WEE1-IN-7 |
WEE1-IN-7 : Inhibitor of WEE1
Probe Summary
Selectivity
Potency
In Vivo
Control Compounds
Chemical Information
References
Vendors
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Probe Summary
| Targets | Biochemical/Biophysical Potency | Cellular Potency |
|---|---|---|
| WEE1 |
|
|
Inhibitor
up to 1 uM
Selectivity
In Vitro Selectivity Assessment
Potency Assay Off-Target:
Kinase profiling was performed at a concentration of 1 μM against 225 kinase targets and found that ...
Potency Cellular
In Vitro
WEE1
Mode of Action: Inhibitor
Structure-Activity-Relationship data available? Yes
DOI Reference: 10.1021/acs.jmedchem.3c02434
In Vivo Validations
Mouse
Dose: 1 mg/Kg
Route of delivery:
Intravenous
Plasma half life:
1.06 h
Systemic clearance:
8.2 L/h/Kg
Area Under the Curve::
118 h·ng/mL
Volume of Distribution at Steady-State:
11.3 L/Kg
DOI Reference: 10.1021/acs.jmedchem.3c02434
Dose: 60 mg/Kg
Route of delivery:
Intragastric
Plasma half life:
5.94 h
Cmax:
498
Area Under the Curve::
4342 h·ng/mL
Bioavailability:
61.46%
DOI Reference: 10.1021/acs.jmedchem.3c02434
Chemical Information
| Molecular Formula | C28H28N10O |
| SMILEs | C=CCn1c(=O)c2cnc(Nc3ccc(N4CCN(C)CC4)cc3)nc2n1-c1cccc(-c2cnccn2)n1 |
| InChI | InChI=1S/C28H28N10O/c1-3-13-37-27(39)22-18-31-28(32-20-7-9-21(10-8-20)36-16-14-35(2)15-17-36)34-26(22)38(37)25-6-4-5-23(33-25)24-19-29-11-12-30-24/h3-12,18-19H,1,13-17H2,2H3,(H,31,32,34) |
| Molecular weight | 520.24 Da |
| AlogP | 3.1156000000000015 |
| HBond acceptors | 11 |
| HBond donors | 1 |
| Atoms | 67 |
| PAINS * | Yes |
* This is an automated alert only, and may not necessarily indicate an issue with this probe. ( Learn more about PAINS )
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