Serina proteasa
Los inhibidores de serina proteasa son compuestos que inhiben las serina proteasas, un grupo de enzimas caracterizadas por un residuo de serina en su sitio activo. Estas proteasas están involucradas en numerosos procesos fisiológicos, incluyendo la digestión, la respuesta inmunitaria, la coagulación sanguínea y la inflamación. Los inhibidores de serina proteasa son fundamentales para estudiar enfermedades en las que estas enzimas están desreguladas, como enfermedades cardiovasculares, cáncer y condiciones inflamatorias. En CymitQuimica, ofrecemos inhibidores de serina proteasa para apoyar su investigación en enzimología, mecanismos de enfermedades e intervenciones terapéuticas.
Se han encontrado 79 productos para "Serina proteasa".
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WNK463
CAS:WNK463 is a pan-WNK-kinase inhibitor. It effectively inhibits the in vitro kinase activity of all four WNK family members (WNK1/2/3/4).Fórmula:C21H24F3N7O2Pureza:>99.99% - ≥95%Forma y color:SolidPeso molecular:463.46Benzamidine hydrochloride
CAS:Benzamidine hydrochloride (Benzamidine HCl) is a reversible inhibitor of serine proteases, including trypsin, plasmin, and thrombin.Fórmula:C7H9ClN2Pureza:99.64% - 99.97%Forma y color:SolidPeso molecular:156.612,4-Dioxaspiro(5.5)undec-8-ene, 3-(2-furanyl)-
CAS:2,4-Dioxaspiro(5.5)undec-8-ene, 3-(2-furanyl)- (Ulinastatin) ,as an urinary trypsin inhibitor (UTI), is a glycoprotein that is isolated from healthy human urineFórmula:C13H16O3Pureza:99.53% - 99.81%Forma y color:SolidPeso molecular:220.26Ref: TM-T8802
1mg82,00€1mL*10mM (DMSO)146,00€5mg168,00€10mg244,00€25mg404,00€50mg567,00€100mg767,00€500mg1.521,00€CH 5450
CAS:CH 5450 (Z-Ile-Glu-Pro-Phe-Ome) (Z-Ile-Glu-Pro-Phe-Ome) is a short peptide inhibitor of chymase in the human heartFórmula:C34H44N4O9Pureza:95.93%Forma y color:SolidPeso molecular:652.73WNK-IN-11
CAS:WNK-IN-11 (Allosteric WNK Kinase Inhibitor) is an allosteric With-No-Lysine (WNK) kinase inhibitor,WNK1(IC50 : 4 nM)Fórmula:C21H21Cl2N5OSPureza:98.32%Forma y color:SolidPeso molecular:462.4Ref: TM-T5456
1mg87,00€5mg172,00€1mL*10mM (DMSO)188,00€10mg280,00€25mg474,00€50mg683,00€100mg964,00€500mg1.918,00€Fulacimstat
CAS:Fulacimstat (BAY1142524) (BAY1142524) is a chymase inhibitor, with IC50s of 3, 4 nM for hamster and human chymase enzyme, respectively.Fórmula:C23H16F3N3O6Pureza:99.77%Forma y color:White SolidPeso molecular:487.38Ref: TM-TQ0035
1mg101,00€5mg215,00€1mL*10mM (DMSO)230,00€10mg313,00€25mg512,00€50mg737,00€100mg973,00€Alvelestat
CAS:Alvelestat (AZD9668) is an orally bioavailable, selective and reversible inhibitor of human neutrophil elastase (NE), with potential anti-inflammatory activity.Fórmula:C25H22F3N5O4SPureza:98% - >99.99%Forma y color:White SolidPeso molecular:545.53Ref: TM-T3107
1mg34,00€2mg43,00€5mg56,00€1mL*10mM (DMSO)74,00€10mg84,00€25mg148,00€50mg219,00€100mg349,00€500mg830,00€ML281
CAS:ML281 is a potent and selective STK33 inhibitor with IC50 of 14 nM.Fórmula:C22H19N3O2SPureza:99.12% - 99.87%Forma y color:SolidPeso molecular:389.47Ref: TM-T3423
1mg34,00€5mg75,00€1mL*10mM (DMSO)84,00€10mg92,00€25mg178,00€50mg295,00€100mg474,00€500mg1.035,00€Galegenimab
