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Eupatorin 5-methyl ether

CAS:

Ref. 3D-FE23208

1g
1,008.00€
100mg
190.00€
250mg
400.00€
500mg
621.00€
Eupatorin 5-methyl ether
Biosynth

Product Information

Name:Eupatorin 5-methyl ether
Synonyms:
  • 2-(3-Hydroxy-4-methoxyphenyl)-5,6,7-trimethoxy-4H-1-benzopyran-4-one3'-Hydroxy-4',5,6,7-tetramethoxyflavone3'-Hydroxy-5,6,7,4'-tet ramethoxyflavone
Brand:Biosynth
Description:Eupatorin 5-methyl ether is a bioactive compound, which is a naturally occurring flavonoid found in certain plant species. This compound is derived from various plants, including those in the Asteraceae family. Eupatorin 5-methyl ether functions primarily through modulating various biochemical pathways, exhibiting anti-inflammatory, antioxidant, and anticancer activities. The specific mode of action involves the inhibition of enzymes and modulation of signaling pathways that are pivotal in the proliferation and survival of cancer cells. It impedes key growth factor receptors and kinases, thereby regulating the cell cycle and promoting apoptosis in malignant cells. Additionally, its antioxidant properties play a crucial role in reducing oxidative stress, a known contributor to numerous chronic diseases. Eupatorin 5-methyl ether is explored extensively in pharmacological and biochemical studies for its potential therapeutic effects. Its applications range across various disciplines, including oncology, where it is evaluated for its efficacy in inhibiting tumor growth, and in chronic disease management due to its anti-inflammatory properties. Researchers continue to investigate its full potential and applicability in the development of new therapeutic agents.
Notice:Our products are intended for lab use only. For any other use, please contact us.

Chemical properties

Molecular weight:358.34 g/mol
Formula:C19H18O7
Purity:Min. 95%
Color/Form:Powder
InChI:InChI=1S/C19H18O7/c1-22-13-6-5-10(7-11(13)20)14-8-12(21)17-15(26-14)9-16(23-2)18(24-3)19(17)25-4/h5-9,20H,1-4H3
InChI key:InChIKey=LYLDPYNWDVVPIQ-UHFFFAOYSA-N
SMILES:COc1ccc(-c2cc(=O)c3c(OC)c(OC)c(OC)cc3o2)cc1O

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