Description
Methyllinderone, isolated from the roots of Lindera aggregata( Sims) Kosterm, showed moderate to weak antifungal activities against various pathogenic fungi. Methyllinderone and methyllucidone selectively inhibited the growth of H-ras-transformed rat-2 cell lines in comparison with normal rat-2 cells with a GI50 value of 0.3 and 0.85 microM, respectively.
Synonyms
4,5-Dimethoxy-2-[(2E)-1-methoxy-3-phenyl-2-propen-1-ylidene]-4-cyclopentene-1,3-dione; 4-Cyclopentene-1,3-dione, 4,5-dimethoxy-2-(1-methoxy-3-phenyl-2-propenylidene)-, (E)-; 4-Cyclopentene-1,3-dione, 4,5-dimethoxy-2-(α-methoxycinnamylidene)-; Linderone, methyl-; Methyl linderone
IUPAC Name
4,5-dimethoxy-2-[(E)-1-methoxy-3-phenylprop-2-enylidene]cyclopent-4-ene-1,3-dione
Molecular Formula
C17H16O5
Canonical SMILES
COC1=C(C(=O)C(=C(/C=C/C2=CC=CC=C2)OC)C1=O)OC
InChI
InChI=1S/C17H16O5/c1-20-12(10-9-11-7-5-4-6-8-11)13-14(18)16(21-2)17(22-3)15(13)19/h4-10H,1-3H3/b10-9+
InChIKey
KXRUALBXWXRUTD-MDZDMXLPSA-N
Boiling Point
570.1±50.0 °C at 760 mmHg
Solubility
Soluble in Acetone, Chloroform, Dichloromethane, DMSO, Ethyl Acetate