Date published: 2025-9-10

1-800-457-3801

SCBT Portrait Logo
Seach Input

C10orf67 Inhibitors

The functional activity of C10orf67 can be inhibited through various chemical compounds that interact with specific pathways or cellular processes. Inhibitors that modulate epigenetic markers play a significant role in this context; for example, compounds that inhibit histone deacetylases can lead to changes in chromatin structure, resulting in a reduced expression of C10orf67. Similarly, compounds that target DNA methylation processes can alter gene expression profiles, potentially diminishing the transcriptional activity of the C10orf67 gene. These epigenetic modulators exert a profound impact on gene expression regulation, which in turn can influence the levels and function of C10orf67 in the cell.

Furthermore, small molecules that target key signaling pathways also serve as effective inhibitors of C10orf67. For instance, compounds that inhibit the mTOR pathway can impede the translation of certain mRNA populations, which would include C10orf67 if it falls under mTOR's regulatory umbrella. Inhibition of the PI3K/Akt pathway, a critical signaling cascade involved in cell survival and proliferation, could also lead to decreased stability or translation of C10orf67. Additionally, inhibitors of the MAPK/ERK and p38 MAPK pathways can suppress the expression of C10orf67 given its regulation is connected to these pathways.

SEE ALSO...

Items 11 to 11 of 11 total

Display:

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Thapsigargin

67526-95-8sc-24017
sc-24017A
1 mg
5 mg
$94.00
$349.00
114
(2)

An inhibitor of the sarcoplasmic/endoplasmic reticulum Ca2+ ATPase (SERCA), which can lead to ER stress and downregulate C10orf67 given its expression is linked to ER stress response.