Cyphostemmin B
Cyphostemmin B
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Identifiers |
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ChemSpider |
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InChI=1S/C28H22O6/c29-18-5-1-15(2-6-18)9-23-24-13-22(33)14-25(34)28(24)27(16-3-7-19(30)8-4-16)26(23)17-10-20(31)12-21(32)11-17/h1-14,26-27,29-34H/b23-9-/t26-,27+/m1/s1 Key: BIQMSWPBPAKGSE-PBSLAQMISA-N
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c1cc(ccc1/C=C\2/c3cc(cc(c3[C@H]([C@@H]2c4cc(cc(c4)O)O)c5ccc(cc5)O)O)O)O
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Properties |
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C28H22O6 |
Molar mass |
454.47 g/mol |
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 B is an oligostilbene found in Cyphostemma crotalarioides (Vitaceae).[1] It is a resveratrol dimer.
References
- ↑ Cyphostemmins A-B, two new antifungal oligostilbenes from Cyphostemma crotalarioides (Vitaceae). Paul-Henri Ducrot, Albert Kollmann, Adil E. Bala, Amel Majira, Lucien Kerhoas, Robert Delorme and Jacques Einhorn, Tetrahedron Letters, Volume 39, Issue 52, 24 December 1998, Pages 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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Trimers | |
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Tetramers | |
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Pentamers | |
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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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