LXS196
Catalog No. A19419
LXS196 is a potent, selective and orally active protein kinase C (PKC) inhibitor, with IC50 values of 1.9 nM, 0.4 nM and 3.1 μM for PKCα, PKCθ and GSK3β, respectively. It can be used for the treatment of uveal melanoma.
Catalog Num | A19419 |
---|---|
M. Wt | 472.47 |
Formula | C22H23F3N8O |
Purity | >98% |
Storage | at -20°C 3 years Powder |
CAS No. | 1874276-76-2 |
Synonyms | LXS 196, LXS-196 |
SMILES | NC1=C(C(NC2=C(N3CCC(C)(N)CC3)C=CC=N2)=O)N=C(C4=NC=CC=C4C(F)(F)F)C=N1 |
LXS196 is a potent, selective and orally active protein kinase C (PKC) inhibitor, with IC50 values of 1.9 nM, 0.4 nM and 3.1 μM for PKCα, PKCθ and GSK3β, respectively. It can be used for the treatment of uveal melanoma.
In vitro | DMSO | 20 mg/mL (42.33 mM) | |
Water | Insoluble | ||
Ethanol | 5 mg/mL (10.58 mM) | ||
* <1 mg/ml means slightly soluble or insoluble. * Please note that Adooq tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations. |
Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
---|---|---|---|
0.1 mM | 21.17 mL | 105.83 mL | 211.65 mL |
0.5 mM | 4.23 mL | 21.17 mL | 42.33 mL |
1 mM | 2.12 mL | 10.58 mL | 21.17 mL |
5 mM | 0.42 mL | 2.12 mL | 4.23 mL |
*The above data is based on the productmolecular weight 472.47. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.