PKA
La proteina chinasi A (PKA) è un enzima chiave nella cascata di segnalazione dei GPCR, attivato dall'AMP ciclico (cAMP) in risposta a vari segnali extracellulari. La PKA regola una vasta gamma di processi cellulari, tra cui il metabolismo, l'espressione genica e la crescita cellulare. La disregolazione dell'attività della PKA è associata a varie malattie, tra cui il cancro, i disturbi metabolici e le condizioni cardiovascolari. I modulatori della PKA sono strumenti preziosi nella ricerca volta a comprendere le vie di segnalazione dei GPCR e a sviluppare nuove strategie terapeutiche. Presso CymitQuimica, offriamo una selezione di modulatori della PKA di alta qualità per supportare la tua ricerca nella trasduzione del segnale, nella regolazione cellulare e nei meccanismi delle malattie.
Trovati 58 prodotti per "PKA".
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STAD 2
CAS:STAD-2 is a cell permeable akap disruptor, selectively binding to pka-rii and blocking the interaction of pka-ri with akapFormula:C102H182N24O22Colore e forma:SolidPeso molecolare:2096.724(2S,4R)-DS89002333
(2S,4R)-DS89002333 is an enantiomer of DS89002333 and functions as an orally active PRKACA inhibitor, exhibiting an IC50 of 0.3 nM.Formula:C22H20ClF2N3O3Peso molecolare:447.11613PKA Inhibitor Fragment (6-22) amide TFA
PKA Inhibitor Fragment (6-22) amide TFA (PKA Inhibitor Fragment (6-22) amide TFA) is an inhibitor of cAMP-dependent protein kinase A (PKA).Formula:C82H131F3N28O26Purezza:99.61% - 99.87%Colore e forma:White SolidPeso molecolare:1982.08Kemptide
CAS:Kemptide is a synthetic heptapeptide, acting as a substrate for cAMP-dependent protein kinase (PK).Formula:C24H46N10O6Purezza:98%Colore e forma:SolidPeso molecolare:570.6854RI-STAD-2
RI-STAD-2 is a high-affinity peptide that interferes with the regulatory subunit RI of protein kinase A (PKA). It disrupts the binding between A-kinase anchoring proteins (AKAPs) and PKA-RI by mimicking the α-helical domain of AKAPs, interacting with the dimerization/docking (D/D) domain of PKA-RI. This disruption affects the activity and intracellular localization of PKA. RI-STAD-2 is utilized in studying the role of AKAPs and PKA-RI interactions in pathological processes such as cardiovascular diseases and cancer.Formula:C109H181N25O35Colore e forma:SolidPeso molecolare:2400.31519PKItide
CAS:PKItide demonstrates an inhibitory concentration 50 (IC50) of 0.2 μM against cAMP-dependent protein kinase (cAMP-PK) [1].Formula:C85H149N31O24Purezza:98%Colore e forma:SolidPeso molecolare:1989.29PKA-IN-1
CAS:PKA-IN-1 is a selective and potent cyclic AMP-dependent protein kinase (PKA) catalytic subunit (cAK) inhibitor (IC50: 0.03 μM).PKA-IN-1 can be used to studyFormula:C13H11N3OPurezza:99.12%Colore e forma:SolidPeso molecolare:225.2459AP-C2
CAS:AP-C2 is a potent small molecule guanosine 3',5'-cyclic monophosphate (cGMP)-dependent protein kinase II (cGKII) inhibitor with a pIC50 of 5.2 for cGKII.Formula:C18H16N4SPurezza:99.99%Colore e forma:SolidPeso molecolare:320.41PKA/AKAP-IN-2
CAS:PKA/AKAP-IN-2 (WAY-298350) is a PKA and AKAP interaction inhibitor, used in metabolic disease research.Formula:C17H17NO3Purezza:99.82%Colore e forma:SolidPeso molecolare:283.3218Detrothyronine
CAS:Detrothyronine is a biochemical.Formula:C15H12I3NO4Purezza:99.64%Colore e forma:SolidPeso molecolare:650.97DT-3 acetate
DT-3 acetate is a cell-permeable peptide that acts as an inhibitor of protein kinase G (PKGIα), effectively blocking the cGMP-PKG signaling pathway.Formula:C152H258N52O28S·xC2H4O2Colore e forma:SolidPeso molecolare:3294.07 (free acid)PKA inhibitor fragment (6-22) amide Acetate
PKA inhibitor fragment (6-22) amide Acetate is a synthetic peptide which selectively inhibits PKA activity by binding to its substrate site (IC50 < 2 nM).Formula:C82H134N28O26Purezza:99.72%Colore e forma:SolidPeso molecolare:1928.11Fasudil dihydrochloride
CAS:Fasudil dihydrochloride inhibits ROCK1/2, PKA, PKC, PKG, and acts as a Ca²⁺ channel blocker and vasodilator, supporting vascular, cardiovascular, and signaling research.Formula:C14H19Cl2N3O2SPurezza:99.86%Colore e forma:White SolidPeso molecolare:364.291Fasudil hydrochloride
CAS:Fasudil hydrochloride (HA-1077) is a potent inhibitor of ROCK1, PKA, PKC, and MLCK with Ki of 0.33 μM, 1.0 μM, 9.3 μM and 55 μM, respectively.Formula:C14H18ClN3O2SPurezza:99.54% - ≥95%Colore e forma:White SolidPeso molecolare:327.83AT13148
CAS:AT13148 is an oral-active and ATP-competitive, multi-AGC kinase inhibitor for Akt1/2/3, p70S6K, PKA, and ROCKI/II.Formula:C17H16ClN3OPurezza:98.04% - ≥95%Colore e forma:SolidPeso molecolare:313.781H-89 dihydrochloride
CAS:H-89 dihydrochloride (5-Isoquinolinesulfonamide) is a potent inhibitor of protein kinase A (PKA; IC50: 0.14 μM, Ki: 48 nM).Formula:C20H22BrCl2N3O2SPurezza:98.22% - >99.99%Colore e forma:SolidPeso molecolare:519.283Staurosporine
CAS:Staurosporine (AM-2282) is a protein kinase inhibitor with ATP-competitive and non-selective inhibitory activity (IC50=6/15/2/3/3000 nM) against PKC, PKA, c-FgrFormula:C28H26N4O3Purezza:99.24% - 99.86%Colore e forma:SolidPeso molecolare:466.53Metadoxine
CAS:Metadoxine (Metadoxil) is a neurotransmitter stimulant.Formula:C13H18N2O6Purezza:99.19%Colore e forma:White SolidPeso molecolare:298.29188-Bromo-cAMP sodium salt
CAS:8-Bromo-cAMP sodium salt (8-Br-Camp sodium salt) is a long-acting derivative of cyclic AMP. 8-Bromo-cAMP is an activator of cyclic AMP-dependent protein kinase.Formula:C10H10BrN5NaO6PPurezza:98% - 99.94%Colore e forma:White SolidPeso molecolare:430.08AT7867
CAS:AT7867 inhibits Akt1/2/3 & p70S6K/PKA (IC50: 32/17/47 nM & 85/20 nM), minimal effect beyond AGC kinases.Formula:C20H20ClN3Purezza:99.63%Colore e forma:SolidPeso molecolare:337.846
