CPXM inhibitors are chemical compounds designed to target and inhibit the function of carboxypeptidase X, M14 family (CPXM), a member of the metallocarboxypeptidase-like proteins. CPXM, unlike other traditional carboxypeptidases, is considered to be catalytically inactive because it lacks critical residues typically required for enzymatic activity. However, despite the absence of catalytic function, CPXM is believed to play an important role in cellular processes through protein-protein interactions. The exact function of CPXM is not fully understood, but it is thought to be involved in extracellular matrix organization, cell adhesion, and other processes related to tissue structure and cell signaling. CPXM contains domains that suggest it may act as a scaffold protein, mediating interactions between various extracellular and membrane proteins.
Inhibitors of CPXM function by binding to the protein and preventing it from interacting with other proteins or stabilizing certain cellular structures. These inhibitors are valuable tools for exploring the non-catalytic roles of CPXM in biological systems. By blocking CPXM's ability to participate in molecular complexes, researchers can investigate how it contributes to processes such as cell adhesion and extracellular matrix remodeling. Such inhibition helps to reveal the protein's role in maintaining tissue architecture and regulating intercellular communication. The study of CPXM inhibitors can provide insights into the structural and regulatory functions of this unique protein, shedding light on how its interaction with other cellular components influences broader physiological processes and structural integrity within tissues.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Trichostatin A | 58880-19-6 | sc-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 | |
Trichostatin A inhibits histone deacetylases, leading to altered chromatin structure and potentially downregulating CPXM1 expression by affecting gene accessibility. | ||||||
5-Azacytidine | 320-67-2 | sc-221003 | 500 mg | $280.00 | 4 | |
5-Azacytidine, a DNA methyltransferase inhibitor, may reduce methylation of the CPXM1 gene promoter, possibly diminishing its transcription. | ||||||
Actinomycin D | 50-76-0 | sc-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 | |
Actinomycin D binds to DNA and inhibits RNA polymerase, possibly leading to decreased CPXM1 mRNA synthesis and lower protein expression. | ||||||
Cycloheximide | 66-81-9 | sc-3508B sc-3508 sc-3508A | 100 mg 1 g 5 g | $41.00 $84.00 $275.00 | 127 | |
Cycloheximide interferes with mRNA translation on ribosomes, potentially reducing CPXM1 protein levels indirectly by preventing new synthesis. | ||||||
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | $63.00 $158.00 $326.00 | 233 | |
Rapamycin inhibits mTOR, a kinase involved in protein synthesis regulation; this could indirectly lower CPXM1 expression by affecting translation control mechanisms. | ||||||
α-Amanitin | 23109-05-9 | sc-202440 sc-202440A | 1 mg 5 mg | $269.00 $1050.00 | 26 | |
Alpha-amanitin inhibits RNA polymerase II, potentially reducing CPXM1 mRNA transcription and, consequently, protein expression. | ||||||
MG-132 [Z-Leu- Leu-Leu-CHO] | 133407-82-6 | sc-201270 sc-201270A sc-201270B | 5 mg 25 mg 100 mg | $60.00 $265.00 $1000.00 | 163 | |
MG132 inhibits proteasomes, potentially leading to feedback inhibition of CPXM1 expression due to accumulation of misfolded proteins and cellular stress responses. | ||||||
Chetomin | 1403-36-7 | sc-202535 sc-202535A | 1 mg 5 mg | $186.00 $674.00 | 10 | |
Chetomin disrupts hypoxia-inducible factor (HIF) pathways, which might downregulate CPXM1 expression by altering transcription under hypoxic conditions. | ||||||
Sodium Butyrate | 156-54-7 | sc-202341 sc-202341B sc-202341A sc-202341C | 250 mg 5 g 25 g 500 g | $31.00 $47.00 $84.00 $222.00 | 19 | |
Sodium Butyrate is a histone deacetylase inhibitor that could decrease CPXM1 expression by changing the chromatin structure surrounding its gene promoter. | ||||||
PD 98059 | 167869-21-8 | sc-3532 sc-3532A | 1 mg 5 mg | $40.00 $92.00 | 212 | |
PD98059 inhibits MEK, which may lead to reduced activation of transcription factors that control CPXM1 gene expression, thereby potentially reducing its expression. | ||||||