Nepetin
Nepetin
![Chemical structure of nepetin](../I/m/Nepetin.svg.png) |
![Ball-and-stick model of nepetin](../I/m/Nepetin_molecule_ball.png) |
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 |
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520-11-6 Y= |
ChEMBL |
ChEMBL172350 N |
ChemSpider |
4476172 N |
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
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Jmol-3D images |
Image |
PubChem |
5317284 |
COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O
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Properties |
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C16H12O7 |
Molar mass |
316.26 g/mol |
Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa) |
N verify (what is: Y/ N?) |
Infobox references |
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Nepetin is 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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| Aglycones | Monohydroxyflavone | |
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| Dihydroxyflavones | |
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| Trihydroxyflavones | |
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| Tetrahydroxyflavones | |
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| Pentahydroxyflavones | |
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| O-methylated flavones | |
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| Glycosides | of apigenin | |
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| of baicalein | |
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| of hypolaetin |
- Hypolaetin 8-glucoside
- Hypolaetin 8-glucuronide
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| of luteolin | |
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| Acetylated |
- Artocarpetin A
- Artoindonesianin P
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| Sulfated glycosides | |
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| Polymers | |
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| Drugs | |
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