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1384424-80-9

1384424-80-9 Structure

1384424-80-9 Structure
IdentificationBack Directory
[Name]

1-(7-Methoxyquinolin-4-yl)-3-[6-(trifluoromethyl)pyridin-2-yl]urea
[CAS]

1384424-80-9
[Synonyms]

A-1070722
N-(7-Methoxy-4-quinolinyl)-N&rsquo
-[6-(trifluoromethyl)-2-pyridinyl]urea
1-(7-Methoxyquinolin-4-yl)-3-[6-(trifluoromethyl)pyridin-2-yl]urea
N-(7-Methoxy-4-quinolinyl)-N'-[6-(trifluoromethyl)-2-pyridinyl]urea
Urea, N-(7-methoxy-4-quinolinyl)-N'-[6-(trifluoromethyl)-2-pyridinyl]-
[Molecular Formula]

C17H13F3N4O2
[MDL Number]

MFCD22580422
[MOL File]

1384424-80-9.mol
[Molecular Weight]

362.31
Chemical PropertiesBack Directory
[Boiling point ]

412.5±45.0 °C(Predicted)
[density ]

1.461±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[solubility ]

DMSO: soluble15mg/mL, clear
[form ]

powder
[pka]

11.57±0.43(Predicted)
[color ]

white to beige
Safety DataBack Directory
[Hazard Codes ]

T
[Risk Statements ]

25-36/37/38
[Safety Statements ]

36/37/39-45
[RIDADR ]

UN 2811 6.1 / PGIII
[WGK Germany ]

3
Hazard InformationBack Directory
[Description]

A-1070722 is an inhibitor of glycogen synthase kinase 3β (GSK3β; IC50 = <100 nM).
[Uses]

N-(7-Methoxy-4-quinolinyl)-N''-[6-(trifluoromethyl)-2-pyridinyl]urea is a neuroprotective agent and a glycogen synthase kinase-3 (GSK-3) inhibitor. GSK-3 is a conserved signaling enzyme that regulates a wide range of biological events (apoptosis, synaptic plasticity, axon formation, and neurogenesis). The enzyme has a conserved catalytic domain for binding ATP and a C-terminal domain with a conserved activation loop for the kinase activity. GSK-3 is a therapeutic target for treating neurodegenerative and psychiatric disorders.
[in vivo]

A 1070722 (10-20 mg/kg, 30 min before cocaine injection or 30 min prior to injection with saline (test day)) decreases spontaneous locomotion, inhibits the expression of conditioned activities but not the acquisition of conditioned activities in Cocaine-paired rats[2].

[IC 50]

GSK-3α: 0.6 nM (Ki); GSK-3β: 0.6 nM (Ki)
[storage]

Store at RT
[References]

[1] CHANTALLE MOOLMAN . Exploration of benzofuran-based compounds as potent and selective Plasmodium falciparum glycogen synthase kinase-3 (PfGSK-3) inhibitors[J]. Bioorganic Chemistry, 2021, 112: Article 104839. DOI: 10.1016/j.bioorg.2021.104839
Spectrum DetailBack Directory
[Spectrum Detail]

1-(7-Methoxyquinolin-4-yl)-3-[6-(trifluoromethyl)pyridin-2-yl]urea(1384424-80-9)1HNMR
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