Cyphostemmin A

Cyphostemmin A
Identifiers

3D model (JSmol)	Interactive image
ChemSpider	58226951
InChI 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
SMILES c1cc(ccc1C2=C([C@@H](c3c(cc(cc3O)O)C2)c4cc(cc(c4)O)O)c5ccc(cc5)O)O
Properties
Chemical formula	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

Cyphostemmin A 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

Dimers

Trimers

Tetramers:

Higher polymers
(five units or more)

Oligomeric forms
of resveratrol

Dimers	Amurensin A and H Ampelopsin A B D and F Balanocarpol Cyphostemmin A and B δ-viniferin ε-viniferin Gnetin A and C Leachinol F Malibatol A Pallidol Parthenocissin A Quadrangularin A Restrytisol A, B and C Vitisinol D
Trimers	α-viniferin Ampelopsin C Amurensin C, D and G Hopeanolin Malaysianol A Miyabenol C Resviniferin A and B trans-diptoindonesin B
Tetramers	Ampelopsin H Amurensin K Caraphenol B Carasinol B Flexuosol A Hopeaphenol Kobophenol A Miyabenol A Vaticanol B and C Vaticaphenol A Vitisin A B and C β-viniferin (cyclic resveratrol tetramer)
Pentamers	Amurensin E and F
Hexamers	Chunganenol
Higher polymers	γ-viniferin Valeriaphenol A

Glycosides or conjugates

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