CAS:Galegenimab (RG 6147) is an Fab targeting HtrA1, capable of blocking proteolytic cleavage of biglycan (an HtrA1 substrate), suitable for AMD research.Pureza:95% - 95.8% (SDS-PAGE); 99.7% (SEC-HPLC)Forma y color:Transparent LiquidPeso molecular:46.87 kDaAnti-Matriptase Antibody
Anti-Matriptase Antibody is a human antibody expressed in CHO cells.Pureza:95.8% (SDS-PAGE); 99.2% (SEC-HPLC) - 95.8% (SDS-PAGE); 99.2% (SEC-HPLC)Forma y color:Transparent LiquidPeso molecular:144.27 kDaLanadelumab
CAS:Lanadelumab (SHP643), a humanized IgG1 antibody, inhibits plasma kallikrein and its interaction with HMWK, supporting hereditary angioedema research.Pureza:95% - 97.4% (SDS-PAGE); 99.2% (SEC-HPLC)Forma y color:Transparent LiquidPeso molecular:145.70 kDaMEGA-9
CAS:MEGA-9 (Nonanoyl-N-Methylglucamide) solubilizes membrane protein and can be used as a nonionic detergent.Fórmula:C16H33NO6Pureza:99.9%Forma y color:White SolidPeso molecular:335.44ZM223 hydrochloride (2031177-48-5 free base)
ZM223 hydrochloride is an orally active, potent non-covalent inhibitor of NEDD8 activating enzyme (NAE), and with excellent anticancer activity.Fórmula:C23H18ClF3N4O2S2Pureza:98%Forma y color:SolidPeso molecular:538.99Nonacog alfa
CAS:Nonacog alfa (BAX326), a recombinant human factor IX, is utilized in the study of hemophilia B [1].Forma y color:LiquidC1 Esterase Inhibitor (Human)
C1 Esterase Inhibitor (Human) is a glycoprotein derived from human plasma and acts as a serine protease inhibitor. It inactivates enzymes like C1r, C1s, and mannose-binding lectin-associated serine proteases (MASP) through covalent binding. This compound possesses anti-inflammatory properties and is utilized to prevent angioedema attacks associated with hereditary angioedema.Forma y color:Odour LiquidLodelaben
CAS:Lodelaben (Declaben, SC-39026) is a reversible, non-competitive,specific inhibitor of human neutrophil elastase (HNE) with high potency (IC50=0.5 μM).Fórmula:C25H41ClO3Pureza:99.62% - >99.99%Forma y color:White SolidPeso molecular:425.04AGLME
CAS:AGLME is used in a direct enzymatic assay for activated Hageman factor measuring the ability of Hageman factor to hydrolyze the cpd.Fórmula:C11H21N3O4Forma y color:SolidPeso molecular:259.3BMS-363131
CAS:BMS-363131 (BMS363131) is a potent and selective trypsin inhibitor with an IC50 value of <1.7 nM.Fórmula:C28H40N6O5Pureza:97.99%Forma y color:SolidPeso molecular:540.65WNK1-IN-1
CAS:WNK1-IN-1, a WNK1 inhibitor (IC50: 1.6 μM), also inhibits OSR1 phosphorylation (IC50: 4.3 μM), used in blood pressure and cancer research.Fórmula:C13H15BrCl2N2O4SPureza:98.09%Forma y color:SolidPeso molecular:446.14Ref: TM-T73295
1mg71,00€5mg152,00€1mL*10mM (DMSO)167,00€10mg236,00€25mg485,00€50mg782,00€100mg1.305,00€ATN-658
ATN-658 is a neutralizing monoclonal antibody targeting the urokinase-type plasminogen activator receptor. ATN-658 demonstrates the capacity to suppress cellular invasion and reduces the formation of metastatic nodules in various human tumor xenograft models during strictly monitored laboratory observation periods without competing with the natural ligand binding site.
