GNE7915 |
Competitive inhibitor of LRRK2
Probe Summary
Selectivity
Potency
In Vivo
Control Compounds
Chemical Information
References
Vendors
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Probe Summary
| Targets | Biochemical/Biophysical Potency | Cellular Potency |
|---|---|---|
| LRRK2 |
|
|
Competitive inhibitor
Up to 100 nM
Selectivity
In Vitro Selectivity Assessment
Potency Assay Off-Target:
In vitro kinase assays, GNE7915 inhibited only 1 kinase >50% at 0.1 uM. In DiscoveRx Kinome scan of ...
Potency Cellular
In Vitro
LRRK2
Mode of Action: Competitive inhibitor
Structure-Activity-Relationship data available? No
In Vivo Validations
Rat
Dose: 0.5 mg/kg
Route of delivery:
Intravenous
Plasma half life:
3.1 hr
Systemic clearance:
8.3 mL/min/kg
Organ of interest (O):
brain
Target engagement assay:
Indirect: inhibition of autophosphorylation
Reference: --
Orthogonal Probes def
MLi-2
Chemical Information
| Molecular Formula | C19H21F4N5O3 |
| SMILEs | CCNc1nc(Nc2cc(F)c(C(=O)N3CCOCC3)cc2OC)ncc1C(F)(F)F |
| InChI | InChI=1S/C19H21F4N5O3/c1-3-24-16-12(19(21,22)23)10-25-18(27-16)26-14-9-13(20)11(8-15(14)30-2)17(29)28-4-6-31-7-5-28/h8-10H,3-7H2,1-2H3,(H2,24,25,26,27) |
| Molecular weight | 443.16 Da |
| AlogP | 0.0 |
| HBond acceptors | 8 |
| HBond donors | 2 |
| Atoms | 52 |
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