
Proteases/Proteasome
Protease and proteasome inhibitors are compounds that block the activity of proteases and the proteasome, which are involved in protein degradation and turnover. These inhibitors are vital for studying the regulation of protein homeostasis, cell cycle control, and apoptosis. Protease and proteasome inhibitors are also used in the treatment of diseases such as cancer, where abnormal protein degradation plays a role in disease progression. By inhibiting proteases or the proteasome, these compounds can induce cell death in cancer cells and are critical tools in both basic research and therapeutic development. At CymitQuimica, we provide a wide range of high-quality protease and proteasome inhibitors to support your research in biochemistry, cell biology, and drug development.
Subcategories of "Proteases/Proteasome"
- Acetyl-CoA Carboxylase(37 products)
- Cysteine Protease(111 products)
- DPP-4(24 products)
- Glutaminase(44 products)
- HIV Protease(502 products)
- PAI-1(26 products)
- Protease Inhibitors(50 products)
- Protease-activated Receptor(54 products)
- Proteasome(89 products)
- Serine Protease(54 products)
- p97(15 products)
Show 3 more subcategories
Found 992 products of "Proteases/Proteasome"
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Setrobuvir
CAS:Setrobuvir (ANA-598) is an orally active non-nucleoside HCV NS5B polymerase inhibitor with inhibitory effects on de novo RNA synthesis and primer extension withFormula:C25H25FN4O6S2Purity:99.95% - 99.97%Color and Shape:SolidMolecular weight:560.62Ref: TM-T28762
1mg229.00€5mg570.00€10mg812.00€25mg1,216.00€50mg1,663.00€100mg2,242.00€500mg4,494.00€1mL*10mM (DMSO)737.00€Cathepsin X-IN-1
CAS:Cathepsin X-IN-1 (compound 25) reduces the migration of PC-3 cell with low cytotoxic that is a potent inhibitor of Cathepsin X (IC 50 = 7.13 μM) [1].
Formula:C15H13N3O3SPurity:99.34%Color and Shape:SolidMolecular weight:315.35Uprifosbuvir
CAS:Uprifosbuvir is an inhibitor of uridine nucleotide analog HCV NS5B polymerase.Formula:C22H29ClN3O9PPurity:99.73% - >99.99%Color and Shape:SolidMolecular weight:545.91VRK-IN-1
CAS:VRK-IN-1 is a potent and selective inhibitor of cowpox-associated kinase 1 (VRK1), which can be used in the study of neurological disorders.Formula:C18H11F4NO2Purity:99.18% - 99.25%Color and Shape:SolidMolecular weight:349.28Ref: TM-T35863
1mg103.00€5mg236.00€10mg379.00€25mg750.00€50mg1,130.00€100mg1,510.00€200mg2,062.00€1mL*10mM (DMSO)259.00€JNJ-10311795
CAS:JNJ-10311795 (RWJ-355871) is an inhibitor of neutrophil elastase G and mast cell chymase, demonstrating significant anti-inflammatory effects.Formula:C40H35N2O6PPurity:97.43%Color and Shape:SolidMolecular weight:670.69DB04760
CAS:DB04760: selective MMP-13 inhibitor, non-zinc-chelating, IC50=8nM, reduces paclitaxel neurotoxicity, anticancer.Formula:C22H20F2N4O2Purity:99.93% - 99.99%Color and Shape:SolidMolecular weight:410.42Ref: TM-T15055
1mg84.00€5mg205.00€10mg309.00€25mg522.00€50mg747.00€100mg1,035.00€500mg2,052.00€1mL*10mM (DMSO)178.00€TG-2-IN-1
CAS:TG-2-IN-1 (Compound D003) is a transglutaminase-2 ( TGM-2 ) inhibitor. TG-2-IN-1 can be used in myopia research[1].Formula:C8H13ClN2OSPurity:98.43%Color and Shape:SolidMolecular weight:220.72BILB-1941
CAS:BILB-1941 (BILB-1941ZW) is an inhibitor of HCV NS5B polymerase and can be used in studies about HCV infection.Formula:C34H34N4O4Purity:99.51% - 99.65%Color and Shape:SolidMolecular weight:562.66Ref: TM-T26815
1mg296.00€5mg718.00€10mg982.00€25mg1,485.00€50mg2,008.00€100mg2,637.00€1mL*10mM (DMSO)1,044.00€(2RS)-FPMPA
CAS:(2RS)-FPMPA(FPMPA) has antiviral activity with an IC50 value of 1.85 μM measured in human MT12 cells infected with SHIV (DH4R).Formula:C9H13FN5O4PPurity:99.9% - >99.99%Color and Shape:SolidMolecular weight:305.2UPGL00004
CAS:UPGL00004: potent GAC inhibitor, IC50=29 nM, Kd=27 nM, suppresses triple-negative breast cancer cell growth.Formula:C25H26N8O2S2Purity:97.93%Color and Shape:SolidMolecular weight:534.66Atevirdine
CAS:Atevirdine is an HIV-1 reverse transcriptase inhibitor with antiviral activity for the study of the AIDS dementia complex (ADC).
