Trimethoxystilbene

Trimethoxystilbene
Product Name Trimethoxystilbene
CAS No.: 22255-22-7
Catalog No.: CFN90874
Molecular Formula: C17H18O3
Molecular Weight: 270.3 g/mol
Purity: >=98%
Type of Compound: Polyphenols
Physical Desc.: Powder
Source: The herbs of Sophora viciifolia.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price: $40/20mg
Trimethoxystilbene has anti-cancer activity, it inhibits cancer cell growth by inducing multipolar cell mitosis.
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Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com

The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
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  • Pak J Pharm Sci.2019, 32(6)
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  • Acta Biochim Pol.2015, 62(2):253-8
  • RSC Advances2017, 86
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    Mol Carcinog. 2017 Mar;56(3):1117-26.
    The resveratrol analogue trimethoxystilbene inhibits cancer cell growth by inducing multipolar cell mitosis.[Pubmed: 27739192 ]
    Natural compounds are extensively studied for their potential use in traditional and non-traditional medicine. Several natural and synthetic Resveratrol analogues have shown interesting biological activities in the field of cancer chemoprevention.
    METHODS AND RESULTS:
    In the present study, we have focused on the ability of Resveratrol and two methoxylated derivatives (Trimethoxystilbene and Pterostilbene) to inhibit human cancer cell growth particularly analyzing their ability to interfere with tubulin dynamics at mitosis. We show that Trimethoxystilbene, differently from Resveratrol and Pterostilbene, alters microtubule polymerization dynamics in HeLa cells specifically inducing multipolar spindles and mitotic arrest coupled to a reduction of cell growth and an increase in apoptotic death by mitotic catastrophe.
    CONCLUSIONS:
    This work demonstrates that the structural modification of Rsv causes substantial changes in the mechanism of action of the derivatives. The presence of three extra methyl groups renders Trimethoxy very efficient in impairing cell proliferation by inducing mitotic catastrophe in cancer cells.
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