1-Methyl-2-nonylquinolin-4(1H)-one
1-Methyl-2-nonylquinolin-4(1H)-one Basic information
- Product Name:
- 1-Methyl-2-nonylquinolin-4(1H)-one
- Synonyms:
-
- 1-Methyl-2-nonylquinolin-4(1H)-one
- 1-Methyl-2-n-nonyl-4(1H) quinolone
- 1-Methyl-2-nonyl-4(1H)-quinolone
- 1-Methyl-2-nonyl-4-quinolinone
- 1-METHYL-2-NONYLQUINOLIN-4(1H)-O
- 4(1H)-Quinolinone, 1-methyl-2-nonyl-
- 1-Methyl-2-nonyl-4(1H)-quinolinone
- 1-methyl-2-nonylquinolin-4-one
- CAS:
- 68353-24-2
- MF:
- C19H27NO
- MW:
- 285.42
- Mol File:
- 68353-24-2.mol
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1-Methyl-2-nonylquinolin-4(1H)-one Chemical Properties
- Melting point:
- 73-75℃
- Boiling point:
- 391.9±42.0 °C(Predicted)
- Density
- 0.990±0.06 g/cm3(Predicted)
- pka
- 2.53±0.70(Predicted)
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1-Methyl-2-nonylquinolin-4(1H)-one Usage And Synthesis
Uses
1-Methyl-2-nonyl-4(1H)-quinolone, a quinolone alkaloid, is a potent and selective MAO-B (monoamine oxidase) inhibitor. 1-Methyl-2-nonyl-4(1H)-quinolone exhibites inhibitory activity on leukotriene biosynthesis, with an IC50 of 12.1 μM[1][2].
Definition
ChEBI: 1-Methyl-2-nonyl-4(1H)-quinolinone is a member of quinolines.
IC 50
MAO-B; MAO-A
References
[1] Han XH, et al. Quinolone alkaloids from evodiae fructus and their inhibitory effects on monoamine oxidase. Arch Pharm Res. 2007 Apr;30(4):397-401. DOI:10.1007/BF02980210
[2] Adams M, et al. Inhibition of leukotriene biosynthesis by quinolone alkaloids from the fruits of Evodia rutaecarpa. Planta Med. 2004 Oct;70(10):904-8. DOI:10.1055/s-2004-832614
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