Date published: 2026-4-1

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KIAA0329 Inhibitors

The term KIAA0329 inhibitors would refer to a category of chemical compounds specifically designed to inhibit the activity of a protein that is encoded by the KIAA0329 gene. The KIAA nomenclature originates from a systematic effort to characterize novel cDNA sequences from human brain tissue by a Japanese consortium. These sequences often received KIAA designations followed by a unique number, and many of these genes were initially of unknown function. Over time, some KIAA genes have been linked to specific biological functions, while others remain less characterized. If the protein product of KIAA0329 has been identified and found to play a significant role in cellular processes, inhibitors developed against it would be aimed at modulating its function for the purpose of scientific inquiry.

To develop KIAA0329 inhibitors, a deep understanding of the protein's structure and function would be essential. Researchers would conduct studies to elucidate its role within the cell, potentially involving gene expression profiling, proteomic analyses to identify interaction partners, and functional assays to determine its activity. Structural studies would be paramount in identifying potential binding sites for inhibitors. These could include enzymatic active sites, binding domains for interaction partners, or allosteric sites that modulate the protein's activity. Advanced techniques such as X-ray crystallography, nuclear magnetic resonance (NMR) spectroscopy, or cryo-electron microscopy could be used to solve the three-dimensional structure of the protein, providing a blueprint for the rational design of inhibitors that can interact with the protein with high specificity.

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Items 1 to 10 of 11 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Puromycin dihydrochloride

58-58-2sc-108071
sc-108071B
sc-108071C
sc-108071A
25 mg
250 mg
1 g
50 mg
$42.00
$214.00
$832.00
$66.00
394
(16)

Puromycin causes premature chain termination during translation by acting as an analog of aminoacyl-tRNA, thus inhibiting protein synthesis.

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 the ribosome.

Chloramphenicol

56-75-7sc-3594
25 g
$90.00
10
(1)

Chloramphenicol binds to bacterial ribosomes and inhibits protein synthesis, and can also affect mitochondrial protein synthesis in eukaryotes.

Anisomycin

22862-76-6sc-3524
sc-3524A
5 mg
50 mg
$99.00
$259.00
36
(2)

Anisomycin interferes with protein synthesis by inhibiting peptide bond formation at the level of the 80S ribosome.

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, preventing mRNA synthesis.

α-Amanitin

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

α-Amanitin inhibits RNA polymerase II, the enzyme responsible for mRNA transcription, leading to decreased gene expression.

Homoharringtonine

26833-87-4sc-202652
sc-202652A
sc-202652B
1 mg
5 mg
10 mg
$52.00
$125.00
$182.00
11
(1)

Harringtonine inhibits protein synthesis by preventing the initial elongation step of translation.

Harringtonin

26833-85-2sc-204771
sc-204771A
sc-204771B
sc-204771C
sc-204771D
5 mg
10 mg
25 mg
50 mg
100 mg
$250.00
$367.00
$548.00
$730.00
$980.00
30
(1)

Homoharringtonine inhibits protein elongation by binding to the ribosome, similar to Harringtonine.

Fusidic acid

6990-06-3sc-215065
1 g
$292.00
(0)

Fusidic acid prevents the turnover of elongation factor G (EF-G) from the ribosome, impeding bacterial protein synthesis.

Tunicamycin

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

Tunicamycin blocks N-linked glycosylation and can inhibit the proper folding and stability of many proteins, leading to decreased expression.