Date published: 2026-5-21

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FAST Inhibitors

FAST inhibitors belong to a class of chemical compounds specifically designed to target and modulate the activity of the FAST protein, which stands for "Fas-activated serine-threonine kinase." FAST is a relatively newly discovered protein that plays a role in cellular processes, particularly in cell signaling pathways associated with apoptosis, or programmed cell death. Apoptosis is a fundamental mechanism in multicellular organisms, regulating tissue development, immune responses, and the elimination of damaged or potentially harmful cells. Inhibitors designed to target FAST are primarily employed in molecular and cellular biology research to investigate the functional properties and regulatory mechanisms associated with this protein's role in apoptosis signaling.

The development of FAST inhibitors typically involves a combination of biochemical, biophysical, and structural approaches aimed at identifying or designing molecules that can selectively interact with FAST and modulate its activity within apoptosis signaling pathways. By inhibiting FAST, these compounds can potentially disrupt its role in regulating apoptosis, affecting cell survival and death decisions. Researchers use FAST inhibitors to explore the intricate roles played by this protein in cellular processes, attempting to unravel its contributions to apoptosis pathways, immune cell responses, and tissue homeostasis.

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Items 1 to 10 of 12 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Actinomycin D

50-76-0sc-200906
sc-200906A
sc-200906B
sc-200906C
sc-200906D
5 mg
25 mg
100 mg
1 g
10 g
$74.00
$243.00
$731.00
$2572.00
$21848.00
53
(3)

Actinomycin D binds to DNA and inhibits RNA polymerase, which could reduce FASTK mRNA synthesis and thus its protein levels.

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 eukaryotic protein synthesis by interfering with the translocation step in protein synthesis, potentially decreasing FASTK protein levels.

Fluorouracil

51-21-8sc-29060
sc-29060A
1 g
5 g
$37.00
$152.00
11
(1)

5-Fluorouracil is metabolized to compounds that can be incorporated into RNA and disrupt its processing, possibly affecting FASTK expression indirectly.

Chloroquine

54-05-7sc-507304
250 mg
$69.00
2
(0)

Chloroquine can elevate lysosomal pH and affect protein degradation pathways, which may influence FASTK protein stability and expression.

2-Deoxy-D-glucose

154-17-6sc-202010
sc-202010A
1 g
5 g
$70.00
$215.00
26
(2)

As a glycolysis inhibitor, 2-Deoxy-D-glucose may disrupt cellular metabolism, potentially downregulating FASTK expression due to energy stress.

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 is a proteasome inhibitor that could lead to reduced degradation of proteins that regulate FASTK expression, indirectly affecting its levels.

Trichostatin A

58880-19-6sc-3511
sc-3511A
sc-3511B
sc-3511C
sc-3511D
1 mg
5 mg
10 mg
25 mg
50 mg
$152.00
$479.00
$632.00
$1223.00
$2132.00
33
(3)

Trichostatin A is a histone deacetylase inhibitor that could alter chromatin structure and modulate the transcription of various genes, including potentially FASTK.

Suberoylanilide Hydroxamic Acid

149647-78-9sc-220139
sc-220139A
100 mg
500 mg
$133.00
$275.00
37
(2)

SAHA is another histone deacetylase inhibitor that may change gene expression profiles, possibly affecting FASTK expression.

α-Amanitin

23109-05-9sc-202440
sc-202440A
1 mg
5 mg
$269.00
$1050.00
26
(2)

α-Amanitin is an inhibitor of RNA polymerase II which could lead to a decrease in mRNA synthesis, affecting the levels of proteins such as FASTK.

Camptothecin

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

Camptothecin inhibits DNA topoisomerase I, which could result in reduced transcription and therefore decrease FASTK expression.