Nepetin
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| Names
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| IUPAC name
3′,4′,5,7-Tetrahydroxy-6-methoxyflavone
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Systematic IUPAC name
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-6-methoxy-4H-1-benzopyran-4-one
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| Other names
6-Methoxyluteolin
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| Identifiers
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| ChEMBL
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| ChemSpider
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| UNII
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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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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
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| Molar mass
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316.26 g/mol
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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N verify (what is Y N ?)
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| Infobox references
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Tracking categories (test):
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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| 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 | |
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| of luteolin | |
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| Acetylated | |
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| Sulfated glycosides | |
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| Polymers | |
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| Drugs | |
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 | Original source: https://en.wikipedia.org/wiki/Nepetin. Read more |