Taxonomic group: plant / Streptophyta
(Phylum: Streptophyta)
NCBI PubMed ID: 10820819Publication DOI: 10.1016/s0031-9422(00)00027-3Journal NLM ID: 0151434Publisher: Elsevier
Correspondence: shoyama
shoyaku.pharm.kyushu-u.ac.jp
Institutions: Graduate School of Pharmaceutical Sciences, Kyushu University, Fukuoka, Japan, Seiwa Pharmaceutical Ltd., Tokyo, Japan
A flavonol glycoside, 3-[[6-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranosyl]oxi]-5,7-dihydroxy-8-[(4-hydroxy-3,5-dimethoxyphenyl)methyl]-2-(3,4-dihydroxypheny)-4H-1-benzopyran-4-one, trivially named goodyerin, was isolated from the whole plant of Goodyera schlechtendaliana, along with three known flavonoids, rutin, kaempferol-3-O-rutinoside and isorhamnetin-3-O-rutinoside. The structures were established by spectroscopic analysis.
flavonoids, Orchidaceae, Goodyera schlechtendaliana, goodyerin
Structure type: oligomer
C
27H
30O
16
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: 13C NMR, 1H NMR, NMR-2D, FAB-MS, TLC, acid hydrolysis, GC, UV, extraction, optical rotation measurement, CC, RP-HPLC, melting point determination, derivatization, evaporation, HR-FAB-MS
Related record ID(s): 65352, 65354, 65355
NCBI Taxonomy refs (TaxIDs): 164262Reference(s) to other database(s): CCSD:
50720, CBank-STR:3399
Show glycosyltransferases
There is only one chemically distinct structure:
Found 
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