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Filorexant(mk-6096)

  Cat. No.:  DC7745   Featured
Chemical Structure
1088991-73-4
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More than 5000 active chemicals with high quality for research!
Field of application
MK-6096 is an orally bioavailable potent and selective reversible antagonist of OX(1)R and OX(2)R currently in clinical development for insomnia.
Chemicals PropertiesBiological activity COA & MSDSRelated productsDatasheet
Cas No.: 1088991-73-4
Chemical Name: MK 6096,MK6096
Synonyms: MK 6096,MK6096
SMILES: CC1=CC(C(N2C[C@H](COC3=CC=C(F)C=N3)CC[C@H]2C)=O)=C(C4=NC=CC=N4)C=C1
Formula: C24H25FN4O2
M.Wt: 420.48
Sotrage: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
Description: Filorexant (MK-6096) is an orally bioavailable potent and selective reversible antagonist of OX1 and OX2 receptor(<3 nM in binding).
In Vivo: Filorexant (MK-6096) dose-dependently reduced locomotor activity and significantly increased sleep in rats (3-30 mg/kg) and dogs (0.25 and 0.5 mg/kg).
In Vitro: In radioligand binding and functional cell based assays Filorexant (MK-6096) demonstrated potent binding and antagonism of both human OX(1)R and OX(2)R (<3 nM in binding, 11 nM in FLIPR), with no significant off-target activities against a panel of >170 receptors and enzymes. Filorexant (MK-6096) occupies 90% of human OX(2)Rs expressed in transgenic rats at a plasma concentration of 142 nM.
MSDS
COA
LOT NO. DOWNLOAD
2018-0101
2018-0101
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