Ampelopsin A
Ampelopsin A
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Identifiers |
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280561-81-1 |
Jmol-3D images |
Image |
Oc1ccc(cc1)C6c2c(cc(O)cc2O)C3c5c(cc(O)cc5OC3c4ccc(O)cc4)C6O
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Properties |
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C28H22O7 |
Molar mass |
470.47 g/mol |
Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa) |
Infobox references |
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Ampelopsin A is a resveratrol dimer found in Ampelopsis brevipedunculata var hancei.[1][2]
References
- ↑ Ampelopsins A, B and C, new oligostilbenes of Ampelopsis brevipedunculata VAR hancei. Yoshiteru Oshima, Yuji Ueno, Hiroshi Hikino, Yang Ling-Ling and Yen Kun-Ying, Tetrahedron, Volume 46, Issue 15, 1990, Pages 5121–5126, doi:10.1016/S0040-4020(01)87819-4
- ↑ Chemical determination of the absolute structures of resveratrol dimers, ampelopsins A, B, D and F. Yoshiaki Takaya, Ke-Xu Yan†, Kenji Terashima, Junko Ito and Masatake Niwa, Tetrahedron, Volume 58, Issue 36, 2 September 2002, Pages 7259–7265, doi:10.1016/S0040-4020(02)00785-8
External links
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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
| | 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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