Cyphostemmin A
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| Names
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| IUPAC name
8-(3,5-dihydroxyphenyl)-6,7-bis(4-hydroxyphenyl)-5,8-dihydronaphthalene-1,3-diol
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| Identifiers
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| ChemSpider
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InChI=1S/C28H22O6/c29-19-5-1-15(2-6-19)24-12-18-11-23(33)14-25(34)27(18)28(17-9-21(31)13-22(32)10-17)26(24)16-3-7-20(30)8-4-16/h1-11,13-14,28-34H,12H2/t28-/m0/s1 Key: ZUOFIYSMCLKBAS-NDEPHWFRSA-N
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c1cc(ccc1C2=C([C@@H](c3c(cc(cc3O)O)C2)c4cc(cc(c4)O)O)c5ccc(cc5)O)O
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| Properties
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C28H22O6
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| Molar mass
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454.478 g·mol−1
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
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Cyphostemmin A is an oligostilbene found in Cyphostemma crotalarioides (Vitaceae).[1]
See also
References
- ^ Ducrot, Paul-Henri; Kollmann, Albert; Bala, Adil E.; Majira, Amel; Kerhoas, Lucien; Delorme, Robert; Einhorn, Jacques (1998). "Cyphostemmins A-B, two new antifungal oligostilbenes from Cyphostemma crotalarioides (Vitaceae)". Tetrahedron Letters. 39 (52): 9655–9658. doi:10.1016/S0040-4039(98)02207-2.
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- 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
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| Dimers |
- Diptoindonesin G
- Jezonodione
- B
- Scirpusin A
- Tibeticanol (piceatannol dimer)
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| Trimers |
- Amurensin B
- Gnetin E
- Gneyulin A
- Johorenol A
- Ampelopsin E
- Vaticanol G
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| Tetramers: |
- Dibalanocarpol
- Gnetin J (3"-hydroxygnetin E)
- Gnetin K (3"-methoxygnetin E)
- Gnetuhainin R (isorhapontigenin tetramer)
- Laetevirenol F and G
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Higher polymers (five units or more) | |
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Oligomeric forms of resveratrol | | Dimers | |
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| Hexamers | |
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| Higher polymers |
- γ-viniferin
- Valeriaphenol A
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| Glycosides or conjugates |
- 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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