ChemicalBook--->CAS DataBase List--->147030-01-1

147030-01-1

147030-01-1 Structure

147030-01-1 Structure
IdentificationBack Directory
[Name]

sodium 3-[1-[(4-chlorophenyl)methyl]-5-(quinolin-2-ylmethoxy)-3-tert-butylsulfanyl-indol-2-yl]-2,2-dimethyl-propanoate
[CAS]

147030-01-1
[Synonyms]

MK 591
Quiflapon SodiuM
QUIFLAPON SODIUM; MK-591; MK 591
sodium 3-[1-[(4-chlorophenyl)methyl]-5-(quinolin-2-ylmethoxy)-3-tert-butylsulfanyl-indol-2-yl]-2,2-dimethyl-propanoate
1-[(4-Chlorophenyl)Methyl]-3-[(1,1-diMethylethyl)thio]-α,α-diMethyl-5-(2-quinolinylMethoxy)-1H-Indole-2-propanoic Acid SodiuM Salt
[Molecular Formula]

C34H34ClN2NaO3S
[MDL Number]

MFCD15143438
[MOL File]

147030-01-1.mol
Chemical PropertiesBack Directory
[storage temp. ]

-20°C
[solubility ]

DMSO : 50 mg/mL (82.08 mM; Need ultrasonic)H2O : < 0.1 mg/mL (insoluble)
[form ]

Powder
[color ]

White to off-white
Hazard InformationBack Directory
[Uses]

Quiflapon is a synthetic compound which specifically inhibits the activity of 5-Lox and is currently under development for the treatment of asthma. Also, Quiflapon, a leukotriene biosynthesis inhibitor, induces apoptosis in prostate cancer cells.
[Biological Activity]

Cell permeable: yes''Primary Target
FLAP
[in vivo]

Hyperoxia groups of mice treated with Quiflapon sodium (MK591) (20, 40 mg/kg) show alveolarization that resembles that of room air controls while untreated hyperoxia groups show definite evidence of aberrant alveolarization but no inflammation[3]. Comparison of the Aβ-immunopositive areas between the placebo and Quiflapon sodium (MK591) (320 mg/kg)-treated group reveals a statistically significant reduction of the amyloid burden in the treated mice. Quiflapon sodium also has a significant reduction in brain levels of IL-1β. Mice treated with Quiflapon sodium show a statistically significant decrease in the steady-state levels of total CREB and its phosphorylated form at Ser133[4].

[target]

FLAP
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