Date published: 2025-9-15

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CMTM2 Activators

Epigallocatechin gallate (EGCG) is known for its ability to modulate protein kinase C (PKC), which plays a pivotal role in cellular signaling and can lead to the upregulation of CMTM2. Dibutyryl-cAMP (db-cAMP) acts as a mimetic of cAMP and engages protein kinase A (PKA), which phosphorylates transcription factors, potentially enhancing the expression of CMTM2. Phorbol 12-myristate 13-acetate (PMA), like EGCG, activates PKC, setting off a cascade of events that can culminate in the upregulation of CMTM2. D-erythro-Sphingosine-1-phosphate, a bioactive lipid, binds to its receptors and can activate signaling pathways that influence the expression levels of CMTM2. Forskolin, by directly stimulating adenylyl cyclase, raises cAMP levels and can enhance the expression of CMTM2.

The calcium ionophore ionomycin increases intracellular calcium, a signal that can lead to the activation of pathways affecting CMTM2. Retinoic acid, which activates retinoic acid receptors, can influence gene expression profiles, including that of CMTM2. Curcumin interacts with multiple signaling pathways, some of which are known to regulate the expression of CMTM2. Sodium butyrate, as a histone deacetylase inhibitor, causes changes in chromatin structure, potentially leading to the activation of CMTM2 gene expression. LY294002, a PI3K inhibitor, and U0126 and PD98059, both MEK inhibitors, impact their respective pathways (AKT and ERK/MAPK) which can affect transcription factors and gene expression profiles related to CMTM2.

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