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Acacetin
	IUPAC名 5,7-dihydroxy-2-(4-methoxyphenyl)chromen-4-one
	別称 5,7-dihydroxy-4′-methoxyflavone; 4'-methoxy-5,7-dihydroxyflavone; Linarigenin; Acacetine; Buddleoflavonol; Linarisenin; 4'-Methoxyapigenin; Apigenin 4'-methyl ether; 5,7-Dioxy-4'-methoxyflavone; 5,7-Dihydroxy-2-(4-methoxyphenyl)-4H-chromen-4-one
識別情報
CAS登録番号	480-44-4
PubChem	5280442
ChemSpider	4444099
ChEBI	CHEBI:15335 ;
ChEMBL	CHEMBL243664
	SMILES COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O; O=C\1c3c(O/C(=C/1)c2ccc(OC)cc2)cc(O)cc3O;
	InChI InChI=1S/C16H12O5/c1-20-11-4-2-9(3-5-11)14-8-13(19)16-12(18)6-10(17)7-15(16)21-14/h2-8,17-18H,1H3 Key: DANYIYRPLHHOCZ-UHFFFAOYSA-N ; InChI=1/C16H12O5/c1-20-11-4-2-9(3-5-11)14-8-13(19)16-12(18)6-10(17)7-15(16)21-14/h2-8,17-18H,1H3 Key: DANYIYRPLHHOCZ-UHFFFAOYAN;
特性
化学式	C16H12O5
モル質量	284.26 g mol−1
精密質量	284.068473 u
	特記なき場合、データは常温 (25 °C)・常圧 (100 kPa) におけるものである。

出典

^ Zhao, J; Dasmahapatra, AK; Khan, SI; Khan, IA (December 2008). “Anti-aromatase activity of the constituents from damiana (Turnera diffusa)”. Journal of Ethnopharmacology 120 (3): 387–393. doi:10.1016/j.jep.2008.09.016. PMID 18948180.
^ Valkama, E; Salminen, J-P; Koricheva, J; Pihlaja, K. “Changes in Leaf Trichomes and Epicuticular Flavonoids during Leaf Development in Three Birch Taxa”. Annals of Botany 94: 233–242. doi:10.1093/aob/mch131.
^ UmiKalsom, Yusuf; Harborne, Jeffrey B. (1991). “Flavonoid distribution in asplenioid ferns”. Pertanika 14 (3): 297–300. http://psasir.upm.edu.my/2863.