PF-05105679 |
PF-05105679 : Antagonist of TRPM8
Probe Summary
Selectivity
Potency
In Vivo
Control Compounds
Chemical Information
References
Vendors
Download
Probe Summary
| Targets | Biochemical/Biophysical Potency | Cellular Potency |
|---|---|---|
| TRPM8 |
|
|
Antagonist
up to 1 uM
Selectivity
In Vitro Selectivity Assessment
Selectivity Assessment Description:
Selectivity within target family: Selective over related family at 10 µM: TRPV1, TRPA1 (Ca+ mobiliza ...
In Vitro Selectivity Assessment
Selectivity Assessment Description:
Clean Kinase panel at 1 uM
Potency Cellular
In Vitro
TRPM8
Mode of Action: Antagonist
Structure-Activity-Relationship data available? No
DOI Reference: 10.1021/ml500479v
In Vivo Validations
Rat
Dose: 2-10 mg/Kg
Route of delivery:
Intravenous
Plasma half life:
3.6 h
Systemic clearance:
19.8 mL/min/Kg
Fb :
98.8%
Bioavailability:
29 (2 mg/Kg) and 62% (10 mg/Kg)
Volume of Distribution at Steady-State:
6.2 L/Kg
DOI Reference: 10.1021/ml500479v
Dog
Dose: 20 mg/Kg
Route of delivery:
Intravenous
Plasma half life:
3.9 h
Systemic clearance:
31 mL/min/Kg
Fb :
96.7%
Bioavailability:
92 %
Volume of Distribution at Steady-State:
7.4 L/Kg
DOI Reference: 10.1021/ml500479v
Negative Control Compounds
Chemical Information
| Molecular Formula | C26H21FN2O3 |
| SMILEs | C[C@H](c1ccc(F)cc1)N(Cc1cccc(C(=O)O)c1)C(=O)c1cnc2ccccc2c1 |
| InChI | InChI=1S/C26H21FN2O3/c1-17(19-9-11-23(27)12-10-19)29(16-18-5-4-7-21(13-18)26(31)32)25(30)22-14-20-6-2-3-8-24(20)28-15-22/h2-15,17H,16H2,1H3,(H,31,32)/t17-/m1/s1 |
| Molecular weight | 428.15 Da |
| AlogP | 0.0 |
| HBond acceptors | 5 |
| HBond donors | 1 |
| Atoms | 53 |
References
Publications
Vendors
Note: This is not an exhaustive list and does not indicate endorsement by the portal.