CP-724714 |
Inhibitor of ERBB2
Probe Summary
Selectivity
Potency
In Vivo
Control Compounds
Chemical Information
References
Vendors
Download
Probe Summary
| Targets | Biochemical/Biophysical Potency | Cellular Potency |
|---|---|---|
| ERBB2 |
|
|
Inhibitor
50 nM - 10 uM
Selectivity
In Vitro Selectivity Assessment
Potency: IC50 - EGFR 6400 nM
Potency Assay Off-Target:
In vitro kinase assay on intracellular domain
>1,000-fold selective for ERBB2 over IGF1R, PDGFRbeta ...
In Cell Selectivity Assessment
Selectivity Assessment Description:
Selective for ERBB2 over EGFR in cells
Potency Cellular
In Vitro
ERBB2
Mode of Action: Inhibitor
Structure-Activity-Relationship data available? No
DOI Reference: 10.1158/0008-5472.CAN-06-3559
In Vivo Validations
Mouse
Dose: 2.5 mg/kg
Route of delivery:
Oral
Organ of interest (O):
xenograft
Target engagement assay:
Indirect: inhibition of protein substrate phosphorylation detected by ex vivo ELISA in xenograft tumor tissue
DOI Reference: 10.1158/0008-5472.CAN-06-3559
Chemical Information
| Molecular Formula | C27H27N5O3 |
| SMILEs | COCC(=O)NC/C=C/c1ccc2ncnc(Nc3ccc(Oc4ccc(C)nc4)c(C)c3)c2c1 |
| InChI | InChI=1S/C27H27N5O3/c1-18-13-21(8-11-25(18)35-22-9-6-19(2)29-15-22)32-27-23-14-20(7-10-24(23)30-17-31-27)5-4-12-28-26(33)16-34-3/h4-11,13-15,17H,12,16H2,1-3H3,(H,28,33)(H,30,31,32)/b5-4+ |
| Molecular weight | 469.21 Da |
| AlogP | 0.0 |
| HBond acceptors | 8 |
| HBond donors | 2 |
| Atoms | 62 |
References
Vendors
- Abcam (383432-38-0)
- Cayman (383432-38-0)
- MCULE
- MedChem Express (383432-38-0)
- MilliporeSigma (383432-38-0)
- Tocris (383432-38-0)
Note: This is not an exhaustive list and does not indicate endorsement by the portal.