MDL | MFCD18782631 |
---|---|
Molecular Weight | 579.49 |
Molecular Formula | C28H23F6N3O4 |
SMILES | O=C1N(C2=CC=CC=C2)C3=C(C(CC(C)(C)C3)=O)C1(C4=C(C)NN(C5=CC=C(OC(F)(F)F)C=C5)C4=O)C(F)(F)F |
ELOVL6-IN-2 is a potent, orally active and selective ELOVL6 inhibitor. ELOVL6-IN-2 inhibits mouse ELOVL6 activities, with an IC 50 value of 34 nM [1] .
IC50: 34 nM (ELOVL6) [1]
ELOVL6-IN-2 (0.1~1mg/kg; p.o.; 2 hours) potently and dose-proportionally suppresses the elongation index in the liver
[1]
.
ELOVL6-IN-2 (10mg/kg; p.o.; 2 hours) demonstrates highly liver penetrable
[1]
.
ELOVL6-IN-2 (1mg/kg; p.o.; 2~24 hours) exhibits sustained plasma exposure
[1]
.
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Animal Model: | Male C57BL/6J mice |
Dosage: | 0.1~1mg/kg |
Administration: | P.o |
Result: | Potently and dose-proportionally suppressed the elongation index in the liver. |
Animal Model: | Male C57BL/6J mice |
Dosage: | 10 mg/kg |
Administration: | P.o |
Result: | Demonstrated highly liver penetrable. |
Animal Model: | Male C57BL/6J mice |
Dosage: | 1 mg/kg |
Administration: | P.o |
Result: | Exhibited sustained plasma exposure. |
Solid
Room temperature in continental US; may vary elsewhere.
Powder | -20°C | 3 years |
---|---|---|
In solvent | -80°C | 6 months |
-20°C | 1 month |
DMSO : 100 mg/mL ( 172.57 mM ; Need ultrasonic)
Concentration Solvent Mass | 1 mg | 5 mg | 10 mg |
---|
1 mM | 1.7257 mL | 8.6283 mL | 17.2566 mL |
5 mM | 0.3451 mL | 1.7257 mL | 3.4513 mL |
10 mM | 0.1726 mL | 0.8628 mL | 1.7257 mL |
Add each solvent one by one: 10% DMSO >> 90% corn oil
Solubility: ≥ 2.5 mg/mL (4.31 mM); Clear solution