PKA IIα reg Inhibitors belong to a distinct chemical class that primarily targets a specific enzyme known as Protein Kinase A (PKA) IIα regulatory subunit. To understand the significance of these inhibitors, it's crucial to delve into the underlying molecular processes. PKA is a critical kinase enzyme involved in cellular signal transduction, and its activity is finely tuned by regulatory subunits, among which PKA IIα is one variant. These inhibitors are designed to specifically interact with and modulate the activity of PKA IIα regulatory subunits, effectively interfering with their regulatory function.
The core mechanism of PKA IIα reg Inhibitors revolves around their ability to bind selectively to the PKA IIα regulatory subunits, disrupting the normal PKA holoenzyme formation. Typically, PKA exists as a tetrameric complex composed of two catalytic subunits and two regulatory subunits. The regulatory subunits keep the catalytic subunits in an inactive state until cAMP (cyclic AMP) is bound, leading to the release of active catalytic subunits. PKA IIα reg Inhibitors, however, disrupt this process by binding tightly to the regulatory subunits, preventing cAMP-induced activation of PKA. This inhibition of PKA activity has far-reaching consequences on various cellular processes, making these inhibitors valuable tools in the study of signal transduction pathways and cell signaling cascades. Researchers utilize PKA IIα reg Inhibitors to gain insights into the roles of PKA in diverse biological contexts, furthering our understanding of cellular regulation and signaling mechanisms.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
H-89 dihydrochloride | 130964-39-5 | sc-3537 sc-3537A | 1 mg 10 mg | $94.00 $186.00 | 71 | |
H-89 is a selective inhibitor of PKA IIα that competes with ATP. It prevents phosphorylation of PKA IIα substrates by binding to the ATP binding site of the kinase, thus inhibiting its catalytic activity. | ||||||
KT 5720 | 108068-98-0 | sc-3538 sc-3538A sc-3538B | 50 µg 100 µg 500 µg | $138.00 $220.00 $972.00 | 47 | |
KT5720 is a potent PKA inhibitor that competes with ATP binding. It prevents PKA IIα activation by blocking the ATP-binding site, inhibiting the phosphorylation of downstream targets. | ||||||
PKA Inhibitor IV | 99534-03-9 | sc-3010 | 0.5 mg | $97.00 | 17 | |
PKI (5-24) is a peptide-based inhibitor that specifically targets the catalytic subunit of PKA IIα. It mimics the PKA substrate and competitively inhibits its phosphorylation by PKA IIα. | ||||||
Rp-8-CPT-cAMPS | 129735-01-9 | sc-215821 | 5 µmol | $726.00 | 2 | |
Rp-8-CPT-cAMPS is a cell-permeable cyclic AMP analog that selectively inhibits PKA IIα by binding to the regulatory subunit and preventing its dissociation from the catalytic subunit. | ||||||
PKI (6-22) amide | 121932-06-7 | sc-201160 | 1 mg | $160.00 | 11 | |
PKI (6-22) is another peptide-based inhibitor, acting as a competitive antagonist of PKA IIα. It mimics PKA substrates and hinders their phosphorylation by PKA IIα. | ||||||
KT5823 | 126643-37-6 | sc-3534 sc-3534A sc-3534B | 100 µg 1 mg 5 mg | $182.00 $1228.00 $4895.00 | 21 | |
KT5823 is a potent and selective inhibitor of PKA IIα. It suppresses PKA IIα activity by blocking the ATP-binding site, preventing the phosphorylation of PKA substrates. | ||||||
PKI (14-22) amide (myristoylated) | 201422-03-9 | sc-471154 | 0.5 mg | $135.00 | 2 | |
PKI (14-22) is a peptide inhibitor that mimics PKA substrates and competitively inhibits PKA IIα by blocking its catalytic activity, preventing substrate phosphorylation. | ||||||
Rp-8-Br-cGMPS | 208445-06-1 | sc-200323 | 500 µg | $275.00 | 9 | |
Rp-8-Br-cGMPS is a cyclic GMP analog that selectively inhibits PKA IIα by binding to the regulatory subunit, preventing its release from the catalytic subunit and inhibiting kinase activity. | ||||||