Gossypetin

Gossypetin

Names
IUPAC name 3,3′,4′,5,7,8-Hexahydroxyflavone
Systematic IUPAC name 2-(3,4-Dihydroxyphenyl)-3,5,7,8-tetrahydroxy-4H-1-benzopyran-4-one
Other names Articulatidin Equisporol 3,5,7,8,3',4'-Hexahydroxyflavone
Identifiers
CAS Number	489-35-0 Y
3D model (JSmol)	Interactive image
ChEBI	CHEBI:16400 N
ChEMBL	ChEMBL253570 N
ChemSpider	4444247 N
PubChem CID	5280647
UNII	SET4M23ZTM Y
CompTox Dashboard (EPA)	DTXSID50197631
InChI 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 N Key: YRRAGUMVDQQZIY-UHFFFAOYSA-N N InChI=1/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 Key: YRRAGUMVDQQZIY-UHFFFAOYAI
SMILES C1=CC(=C(C=C1C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)O)O)O)O
Properties
Chemical formula	C15H10O8
Molar mass	318.23 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N verify (what is YN ?) Infobox references

Gossypetin, also known as 3,5,7,8,3',4'-hexahydroxyflavone, is a flavonol, a type of flavonoid. It has been isolated from the flowers and the calyx of Hibiscus sabdariffa (roselle) and exhibits a strong antibacterial activity.^[1][2] The compound has also been found to act as an antagonist of TrkB.^[3] Gossypetin has radioprotective activity.^{[citation needed]}

The enzyme 8-hydroxyquercetin 8-O-methyltransferase uses S-adenosyl methionine and gossypetin to produce S-adenosylhomocysteine and 3,5,7,3',4'-pentahydroxy-8-methoxyflavone.^{[citation needed]}

In 2022, a study in an animal model using intragastric administration suggested that the flavonoid gossypetin facilitated the clearance of beta-amyloid in the brain and is a promising target for the study of treatments for Alzheimer's Disease by enhancing microglial phagocytic activity against Aβ.^[4]

• Tropomyosin receptor kinase B § Antagonists

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