A flavonoid with diverse biological activities
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Gossypetin

Item No. 33840

Technical Information
Formal Name
2-(3,4-dihydroxyphenyl)-3,5,7,8-tetrahydroxy-4H-1-benzopyran-4-one
CAS Number
489-35-0
Synonyms
  • C.I. 75750
  • 8-hydroxy Quercetin
Molecular Formula
C15H10O8
Formula Weight
Purity
≥98%
A solid
DMSO: solubleEthanol: soluble
λmax
262, 388 nm
SMILES
OC(C=C(C(OC1=C(C(O)=CC(O)=C1O)C2=O)=C2O)C=C3)=C3O
InChi Code
InChI=1S/C15H10O8/c16-6-2-1-5(3-7(6)17)14-13(22)12(21)10-8(18)4-9(19)11(20)15(10)23-14/h1-4,16-20,22H
InChi Key
YRRAGUMVDQQZIY-UHFFFAOYSA-N
Origin
Synthetic
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    Gossypetin is a flavonoid that has been found in H. sabdariffa and has diverse biological activities.1,2,3 It inhibits the MAP2K kinases MKK3 and MKK6 in a concentration-dependent manner, as well as induces apoptosis and cell cycle arrest at the G2 phase in KYSE-450 and KYSE-510 esophageal cancer cells when used at a concentration of 20 µM.1 Gossypetin scavenges DPPH (Item No. 14805) radicals and inhibits copper-induced lipid peroxidation in cell-free assays.2 It reduces high-fat diet-induced increases in serum cholesterol, triglycerides, and LDL-cholesterol levels, as well as decreases aortic extracellular lipid and foam cell deposits in a rabbit model of atherosclerosis when administered at a dose of 10 mg/kg.3

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Xie, X., Liu, K., Liu, F., et alGossypetin is a novel MKK3 and MKK6 inhibitor that suppresses esophageal cancer growth in vitro and in vivo. Cancer Lett. 442, 126-136 (2019).

    2. Chen, J.-H., Tsai, C.-W., Wang, C.-P., et alAnti-atherosclerotic potential of gossypetin via inhibiting LDL oxidation and foam cell formation. Toxicol. Appl. Pharmacol. 272(2), 313-324 (2013).

    3. Lin, H.-H. In vitro and in vivo atheroprotective effects of gossypetin against endothelial cell injury by induction of autophagy. Chem. Res. Toxicol. 28(2), 202-215 (2015).