Date published: 2025-11-1

1-800-457-3801

SCBT Portrait Logo
Seach Input

dcTRAILR1 Inhibitors

dcTRAILR1 inhibitors encompass a range of chemicals targeting crucial signaling pathways associated with apoptosis and cell survival. Curcumin, a natural polyphenol, inhibits NF-κB signaling by stabilizing IκBα, indirectly promoting apoptosis in cancer cells by modulating dcTRAILR1-associated processes related to cell survival and death. Sorafenib, a multi-kinase inhibitor, disrupts Raf/MEK/ERK signaling pathways, indirectly influencing dcTRAILR1 by altering MAPK signaling and impacting processes related to apoptosis and cell survival. Bortezomib, a proteasome inhibitor, stabilizes IκBα, disrupting NF-κB-driven anti-apoptotic signals and promoting apoptosis in cancer cells through its influence on dcTRAILR1-associated processes. LY294002, a PI3K inhibitor, disrupts the PI3K-Akt-mTOR pathway, indirectly affecting dcTRAILR1 by altering downstream events and influencing processes related to apoptosis and cell survival. Thalidomide, an immunomodulatory drug, promotes IκBα stabilization, disrupting NF-κB-driven anti-apoptotic signals and impacting dcTRAILR1-associated processes.

SB203580, a p38 MAPK inhibitor, disrupts p38 MAPK signaling, indirectly influencing dcTRAILR1 by altering downstream events and impacting processes related to apoptosis and cell survival. Dasatinib, a dual BCR-ABL and Src family kinase inhibitor, modulates tyrosine kinase signaling, indirectly affecting dcTRAILR1-associated processes. Rapamycin, an mTOR inhibitor, disrupts the mTOR signaling pathway, indirectly influencing dcTRAILR1 by altering downstream events and impacting processes related to apoptosis and cell survival. Cisplatin, a DNA cross-linking agent, induces DNA damage and activates JNK signaling, indirectly modulating dcTRAILR1-associated processes. Trametinib, a MEK1/2 inhibitor, disrupts the MAPK pathway, indirectly affecting dcTRAILR1 by altering downstream events and influencing processes related to apoptosis and cell survival. Obatoclax, a Bcl-2 family inhibitor, disrupts mitochondrial membrane potential, promoting intrinsic apoptosis and impacting dcTRAILR1-associated processes. Imatinib, a tyrosine kinase inhibitor, targets Bcr-Abl and c-Kit signaling pathways, indirectly affecting dcTRAILR1 by altering downstream events and influencing processes related to apoptosis and cell survival. This diverse set of inhibitors provides valuable tools for dissecting the intricate regulatory networks associated with dcTRAILR1 and its role in cellular processes pivotal for various pathological conditions.

SEE ALSO...

Items 1 to 10 of 12 total

Display:

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Curcumin

458-37-7sc-200509
sc-200509A
sc-200509B
sc-200509C
sc-200509D
sc-200509F
sc-200509E
1 g
5 g
25 g
100 g
250 g
1 kg
2.5 kg
$36.00
$68.00
$107.00
$214.00
$234.00
$862.00
$1968.00
47
(1)

Curcumin, a natural polyphenol, inhibits NF-κB signaling by suppressing IκBα degradation. Its action indirectly modulates dcTRAILR1 by preventing NF-κB-driven anti-apoptotic signals, promoting apoptosis in cancer cells. This influences dcTRAILR1-associated processes related to cell survival and death.

Sorafenib

284461-73-0sc-220125
sc-220125A
sc-220125B
5 mg
50 mg
500 mg
$56.00
$260.00
$416.00
129
(3)

Sorafenib, a multi-kinase inhibitor, targets Raf/MEK/ERK signaling pathways. Its impact on the MAPK pathway indirectly influences dcTRAILR1 by altering downstream signaling, impacting dcTRAILR1-associated processes related to apoptosis and cell survival.

Bortezomib

179324-69-7sc-217785
sc-217785A
2.5 mg
25 mg
$132.00
$1064.00
115
(2)

Bortezomib, a proteasome inhibitor, prevents NF-κB activation by stabilizing IκBα. Its action indirectly modulates dcTRAILR1 by disrupting NF-κB-driven anti-apoptotic signals, promoting apoptosis in cancer cells. This influences dcTRAILR1-associated processes related to cell survival and death.

LY 294002

154447-36-6sc-201426
sc-201426A
5 mg
25 mg
$121.00
$392.00
148
(1)

LY294002, a PI3K inhibitor, disrupts the PI3K-Akt-mTOR pathway. Its influence on PI3K-mediated signaling indirectly affects dcTRAILR1 by altering downstream events, impacting dcTRAILR1-associated processes related to apoptosis and cell survival.

Thalidomide

50-35-1sc-201445
sc-201445A
100 mg
500 mg
$109.00
$350.00
8
(0)

Thalidomide, an immunomodulatory drug, inhibits NF-κB activation by promoting IκBα stabilization. Its action indirectly modulates dcTRAILR1 by disrupting NF-κB-driven anti-apoptotic signals, promoting apoptosis in cancer cells. This influences dcTRAILR1-associated processes related to cell survival and death.

SB 203580

152121-47-6sc-3533
sc-3533A
1 mg
5 mg
$88.00
$342.00
284
(5)

SB203580, a p38 MAPK inhibitor, disrupts the p38 MAPK signaling pathway. Its impact on p38 MAPK-mediated signaling indirectly influences dcTRAILR1 by altering downstream events, impacting dcTRAILR1-associated processes related to apoptosis and cell survival.

Dasatinib

302962-49-8sc-358114
sc-358114A
25 mg
1 g
$47.00
$145.00
51
(1)

Dasatinib, a dual BCR-ABL and Src family kinase inhibitor, modulates tyrosine kinase signaling. Its impact on Src family kinases indirectly influences dcTRAILR1 by altering downstream events, impacting dcTRAILR1-associated processes related to apoptosis and cell survival.

Rapamycin

53123-88-9sc-3504
sc-3504A
sc-3504B
1 mg
5 mg
25 mg
$62.00
$155.00
$320.00
233
(4)

Rapamycin, an mTOR inhibitor, disrupts the mTOR signaling pathway. Its influence on mTOR-mediated signaling indirectly affects dcTRAILR1 by altering downstream events, impacting dcTRAILR1-associated processes related to apoptosis and cell survival.

Cisplatin

15663-27-1sc-200896
sc-200896A
100 mg
500 mg
$76.00
$216.00
101
(4)

Cisplatin, a DNA cross-linking agent, induces DNA damage and activates JNK signaling. Its action indirectly modulates dcTRAILR1 by altering JNK-mediated signaling, impacting dcTRAILR1-associated processes related to apoptosis and cell survival.

Trametinib

871700-17-3sc-364639
sc-364639A
sc-364639B
5 mg
10 mg
1 g
$112.00
$163.00
$928.00
19
(1)

Trametinib, a MEK1/2 inhibitor, disrupts the MAPK pathway. Its impact on MEK-mediated signaling indirectly influences dcTRAILR1 by altering downstream events, impacting dcTRAILR1-associated processes related to apoptosis and cell survival.