CAS 22255-22-7

Resveratrol trimethyl ether

Description:

Resveratrol trimethyl ether, with the CAS number 22255-22-7, is a derivative of resveratrol, a naturally occurring polyphenolic compound found in various plants, particularly in grapes and berries. This compound is characterized by the presence of three methoxy groups (-OCH3) attached to the resveratrol structure, which enhances its lipophilicity and potentially alters its biological activity compared to its parent compound. Resveratrol trimethyl ether exhibits antioxidant properties, contributing to its potential health benefits, including anti-inflammatory and cardioprotective effects. It is often studied for its role in promoting cellular health and longevity, as well as its potential in cancer prevention. The compound is typically soluble in organic solvents, reflecting its modified structure, and may have varying stability and reactivity compared to resveratrol. Research into its pharmacological properties continues, as scientists explore its mechanisms of action and therapeutic applications in various health conditions.

Formula: C₁₇H₁₈O₃

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+

InChI key: InChIKey=GDHNBPHYVRHYCC-SNAWJCMRSA-N

SMILES: C(=C/C1=CC=C(OC)C=C1)\C2=CC(OC)=CC(OC)=C2

Synonyms:

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

3,4',5-Trimethoxy-trans-stilbene

CAS: 22255-22-7

Formula: C₁₇H₁₈O₃

Purity: >98.0%(GC)

Color and Shape: White to Light yellow powder to crystal

Molecular weight: 270.33

Ref: 3B-T1829

Benzene, 1,​3-​dimethoxy-​5-​[(1E)​-​2-​(4-​methoxyphenyl)​ethenyl]​-

CAS: 22255-22-7

Formula: C₁₇H₁₈O₃

Purity: 98%

Color and Shape: Solid

Molecular weight: 270.3230

Ref: IN-DA007P14

trans-Trimethoxyresveratrol

CAS: 22255-22-7

trans-Trimethoxyresveratrol

Purity: ≥98%

Molecular weight: 270.32g/mol

Ref: 54-BUP14461

(E)-1,3-Dimethoxy-5-(4-Methoxystyryl)Benzene

CAS: 22255-22-7

(E)-1,3-Dimethoxy-5-(4-Methoxystyryl)Benzene

Purity: 98%

Molecular weight: 270.32g/mol

Ref: 54-OR1008330

E-Resveratrol trimethyl ether

CAS: 22255-22-7

Formula: C₁₇H₁₈O₃

Color and Shape: White to light yellow crystalline powder

Molecular weight: 270.32

Ref: 7W-GL5652

3,4',5-Trimethoxystilbene

CAS: 22255-22-7

Formula: C₁₇H₁₈O₃

Purity: 95%~99%

Molecular weight: 270.328

Ref: BP-BP3718

trans-Trimethoxyresveratrol

CAS: 22255-22-7

trans-Trimethoxyresveratrol (MR-3), a natural methoxylated analog of resveratrol, inhibits breast Y cell invasiveness by reversal of EMT.

Formula: C₁₇H₁₈O₃

Purity: 99.83%

Color and Shape: Pale Yellow Oil

Molecular weight: 270.32

Ref: TM-T3330

TRIMETHOXYSTILBENE

CAS: 22255-22-7

Formula: C₁₇H₁₈O₃

Purity: 98%

Color and Shape: Liquid, No data available.

Molecular weight: 270.328

Ref: 10-F386383

Resveratrol Trimethyl Ether

Controlled Product

CAS: 22255-22-7

Applications 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.
References Cushman, M., et al.: J. Med. Chem., 34, 2579 (1991), Shimada, T., et al.: Cancer Res., 56, 2979 (1996), Cardile, V., etal.: Bioorg. Chem. 33, 22 (2005).

Formula: C₁₇H₁₈O₃

Color and Shape: Neat

Molecular weight: 270.32

Ref: TR-R150050

3,4',5-Trimethoxystilbene

CAS: 22255-22-7

3,4',5-Trimethoxystilbene is a coumarin derivative that has been found to have inhibitory properties for mitochondrial functions. It also inhibits the production of epidermal growth factor and collagen synthesis in cells. 3,4',5-Trimethoxystilbene may be useful in treating skin conditions such as psoriasis and ichthyosis. This compound has been shown to bind to protein targets in the mitochondria and inhibit mitochondrial membrane potential by hydroxyl group reaction with proteins. 3,4',5-Trimethoxystilbene also binds to dna duplexes, which may affect its biological properties.

Formula: C₁₇H₁₈O₃

Purity: Min. 95%

Molecular weight: 270.32 g/mol

Ref: 3D-FT43010