Procyanidin B2
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| Names | |
|---|---|
| IUPAC name
[(2R,3R,4R)-Flavan-3,3′,4′,5,7-pentol]-(4→8)-[(2R,3R)-flavan-3,3′,4′,5,7-pentol]
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| Systematic IUPAC name
(2R,2′R,3R,3′R,4R)-2,2′-Bis(3,4-dihydroxyphenyl)-3,3′,4,4′-tetrahydro-2H,2′H-[4,8′-bi-1-benzopyran]-3,3′,5,5′,7,7′-hexol | |
| Other names
Procyanidin-B2
(−)- Epicatechin -(4β→8)-(−)-epicatechin | |
| Identifiers | |
3D model (
JSmol ) |
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| ChEBI | |
| ChemSpider | |
PubChem CID
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| UNII | |
CompTox Dashboard (EPA)
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SMILES
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| Properties | |
| C30H26O12 | |
| Molar mass | 578.52 g/mol |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Procyanidin B2 is a
Epicatechin
-(4β→8)-(−)-epicatechin.
Procyanidin B2 can be found in Ecdysanthera utilis.[4]
Procyanidin B2 can be converted into
1,1-diphenyl-2-picrylhydrazyl (DPPH) radicals under neutral conditions.[5]
Procyanidin B2 has been shown to inhibit the formation of the advanced glycation end-products pentosidine, carboxymethyllysine (CML), and methylglyoxal (MGO).[6]
See also
References
- ^ Proanthocyanidin-B2 on liberherbarum.com
- ^ Immunomodulatory and anticancer activities of flavonoids extracted from litchi (Litchi chinensis Sonn.) pericarp. Mouming Zhao; Bao Yang; Jinshui Wang; Yang Liu; Limei Yu; Yueming Jiang, 2007
- ^ Proanthocyanidin-B2 on fuzing.com
- PMID 11975489.
- .
- PMID 20476737.