PT2385 |
Antagonist of EPAS1
Probe Summary
Selectivity
Potency
In Vivo
Control Compounds
Chemical Information
References
Vendors
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Probe Summary
| Targets | Biochemical/Biophysical Potency | Cellular Potency |
|---|---|---|
| EPAS1 |
|
|
Antagonist
up to 1 uM
Selectivity
In Vitro Selectivity Assessment
Potency: HIF-1alpha - not detected
Potency Assay Off-Target:
ITC
In Cell Selectivity Assessment
Selectivity Assessment Description:
0/40 kinase selectivity (<70% activity remaining at 10 μM)
Potency Cellular
In Vitro
EPAS1
Mode of Action: Antagonist
Structure-Activity-Relationship data available? No
DOI Reference: 10.1021/acs.jmedchem.8b01196
In Vivo Validations
Mouse, Rat, Dog
Dose: 3 mg/Kg (IV), 10 mg/Kg (PO)
Route of delivery:
Intravenous, Oral
Plasma half life:
3.3 h (M, R), 11 h (Dog)
Systemic clearance:
19.9 (M), 34.6 (R), 21.5. (D) mL/min/kg
DOI Reference: 10.1021/acs.jmedchem.8b01196
Negative Control Compounds
9a
Chemical Information
| Molecular Formula | C17H12F3NO4S |
| SMILEs | CS(=O)(=O)c1ccc(Oc2cc(F)cc(C#N)c2)c2c1[C@H](O)C(F)(F)C2 |
| InChI | InChI=1S/C17H12F3NO4S/c1-26(23,24)14-3-2-13(12-7-17(19,20)16(22)15(12)14)25-11-5-9(8-21)4-10(18)6-11/h2-6,16,22H,7H2,1H3/t16-/m0/s1 |
| Molecular weight | 383.04 Da |
| AlogP | 3.117980000000002 |
| HBond acceptors | 5 |
| HBond donors | 1 |
| Atoms | 38 |
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