Taxonomic group: plant / Streptophyta
(Phylum: Streptophyta)
Organ / tissue: leaf,
stem
NCBI PubMed ID: 10820807Publication DOI: 10.1016/s0031-9422(99)00447-1Journal NLM ID: 0151434Publisher: Elsevier
Correspondence: mkamel
mailcity.com
Institutions: Department of Pharmacognosy, Faculty of Pharmacy, Assiut University, Assiut, Egypt, Faculty of Medicine, Institute of Pharmaceutical Sciences, Hiroshima University, Hiroshima, Japan, Department of Pharmacognosy, Faculty of Pharmacy, Al-Azhar University, Assiut, Egypt
From the aerial parts of Solenostemma argel, two monoterpene glucosides have been isolated and identified as 6,7-dihydroxy-dihydrolinalool 3-O-β-glucopyranoside and 6,7-dihydroxy-dihydrolinalool 7-O-β- glucopyranoside. A pregnane glucoside was also isolated and assigned as pregn-5-ene-3,14-β-dihydroxy-7,20-dione 3-O-β-glucopyranoside together with the known compounds benzyl alcohol O-β-apiofuranosyl-(1→6)-β-glucopyranoside, 2-phenylethyl O-α-arabinopyranosyl-(1→6)-β-glucopyranoside, astragalin and kaempferol-3-O-α-rhamnopyranosyl-(1→2)-β-glucopyranoside.
Asclepiadaceae, Solenostemma argel, monoterpene, pregnane glucosides
Structure type: monomer
Location inside paper: p. 939, left column, paragraph 2
Trivial name: astragalin, kaempferol 3-O-glucoside
Compound class: glycoside, flavonoid glycoside, flavonol glycoside, flavone glycoside
Contained glycoepitopes: IEDB_142488,IEDB_146664,IEDB_983931,SB_192
Methods: 13C NMR, 1H NMR, NMR-2D, TLC, GLC, HPLC, enzymatic digestion, extraction, optical rotation measurement, CC, derivatization, evaporation, HR-FAB-MS
Related record ID(s): 66496, 66497, 66498, 66499, 66500, 66502
NCBI Taxonomy refs (TaxIDs): 219273Reference(s) to other database(s): CCSD:
49928, CBank-STR:4070
Show glycosyltransferases
There is only one chemically distinct structure:
Found 
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