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Biological Activity
CH5424802 is a potent, selective, and orally available ALK inhibitor with a unique chemical scaffold, showing preferential antitumor activity against cancers with gene alterations of ALK.
Targets
Target | Value |
---|---|
ALK(F1174L) | IC50: 1nM |
ALK | IC50: 1.9nM |
ALK(R1275Q) | IC50: 3.5nM |
INSR | IC50: 550nM |
KDR | IC50: 1.4μM |
Abl | IC50: >5μM |
EGFR | IC50: >5μM |
FGFR2 | IC50: >5μM |
HER2 | IC50: >5μM |
IGF-1R | IC50: >5μM |
JAK1 | IC50: >5μM |
Kit | IC50: >5μM |
Met | IC50: >5μM |
PDGFRβ | IC50: >5μM |
Src | IC50: >5μM |
Akt1 | IC50: >5μM |
Akt2 | IC50: >5μM |
Akt3 | IC50: >5μM |
AuroraA | IC50: >5μM |
CDK1 | IC50: >5μM |
CDK2 | IC50: >5μM |
MEK1 | IC50: >5μM |
PKA | IC50: >5μM |
PKCα | IC50: >5μM |
PKCβ1 | IC50: >5μM |
PKCβ2 | IC50: >5μM |
Raf-1 | IC50: >5μM |
In vitro | DMSO | Warmed: 0.5 mg/mL (1.03 mM) | |
Water | Insoluble | ||
Ethanol | Insoluble | ||
* <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 | 20.72 mL | 103.61 mL | 207.21 mL |
0.5 mM | 4.14 mL | 20.72 mL | 41.44 mL |
1 mM | 2.07 mL | 10.36 mL | 20.72 mL |
5 mM | 0.41 mL | 2.07 mL | 4.14 mL |
*The above data is based on the productmolecular weight 482.6 . 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.
Catalog Num | A11134 |
---|---|
Actions | Inhibitor |
CAS No. | 1256580-46-7 |
Formula | C30H34N4O2 |
M. Wt | 482.6 |
Purity | >98% |
Synonyms | CH-5424802 |
SMILES | CCC1=C(C=C2C(=C1)C(=O)C3=C(C2(C)C)NC4=C3C=CC(=C4)C#N)N5CCC(CC5)N6CCOCC6 |
Storage | Store lyophilized at -20ºC, keep desiccated. |
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