Nepetin

Nepetin
Names
	IUPAC name 3′,4′,5,7-Tetrahydroxy-6-methoxyflavone
	Systematic IUPAC name 2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-6-methoxy-4H-1-benzopyran-4-one
	Other names 6-Methoxyluteolin
Identifiers
CAS Number	520-11-6 ;
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL172350 ;
ChemSpider	4476172 ;
PubChem CID	5317284;
UNII	I3O7LF3GED ;
CompTox Dashboard (EPA)	DTXSID10199959 ;
	InChI InChI=1S/C16H12O7/c1-22-16-11(20)6-13-14(15(16)21)10(19)5-12(23-13)7-2-3-8(17)9(18)4-7/h2-6,17-18,20-21H,1H3 Key: FHHSEFRSDKWJKJ-UHFFFAOYSA-N ; InChI=1/C16H12O7/c1-22-16-11(20)6-13-14(15(16)21)10(19)5-12(23-13)7-2-3-8(17)9(18)4-7/h2-6,17-18,20-21H,1H3 Key: FHHSEFRSDKWJKJ-UHFFFAOYAR;
	SMILES COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O;
Properties
Chemical formula	C16H12O7
Molar mass	316.26 g/mol
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

Nepetin is the 6-methoxy derivative of the pentahydroxyflavone 6-hydroxyluteolin, an O-methylated flavone. It can be found in Eupatorium ballotaefolium.^[1]

Glycosides

Nepitrin is the 7-glucoside of nepetin.

References

^ "Cytotoxic activity of nepetin, a flavonoid from Eupatorium ballotaefolium HBK. Militao G. C. G., Albuquerque M. R. J. R., Pessoa O. D. L., Pessoa C., Moraes M. E. A., De Moraes M. O., Costa-Lotufo L. V., Pharmazie, 2004, vol. 59, no12, pp. 965-966". Archived from the original on 2012-08-28. Retrieved 2010-04-06.

[1] "Cytotoxic activity of nepetin, a flavonoid from Eupatorium ballotaefolium HBK. Militao G. C. G., Albuquerque M. R. J. R., Pessoa O. D. L., Pessoa C., Moraes M. E. A., De Moraes M. O., Costa-Lotufo L. V., Pharmazie, 2004, vol. 59, no12, pp. 965-966". Archived from the original on 2012-08-28. Retrieved 2010-04-06.

[1]