1. Apoptosis
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  3. 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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Anticancer agent 55 Chemical Structure

Anticancer agent 55 Chemical Structure

CAS No. : 2408800-91-7

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Description

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[1].

Cellular Effect
Cell Line 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]
In Vitro

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.

Cell Viability Assay[1]

Cell Line: PC-3, MCF-7 cells
Concentration: 0-100 µM
Incubation Time: 48 h
Result: Significantly inhibited cell viability of PC-3, MCF-7 cells with IC50s of 1.18 µM and 1.95 µM, respectively.

Apoptosis Analysis[1]

Cell Line: PC-3, MCF-7 cells
Concentration: 0, 1, 3, 10 µM
Incubation Time: PC-3 for 12 h; MCF-7 for 24 h
Result: Induced apoptosis by increased the caspase-3 activity in a concentration-dependent manner.

Western Blot Analysis[1]

Cell Line: PC-3, MCF-7 cells
Concentration: 0, 1, 3, 10 µM
Incubation Time: PC-3 for 12 h; MCF-7 for 24 h
Result: Increased cleaved PARP levels in a dose-dependent manner in PC-3 and MCF-7 cells.
Molecular Weight

596.28

Formula

C28H21Br2FN2O2

CAS No.
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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Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation
References
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Anticancer agent 55 Related Classifications

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Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Anticancer agent 55
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HY-146433
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