Chunganenol
Chunganenol
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Identifiers |
3D model (Jmol) |
Interactive image |
[H][C@@]12[C@H]([C@@H](C3=C(O)C=C4O[C@H](C5=CC=C(O)C=C5)[C@]([H])(C4=C13)C1=CC(O)=CC(O)=C1[C@@H]2C1=CC=C(O)C=C1)C1=C(CC2=C(O)C=C(C=C2O)[C@@H]2[C@H](OC3=C2C(\C=C\C2=CC=C(O)C=C2)=C2[C@@H]([C@H](OC2=C3)C2=CC=C(O)C=C2)C2=CC(O)=CC(O)=C2)C2=CC=C(O)C=C2)C(O)=CC(O)=C1)C1=CC=C(O)C=C1
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Properties |
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C85H64O18 |
Molar mass |
1,373.43 g·mol−1 |
Appearance |
Colorless amorphous powder |
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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Chunganenol is a resveratrol hexamer found in Vitis chunganensis.[1]
References
- ↑ Shan He; Liyan Jiang; Bin Wu; Chang Li; Yuanjiang Pan (2009). "Chunganenol: An Unusual Antioxidative Resveratrol Hexamer from Vitis chunganensis". J. Org. Chem. 74 (20): 7966–7969. doi:10.1021/jo901354p. PMID 19757796.
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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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