Date published: 2025-9-14

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UBAP1L Activators

UBAP1L Activators are a diverse set of chemical compounds that indirectly augment the functional activity of UBAP1L through the modulation of various signaling pathways. Compounds like Forskolin and Epigallocatechin gallate (EGCG) work by activating adenylate cyclase to increase cAMP levels or inhibiting certain kinases, respectively. These actions can lead to the activation of pathways that involve PKA or reduce competitive kinase signaling, which may result in an environment where UBAP1L's role in cellular processes, such as endocytic trafficking, is enhanced. Similarly, bioactive lipids like Sphingosine-1-phosphate (S1P) and calcium ionophores such as Ionomycin and A23187 indirectly influence UBAP1L's activity by engaging S1P receptors or elevating intracellular calcium levels, thereby affecting cytoskeletal rearrangements and protein sorting, where UBAP1L may play crucial roles. Phorbol 12-myristate 13-acetate (PMA) activates PKC, leading to a downstream effect on cell signaling that could amplify UBAP1L-mediated endocytic pathways, while LY294002 and U0126 target the PI3K/Akt and MAPK/ERK pathways, potentially allowing for greater UBAP1L activity by decreasing inhibitory influences within those pathways.

The activity of UBAP1L is further influenced by inhibitors like Staurosporine, which, despite its broad-spectrum kinase inhibition, may inadvertently favor UBAP1L's involvement by lifting the inhibition of kinases that negatively regulate UBAP1L-associated signaling. The calmodulin antagonist W-7 and the selective PKC inhibitor Gö6976 also play a role in modulating signaling networks that could lead to the enhancement of UBAP1L's function by disrupting calcium-calmodulin-dependent processes or conventional PKCs, respectively. These compounds collectively contribute to a signaling milieu that can indirectly enhance the functional activity of UBAP1L, by either promoting signaling events that require UBAP1L-mediated processes or by altering the cellular context to necessitate UBAP1L's roles in processes such as ubiquitin-dependent signaling, endosomal sorting, and vesicle trafficking.

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