
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
Show 4 more subcategories
Products of "Proteases/Proteasome"
Sort by
U18666A
CAS:U18666A is a cell-permeable drug and is a cholesterol synthesis and transport inhibitor.Formula:C25H42ClNO2Purity:98.99%Color and Shape:SolidMolecular weight:424.06Ref: TM-T17190
1mg35.00€2mg47.00€5mg70.00€10mg97.00€25mg185.00€50mg301.00€100mg454.00€200mg650.00€1mL*10mM (DMSO)77.00€CASP3 Activator 1541
CAS:CASP3 Activator 1541 is an activator of the proenzyme forms of caspase-3, and induces cell death.Formula:C24H17N3O4Purity:98.84%Color and Shape:SolidMolecular weight:411.41L 756423
CAS:L756423 is a potent, selective HIV protease inhibitor (Ki=0.049 nM), effective against HIV spread in MT25 lymphocytes at 0.1-0.5 nM, useful for AIDS research.Formula:C39H48N4O5Purity:100% - 100%Color and Shape:SolidMolecular weight:652.82TAPI1
CAS:TAPI1 (TAPI) , an ADAM17/TACE inhibitor, inhibits shedding of cytokine receptors.Formula:C26H37N5O5Purity:≥95%Color and Shape:SolidMolecular weight:499.6Setrobuvir
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:100% - 99%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€Efavirenz
CAS:Efavirenz (DMP 266) is an HIV-1 inhibitor, affecting reverse transcriptase and various cytochrome P450 enzymes.Formula:C14H9ClF3NO2Purity:99.2% - 99.83%Color and Shape:White To Slightly Pink Crystalline PowderMolecular weight:315.67Ref: TM-T2393
1g404.00€5mg42.00€10mg52.00€25mg71.00€50mg89.00€100mg116.00€500mg273.00€1mL*10mM (DMSO)49.00€Doxycycline hydrochloride
CAS:Doxycycline hydrochloride (Hyclate) is a synthetic tetracycline derivative with similar antimicrobial activity.Formula:C22H24N2O8·HClPurity:98.77%Color and Shape:Yellow Hygroscopic Crystalline PowderMolecular weight:480.9Atazanavir
CAS:Formula:C38H52N6O7Purity:>95.0%(HPLC)Color and Shape:White to Light yellow powder to crystalMolecular weight:704.87Mk-6186 HCl
MK-6186 HCl, a novel non-nucleoside reverse transcriptase inhibitor with antiviral activity, can be used to study HIV.Formula:C21H13Cl3N6OPurity:98.19%Color and Shape:SoildMolecular weight:471.73Trelagliptin
CAS:Trelagliptin (SYR-472) is a highly specific and long-acting DPP-4 inhibitor.Formula:C18H20FN5O2Purity:98.88%Color and Shape:SolidMolecular weight:357.38ACH-806
CAS:ACH-806 is an NS4A antagonist. It can inhibit Hepatitis C Virus (HCV) replication with an EC50 of 14 nM.Formula:C19H20F3N3O2SPurity:98%Color and Shape:SolidMolecular weight:411.44Sofosbuvir impurity K
CAS:Sofosbuvir impurity K is an diastereoisomer of Sofosbuvir.Sofosbuvir is an HCV RNA replication inhibitor, with potent anti-hepatitis C virus activity.Formula:C22H29ClN3O9PPurity:98%Color and Shape:SolidMolecular weight:545.91NBD-557
CAS:NBD-557 is a potentially HIV-1 inhibitor.Formula:C17H24BrN3O2Purity:99.52%Color and Shape:SolidMolecular weight:382.3Ref: TM-T7382
1mg48.00€5mg97.00€10mg156.00€25mg301.00€50mg437.00€100mg620.00€200mg843.00€1mL*10mM (DMSO)105.00€Ilomastat
CAS:Formula:C20H28N4O4Purity:>95.0%(HPLC)(qNMR)Color and Shape:White to Light yellow powder to crystalMolecular weight:388.472-Amino-6-bromopyridine
CAS:2-Amino-6-bromopyridine has inhibitory effect on HIV-68 protease.Formula:C5H5BrN2Purity:99.87%Color and Shape:SolidMolecular weight:173.013,3′-Bisdemethylpinoresinol
CAS:3,3′-Bisdemethylpinoresinol, a natural lignin derivative, exhibits MMP-1 inhibitory activity in UVA-irradiated human dermal fibroblasts and can be isolated fromFormula:C18H18O6Purity:98%Color and Shape:SolidMolecular weight:330.33LY 3000328
CAS:LY 3000328 (Cathepsin S inhibitor) is a selective inhibitor of cathepsin S.Cost-effective and quality-assured.Formula:C25H29FN4O5Purity:97.83% - 99.54%Color and Shape:SolidMolecular weight:484.52Ref: TM-TQ0116
1mg96.00€2mg137.00€5mg210.00€10mg278.00€25mg487.00€50mg708.00€100mg998.00€1mL*10mM (DMSO)220.00€NNRTIs-IN-3
NNRTIs-IN-3 (compound 8) is an HIV-1 non-nucleoside reverse transcriptase inhibitor, displaying potent efficacy with an EC50 value of 0.01 µM [1].Formula:C17H20ClN5OPurity:98%Color and Shape:SolidMolecular weight:345.83NP-313
CAS:NP-313 (NSC-4264) is a potent antithrombotic that blocks platelet aggregation via thromboxane A2 synthesis inhibition and targets SOCC-mediated Ca2+ efflux.Formula:C12H8ClNO3Purity:98.97%Color and Shape:SolidMolecular weight:249.65