Nepetin

Nepetin
Names
	IUPAC name 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-methoxychromen-4-one
	Other names 6-Methoxyluteolin; 6-methoxy 5,7,3',4'-tetrahydroxyflavone
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).
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	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

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[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