| MDL | - |
|---|---|
| Molecular Weight | 456.63 |
| Molecular Formula | C16H11Cl3F3N3O3 |
| SMILES | O=C(C1=C(C(F)(F)F)N(C2=CC=C(NC(/C(Cl)=C(Cl)/Cl)=O)C=C2)N=C1)OCC |
Pyr3 is a selective inhibitor of transient receptor potential canonical channel 3 (TRPC3) , with an IC 50 of 700 nM for TRPC3-mediated Ca 2+ influx.
IC50: 700 nM (TRPC3) [1] .
Pyr3 selectively and directly inhibits TRPC3 channels among TRPC family members. Application of Pyr3 inhibits TRPC3-mediated Ca 2+ influx in a dose-dependent manner with the IC 50 value of 700 nM. Pyr3 becomes apparent at 0.3 μM, and is almost complete at 3 μM. Interestingly, Ca 2+ influx is inhibited by Pyr3 in cells co-expressing TRPC3 plus TRPC6 but not in cells coexpressing TRPC1 plus TRPC5. The Ang II-induced NFAT translocation is suppressed by Pyr3, but weakly by Pyr2 in a concentration-dependent manner (IC 50 value was 0.05 μM for Pyr3 and 2 μM for Pyr2) [1] .
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Solid
Room temperature in continental US; may vary elsewhere.
| Powder | -20°C | 3 years |
|---|---|---|
| 4°C | 2 years | |
| In solvent | -80°C | 6 months |
| -20°C | 1 month |
DMSO : ≥ 125 mg/mL ( 273.74 mM )
* "≥" means soluble, but saturation unknown.
| Concentration Solvent Mass | 1 mg | 5 mg | 10 mg |
|---|
| 1 mM | 2.1900 mL | 10.9498 mL | 21.8996 mL |
| 5 mM | 0.4380 mL | 2.1900 mL | 4.3799 mL |
| 10 mM | 0.2190 mL | 1.0950 mL | 2.1900 mL |