AWP1 Activators comprise a diverse array of chemical compounds that specifically enhance the functional activity of AWP1 through various signaling pathways, most notably those mediated by cyclic nucleotide second messengers. Forskolin, for example, is known to increase intracellular cAMP, thereby indirectly activating protein kinase A, which can phosphorylate AWP1 or proteins associated with AWP1, boosting its functional activity. Similarly, phosphodiesterase (PDE) inhibitors like IBMX and Rolipram increase cAMP levels, potentially enhancing AWP1's activity through the same PKA-mediated mechanisms. The PDE5 inhibitors Sildenafil and Zaprinast elevate cGMP levels, which may bolster AWP1 activity via cGMP-dependent protein kinase pathways. The intricate relationship between cyclic nucleotide signaling and AWP1 is further exemplified by L-NAME, which, by inhibiting nitric oxide synthase, may affect nitric oxide signaling pathways that have downstream effects on AWP1's activity.
Moreover, YC-1, through its sensitization of soluble guanylyl cyclase to nitric oxide, enhances cGMP synthesis that could indirectly upregulate AWP1 activity via PKG signaling. Anagrelide and cilostamide, both PDE3 inhibitors, raise cAMP levels that could lead to an increase in AWP1 activity, through mechanisms that involve cAMP-dependent pathways. Milrinone, another selective PDE3 inhibitor, and trequinsin, with its potent PDE3 inhibitory action, work similarly by elevating cAMP levels and thereby potentially enhancing AWP1 activity through PKA-dependent signaling. Vardenafil, as a PDE5 inhibitor, also playsa role in this intricate network by increasing cGMP levels, which could lead to an enhancement of AWP1 activity through cGMP-dependent signaling. Collectively, these AWP1 Activators work through nuanced molecular mechanisms that converge on the enhancement of AWP1 function by modulating the levels of key second messengers and the activity of associated kinases. The specificity and diversity of these chemical activators underscore the complex regulatory environment in which AWP1 operates, emphasizing the multifaceted nature of its activation and the potential precision with which its activity
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
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 potent activator of protein kinase C (PKC) which can modulate the activity of downstream proteins by phosphorylation. PKC-mediated phosphorylation could potentially enhance the functional activity of AWP1 by altering its interaction with binding partners or substrates. | ||||||
Forskolin | 66575-29-9 | sc-3562 sc-3562A sc-3562B sc-3562C sc-3562D | 5 mg 50 mg 1 g 2 g 5 g | $78.00 $153.00 $740.00 $1413.00 $2091.00 | 73 | |
Forskolin activates adenylate cyclase, leading to an increase in cAMP levels and subsequent activation of PKA. PKA can phosphorylate various proteins, potentially including AWP1, thereby enhancing its activity. | ||||||
Ionomycin, free acid | 56092-81-0 | sc-263405 sc-263405A | 1 mg 5 mg | $96.00 $264.00 | 2 | |
Ionomycin is a calcium ionophore that increases intracellular calcium levels, which can activate calcium-dependent protein kinases. These kinases could phosphorylate and enhance the activity of AWP1 within calcium-signaling pathways. | ||||||
8-Bromoadenosine 3′,5′-cyclic monophosphate | 23583-48-4 | sc-217493B sc-217493 sc-217493A sc-217493C sc-217493D | 25 mg 50 mg 100 mg 250 mg 500 mg | $108.00 $169.00 $295.00 $561.00 $835.00 | 2 | |
This cAMP analog is resistant to degradation and activates PKA, leading to the phosphorylation of substrates that might include AWP1, potentially enhancing its 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 known to inhibit certain protein kinases. By inhibiting kinases that usually phosphorylate inhibitory sites, EGCG could indirectly enhance AWP1 activity by reducing its inhibitory phosphorylation. | ||||||
Dibutyryl-cAMP | 16980-89-5 | sc-201567 sc-201567A sc-201567B sc-201567C | 20 mg 100 mg 500 mg 10 g | $47.00 $136.00 $492.00 $4552.00 | 74 | |
As another cAMP analog, dibutyryl cAMP activates PKA, potentially leading to the phosphorylation and activation of AWP1. | ||||||
Calyculin A | 101932-71-2 | sc-24000 sc-24000A | 10 µg 100 µg | $163.00 $800.00 | 59 | |
Calyculin A is an inhibitor of protein phosphatases 1 (PP1) and 2A (PP2A), which prevents the dephosphorylation of proteins. By inhibiting these phosphatases, AWP1 phosphorylation state could be maintained, thus enhancing 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 engages with G-protein-coupled receptors to activate downstream kinases, including PKC, possibly leading to the enhanced activity of AWP1 through phosphorylation. | ||||||
Okadaic Acid | 78111-17-8 | sc-3513 sc-3513A sc-3513B | 25 µg 100 µg 1 mg | $291.00 $530.00 $1800.00 | 78 | |
Similar to Calyculin A, Okadaic Acid is a potent inhibitor of PP1 and PP2A, potentially leading to an increased phosphorylation state and enhanced activity of AWP1. | ||||||
Anisomycin | 22862-76-6 | sc-3524 sc-3524A | 5 mg 50 mg | $99.00 $259.00 | 36 | |
Anisomycin is a protein synthesis inhibitor that can activate stress-activated protein kinases (SAPKs) indirectly. These kinases might phosphorylate AWP1, enhancing its activity as a response to stress signals. | ||||||