Date published: 2025-9-18

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FAM26D Inhibitors

Chemical inhibitors of FAM26D can achieve functional inhibition through various intracellular signaling pathways. Staurosporine is a broad-spectrum kinase inhibitor with high affinity for protein kinase C, which is a pivotal enzyme in numerous cellular processes, including those that may regulate the activity of FAM26D. By inhibiting protein kinase C, Staurosporine can disrupt the phosphorylation events necessary for FAM26D to function properly within its cellular context. Similarly, GF109203X targets protein kinase C, which likely influences the functional state of FAM26D by preventing necessary phosphorylation. Wortmannin and LY294002 both act as inhibitors of phosphoinositide 3-kinases (PI3K), a family of enzymes involved in cellular functions such as proliferation, differentiation, and survival. By blocking PI3K activity, these inhibitors can suppress downstream signaling events that would otherwise contribute to the normal function of FAM26D. This suppression can lead to a decrease in FAM26D activity, which is integral to its role in cellular signaling pathways.

Moreover, U0126, SB203580, PD98059, and SP600125 target different kinases within the mitogen-activated protein kinase (MAPK) pathway, such as MEK1/2, p38 MAP kinase, and c-Jun N-terminal kinase (JNK). These kinases are integral to cellular responses like inflammation, differentiation, and apoptosis, all of which can intersect with the functional role of FAM26D. Specifically, U0126 and PD98059 block MEK, which in turn prevents the activation of ERK, potentially inhibiting processes that require FAM26D activity. SB203580's selective inhibition of p38 MAP kinase, and SP600125's inhibition of JNK, can also alter the cellular environment in a way that inhibits the function of FAM26D. Rapamycin, an mTOR inhibitor, disrupts a central regulatory pathway for cell growth, which can indirectly lead to the inhibition of FAM26D by altering the cellular growth conditions in which FAM26D operates. Lastly, PP2 and AG490 inhibit Src family kinases and JAK2, respectively, both of which are involved in pathways that regulate cellular proliferation, differentiation, and the immune response, all potentially intersecting with FAM26D's role within these pathways. PD173074's inhibition of FGFR and VEGFR, kinases involved in processes such as angiogenesis, can also perturb the signaling milieu of FAM26D, leading to its inhibition.

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