| Cat.No. | Name | Information |
|---|---|---|
| M52552 | Microcystin-RR | Microcystin-RR (Cyanoviridin RR) is a potent and orally active protein phosphatase inhibitor. |
| M52551 | 11R-CaN-AID | 11R-CaN-AID is a potent and cell permeant inhibitor of calcineurin. |
| M52549 | Z-Pro-Pro-aldehyde-dimethyl acetal | Z-Pro-Pro-aldehyde-dimethyl acetal is a potent inhibitor of prolyl endopeptidase (PREP), a cytoplasmic serine endoprotease (IC50= 12 nM). |
| M52548 | Suc-Ala-Pro-pNA | Suc-Ala-Pro-pNA is a peptide that serves as a substrate to detect the activity and stability of prolyl endopeptidase (PEP). |
| M52547 | Z-Pro-Pro-CHO | Z-Pro-Pro-CHO is a prolyl oligopeptidase inhibitor (IC50: 0.16 μM and 0.01 μM for human and Schistosoma Mansoni prolyl oligopeptidase respectively). |
| M52546 | Poststatin | Poststatin is a pecific prolyl endopeptidase (PEP) inhibitor. |
| M52545 | PR-39 | PR-39, a natural proline- and arginine-rich antibacterial peptide, is a noncompetitive, reversible and allosteric proteasome inhibitor. |
| M52544 | PSI | PSI (Proteasome Inhibitor 1) is a potent proteasome inhibitor. |
| M52543 | Suc-Ala-Ala-Pro-Phe-SBzl | Suc-Ala-Ala-Pro-Phe-SBzl can be used as the substrate of rat intestinal mast cell protease (RMCP I), rat skeletal muscle mast cell protease (RMCP II) and Chymotrypsin. |
| M52542 | Ac-Leu-Leu-Norleucinol | Ac-Leu-Leu-Norleucinol (ALLN) is a calpain inhibitor, can be used for research of Acetaminophen induced acute liver damage, and lowers glutamic-oxalacetic transaminease (ALT) and glutamic-pyruvic transaminase (AST). |
| M52541 | MeOSuc-Gly-Leu-Phe-AMC | MeOSuc-Gly-Leu-Phe-AMC is a peptide substrate of proteasomal. |
| M52540 | Z-Gly-Pro-Phe-Leu-CHO | Z-Gly-Pro-Phe-Leu-CHO (Z-GPFL-CHO) is a tetrapeptide aldehyde that acts as a highly selective and potent proteasomal inhibitor. |
| M52539 | Suc-Gly-Gly-Phe-pNA | Suc-Gly-Gly-Phe-pNA is the chymotrypsin substrate with an Km value of 1.6 mM. |
| M52538 | Z-Leu-Leu-Tyr-COCHO | Z-Leu-Leu-Tyr-COCHO is a potent chymotrypsin-like activity inhibitor with a Ki value of 3.0 nM. |
| M52537 | Z-Ala-Arg-Arg-AMC | Z-Ala-Arg-Arg-AMC (Fluorogenic Proteasome Substrate) is a fluorogenic substrate for assaying trypsin-like activity of proteasome. |
| M52536 | Z-Leu-Leu-Glu-AMC | Z-Leu-Leu-Glu-AMC is a substrate peptide, and can be used for determination of postacidic-like hydrolysing activity of 20S proteasome. |
| M52535 | Z-Leu-Leu-Glu-βNA | Z-Leu-Leu-Glu-βNA (Z-Leu-Leu-Glu-β-naphthylamide) is a substrate for determination of the glutamylpeptidyl-peptide hydrolase activity of the 20S proteasome. |
| M52534 | Z-Leu-Leu-Leu-AMC | Z-Leu-Leu-Leu-AMC is a fluorogenic substrate for measuring the chymotrypsin-like protease activity of the 20S proteasome. |
| M52533 | Baceridin | Baceridin is a proteasome inhibitor and a cyclic hexapeptide. |
| M52532 | Z-LLF-CHO | Z-LLF-CHO (Z-Leu-Leu-Phe-CHO) is a potent inhibitor of the chymotrypsin-like activity of the pituitary multicatalytic proteinase complex (Ki = 460 nM). |
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