PHA-793887
Important Notice: For research use only. We do not sell to patients.
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Important Notice: For research use only. We do not sell to patients.
Not your Region? View all Distributors
Discription | PHA-793887, a novel potent inhibitor of Cdk, target on kinds of cyclin-dependent kinase under low concentrations and poses high activity against several cancer cell lines. | ||
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Targets |
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Catalog Num | A10716 |
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Formula | C19H31N5O2 |
Molecular Weight | 361.5 |
CAS Number | 718630-59-2 |
SMILES | CC(C)CC(=O)NC1=NNC2=C1CN(C2(C)C)C(=O)C3CCN(CC3)C |
Storage | Store lyophilized at -20ºC, keep desiccated. |
In vitro (25°C) | DMSO | 61 mg/mL (168.75 mM) | |
Water | Insoluble | ||
Ethanol | 61 mg/mL (168.75 mM) | ||
In vivo | 30% propylene glycol, 5% Tween 80, 65% D5W | 14 mg/mL | |
* <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 |
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0.1 mM | 27.66 mL | 138.31 mL | 276.63 mL |
0.5 mM | 5.53 mL | 27.66 mL | 55.33 mL |
1 mM | 2.77 mL | 13.83 mL | 27.66 mL |
5 mM | 0.55 mL | 2.77 mL | 5.53 mL |
Calculate the dilution required to prepare a stock solution. This equation is commonly abbreviated as: C1V1 = C2V2