ABT-100 |
Inhibitor of FNTB
Probe Summary
Selectivity
Potency
In Vivo
Control Compounds
Chemical Information
References
Vendors
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Probe Summary
| Targets | Biochemical/Biophysical Potency | Cellular Potency |
|---|---|---|
| FNTB |
|
|
Inhibitor
10-1000 nM
Selectivity
In Vitro Selectivity Assessment
Selectivity Assessment Description:
>100 000-fold selective for FNTB over the closely related enzyme PGGT1B (GGTase I)
In Cell Selectivity Assessment
Selectivity Assessment Description:
No activity in panel of 75 off-targets @10 µM; closest hit: phencyclidine PCP receptor IC50 = 3 μ ...
Potency Cellular
In Vitro
FNTB
Mode of Action: Inhibitor
Structure-Activity-Relationship data available? No
In Vivo Validations
Rat, Dog
Dose: 5 mg/kg (Rat), 2.5 mg/kg (Dog), up to 25 mg/kg (PO)
Route of delivery:
Intravenous, Oral
Plasma half life:
2.3 h (Rat), 6.8 h (Dog)
Systemic clearance:
1.2 (Rat) and 0.34 (Dog) l/h/kg
Reference: --
Negative Control Compounds
ABT-108
Chemical Information
| Molecular Formula | C27H19F3N4O3 |
| SMILEs | Cn1cncc1[C@](O)(COc1ccc(C#N)cc1-c1ccc(OC(F)(F)F)cc1)c1ccc(C#N)cc1 |
| InChI | InChI=1S/C27H19F3N4O3/c1-34-17-33-15-25(34)26(35,21-7-2-18(13-31)3-8-21)16-36-24-11-4-19(14-32)12-23(24)20-5-9-22(10-6-20)37-27(28,29)30/h2-12,15,17,35H,16H2,1H3/t26-/m0/s1 |
| Molecular weight | 504.14 Da |
| AlogP | 5.043960000000004 |
| HBond acceptors | 7 |
| HBond donors | 1 |
| Atoms | 56 |
Vendors
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