Alnetin
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Names
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IUPAC name
5-Hydroxy-6,7,8-trimethoxyflavone
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Systematic IUPAC name
5-Hydroxy-6,7,8-trimethoxy-2-phenyl-4H-1-benzopyran-4-one
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Other names
5-Hydroxy-6,7,8-trimethoxy-2-phenyl-4H-chromen-4-one
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Identifiers
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ChemSpider
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UNII
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InChI=1S/C18H16O6/c1-21-16-14(20)13-11(19)9-12(10-7-5-4-6-8-10)24-15(13)17(22-2)18(16)23-3/h4-9,20H,1-3H3 Key: VOLPCZWHFBZDQT-UHFFFAOYSA-N InChI=1/C18H16O6/c1-21-16-14(20)13-11(19)9-12(10-7-5-4-6-8-10)24-15(13)17(22-2)18(16)23-3/h4-9,20H,1-3H3 Key: VOLPCZWHFBZDQT-UHFFFAOYAZ
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O=C\1c3c(O/C(=C/1)c2ccccc2)c(OC)c(OC)c(OC)c3O
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Properties
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C18H16O6
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Molar mass
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328.316
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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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Infobox references
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Tracking categories (test):
Alnetin is a flavone isolated from Lindera lucida.[1]
References
- ↑ A dihydrochalcone from Lindera lucida. Yuan-Wah Leong, Leslie J. Harrison, Graham J. Bennett, Azizol A. Kadir and Joseph D. Connolly, Phytochemistry, Volume 47, Issue 5, March 1998, Pp. 891-894, doi:10.1016/S0031-9422(97)00947-3
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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/Alnetin. Read more |