1-Methyl-2-nonylquinolin-4(1H)-one
- Product Name
- 1-Methyl-2-nonylquinolin-4(1H)-one
- CAS No.
- 68353-24-2
- Chemical Name
- 1-Methyl-2-nonylquinolin-4(1H)-one
- Synonyms
- N-methyl-2-nonyl-4-quinolone;1-methyl-2-nonylquinolin-4-one;1-Methyl-2-nonyl-4-quinolinone;1-METHYL-2-NONYLQUINOLIN-4(1H)-O;1-Methyl-2-nonyl-4(1H)-quinolone;1-Methyl-2-n-nonyl-4(1H) quinolone;1-Methyl-2-nonylquinolin-4(1H)-one;1-Methyl-2-nonyl-4(1H)-quinolinone;4(1H)-Quinolinone, 1-methyl-2-nonyl-
- CBNumber
- CB12681183
- Molecular Formula
- C19H27NO
- Formula Weight
- 285.42
- MOL File
- 68353-24-2.mol
1-Methyl-2-nonylquinolin-4(1H)-one Property
- 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)
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- AS204872
- Product name
- 1-Methyl-2-nonylquinolin-4(1H)-one
- Packaging
- 5mg
- Price
- $316
- Updated
- 2021/12/16
- Product number
- CD32000621
- Product name
- 1-Methyl-2-nonylquinolin-4(1H)-one
- Purity
- 95+%
- Packaging
- 5mg
- Price
- $810
- Updated
- 2021/12/16
- Product number
- 68353242
- Product name
- 1-Methyl-2-nonylquinolin-4(1H)-one
- Packaging
- 5mg
- Price
- $834.3
- Updated
- 2021/12/16
1-Methyl-2-nonylquinolin-4(1H)-one Chemical Properties,Usage,Production
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
1-Methyl-2-nonylquinolin-4(1H)-one Preparation Products And Raw materials
Raw materials
Preparation Products
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