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Details

Stereochemistry ACHIRAL
Molecular Formula C20H20O8
Molecular Weight 388.368
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ARTEMETIN

SMILES

COC1=CC2=C(C(=O)C(OC)=C(O2)C3=CC(OC)=C(OC)C=C3)C(O)=C1OC

InChI

InChIKey=RIGYMJVFEJNCKD-UHFFFAOYSA-N
InChI=1S/C20H20O8/c1-23-11-7-6-10(8-12(11)24-2)18-20(27-5)17(22)15-13(28-18)9-14(25-3)19(26-4)16(15)21/h6-9,21H,1-5H3

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Flavonoids from Vitex trifolia L. inhibit cell cycle progression at G2/M phase and induce apoptosis in mammalian cancer cells.
2005 Aug
New antifungal flavonoid glycoside from Vitex negundo.
2007 Jan 1
Antiproliferative effect of flavonoids and sesquiterpenoids from Achillea millefolium s.l. on cultured human tumour cell lines.
2009 May
A high-speed counter-current chromatography- HPLC-DAD method for preparative isolation and purification of two polymethoxylated flavones from Taraxacum mongolicum.
2009 May-Jun
Hypotensive mechanism of the extracts and artemetin isolated from Achillea millefolium L. (Asteraceae) in rats.
2011 Jul 15
Name Type Language
ARTEMETIN
Common Name English
5-HYDROXY-3,3',4',6,7-PENTAMETHOXY-FLAVONE
Systematic Name English
5-HYDROXY-3,3',4',6,7-PENTAMETHOXYFLAVONE
Systematic Name English
Code System Code Type Description
FDA UNII
73KMT7R64H
Created by admin on Fri Dec 15 17:50:47 GMT 2023 , Edited by admin on Fri Dec 15 17:50:47 GMT 2023
PRIMARY
CAS
479-90-3
Created by admin on Fri Dec 15 17:50:47 GMT 2023 , Edited by admin on Fri Dec 15 17:50:47 GMT 2023
PRIMARY
MESH
C054132
Created by admin on Fri Dec 15 17:50:47 GMT 2023 , Edited by admin on Fri Dec 15 17:50:47 GMT 2023
PRIMARY
EPA CompTox
DTXSID20197325
Created by admin on Fri Dec 15 17:50:47 GMT 2023 , Edited by admin on Fri Dec 15 17:50:47 GMT 2023
PRIMARY
PUBCHEM
5320351
Created by admin on Fri Dec 15 17:50:47 GMT 2023 , Edited by admin on Fri Dec 15 17:50:47 GMT 2023
PRIMARY