Catalog name Description price
R-C-1727 Boceprevir (SCH-503034) CAS:394730-60-0 Boceprevir(EBP 520)is a potent, highly selective,orally bioavailable HCV NS3 protease inhibitor with a Ki of 14nM in both enzyme assay and an EC90 of 350nM in cell-based replicon assay.Boceprevir inhibits SARS-CoV-2 3CLpro activity. price>
R-C-1763 GK921 CAS:1025015-40-0 GK921 is a transglutaminase 2(TGase)inhibitor with an IC50 of 7.71μM for human recombinant TGase 2. price>
R-C-1832 MG-132 CAS:1211877-36-9 MG132(Z-Leu-Leu-Leu-al)is a potent cell-permeable proteasome and calpain inhibitor with IC50s of 0.1μM and 1.2μM for the inhibition of proteasome and calpain,respectively.MG132 activates autophagy and induces apoptosis in tumor cells. price>
R-C-1893 Fostemsavir(BMS-663068) CAS:864953-29-7 Fostemsavir(BMS-663068,Rukobia),the phosphonooxymethyl prodrug of BMS626529,is an attachment inhibitor that targets HIV-1 gp120 and prevents its binding to CD4+ T cells with EC50 of<10nM. price>
R-C-1896 Glecaprevir CAS:1365970-03-1 Glecaprevir(ABT-493,A-1282576)is a novel HCV NS3/4A protease inhibitor,with IC50 values ranging from 3.5 to 11.3nM. price>
R-C-1933 ALVELESTAT (AZD 9668) CAS:848141-11-7 Alvelestat(AZD9668,Avelestat)is an oral,highly selective inhibitor of neutrophil elastase(NE)with IC50 and Ki of 12nM and 9.4nM,at least 600-fold more selective over other serine proteases.  price>
R-C-1957 Calpeptin CAS:117591-20-5 Calpeptin is a potent,cell-permeable calpain inhibitor with ID50 of 52 nM, 34 nM,138nM,and 40 nM for Calpain I(porcine erythrocytes),Calpain II(porcine kidney),Papainb,and Calpain I(human platelets),respectively.Calpeptin attenuates apoptosis and intracellular inflammatory changes in muscle cells. price>
R-C-1962 CD437 CAS:125316-60-1 CD437 is a selective Retinoic Acid Receptor γ(RARγ)agonist. price>
R-C-1972 LSN3154567(Nampt-IN-1) CAS:1698878-14-6 Nampt-IN-1(LSN3154567)is a potent and selective NAMPT inhibitor.Nampt-IN-1 inhibits purified NAMPT with an IC50 of 3.1nM. price>
R-C-1973 CVT-12012 CAS:1018675-35-8 CVT-12012 is a potent and orally bioavailable stearoyl-coA desaturase(SCD)inhibitor, with IC50s of 38 nM,6.1nM for rat microsomal and human HEPG2. price>