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ChemicalBook--->CAS DataBase List--->442898-34-2

442898-34-2

442898-34-2 Structure

442898-34-2 Structure
IdentificationBack Directory
[Name]

NCGC00092410
[CAS]

442898-34-2
[Synonyms]

ML008
NCGC00092410
[Molecular Formula]

C21H27N3O2
[MDL Number]

MFCD14719081
[MOL File]

442898-34-2.mol
[Molecular Weight]

353.46
Chemical PropertiesBack Directory
[Boiling point ]

627.9±55.0 °C(Predicted)
[density ]

1.210±0.06 g/cm3(Predicted)
[solubility ]

DMSO : 41.67 mg/mL (117.89 mM; Need ultrasonic)
[form ]

Solid
[pka]

14.93±0.20(Predicted)
[color ]

Light yellow to yellow
Hazard InformationBack Directory
[Definition]

ChEBI: N-[4-methyl-2-(4-morpholinyl)-6-quinolinyl]cyclohexanecarboxamide is an aminoquinoline.
[Biological Activity]

NCGC00092410 is a potent, selective, and nonsugar glucocerebrosidase (GC) inhibitor, with an IC50 of 31 nM. NCGC00092410 shows no activity against the related hydrolases at concentrations up to 77 μM. NCGC00092410, a GC chaperone, and increases the activity and lysosomal localization of glucocerebrosidase in mutant cell lines. NCGC00092410 can be used for the research of Gaucher disease[1]. NCGC00092410 (7.3-130 nM; 25 min) inhibits the GC activity at various substrate concentrations (10-150 μM) in a dose-dependent manner[1].NCGC00092410 (55-40 μM; 2 d) increases the GC activity in the N370S mutant fibroblasts[1].NCGC00092410 (40 μM; 60-72 h) increases the lysosomal localization of GC in gaucher fibroblasts[1].
[References]

[1]. Zheng W, et, al. Three classes of glucocerebrosidase inhibitors identified by quantitative high-throughput screening are chaperone leads for Gaucher disease. Proc Natl Acad Sci U S A. 2007 Aug 7;104(32):13192-7.
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