![]() | |
Names | |
---|---|
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)
|
|
ChEBI | |
ChEMBL | |
ChemSpider | |
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
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 viticola in Vitis vinifera and Vitis riparia. [4] It has been shown to inhibit acetylcholinesterase. [1]
![]() | |
Names | |
---|---|
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)
|
|
ChEBI | |
ChEMBL | |
ChemSpider | |
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
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 viticola in Vitis vinifera and Vitis riparia. [4] It has been shown to inhibit acetylcholinesterase. [1]