
Chinasi di serina/treonina
Gli inibitori delle chinasi serina/treonina sono composti che prendono di mira gli enzimi responsabili della fosforilazione dei residui di serina e treonina sulle proteine, i quali svolgono un ruolo cruciale nella regolazione dell'apoptosi e di altri processi cellulari. Queste chinasi sono coinvolte in vie di segnalazione che controllano la crescita, la divisione e la morte cellulare programmata. Inibire specifiche chinasi serina/treonina può alterare l'equilibrio tra sopravvivenza cellulare e apoptosi, rendendo questi inibitori strumenti essenziali nella ricerca sul cancro e in altre aree della biologia cellulare. Presso CymitQuimica, offriamo una selezione completa di inibitori delle chinasi serina/treonina di alta qualità per supportare la tua ricerca in apoptosi, trasduzione del segnale e meccanismi delle malattie.
Trovati 20 prodotti per "Chinasi di serina/treonina".
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BMT-124110 Formate
BMT-124110 Formate is a selective AAK1 inhibitor (IC50: 0.9 nM) with anti-injury sensory activity.BMT-124110 Formate inhibits the BMP-2-inducible protein kinase
Formula:C22H20N2O2Purezza:99.52%Colore e forma:SoildPeso molecolare:344.41CRA-2059
CAS:CRA-2059 is a selective and reversible inhibitor of human tryptase beta, exhibiting a Ki value of 620 pM against recombinant human tryptase beta (rHTβ).Formula:C34H46N12O8Purezza:97.68% - 99.29%Colore e forma:White SolidPeso molecolare:750.82TLK1-IN-1
TLK1-IN-1 (Compound 5n) is a TLK1 inhibitor with an IC50 of 7.2 μM for TLK1B and a GI50 of 2.7 μM for LNCaP cells. It induces DNA damage and apoptosis (Apoptosis) in cancer cells and is applicable in prostate cancer research.Formula:C24H23BrClN5O3Colore e forma:SoildPeso molecolare:544.831,8-Diazanaphthalene
CAS:1,8-Diazanaphthalene inhibits Protein Kinase B with a binding constant Ka=407 μM.Formula:C8H6N2Colore e forma:SolidPeso molecolare:130.15Tilpisertib
CAS:Tilpisertib is a serine/threonine kinase inhibitor (WO2017007689).Formula:C33H33ClN8OColore e forma:SolidPeso molecolare:593.13kb NB 142-70
CAS:kb NB 142-70 is a selective protein kinase D (PKD) inhibitor (IC50 values are 28.3, 58.7 and 53.2 nM for PKD1, 2 and 3 respectively).Formula:C11H9NO2S2Purezza:98.15% - ≥95%Colore e forma:SolidPeso molecolare:251.32GAK inhibitor 49
CAS:GAK inhibitor 49 is a highly selective and ATP-competitive cyclin G associated kinase (GAK) inhibitor (IC50: 56 nM; Ki: 0.54 nM ).Formula:C20H22N2O5Purezza:98.71%Colore e forma:SolidPeso molecolare:370.4Ref: TM-T8535
1mg54,00€5mg111,00€1mL*10mM (DMSO)128,00€10mg177,00€25mg299,00€50mg430,00€100mg587,00€200mg792,00€1-Naphthyl PP1
CAS:1-Naphthyl PP1 (1-NA-PP 1) is a selective src inhibitor(v-Src and c-Fyn, c-Abl, CDK2 and CAMK II with IC50s of 1.0, 0.6, 0.6, 18 and 22 μM, respectively)Formula:C19H19N5Purezza:99.85%Colore e forma:White Cyrstalline SolidPeso molecolare:317.39CID 2011756
CAS:CID 2011756 is an ATP-competitive and specific PKD1 inhibitor.Formula:C22H21ClN2O3Purezza:98.15% - ≥95%Colore e forma:SolidPeso molecolare:396.87SPHINX31
CAS:SPHINX31 is a potent inhibitor of serine/arginine-rich protein kinase 1 (SRPK1; IC50: 5.9 nM).Formula:C27H24F3N5O2Purezza:99.3% - 99.87%Colore e forma:SolidPeso molecolare:507.51Ref: TM-T5194
1mg38,00€5mg79,00€10mg92,00€1mL*10mM (DMSO)93,00€25mg170,00€50mg255,00€100mg408,00€500mg945,00€SGC-GAK-1
CAS:SGC-GAK-1 is a selective cyclin G-associated kinase (GAK) inhibitor (Ki: 3.1 nM).Formula:C18H17BrN2O3Purezza:99.85%Colore e forma:SolidPeso molecolare:389.24CID755673
CAS:CID755673 inhibits PKD (IC50: 182 nM), with selectivity over PLK1, AKT, CAMKIIα, CAK, PKC.Formula:C12H11NO3Purezza:97.68% - 99.84%Colore e forma:SolidPeso molecolare:217.22PKD-IN-1
CAS:CRT0066101 is an inhibitor of PKD.Formula:C18H19ClN4OPurezza:98%Colore e forma:SolidPeso molecolare:342.82MLCK inhibitor peptide 18 acetate
MLCK inhibitor peptide 18 acetate: Selective (IC50=50nM), 4000x more than CaM kinase II. Does not block PKA. Cell-permeable.Formula:C62H109N23O13Purezza:99.57%Colore e forma:SolidPeso molecolare:1384.67SRPIN340
CAS:SRPIN340 (SRPK inhibitor), a serine/arginine-rich protein kinase (SRPK)-specific inhibitor, is potent for SRPK1 (IC50 = 0.89 uM).Formula:C18H18F3N3OPurezza:99.79% - 99.96%Colore e forma:SolidPeso molecolare:349.35Ref: TM-T1954
2mg44,00€5mg65,00€1mL*10mM (DMSO)71,00€10mg100,00€25mg177,00€50mg324,00€100mg421,00€500mg945,00€SRPKIN-1
CAS:SRPKIN-1 is a covalent and irreversible inhibitor of SRPK1/2 (IC50s: 35.6 and 98 nM, respectively).Formula:C27H21FN2O3SPurezza:98%Colore e forma:SolidPeso molecolare:472.53Protein kinase inhibitor 14
CAS:Protein kinase inhibitor 14 (Compound 13) exhibits inhibitory effects on various serine/threonine kinases and receptor/non-receptor tyrosine kinases.Formula:C22H22F2N6OColore e forma:SolidPeso molecolare:424.447Anti-neuroinflammation agent 3
CAS:Compound A.10.3 (Anti-neuroinflammation agent 3) exhibits inhibitory activity against various Ser/Thr kinases or receptor/non-receptor tyrosine kinases.Formula:C22H23FN6O2Colore e forma:SolidPeso molecolare:422.455MASTL-IN-3
CAS:MASTL-IN-3 (compound 60) is an effective MASTL inhibitor (pIC50 = 9.10 M) exhibiting antiproliferative activity.Formula:C17H17F2N9Purezza:99.57%Peso molecolare:385.37Ofirnoflastum
CAS:Ofirnoflastum (Ofirnoflast) is a selective serine/threonine-protein kinase Nek7 inhibitor that exerts potent anti-inflammatory effects by suppressing Nek7-dependent NLRP3 inflammasome activation, reducing caspase-1 cleavage, IL-1β and IL-18 secretion, and pyroptotic cell death in vitro, while significantly attenuating cytokine production and tissue injury in animal models of acute and chronic inflammation, supporting its therapeutic potential in autoimmune and inflammatory diseases.Formula:C23H19F4N7O2Colore e forma:SolidPeso molecolare:501.44

