6-Hydroxyflavone

6-Hydroxyflavone

IUPAC name 6-hydroxy-2-phenylchromen-4-one
Other names 6-Monohydroxyflavone; 6-Hydroxy-2-phenyl-4-benzopyrone
Identifiers
CAS number	6665-83-4
PubChem	72279
ChemSpider	65233^Y
EC-number	229-704-8
KEGG	C14137^Y
ChEMBL	CHEMBL138649^Y
Jmol-3D images	Image 1 Image 2
SMILES C1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=CC(=C3)O O=C\1c3c(O/C(=C/1)c2ccccc2)ccc(O)c3
InChI InChI=1S/C15H10O3/c16-11-6-7-14-12(8-11)13(17)9-15(18-14)10-4-2-1-3-5-10/h1-9,16H^Y Key: GPZYYYGYCRFPBU-UHFFFAOYSA-N^Y InChI=1/C15H10O3/c16-11-6-7-14-12(8-11)13(17)9-15(18-14)10-4-2-1-3-5-10/h1-9,16H Key: GPZYYYGYCRFPBU-UHFFFAOYAV
Properties
Molecular formula	C₁₅H₁₀O₃
Molar mass	238.24 g mol⁻¹
Exact mass	238.062994 g mol⁻¹
Melting point	234-236 °C, 507-509 K, 453-457 °F
Y (verify) (what is: Y/N?) Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)
Infobox references

6-Hydroxyflavone is a flavone, a type of chemical compound. It is one of the noncompetitive inhibitors of cytochrome P450 2C9. It is reported in leaves of Barleria prionitis Linn. (a common Acanthaceae from India)^[1]. 6-Hydroxyflavone may have a potential as a therapeutic drug capable for the treatment of anxiety-like disorders^[2].

References

External links

Flavones and their glycosides

Flavones	Apigenin \| Baicalein \| Chrysin \| 6-Hydroxyflavone \| Luteolin \| Scutellarein

O-methylated flavones	Acacetin \| Diosmetin \| Eupatilin \| Genkwanin \| Nepetin \| Nobiletin \| Oroxylin A \| Sinensetin \| Tangeritin \| Techtochrysin \| Tricin \| Wogonin

Glycosides	Apiin \| Apigetrin \| Baicalin \| Cynaroside \| Diosmin \| Giraldiin A and B \| Nepitrin (Nepetin 7-glucoside) \| Orientin (Isoorientin) \| Oroxindin \| Rhoifolin \| Saporanin (Isovitexin-7-O-glucoside) \| Schaftoside \| Scutellarin \| Tetuin \| Veronicastroside \| Vicenin-2 \| Vitexin (Isovitexin)

acetylated	Artoindonesianin P

Synthetic	Diosmin \| Flavoxate \| Hidrosmin