1. Apoptosis Epigenetics Cell Cycle/DNA Damage
  2. Apoptosis Caspase PARP Bcl-2 Family
  3. Anticancer agent 64

Anticancer agent 64 (compound 5m) shows cytotoxic activity in CCRF-CEM cells, with IC50 of 2.4 μM. Anticancer agent 64 shows good anticancer activity through apoptosis induction. Anticancer agent 64 induces caspase 3 and 7 activation and PARP cleavage. Anticancer agent 64 induces significant effect of mitochondria depolarization.

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Anticancer agent 64 Chemical Structure

Anticancer agent 64 Chemical Structure

CAS No. : 2387902-92-1

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Description

Anticancer agent 64 (compound 5m) shows cytotoxic activity in CCRF-CEM cells, with IC50 of 2.4 μM. Anticancer agent 64 shows good anticancer activity through apoptosis induction. Anticancer agent 64 induces caspase 3 and 7 activation and PARP cleavage. Anticancer agent 64 induces significant effect of mitochondria depolarization[1].

IC50 & Target

Caspase 3

 

Caspase-7

 

Bcl-2

 

Bax

 

PARP

 

Cellular Effect
Cell Line Type Value Description References
A549 IC50
38.4 μM
Compound: 5m
Cytotoxicity against human A549 cells incubated for 72 hrs by MTS assay
Cytotoxicity against human A549 cells incubated for 72 hrs by MTS assay
[PMID: 31677446]
BJ IC50
> 50 μM
Compound: 5m
Cytotoxicity against human BJ cells incubated for 72 hrs by MTS assay
Cytotoxicity against human BJ cells incubated for 72 hrs by MTS assay
[PMID: 31677446]
CCRF-CEM IC50
2.4 μM
Compound: 5m
Cytotoxicity against human CCRF-CEM cells incubated for 72 hrs by MTS assay
Cytotoxicity against human CCRF-CEM cells incubated for 72 hrs by MTS assay
[PMID: 31677446]
HCT-116 IC50
36.5 μM
Compound: 5m
Cytotoxicity against human HCT116 cells incubated for 72 hrs by MTS assay
Cytotoxicity against human HCT116 cells incubated for 72 hrs by MTS assay
[PMID: 31677446]
HCT-116 IC50
48.3 μM
Compound: 5m
Cytotoxicity against p53 knockout human HCT116 cells incubated for 72 hrs by MTS assay
Cytotoxicity against p53 knockout human HCT116 cells incubated for 72 hrs by MTS assay
[PMID: 31677446]
K562 IC50
> 50 μM
Compound: 5m
Cytotoxicity against human K562 cells incubated for 72 hrs by MTS assay
Cytotoxicity against human K562 cells incubated for 72 hrs by MTS assay
[PMID: 31677446]
MRC5 IC50
> 50 μM
Compound: 5m
Cytotoxicity against human MRC5 cells incubated for 72 hrs by MTS assay
Cytotoxicity against human MRC5 cells incubated for 72 hrs by MTS assay
[PMID: 31677446]
U2OS IC50
48 μM
Compound: 5m
Cytotoxicity against human U2OS cells incubated for 72 hrs by MTS assay
Cytotoxicity against human U2OS cells incubated for 72 hrs by MTS assay
[PMID: 31677446]
In Vitro

Anticancer agent 64 (compound 5m) increases BAX expression and decreases Bcl-2 protein expression[1].
. Anticancer agent 64 shows significant increasement in cells accumulation in the G2/M phase of the cell cycle, while proportion of cells in S phase is reduced[1].

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

Molecular Weight

510.77

Formula

C31H46N2O2S

CAS No.
SMILES

OC([C@]12[C@@]([C@@H](CC2)C(C)=C)([H])[C@]3([H])[C@@](CC1)([C@]4([C@]([C@@]5([C@@](C(C)(C6=C(SC(N)=N6)C5)C)([H])CC4)C)([H])CC3)C)C)=O

Shipping

Room temperature in continental US; may vary elsewhere.

Storage

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

Purity & Documentation
References
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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 64
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HY-147514
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