BC023882 Activators are a collection of chemical compounds that indirectly enhance the functional activity of BC023882 through various signaling pathways. Compounds such as Forskolin and IBMX raise intracellular cAMP levels, with Forskolin activating adenylyl cyclase and IBMX inhibiting phosphodiesterases. The resulting increased cAMP may activate protein kinase A (PKA), which could then phosphorylate and activate BC023882 should it serve as a PKA substrate. Similarly, PMA's role as a protein kinase C (PKC) activator could promote the phosphorylation of BC023882, assuming it is a target of PKC-mediated signaling. The impact of Okadaic acid, as an inhibitor of phosphatases, could also lead to the augmentation of BC023882 activity by preventing its dephosphorylation. Meanwhile, Epigallocatechin gallate (EGCG) and Sphingosine-1-phosphate (S1P) could modulate oxidative stress and sphingolipid receptor pathways, respectively,to enhance BC023882's activity if it is integrated into these response mechanisms.
Furthermore, the use of specific kinase inhibitors like LY294002, U0126, SB203580, and Genistein could indirectly enhance BC023882's activity by inhibiting dominant pathways and thus potentially activating compensatory mechanisms that involve BC023882. LY294002 and U0126, which target PI3K and MEK respectively, may lead to the upregulation of alternative pathways that impinge upon BC023882's functionality. SB203580's inhibition of p38 MAPK and Genistein's inhibition of tyrosine kinases also provide a potential for shifting signaling dynamics in favor of pathways that activate BC023882. Additionally, A23187 (Calcimycin) and KN-93, through their actions on calcium signaling, could influence BC023882's activity; A23187 by increasing intracellular calcium levels and thereby activating calcium-sensitive pathways, and KN-93 by inhibiting CaMKII, possibly leading to the activation of BC023882 through alternative calcium-responsive routes. Collectively, these chemical activators, by targeting specific pathways, create a conducive cellular environment for the enhanced activity of BC023882, showcasing a complex network of indirect activations.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
IBMX | 28822-58-4 | sc-201188 sc-201188B sc-201188A | 200 mg 500 mg 1 g | $260.00 $350.00 $500.00 | 34 | |
IBMX is a non-selective inhibitor of phosphodiesterases, which degrade cAMP and cGMP. By preventing cAMP degradation, IBMX can indirectly enhance the activation of PKA, which in turn could lead to the phosphorylation and activation of BC023882. | ||||||
PMA | 16561-29-8 | sc-3576 sc-3576A sc-3576B sc-3576C sc-3576D | 1 mg 5 mg 10 mg 25 mg 100 mg | $41.00 $132.00 $214.00 $500.00 $948.00 | 119 | |
PMA is a diacylglycerol analog that activates protein kinase C (PKC). If BC023882 is regulated by PKC-mediated phosphorylation, PMA could enhance its activity. | ||||||
Okadaic Acid | 78111-17-8 | sc-3513 sc-3513A sc-3513B | 25 µg 100 µg 1 mg | $291.00 $530.00 $1800.00 | 78 | |
Okadaic acid is a potent inhibitor of protein phosphatases 1 and 2A, leading to increased phosphorylation levels in the cell. If BC023882's activity is regulated by phosphorylation, okadaic acid could enhance its functional activity. | ||||||
(−)-Epigallocatechin Gallate | 989-51-5 | sc-200802 sc-200802A sc-200802B sc-200802C sc-200802D sc-200802E | 10 mg 50 mg 100 mg 500 mg 1 g 10 g | $43.00 $73.00 $126.00 $243.00 $530.00 $1259.00 | 11 | |
EGCG is a catechin found in green tea with antioxidant properties. It can modulate various signaling pathways, and if BC023882 is involved in oxidative stress response, EGCG could enhance its activity. | ||||||
D-erythro-Sphingosine-1-phosphate | 26993-30-6 | sc-201383 sc-201383D sc-201383A sc-201383B sc-201383C | 1 mg 2 mg 5 mg 10 mg 25 mg | $165.00 $322.00 $570.00 $907.00 $1727.00 | 7 | |
S1P is a bioactive lipid that activates sphingosine-1-phosphate receptors, leading to diverse cellular responses. If BC023882 is part of the S1P signaling pathway, S1P could enhance its activity. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $123.00 $400.00 | 148 | |
LY294002 is an inhibitor of phosphoinositide 3-kinases (PI3K). By inhibiting PI3K, it may lead to activation of compensatory pathways that could enhance the activity of BC023882 if it is a part of such pathways. | ||||||
U-0126 | 109511-58-2 | sc-222395 sc-222395A | 1 mg 5 mg | $64.00 $246.00 | 136 | |
U0126 is an inhibitor of mitogen-activated protein kinase kinase (MEK), which may lead to the activation of alternative pathways that could enhance BC023882 activity if it is associated with those pathways. | ||||||
SB 203580 | 152121-47-6 | sc-3533 sc-3533A | 1 mg 5 mg | $90.00 $349.00 | 284 | |
SB203580 is an inhibitor of p38 MAPK. Inhibition of p38 MAPK can shift the signaling balance to activate alternative pathways, potentially enhancing the activity of BC023882 if it is connected to these pathways. | ||||||
A23187 | 52665-69-7 | sc-3591 sc-3591B sc-3591A sc-3591C | 1 mg 5 mg 10 mg 25 mg | $55.00 $131.00 $203.00 $317.00 | 23 | |
A23187 is a calcium ionophore that increases intracellular calcium levels, which could activate calcium-dependent signaling pathways and thereby enhance the activity of BC023882 if it is calcium-sensitive. | ||||||
KN-93 | 139298-40-1 | sc-202199 | 1 mg | $182.00 | 25 | |
KN-93 is an inhibitor of calcium/calmodulin-dependent protein kinase II (CaMKII). Inhibition of CaMKII can lead to activation of alternative pathways that could enhance the activity of BC023882 if it is part of such pathways. | ||||||