Epsilon-Viniferin
From Wikipedia, the free encyclopedia
| ε-Viniferin | |
|---|---|
 (-)-Trans-epsilon-viniferin | |
| IUPAC name 5-[(2R,3R)-6-Hydroxy-2-(4-hydroxyphenyl)-4-[(E)-2-(4-hydroxyphenyl)ethenyl]-2,3-dihydro-1-benzofuran-3-yl]benzene-1,3-diol | |
| Identifiers | |
| CAS number | 62218-08-0  |
| PubChem | 5281728 |
| ChemSpider | 4445043  |
| ChEMBL | CHEMBL1224875 |
| Jmol-3D images | Image 1 |
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| Properties | |
| Molecular formula | C28H22O6 |
| Molar mass | 454.47 g/mol |
| (verify) (what is: /?) Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa) | |
| Infobox references | |
ε-Viniferin is a naturally occurring phenol, belonging to the stilbenoids family. It is a resveratrol dimer.
It is found in Vitis vinifera[4] grapevines,[5] in wines,[6] in the Oriental medicinal plant Vitis coignetiae and in the stem bark of Dryobalanops aromatica.[7]
Cis-epsilon-viniferin can be found in Paeonia lactiflora.[3]
It shows a human cytochrome P450 enzymes inhition activity.[8]
Glycosides
Diptoindonesin A is a C-glucoside of ε-viniferin.
See also
References
- ↑ Yáñez, M.; Fraiz, N.; Cano, E.; Orallo, F. (2006). "(−)-Trans-ε-viniferin, a polyphenol present in wines, is an inhibitor of noradrenaline and 5-hydroxytryptamine uptake and of monoamine oxidase activity". European Journal of Pharmacology 542 (1–3): 54–60. doi:10.1016/j.ejphar.2006.06.005. PMID 16828740.
- ↑ Cornacchione, S.; Sadick, N. S.; Neveu, M.; Talbourdet, S.; Lazou, K.; Viron, C.; Renimel, I.; De Quéral, D.; Kurfurst, R.; Schnebert, S.; Heusèle, C.; André, P.; Perrier, E. (2007). "In vivo skin antioxidant effect of a new combination based on a specific Vitis vinifera shoot extract and a biotechnological extract". Journal of drugs in dermatology : JDD 6 (6 Suppl): s8–13. PMID 17691204.
- ↑ 3.0 3.1 Kim, H. J.; Chang, E. J.; Cho, S. H.; Chung, S. K.; Park, H. D.; Choi, S. W. (2002). "Antioxidative Activity of Resveratrol and Its Derivatives Isolated from Seeds of Paeonia lactiflora". Bioscience, Biotechnology, and Biochemistry 66 (9): 1990–3. doi:10.1271/bbb.66.1990. PMID 12400706.
- ↑ Privat, C.; Telo, J. O. P.; Bernardes-Genisson, V.; Vieira, A.; Souchard, J. P.; Nepveu, F. O. (2002). "Antioxidant Properties oftrans-ε-Viniferin As Compared to Stilbene Derivatives in Aqueous and Nonaqueous Media". Journal of Agricultural and Food Chemistry 50 (5): 1213–1217. doi:10.1021/jf010676t. PMID 11853506.
- ↑ Langcake, P.; Pryce, R. J. (1977). "A new class of phytoalexins from grapevines". Experientia 33 (2): 151–152. doi:10.1007/BF02124034. PMID 844529.
- ↑ Vitrac, X.; Bornet, A. L.; Vanderlinde, R.; Valls, J.; Richard, T.; Delaunay, J. C.; Mérillon, J. M.; Teissédre, P. L. (2005). "Determination of Stilbenes (δ-viniferin,trans-astringin,trans-piceid,cis- andtrans-resveratrol, ε-viniferin) in Brazilian Wines". Journal of Agricultural and Food Chemistry 53 (14): 5664–5669. doi:10.1021/jf050122g. PMID 15998130.
- ↑ Wibowo, A.; Ahmat, N.; Hamzah, A. S.; Sufian, A. S.; Ismail, N. H.; Ahmad, R.; Jaafar, F. M.; Takayama, H. (2011). "Malaysianol A, a new trimer resveratrol oligomer from the stem bark of Dryobalanops aromatica". Fitoterapia 82 (4): 676–681. doi:10.1016/j.fitote.2011.02.006. PMID 21338657.
- ↑ Piver, B.; Berthou, F. O.; Dreano, Y.; Lucas, D. L. (2003). "Differential inhibition of human cytochrome P450 enzymes by ε-viniferin, the dimer of resveratrol: Comparison with resveratrol and polyphenols from alcoholized beverages". Life Sciences 73 (9): 1199–1213. doi:10.1016/S0024-3205(03)00420-X. PMID 12818727.
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