PKR Inhibitor
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.
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Discription | PKR Inhibitor is an oxindole/imidazole derivative that binds the ATP-binding site of PKR and blocks autophosphorylation with an IC50 value of 186-210 nM.3 PKR Inhibitor protects human neuroblastoma cells against cell damage triggered by tunicamycin-mediated endoplasmic reticulum stress. |
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Catalog Num | A13538 |
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Formula | C13H8N4OS |
Molecular Weight | 268.3 |
CAS Number | 608512-97-6 |
SMILES | C1=CC2=C(C\3=C1NC(=O)/C3=C\C4=CN=CN4)SC=N2 |
Synonyms | C16, GW 506033X |
Storage | Store lyophilized at -20ºC, keep desiccated. |
In vitro | DMSO | 13 mg/mL (48.45 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 |
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0.1 mM | 37.27 mL | 186.36 mL | 372.72 mL |
0.5 mM | 7.45 mL | 37.27 mL | 74.54 mL |
1 mM | 3.73 mL | 18.64 mL | 37.27 mL |
5 mM | 0.75 mL | 3.73 mL | 7.45 mL |
Calculate the dilution required to prepare a stock solution. This equation is commonly abbreviated as: C1V1 = C2V2