
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
- Cysteine Protease
- DPP-4
- Glutaminase
- HCV Protease
- HIV Protease
- p97
- PAI-1
- Protease-activated Receptor
- Protease Inhibitors
- Proteasome
- Serine Protease
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Products of "Proteases/Proteasome"
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BILB-1941
CAS:BILB-1941 (BILB-1941ZW) is an inhibitor of HCV NS5B polymerase and can be used in studies about HCV infection.Formula:C34H34N4O4Purity:98.34% - 99.24%Color and Shape:SolidMolecular weight:562.66Ref: TM-T26815
1mg313.00€5mg758.00€10mg1,035.00€25mg1,568.00€50mg2,118.00€100mg2,783.00€1mL*10mM (DMSO)1,103.00€Faldaprevir
CAS:Faldaprevir is an orally effective, selective, non-covalent HCV NS3/4A protease inhibitor with high inhibitory activity against HCV 1a and 1b genotype.Formula:C40H49BrN6O9SPurity:100% - 100%Color and Shape:SolidMolecular weight:869.82Tyrosinase-IN-19
Tyrosinase-IN-19 (compound 9), a competitive tyrosinase inhibitor, exhibits potent antioxidant activities by neutralizing ROS, ABTS+, and DPPH radicals andPurity:98%Color and Shape:Odour SolidEP1013
CAS:EP1013 is a broad-spectrum selective inhibitor of Caspase used in the study of type 1 diabetes.Formula:C18H23FN2O6Purity:98%Color and Shape:SolidMolecular weight:382.38Doxycycline
CAS:Doxycycline (Doxiciclina) belongs to the tetracycline class of antibiotics and is a broad-spectrum metalloproteinase (MMP) inhibitor with oral activity.Formula:C22H24N2O8Purity:97.51% - 99.88%Color and Shape:Yellow Crystalline Powder SolidMolecular weight:444.43BCX 1470 hydrochloride
BCX 1470 hydrochloride is a serine protease inhibitor with anti-inflammatory activity that inhibits factor D hemolytic activity and may be used to study edema.Formula:C14H11ClN2O2S2Purity:98.76%Color and Shape:SoildMolecular weight:338.83Ref: TM-T13568L
1mg137.00€5mg329.00€10mg520.00€25mg825.00€50mg1,111.00€100mg1,491.00€500mg3,002.00€1mL*10mM (DMSO)363.00€Ac-AAVALLPAVLLALLAP-LEHD-CHO
CAS:Ac-AAVALLPAVLLALLAP-LEHD-CHO is a caspase inhibitor targeting caspases 4, 5, and 9, demonstrating protective effects in MCF-7 cells treated withFormula:C97H162N22O25Purity:98%Color and Shape:SolidMolecular weight:2036.46MMP3 inhibitor 1
CAS:MMP3 inhibitor 1 is a potent and highly selective inhibitor of MMP-3 (IC50 of 1 nM).Formula:C23H31N3O6SPurity:98%Color and Shape:SolidMolecular weight:477.57S-methyl-KE-298
CAS:S-methyl-KE-298 is the second main metabolite in plasma,is a methyl conjugate of deacetyl-KE-298.KE-298 inhibits matrix metalloproteinase (MMP-1) productionFormula:C13H16O3SPurity:96.90%Color and Shape:SolidMolecular weight:252.33Ono-3307 mesylate
CAS:no-3307 mesylate is a protease inhibitor that inhibits a variety of proteases and may be used to study pancreatitis.Formula:C15H18N4O7S2Purity:98.02% - 98.16%Color and Shape:SolidMolecular weight:430.46Ac-AAVALLPAVLLALLAP-LEVD-CHO
CAS:Ac-AAVALLPAVLLALLAP-LEVD-CHO is a cell-permeable inhibitor of caspase-4 that exhibits antitumor activity [1].Formula:C96H164N20O25Purity:98%Color and Shape:SolidMolecular weight:1998.45PTACH
CAS:PTACH (Cpd 51) (NCH-51) is a SAHA-based inhibitor of human HDAC. It can potently inhibit the growth of various human Y cells (EC50: 1 to 10 μM).Formula:C20H26N2O2S2Purity:87.44% - 99.74%Color and Shape:SolidMolecular weight:390.56Ref: TM-T3199
1mg50.00€5mg97.00€10mg154.00€25mg298.00€50mg447.00€100mg620.00€200mg843.00€1mL*10mM (DMSO)111.00€Brazilein
CAS:Brazilein, a natural antioxidant, inhibits adipocyte differentiation by inhibiting PPAR γ induction, inhibits skin cancer cells through increasing caspase-3 .Formula:C16H12O5Color and Shape:SolidMolecular weight:284.26HIV-1 TAT (48-60) Acetate
Lilotomab (HH1) is a murine anti-CD37 antibody that can be used to synthesize anti-CD37 antibody-radionuclide couplings.Formula:C72H135N35O18Purity:99.93%Color and Shape:SoildMolecular weight:1779.07ST7612AA1
CAS:ST7612AA1: potent, oral HDAC inhibitor; reactivates HIV-1 latency; shows antitumor effects; may study malaria.Formula:C20H27N3O4SPurity:100%Color and Shape:SolidMolecular weight:405.51Salvianolic acid A
CAS:Salvianolic acid A (Dan Phenolic Acid A) is an MMP-9 inhibitor. Salvianolic acid A has anti-inflammatory activity. Cost-effective and quality-assured.Formula:C26H22O10Purity:100% - 99.08%Color and Shape:Yellow SolidMolecular weight:494.45Nelfinavir
CAS:Nelfinavir (AG1341), with Ki=2 nM, is an HIV treatment and broad-spectrum anticancer drug.Formula:C32H45N3O4SPurity:98.16% - 99.5%Color and Shape:White To Off-White Crystalline PowderMolecular weight:567.78Ref: TM-T7779
1mg43.00€2mg56.00€5mg88.00€10mg111.00€25mg168.00€50mg216.00€100mg285.00€1mL*10mM (DMSO)97.00€Raltegravir
CAS:Raltegravir (MK-0518) is a pyrrolidinone derivative and HIV INTEGRASE INHIBITOR that is used in combination with other ANTI-HIV AGENTS for the treatment of HIVFormula:C20H21FN6O5Purity:100% - 99.86%Color and Shape:SolidMolecular weight:444.42AC1NS4RE
CAS:It is a tyrosine kinase inhibitor.Formula:C15H13ClN2OPurity:99.53%Color and Shape:SolidMolecular weight:272.73