PFI-653 |
PFI-653 : Inhibitor of VNN1
Probe Summary
Selectivity
Potency
In Vivo
Control Compounds
Chemical Information
References
Vendors
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Probe Summary
| Targets | Biochemical/Biophysical Potency | Cellular Potency |
|---|---|---|
| VNN1 |
|
|
Inhibitor
1 uM
Selectivity
In Vitro Selectivity Assessment
Selectivity Assessment Description:
Selectivity within target family - Nitrilase family selectivity: BTD (Biotinidase): IC50 > 50 µM (>7 ...
Potency Cellular
In Vitro
VNN1
Mode of Action: Inhibitor
Structure-Activity-Relationship data available? No
Other Reference: not yet published
In Vivo Validations
Rat
Dose: 2 mg/kg IV, 10 mg/kg PO
Route of delivery:
Invitrous, Oral
Plasma half life:
1 h (IV)
Area Under the Curve::
1790 ng h/mL IV, 8540 h/mL PO
Fb :
96% (PO)
Target engagement assay:
PO: Dose vehicle: 10% DMSO / 30% PEG400 / 60% Water. Rat fu = 0.87
Other Reference: not yet published
Negative Control Compounds
CANSAR3511558
Notes: PFI-653-N: Human VNN1 assay: IC50 > 17.6 µM Human plasma VNN1 assay: IC50 > 3 µM
Chemical Information
| Molecular Formula | C18H22N6O2 |
| SMILEs | O=C(c1cnc(NCc2cnccn2)nc1)N1CCC2(CCOCC2)C1 |
| InChI | InChI=1S/C18H22N6O2/c25-16(24-6-1-18(13-24)2-7-26-8-3-18)14-9-21-17(22-10-14)23-12-15-11-19-4-5-20-15/h4-5,9-11H,1-3,6-8,12-13H2,(H,21,22,23) |
| Molecular weight | 354.18 Da |
| AlogP | 0.0 |
| HBond acceptors | 8 |
| HBond donors | 1 |
| Atoms | 48 |