68353-24-2

68353-24-2 structure
68353-24-2 structure
  • Name: 1-Methyl-2-nonylquinolin-4(1H)-one
  • Chemical Name: 1-methyl-2-nonylquinolin-4-one
  • CAS Number: 68353-24-2
  • Molecular Formula: C19H27NO
  • Molecular Weight: 285.424
  • Catalog: Natural product Alkaloid
  • Create Date: 2017-12-18 17:02:07
  • Modify Date: 2024-01-11 09:41:25
  • 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].

Name 1-methyl-2-nonylquinolin-4-one
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].
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

[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.

[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.

Density 1.0±0.1 g/cm3
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

~10%

68353-24-2 structure

68353-24-2

Literature: Somanathan; Smith Journal of Heterocyclic Chemistry, 1981 , vol. 18, # 6 p. 1077 - 1079

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68353-24-2 structure

68353-24-2

Literature: Somanathan; Smith Journal of Heterocyclic Chemistry, 1981 , vol. 18, # 6 p. 1077 - 1079

~%

68353-24-2 structure

68353-24-2

Literature: Somanathan; Smith Journal of Heterocyclic Chemistry, 1981 , vol. 18, # 6 p. 1077 - 1079

~%

68353-24-2 structure

68353-24-2

Literature: Somanathan; Smith Journal of Heterocyclic Chemistry, 1981 , vol. 18, # 6 p. 1077 - 1079

~%

68353-24-2 structure

68353-24-2

Literature: Somanathan; Smith Journal of Heterocyclic Chemistry, 1981 , vol. 18, # 6 p. 1077 - 1079

~%

68353-24-2 structure

68353-24-2

Literature: Coppola, Gary M. Journal of Heterocyclic Chemistry, 1985 , vol. 22, p. 491 - 494