Date published: 2026-1-23

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BI-1 Inhibitors

BI-1 inhibitors belong to a distinctive chemical class known for their ability to modulate cellular processes by targeting a specific protein called Bax Inhibitor-1 (BI-1). These inhibitors are a group of small molecules or compounds that have been designed and synthesized to interact with BI-1, altering its function within the cell. BI-1 itself is a transmembrane protein primarily found in the endoplasmic reticulum (ER), a crucial cellular organelle responsible for protein folding and calcium storage. The primary role of BI-1 is to suppress programmed cell death, also known as apoptosis, by activation of Bax, a pro-apoptotic protein. BI-1 inhibitors act by binding to BI-1 and modulating its activity, thereby influencing the apoptotic pathways and potentially impacting cell survival. These inhibitors are of particular interest in the field of cell biology and molecular pharmacology due to their potential to elucidate the intricate mechanisms involved in cell death regulation. Researchers utilize BI-1 inhibitors as valuable tools to explore the fundamental biology of apoptosis and its implications in various cellular processes. By studying the effects of BI-1 inhibitors on cell survival and apoptosis, scientists aim to gain insights into the underlying molecular pathways that govern these processes. Moreover, BI-1 inhibitors have been employed in experimental settings to investigate their impact on cellular stress responses and the ER stress pathway.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

3′-Azido-3′-deoxythymidine

30516-87-1sc-203319
10 mg
$61.00
2
(1)

NSC 66811 inhibits TMBIM6 by binding to its hydrophobic pocket, possibly disrupting its anti-apoptotic function.

Vinorelbine ditartrate

125317-39-7sc-361397B
sc-361397
sc-361397A
sc-361397C
sc-361397D
5 mg
10 mg
50 mg
1 g
5 g
$92.00
$131.00
$547.00
$2448.00
$9180.00
6
(1)

NSC 68353 targets TMBIM6 by intercalating into the membrane and altering its stability or oligomerization state.

Quercetin

117-39-5sc-206089
sc-206089A
sc-206089E
sc-206089C
sc-206089D
sc-206089B
100 mg
500 mg
100 g
250 g
1 kg
25 g
$11.00
$17.00
$110.00
$250.00
$936.00
$50.00
33
(2)

Quercetin interacts with TMBIM6 and may inhibit its function by modulating its protein conformation or protein-protein interactions.

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 affects TMBIM6 indirectly by disrupting the Golgi apparatus structure, potentially impacting TMBIM6 trafficking or stability.

MG-132 [Z-Leu- Leu-Leu-CHO]

133407-82-6sc-201270
sc-201270A
sc-201270B
5 mg
25 mg
100 mg
$60.00
$265.00
$1000.00
163
(3)

MG-132 can lead to the accumulation of misfolded TMBIM6 proteins by inhibiting the proteasome, which may reduce its functional levels in the cell.

PIK-75, hydrochloride

372196-77-5sc-296089
sc-296089A
1 mg
5 mg
$29.00
$124.00
(1)

Eeyarestatin I can indirectly inhibit TMBIM6 by blocking the ER-associated degradation (ERAD) pathway, affecting protein folding and stability.

Cycloheximide

66-81-9sc-3508B
sc-3508
sc-3508A
100 mg
1 g
5 g
$41.00
$84.00
$275.00
127
(6)

Cycloheximide inhibits protein synthesis, indirectly reducing TMBIM6 levels by preventing its synthesis.

Salubrinal

405060-95-9sc-202332
sc-202332A
1 mg
5 mg
$34.00
$104.00
87
(2)

Salubrinal indirectly targets TMBIM6 by inhibiting dephosphorylation of eIF2α, which may alter TMBIM6 translation or stress response.

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
$37.00
$69.00
$109.00
$218.00
$239.00
$879.00
$1968.00
47
(1)

Curcumin can inhibit TMBIM6 by modulating its expression or interfering with its anti-apoptotic activity.

Celastrol, Celastrus scandens

34157-83-0sc-202534
10 mg
$158.00
6
(1)

Celastrol can disrupt TMBIM6 function by inducing heat shock response and potentially modulating its protein levels or activity.