CPUL1
CPUL1 is a TrxR inhibitor, which shows proliferation-inhibitory and anti-metastatic activity against A549 cells. CPUL1 influences EMT (epithelial-mesenchymal transition) via inducing ROS-mediated ERK/JNK signaling by inhibiting TrxR1 enzyme activity. CPUL1 in combination with α-Lipoic Acid (HY-N0492) or Dithiodipropionic acid (HY-W014395) is more effective.
For research use only. We do not sell to patients.
- CAS No.: 2043660-80-4
- Formula: C22H13Cl2N5O
- Molecular Weight:434.28
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
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Cell Line
|
Type | Value | Description | References |
|---|---|---|---|---|
| A549 | IC50 |
6.8 μM
Compound: 1i
|
Antiproliferative activity against human A549 cells after 48 hrs by MTT assay
Antiproliferative activity against human A549 cells after 48 hrs by MTT assay
|
[PMID: 27836197] |
| HCT-116 | IC50 |
8 μM
Compound: 1i
|
Antiproliferative activity against human HCT116 cells after 48 hrs by MTT assay
Antiproliferative activity against human HCT116 cells after 48 hrs by MTT assay
|
[PMID: 27836197] |
| HepG2 | IC50 |
2.1 μM
Compound: 1i
|
Antiproliferative activity against human HepG2 cells after 48 hrs by MTT assay
Antiproliferative activity against human HepG2 cells after 48 hrs by MTT assay
|
[PMID: 27836197] |
| MCF7 | IC50 |
7.3 μM
Compound: 1i
|
Antiproliferative activity against human MCF7 cells after 48 hrs by MTT assay
Antiproliferative activity against human MCF7 cells after 48 hrs by MTT assay
|
[PMID: 27836197] |
CPUL1 (2.5, 5, 10, 20, 40 μM; 48 h) inhibits A549 cell proliferation and (2, 4, 8 μM; 48 h) colony formation[1].
CPUL1 (4, 8 μM; 0, 24, 48 h) inhibits A549 cells migration and (2, 4, 8 μM; 48 h) invasion[1].
CPUL1 hinders EMT (epithelial-mesenchymal transition) progress and affects MAPK pathway in A549 cells[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Cell Line:A549 cells
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Concentration:2.5, 5, 10, 20, 40 μM
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Incubation Time:48 h
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Result:Showed a dose-dependent cytotoxicity, with an IC50 value of 7.61 μM.
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Cell Line:A549 cells
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Concentration:2, 4, 8 μM
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Incubation Time:48 h
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Result:Significantly abolished the capacity of A5459 cells to form colonies at the dose-dependent concentration.
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Cell Line:A549 cells
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Concentration:4, 8 μM
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Incubation Time:0, 24, 48 h
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Result:Inhibited the migration of A549 cells in a dose- and time-dependent manner.
Chemical Information
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CAS No. 2043660-80-4
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Molecular Weight 434.28
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Formula C22H13Cl2N5O
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SMILES
N#CC1=C(OC2=C(C1C3=CC(Cl)=C(Cl)C=C3)C4=NC5=CC=CC=C5N=C4C=C2N)N
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)