CPI-17 activators are a class of chemical compounds with the unique ability to interact with and modulate the activity of protein kinase C-potentiated myosin phosphatase inhibitor 1 (CPI-17). CPI-17 is a regulatory protein involved in the modulation of smooth muscle contraction, and plays an essential role in the regulation of various physiological processes, particularly in the smooth muscle tissues of the cardiovascular and gastrointestinal systems. CPI-17 activators are compounds that can influence CPI-17 activation, phosphorylation or interactions, thereby impacting smooth muscle tone, contractility and other cellular processes associated with the regulation of muscle function.
The mechanism of action of CPI-17 activators generally involves their ability to modulate the phosphorylation state of CPI-17. CPI-17 functions as an inhibitor of myosin phosphatase, a key enzyme responsible for the dephosphorylation of myosin light chain (MLC) in smooth muscle cells. When CPI-17 is phosphorylated, it becomes active and inhibits myosin phosphatase, resulting in increased levels of phosphorylated MLC and enhanced smooth muscle contraction. Activators can increase or inhibit IPC-17 phosphorylation, thus affecting its activity and ability to modulate smooth muscle contractility. In addition, they may influence the interactions of CPI-17 with other regulatory or scaffolding proteins, which may further regulate its function in smooth muscle tissue. Understanding the properties and effects of CPI-17 activators is important in the field of smooth muscle physiology and contractility, as it enhances our understanding of the molecular mechanisms that govern muscle tone and contraction, which are essential for various physiological processes such as blood vessel constriction and gastrointestinal motility. It contributes to our understanding of how specific compounds can modulate muscle function and influence the regulation of smooth muscle contractility.
VOIR ÉGALEMENT...
| Nom du produit | CAS # | Ref. Catalogue | Quantité | Prix HT | CITATIONS | Classement |
|---|---|---|---|---|---|---|
PMA | 16561-29-8 | sc-3576 sc-3576A sc-3576B sc-3576C sc-3576D | 1 mg 5 mg 10 mg 25 mg 100 mg | $40.00 $129.00 $210.00 $490.00 $929.00 | 119 | |
La PMA est un puissant activateur de la protéine kinase C (PKC), qui peut à son tour phosphoryler et activer l'IPC-17. | ||||||
Rottlerin | 82-08-6 | sc-3550 sc-3550B sc-3550A sc-3550C sc-3550D sc-3550E | 10 mg 25 mg 50 mg 1 g 5 g 20 g | $82.00 $163.00 $296.00 $2050.00 $5110.00 $16330.00 | 51 | |
La rottlerine est connue pour moduler la PKC, en particulier la PKC delta, ce qui peut indirectement influencer l'activité de l'IPC-17. | ||||||
Calyculin A | 101932-71-2 | sc-24000 sc-24000A sc-24000C | 10 µg 100 µg 1 mg | $160.00 $750.00 $3000.00 | 59 | |
La caliculine A inhibe les protéines phosphatases, telles que PP1, ce qui pourrait accroître l'inhibition de la MLCP médiée par l'IPC-17. | ||||||
Okadaic Acid | 78111-17-8 | sc-3513 sc-3513A sc-3513B | 25 µg 100 µg 1 mg | $285.00 $520.00 $1300.00 | 78 | |
Comme la caliculine A, l'acide okadaïque inhibe PP1 et PP2A, ce qui renforce indirectement l'activité de l'IPC-17. | ||||||
Ruboxistaurin | 169939-94-0 | sc-507364 | 25 mg | $1080.00 | ||
La ruboxistaurine est un inhibiteur sélectif de la PKC bêta, qui pourrait moduler indirectement la fonction de l'IPC-17. | ||||||
Balanol | 63590-19-2 | sc-503251 | 10 mg | $13500.00 | ||
Le balanol est un inhibiteur ATP-compétitif de la PKC, qui affecte indirectement l'activité de l'IPC-17. | ||||||
LY-333,531 Hydrochloride | 169939-93-9 | sc-364215 sc-364215A | 1 mg 5 mg | $92.00 $281.00 | 6 | |
Également connu sous le nom de Ruboxistaurin, il inhibe sélectivement la PKC bêta, affectant potentiellement le CPI-17. | ||||||