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Alnetin
Names
IUPAC name
5-Hydroxy-6,7,8-trimethoxyflavone
Preferred IUPAC name
5-Hydroxy-6,7,8-trimethoxy-2-phenyl-4H -1-benzopyran-4-one
Other names
5-Hydroxy-6,7,8-trimethoxy-2-phenyl-4H -chromen-4-one
Identifiers
3D model (JSmol )
ChemSpider
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
O=C\1c3c(O/C(=C/1)c2ccccc2)c(OC)c(OC)c(OC)c3O
Properties
C18 H16 O6
Molar mass
328.316
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
Chemical compound
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
Aglycones
Monohydroxyflavone Dihydroxyflavones Trihydroxyflavones Tetrahydroxyflavones Pentahydroxyflavones O-methylated flavones
Glycosides
of apigenin of baicalein of hypolaetin of luteolin
Acetylated
Sulfated glycosides Polymers Drugs
Categories :
Flavones Aromatic compound stubs Hidden categories:
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