Anticancer agent 55
Anticancer agent 55 is a potent anticancer agent. Anticancer agent 55 shows anticancer activity via reducing the cell viability and cell migration in a dose-dependent manner. Anticancer agent 55 induces apoptosis. Anticancer agent 55 has the potential for the research of prostate cancer and breast cancer.
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- CAS 番号: 2408800-91-7
- 分子式: C28H21Br2FN2O2
- 分子量:596.28
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保管条件:
Please store the product under the recommended conditions in the Certificate of Analysis.
生物活性
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Cell Line
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Type | Value | Description | References |
|---|---|---|---|---|
| MCF7 | IC50 |
1.95 μM
Compound: 3h
|
Cytotoxicity against human MCF7 cells assessed as reduction cell viability incubated for 48 hrs by MTS assay
Cytotoxicity against human MCF7 cells assessed as reduction cell viability incubated for 48 hrs by MTS assay
|
[PMID: 31901746] |
| PC-3 | IC50 |
1.18 μM
Compound: 3h
|
Cytotoxicity against human PC-3 cells assessed as reduction in cell viability incubated for 48 hrs by MTS assay
Cytotoxicity against human PC-3 cells assessed as reduction in cell viability incubated for 48 hrs by MTS assay
|
[PMID: 31901746] |
Anticancer agent 55 (compound 3h) (0-100 μM; 48 h) inhibits cell viability with IC50s of 1.18 μM and 1.95 μM for PC-3, MCF-7 cells, respectively[1].
Anticancer agent 55 (0, 1, 3, 10 μM; 24 h) inhibits cell migration of PC-3 cells and MCF-7 cells in a dose-dependent manner[1].
Anticancer agent 55 (0, 1, 3, 10 μM; 12, 24 h) induces apoptosis by increases the caspase-3 activity and cleaved PARP levels[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Cell Line:PC-3, MCF-7 cells
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Concentration:0-100 µM
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Incubation Time:48 h
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Result:Significantly inhibited cell viability of PC-3, MCF-7 cells with IC50s of 1.18 µM and 1.95 µM, respectively.
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Cell Line:PC-3, MCF-7 cells
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Concentration:0, 1, 3, 10 µM
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Incubation Time:PC-3 for 12 h; MCF-7 for 24 h
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Result:Induced apoptosis by increased the caspase-3 activity in a concentration-dependent manner.
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Cell Line:PC-3, MCF-7 cells
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Concentration:0, 1, 3, 10 µM
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Incubation Time:PC-3 for 12 h; MCF-7 for 24 h
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Result:Increased cleaved PARP levels in a dose-dependent manner in PC-3 and MCF-7 cells.
化学情報
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CAS 番号 2408800-91-7
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分子量 596.28
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分子式 C28H21Br2FN2O2
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SMILES
O=C(C1=CC=CC=C1)C[N+]2=CC3=CC=CN3[C@@H](C2C4=CC=C(C=C4)Br)C(C5=CC=C(C=C5)F)=O.[Br-]
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輸送条件
Room temperature in continental US; may vary elsewhere.
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保管条件
Please store the product under the recommended conditions in the Certificate of Analysis.
純度とドキュメンテーション
参考文献
Calculators
濃度 (開始) × 体積 (開始) = 濃度 (終了) × 体積 (終了)