MK-3901
MK-3901 is a selective P2X3 receptor antagonist with an IC50 of 24 nM. MK-3901 inhibits UGT1A1 (with an IC50 of 1 μM) and CYP2C9 (with an IC50 of 5.7 μM). MK-3901 activates PXR. MK-3901 induces hyperbilirubinemia. MK-3901 can be used for the research of inflammatory pain.
Para uso exclusivo en investigación. No vendemos a pacientes.
- No. CAS: 1149750-69-5
- Fòrmula: C28H24FN5O2
- Peso molecular:481.53
-
Almacenamiento:
Please store the product under the recommended conditions in the Certificate of Analysis.
Ver todos los productos específicos de isoformas P2X Receptor
More
Actividad biológica
|
P2X3 Receptor 24 nM (IC50) |
CYP2C9 5.7 μM (IC50) |
UGT1A1 1 μM (IC50) |
MK-3901 potently antagonizes the P2X3 receptor in a cell-based patch clamp electrophysiology assay with an IC50 of 24 nM[1].
MK-3901 inhibits UGT1A1 enzyme activity in a cell-free biochemical assay with an IC50 of 1 μM[1].
MK-3901 inhibits CYP2C9 enzyme activity in a human liver microsome-based cell-free biochemical assay with an IC50 of 5.7 μM[1].
MK-3901 (10 μM) activates the pregnane X receptor (PXR) by 47%[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
-
No. CAS 1149750-69-5
-
Peso molecular 481.53
-
Fòrmula C28H24FN5O2
-
SMILES
C(N[C@H](C)C1=CC=C(F)C=N1)(=O)C2=CC(=CC(=C2)C3=CC=C(C)C=N3)C=4C[C@H](ON4)C5=CC=CC=N5
-
Envío
Room temperature in continental US; may vary elsewhere.
-
Almacenamiento
Please store the product under the recommended conditions in the Certificate of Analysis.
Pureza y Documentación
Referencias
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)