(2Z,3Z)-U0126
(2Z,3Z)-U0126 is a selective inhibitor of MEK1 and MEK2, demonstrating potent antiinflammatory effects by noncompetitively inhibiting AP-1 transcriptional activity with IC50 values of 72 nM for MEK1 and 58 nM for MEK2. (2Z,3Z)-U0126 also inhibits anchorage-independent growth of Ki-ras-transformed rat fibroblasts by blocking both the extracellular signal-regulated kinase and mammalian target of rapamycin pathways. Additionally, (2Z,3Z)-U0126 can undergo isomerization and cyclization, resulting in various products that show reduced affinity for MEK and diminished AP-1 inhibition compared to the parent compound.
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- CAS. Nr.: 218601-62-8
- Formel: C18H16N6S2
- Molecular Weight:380.49
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Speicherung:
Please store the product under the recommended conditions in the Certificate of Analysis.
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Biologische Aktivität
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Cell Line
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Type | Value | Description | References |
|---|---|---|---|---|
| A-375 | IC50 |
1.1 μM
Compound: U0126
|
Antiproliferative activity against human A375 cells assessed as cell viability incubated for 72 hrs by cell titer-glo luminescent cell viability assay (Rvb = > 100 uM)
Antiproliferative activity against human A375 cells assessed as cell viability incubated for 72 hrs by cell titer-glo luminescent cell viability assay (Rvb = > 100 uM)
|
[PMID: 31252285] |
| A549 | IC50 |
32.2 μM
Compound: U0126
|
Antiproliferative activity against human A549 cells assessed as cell viability incubated for 72 hrs by cell titer-glo luminescent cell viability assay (Rvb = > 100 uM)
Antiproliferative activity against human A549 cells assessed as cell viability incubated for 72 hrs by cell titer-glo luminescent cell viability assay (Rvb = > 100 uM)
|
[PMID: 31252285] |
| COS-7 | IC50 |
1 μM
Compound: U-0126
|
Inhibitory concentration against AP-1 transcription in COS-7 cells
Inhibitory concentration against AP-1 transcription in COS-7 cells
|
[PMID: 15006386] |
| DLD-1 | IC50 |
1.14 μM
Compound: 40; U0126
|
Anticancer activity against human DLD-1 cells assessed as reduction in cell viability incubated for 24 hrs by Cell Titer-Glo assay
Anticancer activity against human DLD-1 cells assessed as reduction in cell viability incubated for 24 hrs by Cell Titer-Glo assay
|
[PMID: 33445154] |
| HCT-116 | GI50 |
19.4 μM
Compound: U-0126
|
Ability of compound to inhibit anchorage independent colony formation (soft agar growth assay) in HCT116 cells
Ability of compound to inhibit anchorage independent colony formation (soft agar growth assay) in HCT116 cells
|
[PMID: 15225706] |
| HCT-116 | IC50 |
0.94 μM
Compound: 40; U0126
|
Anticancer activity against human HCT-116 cells assessed as reduction in cell viability incubated for 24 hrs by Cell Titer-Glo assay
Anticancer activity against human HCT-116 cells assessed as reduction in cell viability incubated for 24 hrs by Cell Titer-Glo assay
|
[PMID: 33445154] |
| HeLa | IC50 |
0.29 μM
Compound: U-0126
|
Inhibition of EGF-stimulated Elk1-luciferase reporter assay in HeLa cells
Inhibition of EGF-stimulated Elk1-luciferase reporter assay in HeLa cells
|
[PMID: 15225706] |
| HL-60 | IC50 |
0.3 μM
Compound: U0126
|
Antiproliferative activity against human HL60 cells assessed as cell viability incubated for 72 hrs by cell titer-glo luminescent cell viability assay (Rvb = > 100 uM)
Antiproliferative activity against human HL60 cells assessed as cell viability incubated for 72 hrs by cell titer-glo luminescent cell viability assay (Rvb = > 100 uM)
|
[PMID: 31252285] |
| MDCK | CC50 |
>50 μM
Compound: 79; U0126
|
Cytotoxicity against MDCK cells
Cytotoxicity against MDCK cells
|
[PMID: 33539089] |
| Sf21 | IC50 |
0.21 μM
Compound: U0126
|
Inhibition of recombinant N-terminal GST-tagged human BRAF (433-726 residues) expressed in baculovirus infected sf21 insect cells/recombinant human full length N-terminal GST-tagged MEK1 expressed in Escherichia coli cascading pathway assessed as reductio
Inhibition of recombinant N-terminal GST-tagged human BRAF (433-726 residues) expressed in baculovirus infected sf21 insect cells/recombinant human full length N-terminal GST-tagged MEK1 expressed in Escherichia coli cascading pathway assessed as reductio
|
[PMID: 31252285] |
| Sf9 | IC50 |
50 μM
Compound: U-0126
|
Inhibition of His-tagged human PRAK expressed in Sf9 cells
Inhibition of His-tagged human PRAK expressed in Sf9 cells
|
[PMID: 10998351] |
| Sf9 | IC50 |
60 μM
Compound: U-0126
|
Inhibition of human PKBalpha expressed in SF9 cells
Inhibition of human PKBalpha expressed in SF9 cells
|
[PMID: 10998351] |
Chemical Information
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CAS. Nr. 218601-62-8
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Molecular Weight 380.49
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Formel C18H16N6S2
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SMILES
NC(C=CC=C1)=C1S/C(N)=C(C#N)/C(C#N)=C(N)/SC2=C(C=CC=C2)N
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Versand
Room temperature in continental US; may vary elsewhere.
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Speicherung
Please store the product under the recommended conditions in the Certificate of Analysis.
Reinheit & Dokumentation
Verweise
Calculators
Konzentration (Stammlösung) × Volumen (Stammlösung) = Konzentration (Ziellösung) × Volumen (Ziellösung)