Miyabenol C
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Names | |
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Preferred IUPAC name (2S,2′R,3S,3′R)-3′-(3,5-Dihydroxyphenyl)-2,2′-bis(4-hydroxyphenyl)-4-[(E)-2-(4-hydroxyphenyl)ethen-1-yl]-2,2′,3,3′-tetrahydro[3,5′-bi-1-benzofuran]-6,7′-diol | |
Other names Z-miyabenol C E-cis-miyabenol C[1] | |
Identifiers | |
CAS Number |
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3D model (JSmol) |
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ChEBI |
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ChemSpider |
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PubChem CID |
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UNII |
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CompTox Dashboard (EPA) |
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InChI
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Properties | |
Chemical formula | C42H32O9 |
Molar mass | 680.69 g/mol |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references |
Chemical compound
Miyabenol C is a stilbenoid. It is a resveratrol trimer. It is found in Vitis vinifera (grape),[2] in Foeniculi fructus (fruit of Foeniculum vulgare),[3] in Caragana sinica.[4]
It shows protein kinase C inhibitor activity.[4]
Foeniculoside I is a glucoside of cis-miyabenol C.
References
- ^ Mattivi, F.; Vrhovsek, U.; Malacarne, G.; Masuero, D.; Zulini, L.; Stefanini, M.; Moser, C.; Velasco, R.; Guella, G. (2011). "Profiling of Resveratrol Oligomers, Important Stress Metabolites, Accumulating in the Leaves of Hybrid Vitis vinifera (Merzling × Teroldego) Genotypes Infected with Plasmopara viticola". Journal of Agricultural and Food Chemistry. 59 (10): 5364–75. doi:10.1021/jf200771y. PMID 21510709.
- ^ Barjot, C.; Tournaire, M.; Castagnino, C.; Vigor, C.; Vercauteren, J.; Rossi, J. F. O. (2007). "Evaluation of antitumor effects of two vine stalk oligomers of resveratrol on a panel of lymphoid and myeloid cell lines: Comparison with resveratrol". Life Sciences. 81 (23–24): 1565–1574. doi:10.1016/j.lfs.2007.08.047. PMID 18001803.
- ^ Ono, M; Ito, Y; Kinjo, J; Yahara, S; Nohara, T; Niiho, Y (1995). "Four new glycosides of stilbene trimer from Foeniculi fructus (fruit of Foeniculum vulgare MILLER)". Chemical and Pharmaceutical Bulletin. 43 (5): 868–871. doi:10.1248/cpb.43.868. INIST 3610745.
- ^ a b Kulanthaivel, P.; Janzen, W.; Ballas, L.; Jiang, J.; Hu, C. Q.; Darges, J.; Seldin, J.; Cofield, D.; Adams, L. (2007). "Naturally Occurring Protein Kinase C Inhibitors; II. Isolation of Oligomeric Stilbenes from Caragana sinica". Planta Medica. 61 (1): 41–44. doi:10.1055/s-2006-957996. PMID 7700990.
External links
- Miyabenol C at www.plant-expert.com
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Oligostilbenoids and their glycosides
- Diptoindonesin C
- Diptoindonesin F
- Gnetin H
- Hemsleyanol D
- Isohopeaphenol
- Laetevirenol A, B, C, D and E
- Suffruticosol A and B
- Viniferal
- E-ω-viniferin
- Z-ω-viniferin
- Diptoindonesin G
- Jezonodione
- B
- Scirpusin A
- Tibeticanol (piceatannol dimer)
- Amurensin B
- Gnetin E
- Gneyulin A
- Johorenol A
- Ampelopsin E
- Vaticanol G
- Dibalanocarpol
- Gnetin J (3"-hydroxygnetin E)
- Gnetin K (3"-methoxygnetin E)
- Gnetuhainin R (isorhapontigenin tetramer)
- Laetevirenol F and G
(five units or more)
- Vaticanol D, H, I and J
of resveratrol
Dimers |
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Trimers |
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Tetramers |
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Pentamers |
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Hexamers | |
Higher polymers |
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- Diptoindonesin A (C-glucoside of ε-viniferin)
- Foeniculoside I (glucoside of miyabenol C), II, III and IV
- Laevifonol (an ε-viniferin-ascorbic acid hybrid compound)
- Laevifoside (O-glucoside of ampelopsin A)
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