PRT062607 |
Inhibitor of SYK
Probe Summary
Selectivity
Potency
In Vivo
Control Compounds
Chemical Information
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Probe Summary
| Targets | Biochemical/Biophysical Potency | Cellular Potency |
|---|---|---|
| SYK |
|
|
Inhibitor
100 nM - 2 uM
Selectivity
In Vitro Selectivity Assessment
Potency: IC50 - FGR 81 nM, MLK1 88 nM, YES 123 nM, FLT3 139 nM, PAK5 166 nM, LYN 192 nM, SRC 244 nM, LCK 249 nM, PYK2 108 nM
Potency Assay Off-Target:
Radiometric assay. At 50 nM, P505-15 was selective for SYK over 270 other kinases; at 300 nM, it inh ...
In Cell Selectivity Assessment
Potency Assay Off-Target:
No activity was detected against LYN substrates in B cells.
Potency Cellular
In Vitro
SYK
Mode of Action: Inhibitor
Structure-Activity-Relationship data available? No
In Vivo Validations
mice
Dose: 30 mg/kg
Route of delivery:
Oral
Organ of interest (O):
B cells
Target engagement assay:
Indirect: inhibition of SYK substrate phosphorylation but not LYN substrate phosphorylation
Reference: --
Orthogonal Probes def
Entospletinib
Chemical Information
| Molecular Formula | C19H23N9O |
| SMILEs | NC(=O)c1cnc(N[C@@H]2CCCC[C@@H]2N)nc1Nc1cccc(-n2nccn2)c1 |
| InChI | InChI=1S/C19H23N9O/c20-15-6-1-2-7-16(15)26-19-22-11-14(17(21)29)18(27-19)25-12-4-3-5-13(10-12)28-23-8-9-24-28/h3-5,8-11,15-16H,1-2,6-7,20H2,(H2,21,29)(H2,22,25,26,27)/t15-,16+/m0/s1 |
| Molecular weight | 393.20 Da |
| AlogP | 1.5815999999999988 |
| HBond acceptors | 10 |
| HBond donors | 6 |
| Atoms | 52 |
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