Names | |
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IUPAC name
3-C-(Hydroxymethyl)-β-D-erythrofuranosyl-(1→3)-β-D-xylopyranosyl-(1→4)-α-L-rhamnopyranosyl-(1→2)-α-L-arabinopyranosyl 3β-(β-D-glucopyranosyloxy)-2β,16α,23,24-hydroxyolean-12-en-28-oate
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Systematic IUPAC name
(12S,13R,14S,15S,32S,33R,34S,35R,36S,52S,53R,54S,55R,72S,73R,74R)-14,15,33,34,53,55,73,74-Octahydroxy-74-(hydroxymethyl)-36-methyl-2,4,6-trioxa-1(3),3(2,5),5(2,4)-tris(oxana)-7(2)-oxolanaheptaphan-12-yl (4aR,5R,6aS,6bR,8aR,10R,11S,12aR,12bR,14bS)-5,11-dihydroxy-9,9-bis(hydroxymethyl)-2,2,6a,6b,12a-pentamethyl-10-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1,3,4,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-octadecahydropicene-4a(2H)-carboxylate | |
Identifiers | |
CAS Number
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3D model (JSmol)
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ChEBI |
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ChEMBL |
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ChemSpider |
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ECHA InfoCard | 100.208.719 |
EC Number |
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KEGG |
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PubChem CID
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UNII |
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CompTox Dashboard (EPA)
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InChI
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SMILES
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Properties | |
Chemical formula
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C57H92O28 |
Molar mass | 1225.335 g·mol−1 |
Hazards | |
GHS labelling: | |
Pictograms
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Signal word
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Warning |
Hazard statements
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H302 |
Precautionary statements
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P264, P270, P301+P312, P330, P501 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
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Platycodin D is a bio-active isolate from roots of Platycodon grandiflorus. It has been studied in vitro for its potential human spermicidal effects[1] and its potential anti-inflammatory properties.[2]