Date published: 2025-10-16

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C14orf124 Inhibitors

The designation C14orf124 inhibitors pertains to a specific category of chemical compounds that interact with the product of the gene symbolized as C14orf124. This nomenclature suggests that the gene is situated on chromosome 14 and is characterized as an 'open reading frame' (orf), which is a segment of DNA potentially coding for a protein; 124 serves as a distinctive identifier within this genomic location. The term inhibitors in this context implies that these compounds are designed to bind to the protein encoded by C14orf124 and impede its activity. The discovery and development of such inhibitors would be based on comprehensive research that delves into the protein's structure, function, and its role in cellular processes, although the specific functions of such genes are often not immediately apparent based solely on their genomic location and open reading frame status.

Developing a class of inhibitors for a protein like that encoded by C14orf124 would require a meticulous approach to understand the protein's role at the molecular level. This would include studies to determine the protein's structure, possibly through crystallography or other imaging techniques, to identify potential active or binding sites. Chemists would then design small molecules that can specifically bind to these sites on the protein. These molecules would be engineered to have a high affinity for the target protein, ensuring that they effectively impede its function. The process of designing these inhibitors is characterized by a cyclical pattern of synthesis, testing, and refinement. This cycle is driven by the need to create a compound with the desired specificity and an ability to stably interact with the protein in question, without adversely affecting other proteins. Once an initial compound is synthesized, it undergoes rigorous testing to confirm its efficacy and specificity. Adjustments are made based on the results of these tests, with the dual goals of maximizing the inhibitor's interaction with the C14orf124 protein while minimizing unintended interactions with other molecular structures.

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Items 1 to 10 of 11 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Cycloheximide

66-81-9sc-3508B
sc-3508
sc-3508A
100 mg
1 g
5 g
$40.00
$82.00
$256.00
127
(5)

Cycloheximide inhibits eukaryotic protein synthesis by interfering with the translocation step in protein elongation, which could reduce SDR39U1 levels.

Fostriecin

87860-39-7sc-202160
50 µg
$260.00
9
(1)

Fostriecin selectively inhibits protein phosphatase 2A, which may affect various signaling pathways and potentially decrease SDR39U1 expression.

Camptothecin

7689-03-4sc-200871
sc-200871A
sc-200871B
50 mg
250 mg
100 mg
$57.00
$182.00
$92.00
21
(2)

Camptothecin inhibits DNA topoisomerase I, leading to DNA damage and potentially affecting transcription and expression of SDR39U1.

Flavopiridol

146426-40-6sc-202157
sc-202157A
5 mg
25 mg
$78.00
$254.00
41
(3)

Flavopiridol is a cyclin-dependent kinase inhibitor, which can modify cell cycle progression and potentially downregulate SDR39U1 expression.

Bortezomib

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

Bortezomib inhibits the 26S proteasome, potentially leading to altered protein turnover and expression levels, including that of SDR39U1.

Betulinic Acid

472-15-1sc-200132
sc-200132A
25 mg
100 mg
$115.00
$337.00
3
(1)

Betulinic acid can trigger various cellular responses, such as apoptosis, possibly affecting SDR39U1 expression indirectly.

Geldanamycin

30562-34-6sc-200617B
sc-200617C
sc-200617
sc-200617A
100 µg
500 µg
1 mg
5 mg
$38.00
$58.00
$102.00
$202.00
8
(1)

Geldanamycin binds to heat shock protein 90 (Hsp90) and disrupts its function, which could impact the stability and expression of client proteins like SDR39U1.

Anisomycin

22862-76-6sc-3524
sc-3524A
5 mg
50 mg
$97.00
$254.00
36
(2)

Anisomycin interferes with protein synthesis by inhibiting peptidyl transferase activity on the 60S ribosomal subunit, potentially reducing SDR39U1 levels.

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

133407-82-6sc-201270
sc-201270A
sc-201270B
5 mg
25 mg
100 mg
$56.00
$260.00
$980.00
163
(3)

MG-132 is a proteasome inhibitor, which can lead to increased protein levels but also affect the transcription of certain genes.

Rocaglamide

84573-16-0sc-203241
sc-203241A
sc-203241B
sc-203241C
sc-203241D
100 µg
1 mg
5 mg
10 mg
25 mg
$270.00
$465.00
$1607.00
$2448.00
$5239.00
4
(1)

Rocaglamide inhibits translation initiation and could thereby decrease the synthesis of proteins, including SDR39U1.