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ChemicalBook--->CAS DataBase List--->1088991-73-4

1088991-73-4

1088991-73-4 Structure

1088991-73-4 Structure
IdentificationBack Directory
[Name]

MK 6096
[CAS]

1088991-73-4
[Synonyms]

MK6096
MK-6096
MK 6096
CS-1825
Filorexant
MK 6096;MK6096
MK-6096(Filorexant)
Filorexant(MK-6096)
filorexant / MK-6096, CID25128145
[(2R,5R)-5-[(5-FLUOROPYRIDIN-2-YL)OXYMETHYL]-2-METHYLPIPERIDIN-1-YL]-(5-METHYL-2-PYRIMIDIN-2-YLPHENYL)METHANONE
[(2R,5R)-5-[[(5-Fluoro-2-pyridinyl)oxy]methyl]-2-methyl-1-piperidinyl][5-methyl-2-(2-pyrimidinyl)phenyl]methanone
Methanone, [(2R,5R)-5-[[(5-fluoro-2-pyridinyl)oxy]methyl]-2-methyl-1-piperidinyl][5-methyl-2-(2-pyrimidinyl)phenyl]-
((2R,5R)-5-(((5-Fluoropyridin-2-yl)oxy)methyl)-2-methylpiperidin-1-yl)(5-methyl-2-(pyrimidin-2-yl)phenyl)methanone MK6096
[Molecular Formula]

C24H25FN4O2
[MDL Number]

MFCD28100674
[MOL File]

1088991-73-4.mol
[Molecular Weight]

420.48
Chemical PropertiesBack Directory
[Boiling point ]

540.2±50.0 °C(Predicted)
[density ]

1.203±0.06 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMF: 10mg/mL; DMF:PBS (pH 7.2) (1:4): 0.2mg/mL; DMSO: 2mg/mL; Ethanol: 5mg/mL
[form ]

A solid
[pka]

1.54±0.22(Predicted)
[color ]

Off-white to brown
Hazard InformationBack Directory
[Description]

Filorexant is a dual antagonist of orexin 1 receptor (OX1R) and OX2R (Kis = 2.5 and 0.31 nM, respectively, for the recombinant human receptors). It selectively inhibits OX1R and OX2R over a panel of more than 170 receptors and enzymes. Filorexant inhibits orexin A-induced calcium mobilization in CHO cells expressing recombinant human OX1R or OX2R (Kb = 11 nM for both). It decreases locomotor activity in rats during the dark cycle when administered at a dose of 10 mg/kg. Filorexant (0.5 mg/kg) reduces the time spent awake and decreases the latency to slow-wave sleep stage 1 (SWS1) and SWS2, but not rapid eye movement (REM) sleep, in dogs. It increases the duration of SWS2, but not SWS1 or REM sleep, in the same model.
[Uses]

Filorexant is a selective dual orexin receptor antagonist with potent sleep-promoting properties. It has advanced into phase II clinical trials for the treatment of insomnia.
[storage]

Store at -20°C
Spectrum DetailBack Directory
[Spectrum Detail]

MK 6096(1088991-73-4)1HNMR
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