, Phoenix rupicola, Phoenix loureirii, Phoenix reclinata, Arecastrum romanzoffianum, steroid saponin
Structure type: oligomer
Location inside paper: III
Trivial name: glucoluteolin
Compound class: saponin glycoside, glycoside, flavonoid glycoside, flavone glycoside
Contained glycoepitopes: IEDB_142488,IEDB_146664,IEDB_613439,IEDB_983931,SB_192
Methods: 13C NMR, 1H NMR, IR, partial acid hydrolysis, TLC, acid hydrolysis, methanolysis, HPLC, enzymatic digestion, methylation analysis
NCBI Taxonomy refs (TaxIDs): 446123,
290277Reference(s) to other database(s): CCSD:
27029, CBank-STR:939
Show glycosyltransferases
There is only one chemically distinct structure: