I-CBP112 |
I-CBP112 : Inhibitor of EP300, CREBBP
Probe Summary
Selectivity
Potency
In Vivo
Control Compounds
Chemical Information
References
Vendors
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Probe Summary
| Targets | Biochemical/Biophysical Potency | Cellular Potency |
|---|---|---|
| EP300 |
| |
| CREBBP |
|
|
Inhibitor
Up to 1 uM
Selectivity
In Vitro Selectivity Assessment
Potency: KD - BRD4 (1) 5.6 uM (2) 20 uM
Potency Assay Off-Target:
ITC, and using biointerferometry, I-CBP112 did not bind to any additional of 40 Bromodomains tested. ...
Selectivity Assessment Description:
Minimal activity against 104 proteins (nuclear receptors, ion channels, kinases, proteases, and p ...
Potency Cellular
In Vitro
EP300
Mode of Action: Inhibitor
Structure-Activity-Relationship data available? Yes
DOI Reference: 10.1158/0008-5472.CAN-15-0236
CREBBP
Mode of Action: Inhibitor
Structure-Activity-Relationship data available? Yes
DOI Reference: 10.1158/0008-5472.CAN-15-0236
In Vivo Validations
Mouse
Dose: 3 mg/mL
Route of delivery:
Intraperitoneal
Plasma half life:
0.6 hr
Organ of interest (O):
bone marrow transplant with MLL-AF9 leukemia cells
DOI Reference: 10.1158/0008-5472.CAN-15-0236
Chemical Information
| Molecular Formula | C27H36N2O5 |
| SMILEs | CCC(=O)N1CCOc2c(cc(-c3ccc(OC)c(OC)c3)cc2OC[C@H]2CCCN(C)C2)C1 |
| InChI | InChI=1S/C27H36N2O5/c1-5-26(30)29-11-12-33-27-22(17-29)13-21(20-8-9-23(31-3)24(14-20)32-4)15-25(27)34-18-19-7-6-10-28(2)16-19/h8-9,13-15,19H,5-7,10-12,16-18H2,1-4H3/t19-/m0/s1 |
| Molecular weight | 468.26 Da |
| AlogP | 4.2224 |
| HBond acceptors | 7 |
| HBond donors | -- |
| Atoms | 70 |
Vendors
- Cayman (I-CBP112 hydrochloride)
- MedChem Express (1640282-31-0)
- MCULE
- MilliporeSigma (ICBP112)
- Tocris (ICBP112)
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