Taxonomic group: plant / Streptophyta
(Phylum: Streptophyta)
Organ / tissue: leaf
NCBI PubMed ID: 10925407Publication DOI: 10.1002/1099-1573(200008)14:5<371::aid-ptr625>3.0.co;2-fJournal NLM ID: 8904486Publisher: Chichester: Wiley
Institutions: Faculty of Pharmacy, Obafemi Awolowo University, Ile-Ife, Nigeria, Institute de Chimie des Substances Naturelles, Centre National de la Recherche Scientific, Gif sur Yvette, France
An activity directed fractionation of a 50% aqueous ethanol extract of A. wilkesiana and A. hispida leaves resulted in the isolation of gallic acid, corilagin and geraniin as the compounds responsible for the observed antimicrobial activity. Quercetin 3-O-rutinoside and kaempferol 3-O-rutinoside were also isolated from the inactive fraction of A. hispida. The structures were established by permethylation, 2D - NMR ((1)H and (13)C) and MS data.
antimicrobial, Acalypha wilkesiana, Acalypha hispida, corilagin, geraniin
Structure type: oligomer
C
27H
30O
16Location inside paper: p. 372, left column, paragraph 1
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, methylation, TLC, ESI-MS, biological assays, extraction, optical rotation measurement, CC, evaporation, antimicrobial assay
Related record ID(s): 64604, 64605, 64607
NCBI Taxonomy refs (TaxIDs): 197604Reference(s) to other database(s): CCSD:
50720, CBank-STR:3399
Show glycosyltransferases
There is only one chemically distinct structure:
Found 
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