BSJ-04-122 is a covalent MKK4/7 dual inhibitor. BSJ-04-122 inhibits MKK4 and MKK7 with IC 50 values of 4 nM and 181 nM, respectively. BSJ-04-122 can be used for the research of cancer In Vitro BSJ-04-122 has inhibitory activity for MKK4 and MKK7 with IC 50 values of 4 nM and 181 nM, respectively. BSJ-04-122 (1, 5, 10 μM; 6 h) induces robust reduction of JNK phosphorylation. BSJ-04-122 (0, 1.25, 2.5, 5, 10, 20 μM; 72 h) shows enhanced antiproliferative effects when combination with JNK-IN-8. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Western Blot AnalysisCell Line: MDA-MB-231 cells Concentration: 1, 5, 10 μM Incubation Time: 6 h Result: Significantly decreased levels of T183/Y185 pJNK at 5 μM. Cell Proliferation AssayCell Line: MDA-MB-231 cells Concentration: 1-100 μM; 0, 1.25, 2.5, 5, 10, 20 μM Incubation Time: 72 h Result: Exhibited antiproliferative effects when combination with JNK-IN-8 in MDA-MB-231 cells. Form:Solid IC50& Target:IC50: 4 nM (MKK4),181 nM (MKK7)
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BSJ-04-122
CAS number：2513289-74-0 molecular formula：C15H12ClN5O
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| Chinese alias | - | ||
| English alias | - | ||
| CAS number | 2513289-74-0 | molecular formula | C15H12ClN5O |
| molecular weight | 313.74 g/mol | Exact mass | ≥99% |
| PSA | - | logp | - |
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