Description
3,4',5-Trimethoxystilbene is isolated from the herbs of Virola cuspidata. 3,4',5-Trimethoxystilbene exerts antiallergic and anti-mitotic properties. It shows antiangiogenic and vascular-disrupting effects in zebrafish through the downregulation of VEGFR2 and cell-cycle modulation. 3,4',5-Trimethoxystilbene is a potent small molecule inducer of autophagy in human umbilical vascular endothelial cells (HUVECs) in the presence of serum. It has anti-inflammatory activity, the ability of it to induce HO-1 expression may provide one of possible mechanisms of its anti-inflammatory action. 3,4',5-Trimethoxystilbene shows potent antitumor and anti-HCV activities without exhibiting cytotoxicity to human hepatocytes in vitro or in mice livers. It acts as an inhibitor of tubulin polymerization.
Synonyms
Resveratrol trimethyl ether
IUPAC Name
1,3-dimethoxy-5-[(E)-2-(4-methoxyphenyl)ethenyl]benzene
Molecular Formula
C17H18O3
Canonical SMILES
COC1=CC=C(C=C1)C=CC2=CC(=CC(=C2)OC)OC
InChI
InChI=1S/C17H18O3/c1-18-15-8-6-13(7-9-15)4-5-14-10-16(19-2)12-17(11-14)20-3/h4-12H,1-3H3/b5-4+
InChIKey
GDHNBPHYVRHYCC-SNAWJCMRSA-N
Boiling Point
423.8±35.0 °C(Predicted)
Density
1.104±0.06 g/cm3(Predicted)
Solubility
DMSO: ≥34mg/mL
Storage
Sealed in dry,2-8°C
Chemical Properties
Pale Yellow Oil
Risk Statements
36/37/38-50/53-41-37/38
Safety Statements
26-36/37/39-61-60-39
Uses
A resveratrol analog with a variety of pharmacology action, including anti-cancer properties, anti-allergic activity, estrogenic activity, antiangiogenic activity, and vascular-targeting activity against microtubule-destabilization