Formula:C21H25N5O2Purity:98.20%Color and Shape:SolidMolecular weight:379.46BDCRB
BDCRB disrupts HCMV DNA maturation by altering terminase cleavage, extending packaging 30 kb until second site.Formula:C12H11BrCl2N2O4Purity:99.41% - 99.85%Color and Shape:SoildMolecular weight:398.04BMS-929075
CAS:BMS-929075 is an orally active HCV NS5B replicase (HCV NS5B replicase) palm site variant inhibitor with potency, high oral bioavailability and pharmacokineticFormula:C31H24F2N4O3Purity:99.81% - 99.94%Color and Shape:SolidMolecular weight:538.54Ref: TM-T26863
1mg172.00€5mg432.00€10mg618.00€25mg973.00€50mg1,333.00€100mg1,791.00€500mg3,529.00€1mL*10mM (DMSO)538.00€BAY-43-9695
CAS:BAY-43-9695 is a non-nucleoside compound with anti-human cytomegalovirus (HCMV) activity. It is the major metabolite of BAY-38-4766.Formula:C22H25N3O4SPurity:99.50% - 99.98%Color and Shape:SolidMolecular weight:427.52TS-021
CAS:TS-021 is a selective dipeptidyl peptidase 4 (DPP-4) inhibitor with antidiabetic activity for the study of type 2 diabetes.Formula:C17H24FN3O5SPurity:>99.99% - >99.99%Color and Shape:SolidMolecular weight:401.45MK-8325
CAS:MK-8325 is a potent and orally available HCV NS5A inhibitor with replicative activity against a wide range of genotypes.MK-8325 has demonstrated bioavailabilityFormula:C43H54Cl2F2N8O6SiPurity:99.61%Color and Shape:SolidMolecular weight:915.93Tyrosinase-IN-2
CAS:Tyrosinase-IN-2, a potent tyrosinase inhibitor, may help in skin lightening and food preservation research.Formula:C8H8N4O2SPurity:99.78%Color and Shape:SolidMolecular weight:224.24Ref: TM-T60278
5mg48.00€10mg71.00€25mg135.00€50mg212.00€100mg340.00€200mg467.00€1mL*10mM (DMSO)49.00€MMP-2/MMP-9 Inhibitor I
CAS:MMP-2/MMP-9-IN-1: oral IV collagenase inhibitor; IC50: 0.24 μM (MMP-9), 0.31 μM (MMP-2); targets cancer.Formula:C21H19NO4SPurity:99.98%Color and Shape:SolidMolecular weight:381.44Ref: TM-T21512
1mg56.00€5mg119.00€10mg177.00€25mg356.00€50mg590.00€100mg888.00€200mg1,198.00€1mL*10mM (DMSO)133.00€2'-C-Methyladenosine
CAS:2'-C-Methyladenosine from C. renalis inhibits HCV, NS5B RNA synthesis (IC50: 0.3, 1.9µM), and LRV1 in L. guyanensis, L. braziliensis.Formula:C11H15N5O4Purity:99.85%Color and Shape:SolidMolecular weight:281.27HIV-1 integrase inhibitor 8
CAS:HIV-1 integrase inhibitor 8 is an inhibitor of HIV-1 integrase. Integration is a required step in HIV replication [1].
Formula:C21H24O2Purity:98.91%Color and Shape:SolidMolecular weight:308.41
