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Names | |
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Preferred IUPAC name
(1R,5bR,6R,10bS,11S,15bR)-1,6,11-Tris(4-hydroxyphenyl)-1,5b,6,10b,11,15b-hexahydrocyclonona[1,2,3-cd:4,5,6-c′d′:7,8,9-c′′d′′]tris([1]benzofuran)-4,9,14-triol | |
Other names
α-Viniferin; (+)-α-Viniferin | |
Identifiers | |
3D model (JSmol) |
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ChEBI | |
ChEMBL | |
ChemSpider |
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PubChem CID |
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UNII | |
CompTox Dashboard (EPA) |
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Properties | |
C42H30O9 | |
Molar mass | 678.693 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). |
α-Viniferin is a stilbene trimer. It can be isolated from Caragana chamlagu[1] and from Caragana sinica[2] and from the stem bark of Dryobalanops aromatica.[3] It is also present in relation to resistance to Botrytis cinerea and Plasmopara viticolainVitis vinifera and Vitis riparia.[4] It has been shown to inhibit acetylcholinesterase.[1]
Oligostilbenoids and their glycosides
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Trimers |
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Higher polymers (five units or more) |
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Oligomeric forms of resveratrol |
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Glycosides or conjugates |
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