Eupatilin

Eupatilin
Clinical data


Dependence liability	None
Routes of administration	Oral
ATC code	none
Legal status
Legal status	CA: not available UK: not available US: not available In general: ℞ (Prescription only)
Identifiers
IUPAC name 2-(3,4-Dimethoxyphenyl)-5,7-dihydroxy-6-methoxychromen-4-one
CAS Number	22368-21-4^Y
PubChem CID	5273755
ChemSpider	4438134^N
Chemical and physical data
Formula	C₁₈H₁₆O₇
Molar mass	344.315 g/mol
3D model (JSmol)	Interactive image
SMILES O=C\1c3c(O)c(OC)c(O)cc3O/C(=C/1)c2ccc(OC)c(OC)c2
InChI InChI=1S/C18H16O7/c1-22-12-5-4-9(6-14(12)23-2)13-7-10(19)16-15(25-13)8-11(20)18(24-3)17(16)21/h4-8,20-21H,1-3H3^N Key:DRRWBCNQOKKKOL-UHFFFAOYSA-N^N
^NY (what is this?) (verify)

Eupatilin (5,7-Dihydroxy-3',4',6-trimethoxyflavone) is an O-methylated flavone, a type of flavonoids. It can be found in Artemisia asiatica (Asteraceae).^[1]

References

↑ Kim, D. H.; Na, H. K.; Oh, T. Y.; Kim, W. B.; Surh, Y. J. (2004). "Eupatilin, a pharmacologically active flavone derived from Artemisia plants, induces cell cycle arrest in ras-transformed human mammary epithelial cells". Biochemical Pharmacology. 68 (6): 1081–1087. PMID 15313404. doi:10.1016/j.bcp.2004.04.027.

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. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.