| Description |
Labelled Resveratrol Trimethyl Ether. Resveratrol Trimethyl Ether is isolated from the herbs of Virola cuspidata. Resveratrol Trimethyl Ether exerts antiallergic and anti-mitotic properties. It shows antiangiogenic and vascular-disrupting effects in zebrafish through the downregulation of VEGFR2 and cell-cycle modulation. Resveratrol Trimethyl Ether 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. Resveratrol Trimethyl Ether 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 |
1,3-Dimethoxy-5-[(1E)-2-(4-methoxyphenyl)ethenyl]benzene-13C6; (E)-1,3-Dimethox-5-(4-methoxystyryl)benzene-13C6; (E)-3,4',5-Trimethoxystilbene-13C6; 3,5,4'-Trimethoxy-trans-stilbene-13C6; Tri-O-methylresveratrol-13C6 |
| IUPAC Name |
1,3-dimethoxy-5-[(E)-2-(4-methoxy(1,2,3,4,5,6-13C6)cyclohexa-1,3,5-trien-1-yl)ethenyl]benzene |
| Related CAS |
22255-22-7 (unlabelled)
|
| 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+/i6+1,7+1,8+1,9+1,13+1,15+1 |
| InChI Key |
GDHNBPHYVRHYCC-CVCCECKZSA-N |
| Purity |
≥95% |
| Solubility |
Soluble in Dichloromethane, Ethyl Acetate |
| Appearance |
Transparent Oil |
![Resveratrol Trimethyl Ether-[13C6]](/isotope.v1/images/structure-default.jpg)
