Chemistry:α-Viniferin
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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
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| Identifiers | |
3D model (JSmol)
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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). | |
 verify (what is   ?)
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| Infobox references | |
Tracking categories (test):
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]
References
- ↑ 1.0 1.1 Sung, Sang Hyun; Kang, So Young; Lee, Ki Yong; Park, Mi Jung; Kim, Jeong Hun; Park, Jong Hee; Kim, Young Chul; Kim, Jinwoong et al. (2002). "(+)-α-Viniferin, a Stilbene Trimer from Caragana chamlague, Inhibits Acetylcholinesterase". Biological & Pharmaceutical Bulletin 25 (1): 125–127. doi:10.1248/bpb.25.125. PMID 11824541.
- ↑ Shu, N; Zhou, H; Hu, C (2006). "Simultaneous determination of the contents of three stilbene oligomers in Caragana sinica collected in different seasons using an improved HPLC method". Biological & Pharmaceutical Bulletin 29 (4): 608–12. doi:10.1248/bpb.29.608. PMID 16595888.
- ↑ 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): 676–81. doi:10.1016/j.fitote.2011.02.006. PMID 21338657.
- ↑ Disease resistance of Vitis spp. and the production of the stress metabolites resveratrol, epsilon -viniferin, alpha -viniferin and pterostilbene. Langcake P, Physiological Plant Pathology, 1981, Vol. 18, No. 2, pages 213-226 (abstract )
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