Date published: 2026-4-23

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CPP32 p11 Activators

CPP32 Activators consist of a diverse array of chemical compounds that can enhance the proteolytic activity of CPP32, an essential executor caspase in the apoptosis pathway. Z-DEVD-FMK, by competitively inhibiting other caspases, can increase the substrate availability for CPP32, thereby augmenting its activity. Similarly, Etoposide and Camptothecin, both DNA-damaging agents, induce apoptosis which entails the activation of CPP32 to dismantle cellular components. Compounds such as Tunicamycin, Thapsigargin, and Brefeldin A stress the endoplasmic reticulum, triggering an apoptotic response that culminates in CPP32 activation. Betulinic Acid and Sulforaphane, through mitochondrial pathway induction, and Arsenic Trioxide, via oxidative stress, also contribute to apoptosis, necessitating the action of CPP32 to execute cell death.

Moreover, Staurosporine, a kinase inhibitor, can initiate apoptosis by a broad mechanism that includes the activation of CPP32. Cycloheximide enhances CPP32 activity by inducing apoptosis due to inhibition of protein synthesis. The incorporation of TRAIL, although a biological ligand, in its synthetic form, directly interacts with death receptors, setting off a cascade that activates CPP32.

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Items 1 to 10 of 11 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Caspase-3 Inhibitor

210344-95-9sc-3075
0.5 mg
$112.00
57
(1)

This is a synthetic peptide that functions as an irreversible inhibitor of caspases. By binding to caspases other than CPP32, it can enhance the activity of CPP32 by reducing competition for substrates, thereby indirectly increasing CPP32's proteolytic activity against its specific substrates.

Staurosporine

62996-74-1sc-3510
sc-3510A
sc-3510B
100 µg
1 mg
5 mg
$82.00
$153.00
$396.00
113
(4)

Staurosporine is a potent non-selective inhibitor of protein kinases. It can induce apoptosis through a pathway that includes the activation of CPP32, leading to the proteolytic cleavage of cellular proteins and the execution phase of cell apoptosis.

Etoposide (VP-16)

33419-42-0sc-3512B
sc-3512
sc-3512A
10 mg
100 mg
500 mg
$51.00
$231.00
$523.00
63
(1)

Etoposide is a topoisomerase II inhibitor that can induce DNA damage and apoptosis. It facilitates the release of cytochrome c from mitochondria, which indirectly activates CPP32 as part of the apoptotic cascade.

Tunicamycin

11089-65-9sc-3506A
sc-3506
5 mg
10 mg
$172.00
$305.00
66
(3)

Tunicamycin inhibits N-linked glycosylation, leading to ER stress and the unfolded protein response, which can trigger apoptosis and consequently activate CPP32.

Thapsigargin

67526-95-8sc-24017
sc-24017A
1 mg
5 mg
$136.00
$446.00
114
(2)

Thapsigargin is an inhibitor of the sarcoplasmic/endoplasmic reticulum Ca2+ ATPase (SERCA), causing calcium release and inducing ER stress, which can lead to the activation of CPP32 as part of the apoptosis pathway.

Brefeldin A

20350-15-6sc-200861C
sc-200861
sc-200861A
sc-200861B
1 mg
5 mg
25 mg
100 mg
$31.00
$53.00
$124.00
$374.00
25
(3)

Brefeldin A disrupts ER-Golgi transport, leading to ER stress and activation of apoptosis signaling pathways that include the activation of CPP32.

Betulinic Acid

472-15-1sc-200132
sc-200132A
25 mg
100 mg
$117.00
$344.00
3
(1)

Betulinic acid induces apoptosis in cancer cells through mitochondrial pathway activation, which includes the activation of CPP32.

D,L-Sulforaphane

4478-93-7sc-207495A
sc-207495B
sc-207495C
sc-207495
sc-207495E
sc-207495D
5 mg
10 mg
25 mg
1 g
10 g
250 mg
$153.00
$292.00
$489.00
$1325.00
$8465.00
$933.00
22
(1)

Sulforaphane can induce apoptosis in certain cancer cell lines, leading to the activation of CPP32 as a component of the apoptotic process.

Camptothecin

7689-03-4sc-200871
sc-200871A
sc-200871B
50 mg
250 mg
100 mg
$58.00
$186.00
$94.00
21
(2)

Camptothecin is a topoisomerase I inhibitor that induces DNA damage and apoptosis, leading to the activation of CPP32 in the apoptotic signaling pathways.

Arsenic(III) oxide

1327-53-3sc-210837
sc-210837A
250 g
1 kg
$89.00
$228.00
(0)

Arsenic trioxide is known to induce apoptosis via reactive oxygen species production and mitochondrial dysfunction, which can lead to the activation of CPP32.