Description
Flavokawain B is a chalcone kavalactone originally found in Piper methysticum (kava plant). Flavokawain B exhibits hepatotoxic and anti-inflammatory activities. This compound inhibits degradation of IκBα and activation of NF-κB.
Product Unit Size | Cost | Quantity | Stock |
---|
Flavokawain B is a chalcone kavalactone originally found in Piper methysticum (kava plant). Flavokawain B exhibits hepatotoxic and anti-inflammatory activities. This compound inhibits degradation of IκBα and activation of NF-κB.
Cas No. | 1775-97-9 |
---|---|
Purity | ≥97% |
Formula | C17H16O4 |
Formula Wt. | 284.31 |
IUPAC Name | (E)-1-(2-hydroxy-4,6-dimethoxyphenyl)-3-phenylprop-2-en-1-one |
Melting Point | 85-87°C |
Solubility | DMSO to 35 mM. Insoluble in water. Soluble in methanol. |
Appearance | Orange/Yellow crystalline powder |
Store Temp | -20°C |
---|---|
Ship Temp | Ambient |
MSDS | |
---|---|
Info Sheet |
Teschke R, Qiu SX, Lebot V. Herbal hepatotoxicity by kava: update on pipermethystine, flavokavain B, and mould hepatotoxins as primarily assumed culprits. Dig Liver Dis. 2011 Sep;43(9):676-81. PMID: 21377431.
Folmer F, Blasius R, Morceau F, et al. Inhibition of TNFalpha-induced activation of nuclear factor kappaB by kava (Piper methysticum) derivatives. Biochem Pharmacol. 2006 Apr 14;71(8):1206-18. PMID: 16464438.
Sakai T, Eskander RN, Guo Y, et al. Flavokawain B, a kava chalcone, induces apoptosis in synovial sarcoma cell lines. J Orthop Res. 2012 Jul;30(7):1045-1050. PMID: 22213202.
Cannabinoid receptor 2 selective agonist.
Trichothecene mycotoxin produced by Fusarium.
Induces ER degradation.
Glycopeptide, metal ion chelator, induces DNA s...
Endogenous neuropeptide, involved in opioid sig...
CHK1 inhibitor.
Diterpene found in brewed, unfiltered coffee; F...
ITC found in cruciferous vegetables.
Terpene lactone found in Ginkgo.
mAChR antagonist.
Endogenous calcitonin-family peptide, involved ...
Agonist of STING.
σ1/2and μ/κ/δ-OR agonist, α3β4/α4β2/α7...
Toxin produced by Aspergillus.
Cannabinoid receptor 2 selective agonist.
Furocoumarin; COX-2 inhibitor.
Casein kinase 1 inhibitor.
c-Raf, RET, VEGFR1 inhibitor, potential HMT inh...
Macrolide; protein synthesis inhibitor.
S-adenosylmethionine nucleoside analog; methylt...