MDL | - |
---|---|
Molecular Weight | 436.51 |
Molecular Formula | C21H16N4O3S2 |
SMILES | O=C(C1=C(CN(C2=NC(C(O)=O)=CS2)CC3)C3=CC=C1)NC4=NC5=C(S4)C=CC=C5 |
Bcl-xL antagonist 2 is a potent, selective, and orally active antagonist of BCL-X L with an IC 50 and K i of 0.091 μM and 65 nM, respectively. Bcl-xL antagonist 2 promotes the apoptosis of cancer cells. Bcl-xL antagonist 2 has the potential for the research of the chronic lymphocytic leukemia (CLL) and non-Hodgkin’s lymphoma (NHL) [1] [2] .
0.091 μM (BCL-X L ) [1]
Assessment of Pharmacokinetics (PK) profile of Bcl-xL antagonist 2 (compound 14) in rat
[1]
.
iv (1 mg/kg) | po (5 mg/kg) | ||
CL p (mL/min/kg) | V ss (L/kg) | t 1/2 (h) | F % |
0.47 | 0.16 | 6.0 | 16 |
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
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 : 62.5 mg/mL ( 143.18 mM ; Need ultrasonic)
Concentration Solvent Mass | 1 mg | 5 mg | 10 mg |
---|
1 mM | 2.2909 mL | 11.4545 mL | 22.9090 mL |
5 mM | 0.4582 mL | 2.2909 mL | 4.5818 mL |
10 mM | 0.2291 mL | 1.1454 mL | 2.2909 mL |
Add each solvent one by one: 10% DMSO >> 90% corn oil
Solubility: ≥ 6.25 mg/mL (14.32 mM); Clear solution