1. Apoptosis
    Epigenetics
    Cell Cycle/DNA Damage
  2. Apoptosis
    Bcl-2 Family
    Caspase
    PARP
  3. Anticancer agent 43

Anticancer agent 43 

Cat. No.: HY-146548
Handling Instructions

Anticancer Agent 43 is a potent anticancer agent. Anticancer Agent 43 induces apoptosis by caspase 3, PARP1, and Bax dependent mechanisms. Anticancer Agent 43 induces DNA damage.

For research use only. We do not sell to patients.

Anticancer agent 43 Chemical Structure

Anticancer agent 43 Chemical Structure

CAS No. : 2470015-35-9

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Description

Anticancer Agent 43 is a potent anticancer agent. Anticancer Agent 43 induces apoptosis by caspase 3, PARP1, and Bax dependent mechanisms. Anticancer Agent 43 induces DNA damage[1].

IC50 & Target[1]

Caspase 3

 

PARP1

 

Bax

 

In Vitro

Anticancer agent 43 (compound 3a) shows selectivity toward human tumor cells (SI50=28.94)[1].
Anticancer agent 43 (45 µM, 24 h) induces apoptosis via caspase 3, PARP1 and Bax dependent pathways in HepG2 cells[1].
Anticancer agent 43 (45 µM, 24 h) shows no effect on the transition of G1/S phases in HepG2 cells[1].
Anticancer agent 43 (0.7, 45, 55 µM) induces DNA damage in HCT116 cells (Tail DNA=16.1%, OTM=3.7), MCF-7 cells, HepG2 cells (Tail DNA=26.2%, OTM=13.2), Balb/c 3T3 cells (Tail DNA = 8.4%, OTM = 3.5)[1].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Cytotoxicity Assay[1]

Cell Line: HepG2, MCF-7, HCT116, HeLa, A549, WM793, THP-1, HaCaT, Balb/c3T3 cells
Concentration: 0, 1, 10, 100 µM
Incubation Time: 72 h
Result: Showed cytotoxic action with GI50s of 12.1, 0.7, 0.8, 49.3, 9.7 µM for for HepG2, MCF-7, HCT116, HeLa, A549 cells, low toxicity towards WM793, THP-1, HaCaT, Balb/c 3T3 cells with GI50s of 80.4, 62.4,98.3,40.8 µM , respectively.

Apoptosis Analysis[1]

Cell Line: HepG2 cells
Concentration: 45 µM
Incubation Time: 24 h
Result: Induced apoptosis in HepG2 cells via caspase 3, PARP1 and Bax dependent pathways.

Western Blot Analysis[1]

Cell Line: HCT116, MCF-7 cells
Concentration: 0.7 µM
Incubation Time: 24 h
Result: Decreased the expression of Cdk2 protein in HCT116 and MCF-7 cells.

Cell Cycle Analysis[1]

Cell Line: HepG2 cells
Concentration: 45 µM
Incubation Time: 24 h
Result: Showed no effect on the transition of G1/S phases in HepG2 cells.
Molecular Weight

336.36

Formula

C14H9FN2O3S2

CAS No.
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