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. |
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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. |
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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. |
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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. |
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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. |
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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. |
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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. |
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R-C-1962 |
CD437 CAS:125316-60-1 |
CD437 is a selective Retinoic Acid Receptor γ(RARγ)agonist. |
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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. |
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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. |
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