Nepetin
|
|
Names
|
IUPAC name 3′,4′,5,7-Tetrahydroxy-6-methoxyflavone |
Systematic IUPAC name2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-6-methoxy-4H-1-benzopyran-4-one |
Other names 6-Methoxyluteolin |
Identifiers
|
|
|
|
|
ChEMBL
|
|
ChemSpider
|
|
|
|
UNII
|
|
|
|
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 NKey: FHHSEFRSDKWJKJ-UHFFFAOYSA-N NInChI=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
|
COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O
|
Properties
|
|
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). |
Chemical compound
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
|
---|
Aglycones | Monohydroxyflavone | |
---|
Dihydroxyflavones | |
---|
Trihydroxyflavones | |
---|
Tetrahydroxyflavones | |
---|
Pentahydroxyflavones | |
---|
O-methylated flavones | |
---|
|
---|
Glycosides | of apigenin | |
---|
of baicalein | |
---|
of hypolaetin | |
---|
of luteolin | |
---|
|
---|
Acetylated | |
---|
Sulfated glycosides | |
---|
Polymers | |
---|
Drugs | |
---|