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Found 2 structures. Displayed structures from 1 to 2
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1. Compound ID: 31158

Compound 31158

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Structure type: monomer
Trivial name: corilagin
Compound class: glycoside
Contained glycoepitopes: IEDB_142488,IEDB_146664,IEDB_983931,SB_192

The structure is contained in the following publication(s):

Article ID: 11977
Adesina SK, Idowu O, Ogundaini AO, Oladimeji H, Olugbade TA, Onawunmi GO, Païs M "Antimicrobial constituents of the leaves of Acalypha wilkesiana and Acalypha hispida" - Phytotherapy Research 14(5) (2000) 371-374

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
NCBI PubMed ID: 10925407
Publication DOI: 10.1002/1099-1573(200008)14:5<371::aid-ptr625>3.0.co;2-f
Journal NLM ID: 8904486
Publisher: 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
Methods: 13C NMR, 1H NMR, methylation, TLC, ESI-MS, biological assays, extraction, optical rotation measurement, CC, evaporation, antimicrobial assay

Acalypha hispida, Acalypha wilkesiana
CSDB ID 64604 (all data & tools)

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2. Compound ID: 31159

Compound 31159

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Structure type: monomer
Trivial name: geraniin
Compound class: glycoside
Contained glycoepitopes: IEDB_142488,IEDB_146664,IEDB_983931,SB_192

The structure is contained in the following publication(s):

Article ID: 11977
Adesina SK, Idowu O, Ogundaini AO, Oladimeji H, Olugbade TA, Onawunmi GO, Païs M "Antimicrobial constituents of the leaves of Acalypha wilkesiana and Acalypha hispida" - Phytotherapy Research 14(5) (2000) 371-374

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
NCBI PubMed ID: 10925407
Publication DOI: 10.1002/1099-1573(200008)14:5<371::aid-ptr625>3.0.co;2-f
Journal NLM ID: 8904486
Publisher: 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
Methods: 13C NMR, 1H NMR, methylation, TLC, ESI-MS, biological assays, extraction, optical rotation measurement, CC, evaporation, antimicrobial assay

Acalypha hispida, Acalypha wilkesiana
CSDB ID 64605 (all data & tools)

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