3,4′-Dihydroxystilbene

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3,4′-Dihydroxystilbene

IUPAC name 3-[2-(4-hydroxyphenyl)ethenyl]phenol
Identifiers
	PubChem	54350316
	Jmol-3D images	Image 1
SMILES C1=CC(=CC(=C1)O)C=CC2=CC=C(C=C2)O
InChI InChI=1S/C14H12O2/c15-13-8-6-11(7-9-13)4-5-12-2-1-3-14(16)10-12/h1-10,15-16H Key: UFGKEFGYNRJIGO-UHFFFAOYSA-N
Properties
Molecular formula	C₁₄H₁₂O₂
Molar mass	212.24 g/mol
Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
Infobox references

3,4′-Dihydroxystilbene is a stilbenoid found in the roots of Hydrangea macrophylla.^[1]

References

↑ Lunularic acid and related compounds in liverworts, algae and Hydrangea. John Gorham, Phytochemistry, 1977, Volume 16, Issue 2, Pages 249–253, doi:10.1016/S0031-9422(00)86795-3

Dihydroxylated

Trihydroxylated

Tetrahydroxylated

O-methylated

4-Methoxyresveratrol Gnetucleistol D (2-methoxyoxyresveratrol) Gnetucleistol E (3-methoxy-isorhapontigenin) Isorhapontigenin (3,4',5-trihydroxy-3'-methoxystilbene) Pterostilbene Rhapontigenin (3,3',5-trihydroxy-4'-methoxystilbene)

Combretastatins:	Combretastatin A-1 Combretastatin A-4

carboxylated

other acetylations

of resveratrol	Piceid (trans-Resveratrol-3-O-glucoside) trans-Resveratrol-3-O-glucuronide Resveratroloside (trans-resveratrol-4'-O-beta-D-glucopyranoside)

of rhapontigenin	Rhapontigenin 3-O-rutinoside 4'-Methoxy-(E)-resveratrol 3-O-rutinoside Rhaponticin (Rhapontigenin glucoside)

Tetramers:

of resveratrol

Dimers	Amurensin A and H Ampelopsin A B D and F δ-viniferin ε-viniferin Leachinol F Pallidol Parthenocissin A Quadrangularin A Restrytisol A B and C

Trimers	α-viniferin Amurensin C D and G Malaysianol A Miyabenol C Resviniferin A and B trans-diptoindonesin B

Tetramers	Amurensin E F and K Gnetuhainin R (isorhapontigenin tetramer) Hopeaphenol Vaticanol B Vitisin A B and C β-viniferin (cyclic resveratrol tetramer)

Pentamers	Amurensin E and F

Higher polymers	γ-viniferin

Oligomeric forms
glycosides or conjugates

Synthetic

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