GRK
Le chinasi dei recettori accoppiati alle proteine G (GRK) sono una famiglia di enzimi che fosforilano i GPCR attivati, portando alla desensibilizzazione dei recettori e alla regolazione della segnalazione dei recettori. Le GRK svolgono un ruolo cruciale nel controllo dell'intensità e della durata della segnalazione dei GPCR, rendendole importanti nella regolazione di vari processi fisiologici, tra cui la funzione cardiovascolare, la risposta immunitaria e la neurotrasmissione. Gli inibitori e gli attivatori delle GRK sono studiati per le loro potenziali applicazioni terapeutiche nell'insufficienza cardiaca, nel cancro e nei disturbi neurologici. Presso CymitQuimica, offriamo una gamma di modulatori delle GRK di alta qualità per supportare la tua ricerca nella trasduzione del segnale, nella regolazione dei recettori e nello sviluppo terapeutico.
Trovati 31 prodotti di "GRK"
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CMPD101
CAS:<p>CMPD101 is a membrane-permeable small-molecule inhibitor of GRK2/3 (IC50: 18 nM and 5.4 nM).</p>Formula:C24H21F3N6OPurezza:99.01% - 99.04%Colore e forma:SolidPeso molecolare:466.46Corazonin
CAS:<p>Corazonin, a neuropeptide in insects, regulates caste identity and behavior, mainly in workers/foragers.</p>Formula:C62H83N17O19Colore e forma:SolidPeso molecolare:1370.42CCG258208 hydrochloride
<p>GRKs-IN-1 HCl (14as) strongly inhibits GRK2 (IC50=130nM) & GRK5 (IC50=7.1μM), is a paroxetine derivative with 100x cardiac boost.</p>Colore e forma:SolidGRL018-21
<p>GRL018-21 is a potent, highly selective inhibitor of G protein-coupled receptor kinase 5 (GRK5), exhibiting an IC50 of 10 nM [1].</p>Colore e forma:Odour SolidGSK270822A
CAS:<p>GSK270822A is a selective ROCK1 inhibitor. GSK270822A exhibits IC50 of 9nM, 1100nM, 1550nM for ROCK1, RSK1, p70S6K, respectively.</p>Formula:C24H20N4O2Purezza:98.64% - 99.78%Colore e forma:SolidPeso molecolare:396.44GRK-IN-1
CAS:<p>4-Amino-5-(bromomethyl)-2-methylpyrimidine used in vitamin B1 analogs and esters synthesis.</p>Formula:C6H10Br3N3Colore e forma:SolidPeso molecolare:363.879Endothelin-3, human, mouse, rabbit, rat
CAS:<p>Endothelin-3, human, mouse, rabbit, rat , is a cyclic 21 amino acid peptide. It is an endogenous neuropeptide and potent vasoconstrictor.</p>Formula:C121H168N26O33S4Purezza:98%Colore e forma:SolidPeso molecolare:2643.04GRK2i
CAS:<p>GRK2 inhibitory polypeptide that specifically inhibits Gβγ activation of GRK2. Corresponds to the Gβγ-binding domain and acts as a cellular Gβγ antagonist.</p>Formula:C153H256N50O41SPurezza:98%Colore e forma:SolidPeso molecolare:3484.08GRK2-IN-1 hydrochloride (2055990-90-2 free base)
<p>GRKs-IN-1 hydrochloride has remarkable potency against and selectivity for G protein-coupled receptor kinase 2 GRK2 (IC50: 130 nM) and GRK5 (IC50: 7.1 μM).</p>Formula:C24H26ClFN4O4Purezza:98%Colore e forma:SolidPeso molecolare:488.94GRL093-22
<p>GRL093-22 is an effective and selective inhibitor of G protein-coupled receptor kinases (GRK), with IC50 values of 60 nM for GRK5 and 40 nM for GRK6. It shows potential for research in heart failure and multiple myeloma.</p>Formula:C33H29FN6O3Colore e forma:SolidPeso molecolare:576.62GSK180736A
CAS:<p>GSK180736A: GRK2 inhibitor (IC50 0.77µM), >100x selectivity vs GRKs, weak at PKA (IC50 30µM), strong vs ROCK1 (IC50 100nM).</p>Formula:C19H16FN5O2Purezza:98.38% - 98.98%Colore e forma:SolidPeso molecolare:365.36CCG215022
CAS:<p>CCG215022 is a G protein-coupled receptor kinases (GRKs) inhibitor with IC50s of 0.15±0.07 μM, 0.38±0.06 μM and 3.9±1 μM for GRK2, 5 and 1, respectively.</p>Formula:C26H22FN7O3Purezza:97.63% - 99.69%Colore e forma:SolidPeso molecolare:499.51-(2,3-DIHYDRO-BENZO[1,4]DIOXIN-6-YL)-5-OXO-PYRROLIDINE-3-CARBOXYLIC ACID
CAS:<p>1-(2,3-DIHYDRO-BENZO[1,4]DIOXIN-6-YL)-5-OXO-PYRROLIDINE-3-CARBOXYLIC ACID targets GRK2.</p>Formula:C13H13NO5Purezza:99.55%Colore e forma:SolidPeso molecolare:263.25Takeda103A
CAS:<p>Takeda103A (CMPD103A) is the GRK2-dependent bovine tubulin oxidation effective inhibitor.</p>Formula:C24H23F2N7OPurezza:97.17%Colore e forma:SolidPeso molecolare:463.48GRK6-IN-2
CAS:<p>GRK6-IN-2 is a potent G protein-coupled receptor kinase 6 (GRK6) inhibitor with potential antitumor activity.GRK6-IN-2 has been studied in multiple myeloma.</p>Formula:C21H21FN6Purezza:98.94%Colore e forma:SolidPeso molecolare:376.43KR-39038
CAS:<p>KR-39038 is an oral GRK5 inhibitor for heart failure research; blocks HDAC5 pathway, IC50: 0.02 μM, fights cardiac hypertrophy.</p>Formula:C24H32ClFN6OColore e forma:SolidPeso molecolare:475.00GRK5-IN-3
CAS:<p>GRK5-IN-3 is a covalent inhibitor of G protein-coupled receptor kinase 5 (GRK5).GRK5-IN-3 significantly inhibits GRK5 (IC50: 0.22 μM) and GRK6 (IC50: 0.41 μM).</p>Formula:C23H21N7O3Colore e forma:SolidPeso molecolare:443.46GSK317354A
CAS:<p>GSK317354A is a GRK2 inhibitor.</p>Formula:C25H18F4N6OColore e forma:SolidPeso molecolare:494.44CCG-271423
CAS:<p>CCG-271423: potent GRK5 inhibitor (IC50: 0.0021 μM), less on GRK2 (IC50: 44 μM); lowers Ca2+ events and heart cell contractility.</p>Formula:C28H26N4O3Colore e forma:SolidPeso molecolare:466.53GRK5-IN-4
CAS:<p>GRK5-IN-4: potent, selective covalent inhibitor of GRK5 (IC50=1.1 μM), 90x more specific than GRK2, useful for heart failure research.</p>Formula:C26H25N7O3Colore e forma:SolidPeso molecolare:483.52
![1-(2,3-DIHYDRO-BENZO[1,4]DIOXIN-6-YL)-5-OXO-PYRROLIDINE-3-CARBOXYLIC ACID](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2FTM%2Fthumb-webp%2FT8913.webp&w=3840&q=75)
