About 13 results found for searched term "Cysteine Protease inhibitor" (0.127 seconds)
| Cat.No. | Name | Target |
|---|---|---|
| M14305 | Cysteine Protease inhibitor | Cathepsin |
| Cysteine Protease inhibitor is an inhibitor of cysteine protease. IC50 & Target: Cysteine Protease | ||
| M14306 | Cysteine Protease inhibitor hydrochloride | Cathepsin |
| Cysteine Protease inhibitor hydrochloride is an inhibitor of cysteine protease. IC50 & Target: Cysteine Protease | ||
| M41233 | Cysteine protease inhibitor-3 | Parasite |
| Cysteine protease inhibitor-3 is a Cysteine protease inhibitor. | ||
| M9353 | N-Ethylmaleimide | Cathepsin |
| NEM | ||
| N-Ethylmaleimide (NEM) is a cysteine protease inhibitor. | ||
| M2376 | Aloxistatin | Cathepsin |
| E64d | ||
| Aloxistatin (E64d) is an irreversible and membrane-permeable cysteine protease inhibitor. | ||
| M2659 | E-64 | Autophagy |
| Proteinase inhibitor E 64 | ||
| E-64 is an irreversible and selective cysteine protease inhibitor with IC50 of 9 nM for papain. | ||
| M2823 | Loxistatin Acid | Cathepsin |
| E-64C; NSC 694279; EP 475 | ||
| Loxistatin Acid (E-64C), a derivative of E-64, is an irreversible and membrane-permeant cysteine protease inhibitor. | ||
| M2952 | PMSF | Serine/Threonine Protease |
| Phenylmethylsulfonyl Fluoride | ||
| PMSF is an irreversible serine/cysteine protease inhibitor. PMSF is commonly used in the preparation of cell lysates. | ||
| M6234 | Z-FA-FMK | Caspase |
| Z-FA-FMK is an irreversible cysteine protease inhibitor, and also inhibits effector caspases. | ||
| M7934 | MDL 28170 | Gamma-secretase/Beta-secretase |
| Calpain Inhibitor III | ||
| Mdl-28170 (Calpain Inhibitor III) is a potent, selective, membrane-permeable Inhibitor of cysteine protease (Calpain Inhibitor III) that can quickly cross the blood-brain barrier after systemic administration. Mdl-28170 also blocks gamma-secretase. | ||
| M29515 | K777 | Cathepsin |
| K777 is a potent, orally active and irreversible cysteine protease inhibitor. K777 is also a potent CYP3A4 inhibitor with an IC50 of 60 nM and a selective CCR4 antagonist featuring the potent chemotaxis inhibition. K777 irreversibly inhibits Cruzain, the major cysteine protease of Trypansoma cruzi, and cathepsins B and L. K777 is a broad-spectrum antiviral by targeting cathepsin-mediated cell entry. K777 inhibits SARS-CoV and EBOV pseudovirus entry with IC50 values of 0.68 nM and 0.87 nM, respectively. | ||
| M52656 | Z-FG-NHO-BzOME | Cathepsin |
| Z-FG-NHO-BzOME is a cysteine protease inhibitor that selectively inhibits cathepsin B, cathepsin L, cathepsin S, and papain. | ||
| M52669 | Z-Leu-Leu-Leu-fluoromethyl ketone | Cathepsin |
| Z-Leu-Leu-Leu-fluoromethyl ketone (Z-LLL-FMK) is a cysteine protease inhibitor. | ||
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