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Resveratrol trimethyl ether

Resveratrol trimethyl ether structure

Resveratrol trimethyl ether 

structure
  • CAS No:

    22255-22-7

  • Formula:

    C17H18O3

  • Chemical Name:

    Resveratrol trimethyl ether

  • Synonyms:

    Benzene,1,3-dimethoxy-5-[(1E)-2-(4-methoxyphenyl)ethenyl]-;Stilbene,3,4′,5-trimethoxy-,(E)-;Benzene,1,3-dimethoxy-5-[2-(4-methoxyphenyl)ethenyl]-,(E)-;1,3-Dimethoxy-5-[(1E)-2-(4-methoxyphenyl)ethenyl]benzene;3,4′,5-Trimethoxy-trans-stilbene;Resveratrol trimethyl ether;Tri-O-methylresveratrol;(E)-3,5,4′-Trimethoxystilbene;3,5,4′-Trimethoxy-trans-stilbene;(E)-1-(4-Methoxyphenyl)-2-(3,5-dimethoxyphenyl)ethene;(E)-2-(3,5-Dimethoxyphenyl)-1-(4-methoxyphenyl)ethene;(E)-1,3-Dimethoxy-5-(4-methoxystyryl)benzene;(E)-3,4′,5-Trimethoxystilbene;trans-Trimethoxyresveratrol;BTM 0512

  • Categories:

    Natural Products  >  Phenols

Description

Trans-Trimethoxyresveratrol is a derivative of Resveratrol (RSV),and it may be a more potent anti-inflammatory, antiangiogenic and vascular-disrupting agent when compared with resveratrol.In vitro: The in vitro study of resveratrol and trans-Trimethoxyresveratrol showed rather weak cytotoxic effects on three cancer cell lines (HepG2, MCF-7, and MDA-MB-231), which contradicted a previous study reporting that resveratrol inhibited MCF-7 cells with an IC50 of about 10?μM. This discrepancy m

Resveratrol trimethyl ether Basic Attributes

270.32

270.32

1312995-182-4

2909309090

Characteristics

27.7

4.1

white to tan

1.1±0.1 g/cm3

55-57 °C

423.8°C at 760 mmHg

144.4±23.2 °C

1.600

DMSO: ≥34mg/mL

-20°C

5.37E-07mmHg at 25°C

Safety Information

UN 3077 9 / PGIII

36/37/38-50/53-41-37/38

26-36/37/39-61-60-39

Xi,N

P261-P273-P280-P305 + P351 + P338-P501

H315-H318-H335-H410

Resveratrol trimethyl ether Use and Manufacturing

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.

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