Diptoindonesin A

Diptoindonesin A
Properties

Chemical formula	C₃₄H₃₂O₁₁
Molar mass	616.61 g/mol
Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
Infobox references

Diptoindonesin A is a C-glucoside of ε-viniferin isolated from the two Dipterocarpaceae Shorea seminis^[1] and Dryobalanops aromatica.^[2]

References

↑ Aminah, N. S.; Achmad, S. A.; Aimi, N.; Ghisalberti, E. L.; Hakim, E. H.; Kitajima, M.; Syah, Y. M.; Takayama, H. (2002). "Diptoindonesin A, a new C-glucoside of ε-viniferin from Shorea seminis (Dipterocarpaceae)". Fitoterapia 73 (6): 501–507. doi:10.1016/S0367-326X(02)00179-X. PMID 12385874.
↑ Wibowo, A.; Ahmat, N.; Hamzah, A. S.; Sufian, A. S.; Ismail, N. H.; Ahmad, R.; Jaafar, F. M.; Takayama, H. (2011). "Malaysianol A, a new trimer resveratrol oligomer from the stem bark of Dryobalanops aromatica". Fitoterapia 82 (4): 676–681. doi:10.1016/j.fitote.2011.02.006. PMID 21338657.

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