Date published: 2025-10-13

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BC002230 Activators

BC002230 activators encompass a diverse set of chemical compounds that amplify the functional activity of BC002230 through distinct signaling pathways. Forskolin, for instance, by raising intracellular cAMP levels, indirectly amplifies BC002230's functional activity by enabling PKA-mediated phosphorylation, a key modification for BC002230 activation. The use of PMA as a PKC activator also contributes to the enhancement of BC002230 by facilitating phosphorylation events that promote BC002230's involvement in cellular proliferation and differentiation pathways. EGCG, through its kinase inhibitory action, allows for the enhanced activity of BC002230 by preventing phosphorylation-mediated inactivation, while sphingosine-1-phosphate boosts BC002230 activity by engaging sphingolipid signaling leading to phosphorylation. Ionomycin's calcium mobilization can further potentiate BC002230 through the activation of calcium-dependent kinases, which underscores the multifaceted nature of BC002230 activation mechanisms.

Once a compound has successfully passed these rigorous initial tests, it undergoes a series of analytical procedures to detail its interaction with BC002230. Structural characterization techniques like X-ray crystallography or nuclear magnetic resonance (NMR) spectroscopy can provide a detailed view of the compound's binding site and reveal the precise nature of its interaction with BC002230. Such structural insights are invaluable as they lay the groundwork for understanding the molecular basis of activation. Alongside these structural studies, biophysical methods such as surface plasmon resonance (SPR) and isothermal titration calorimetry (ITC) offer quantitative data on the binding kinetics and thermodynamics. These data points are critical for elucidating how readily and robustly the activators associate and dissociate from BC002230, which can inform the development of compounds with optimal binding characteristics. In parallel, structure-activity relationship (SAR) studies are conducted to dissect the relationship between the activators' chemical structure and their ability to modulate BC002230.

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