MDL | - |
---|---|
Molecular Weight | 428.29 |
Molecular Formula | C17H10F6N6O |
SMILES | O=C(N)/C(C1=CN=CN=C1)=C\N2N=C(C3=CC(C(F)(F)F)=CC(C(F)(F)F)=C3)N=C2 |
Eltanexor Z-isomer (KPT-8602 Z-isomer) is the less active isomer of KPT-8602. KPT-8602 is a potent CRM1 inhibitor. IC50: In Vitro: Eltanexor Z-isomer exhibits different inhibitory effects on Z138, MM15, 3T3 cell lines, with IC 50 s of 100 nM-50 μM, < 100 nM, > 30 μM, respectively [1] . In Vivo:
Solid
Room temperature in continental US; may vary elsewhere.
Powder | -20°C | 3 years |
---|---|---|
4°C | 2 years | |
In solvent | -80°C | 6 months |
-20°C | 1 month |
DMSO : 50 mg/mL ( 116.74 mM ; Need ultrasonic)
Concentration Solvent Mass | 1 mg | 5 mg | 10 mg |
---|
1 mM | 2.3349 mL | 11.6743 mL | 23.3487 mL |
5 mM | 0.4670 mL | 2.3349 mL | 4.6697 mL |
10 mM | 0.2335 mL | 1.1674 mL | 2.3349 mL |