Name | 1-methyl-2-nonylquinolin-4-one |
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Synonyms |
1-Methyl-2-nonyl-4(1H)-quinolinone
4(1H)-Quinolinone, 1-methyl-2-nonyl- N-methyl-2-nonyl-4-quinolone 1-Methyl-2-nonyl-4(1H)-quinolone 1-Methyl-2-n-nonyl-4-chinolon 1-methyl-2-nonyl-1H-quinolin-4-one |
Description | 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]. |
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Related Catalog | |
Target |
MAO-B MAO-A |
In Vitro | 1-Methyl-2-nonyl-4(1H)-quinolone shows more potent inhibitory effects against MAO-B compared to MAO-A[1]. |
References |
Density | 1.0±0.1 g/cm3 |
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Boiling Point | 391.9±42.0 °C at 760 mmHg |
Melting Point | 73-75℃ |
Molecular Formula | C19H27NO |
Molecular Weight | 285.424 |
Flash Point | 132.6±17.3 °C |
Exact Mass | 285.209259 |
PSA | 22.00000 |
LogP | 6.09 |
Vapour Pressure | 0.0±0.9 mmHg at 25°C |
Index of Refraction | 1.524 |
Hazard Codes | Xi |
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~10% 68353-24-2 |
Literature: Somanathan; Smith Journal of Heterocyclic Chemistry, 1981 , vol. 18, # 6 p. 1077 - 1079 |
~% 68353-24-2 |
Literature: Somanathan; Smith Journal of Heterocyclic Chemistry, 1981 , vol. 18, # 6 p. 1077 - 1079 |
~% 68353-24-2 |
Literature: Somanathan; Smith Journal of Heterocyclic Chemistry, 1981 , vol. 18, # 6 p. 1077 - 1079 |
~% 68353-24-2 |
Literature: Somanathan; Smith Journal of Heterocyclic Chemistry, 1981 , vol. 18, # 6 p. 1077 - 1079 |
~% 68353-24-2 |
Literature: Somanathan; Smith Journal of Heterocyclic Chemistry, 1981 , vol. 18, # 6 p. 1077 - 1079 |
~% 68353-24-2 |
Literature: Coppola, Gary M. Journal of Heterocyclic Chemistry, 1985 , vol. 22, p. 491 - 494 |
Precursor 7 | |
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DownStream 0 |