| Structure | Cat No. | Product Name | CAS No. | Product Description |
|---|---|---|---|---|
|
V0706 | Calpeptin | 117591-20-5 | Calpeptin(sequence: Z-Leu-nLeu-H) is a novel, potent, cell-permeable calpain inhibitor with anti-fibrotic activity. |
|
V0699 | Cathepsin Inhibitor 1 | 225120-65-0 | Cathepsin Inhibitor 1 (CTS-IN-1) is a novel and potent inhibitor of Cathepsin (L, L2, S, K, B) with the potential to be used in the treatment of osteoarthritis. |
|
V33611 | Cruzain-IN-1 | 1199523-24-4 | Cruzain-IN-1 is a covalent reversible inhibitor of Trypanosoma cruzi cysteine protease (Cruzain) with IC50 of 10 nM. |
|
V0708 | E-64 | 66701-25-5 | E-64 (also known as Proteinase inhibitor E 64), a naturally occuring compound isolated from cultures of Aspergillus, is a novel, potent, irreversible and selective cysteine protease inhibitorwith potential antineoplastic andantiparasitic activity. |
|
V3163 | N-Ethylmaleimide (NEM) | 128-53-0 | N-Ethylmaleimide (also known as NEM) is an organic biochemical compound that is derived from maleic acid. |
![NALPHA-[(苄氧基)羰基]-N-(4-氟-3-氧代-2-丁烷基)苯丙氨酰胺](http://www.invivochem.com/upload/0201/CgAGTF2gbDeAZPQUAABBryHdvWA475.png)
|
V0702 | Z-FA-FMK | 197855-65-5 | Z-FA-FMK, a control peptidic fluoromethylketone (boc-Thr-CH2F), is a novel and irreversible cysteine protease inhibitor, and also inhibits effector caspases. |
|
V0704 | PD 151746 | 179461-52-0 | PD 151746 (PD-151746) is a novel, potent, selective, andcell-permeable calpain inhibitor with important biological activity. |
|
V0703 | Leupeptin Hemisulfate (NK381) | 103476-89-7 | Leupeptin Hemisulfate (NK-381; N-acetyl-L-leucyl-L-leucyl-L-argininal) is a naturally occurring, membrane-permeable, reversible and competitive inhibitor of the serine and cysteine proteases with potential antioxidant and anti-inflammatory activity. |
|
V0705 | MG-101 (ALLN) | 110044-82-1 | MG-101 (also known as MG101; Calpain Inhibitor I and ALLN) is a novel, cell-permeable and potent inhibitor of cysteine proteases including calpains and lysosomal cathepsins with potential antitumor activity. |
|
V0696 | Odanacatib (MK0822) | 603139-19-1 | Odanacatib (also known as MK-0822) is a potent, selective, and neutral inhibitor of cathepsin K (human/rabbit) with the potential to be used for thetreatment for osteoporosis and bone metastasis. |
|
V4361 | BALICATIB | 354813-19-7 | Balicatib (also known as AAE-581) is a novel, potent and selective inhibitor of cathepsin K with 10-100 fold higher potency in cell-based enzyme occupancy assays than against cathepsin B, L, and S. |
|
V0701 | PMSF | 329-98-6 | PMSF (full name: Phenylmethanesulfonyl fluoride) is a potent and irreversible inhibitor of serine/cysteine protease (e.g. thrombin, trypsin and chymotrypsin) with potential analgesic effects. |
|
V28953 | MDL-28170 | 88191-84-8 | MDL-28170 (Calpain Inhibitor III) is a novel potent, selective and membrane-permeable cysteine protease inhibitor of calpain that rapidly penetrates the blood-brain barrier following systemic administration. |
|
V0698 | Aloxistatin (Loxistatin; E64d, NSC-694281) | 88321-09-9 | Aloxistatin (also known asE-64d,E-64c ethyl ester; EST, Loxistatin; NSC 694281) is a novel, potent, selective, irreversible,broad-spectrum and cell membrane-permeable cysteine protease inhibitor with anticoagulant activities. |
|
V0700 | Loxistatin Acid (E-64C; NSC694279; EP475) | 76684-89-4 | Loxistatin Acid (formerly also known as E-64C; NSC-694279; EP-475), an analog of E-64, is a novel, potent, irreversible and membrane-permeable cysteine protease inhibitor with important biological activity. |
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