Acacetin

Acacetin
Names


Preferred IUPAC name 5,7-dihydroxy-2-(4-methoxyphenyl)-4H-1-benzopyran-4-one
Other names 5,7-dihydroxy-2-(4-methoxyphenyl)-4H-chromen-4-one 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
Identifiers
CAS Number	480-44-4^N
3D model (Jmol)	Interactive image Interactive image
ChEBI	CHEBI:15335^Y
ChEMBL	ChEMBL243664^Y
ChemSpider	4444099^Y
ECHA InfoCard	100.006.867
PubChem	5280442
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^Y Key: DANYIYRPLHHOCZ-UHFFFAOYSA-N^Y 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
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
Properties
Chemical formula	C₁₆H₁₂O₅
Molar mass	284.26 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is ^YN ?)
Infobox references

Acacetin is an O-methylated flavone found in Robinia pseudoacacia (black locust), Turnera diffusa (damiana),^[1] Betula pendula (silver birch),^[2] and in the fern Asplenium normale.^[3]

References

↑ 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.

Flavones and their conjugates

Aglycones

Monohydroxyflavone	6-Hydroxyflavone

Dihydroxyflavones	Chrysin 4',7-Dihydroxyflavone 7,8-Dihydroxyflavone

Trihydroxyflavones	Apigenin Baicalein Norwogonin

Tetrahydroxyflavones	Isoscutellarein Luteolin Norartocarpetin Scutellarein

Pentahydroxyflavones	6-Hydroxyluteolin Hypolaetin Tricetin

O-methylated flavones	Acacetin Alnetin Artocarpetin Chrysoeriol Cirsilineol Cirsiliol Cirsimaritin Diosmetin Eupatilin Genkwanin Hispidulin Nepetin Nobiletin Oroxylin A Pratol Salvigenin Sinensetin Tangeritin Techtochrysin Tricin Wogonin Zapotin

of apigenin	Apiin Apigetrin Isovitexin Rhoifolin Saponarin Schaftoside Vicenin-2 Vitexin

of baicalein	Baicalin Tetuin

of hypolaetin	Hypolaetin 8-glucoside Hypolaetin 8-glucuronide

of luteolin	Cynaroside Isoorientin Orientin Veronicastroside Luteolin-7-O-glucuronide

Acetylated

Sulfated glycosides

Polymers

Drugs

This article is issued from Wikipedia - version of the 9/5/2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.