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| | 3,4',5-Trimethoxy-trans-stilbene Basic information |
| Product Name: | 3,4',5-Trimethoxy-trans-stilbene | | Synonyms: | (E)-1,3-Dimethoxy-5-(4-methoxystyryl)benzene;(E)-3,4',5-Trimethoxystilbene;3,5,4'-Trimethoxy-trans-stilbene;Trimethoxystilbene;3,4,5-TRIMETHOXY-TRANS-STILBENE 95+%;TRANS-1-(3,5-DIMETHOXYPHENYL)-2-(4-METHOXYPHENYL)ETHYLENE;TRISMETHOXY RESVERATROL;1,3-DIMETHOXY-5-[(E)-2-(4-METHOXY-PHENYL)-VINYL]-BENZENE | | CAS: | 22255-22-7 | | MF: | C17H18O3 | | MW: | 270.32 | | EINECS: | 694-659-7 | | Product Categories: | Resveratrol;Intermediates & Fine Chemicals;Pharmaceuticals;Stilbenes | | Mol File: | 22255-22-7.mol |  |
| | 3,4',5-Trimethoxy-trans-stilbene Chemical Properties |
| Melting point | 57°C | | Boiling point | 423.8±35.0 °C(Predicted) | | density | 1.104±0.06 g/cm3(Predicted) | | storage temp. | Sealed in dry,2-8°C | | solubility | DMSO: ≥34mg/mL | | form | powder to crystal | | color | white to tan | | 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 | | SMILES | C1(OC)=CC(/C=C/C2=CC=C(OC)C=C2)=CC(OC)=C1 | | CAS DataBase Reference | 22255-22-7 |
| | 3,4',5-Trimethoxy-trans-stilbene Usage And Synthesis |
| Description | trans-trismethoxy Resveratrol is a polyketide synthase-derived stilbene originally isolated from Virola cuspidata that has diverse biological activities. It is cytotoxic to several cancer cell lines, including PC3, KB, HT-29, SW480, and HL-60 cells (IC50s =3.6, 10.2, 16.1, 54, and 2.5 μM, respectively). trans-trismethoxy Resveratrol (15 μM) inhibits TNF-α-induced activation of NF-κB in HEK293T cells in a reporter assay. It inhibits angiogenesis in zebrafish embryos when used at a concentration of 0.1 μM. | | Chemical Properties | Pale Yellow Oil | | 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 | | Uses | A resveratrol analog with a variety of pharmacology action, including
inst microtubule-destabilization | | Uses | Phenolic compounds, particularly flavonoids, from plant sources have long been observed to have antioxidant activity with potential benefits for human health. Resveratrol is a potent phenolic antioxidant found in grapes and red wine that also has antiproliferative and anti-inflammatory activity. When the three phenolic hydroxyl groups of resveratrol are converted to methyl ethers, the inhibition of cell growth and pro-apoptotic activities of resveratrol are enhanced. | | References | [1] MICHAEL B. AUSTIN Joseph P N. The Chalcone Synthase Superfamily of Type III Polyketide Synthases[J]. ChemInform, 2003, 34 17. DOI: 10.1002/chin.200317284
[2] FAHAD S ALDAWSARI Carlos A V M. 3,4’,5-trans-Trimethoxystilbene; a natural analogue of resveratrol with enhanced anticancer potency.[J]. Investigational New Drugs, 2015, 33 3: 775-786. DOI: 10.1007/s10637-015-0222-x
[3] JUSTIN J. HEYNEKAMP. Substituted trans-Stilbenes, Including Analogues of the Natural Product Resveratrol, Inhibit the Human Tumor Necrosis Factor Alpha-Induced Activation of Transcription Factor Nuclear Factor KappaB[J]. Journal of Medicinal Chemistry, 2006, 49 24: 7182-7189. DOI: 10.1021/jm060630x
[4] MIRELLA BELLERI. Antiangiogenic and vascular-targeting activity of the microtubule-destabilizing trans-resveratrol derivative 3,5,4’-trimethoxystilbene.[J]. Molecular Pharmacology, 2005, 67 5: 1451-1459. DOI: 10.1124/mol.104.009043 |
| | 3,4',5-Trimethoxy-trans-stilbene Preparation Products And Raw materials |
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