About 15 results found for searched term "CALP2" (0.122 seconds)
| Cat.No. | Name | Target |
|---|---|---|
| M28012 | Acetyl-Calpastatin(184-210)(human) | Proteasome |
| Acetyl-Calpastatin(184-210)(human) is a potent, selective and reversible calpain inhibitor with Ki values of 0.2 nM and 6 μM for µ-calpain and cathepsin L, respectively. | ||
| M31060 | Acetyl-Calpastatin(184-210)(human) TFA | Proteasome |
| Acetyl-Calpastatin(184-210)(human) TFA is a potent, selective and reversible calpain inhibitor with Ki values of 0.2 nM and 6 μM for µ-calpain and cathepsin L, respectively. | ||
| M52790 | CALP2 | Others |
| CALP2 is a calmodulin (CaM) antagonist ( (Kd of 7.9 µM)) with high affinity for binding to the CaM EF-hand/Ca2+-binding site. | ||
| M5167 | Calpeptin | Akt |
| Calpeptin is a potent, cell-permeable inhibitor of the Ca2+-dependent protease, calpain. | ||
| M5221 | MG-101 | Proteasome |
| Calpain inhibitor I; Ac-LLnL-CHO; ALLN | ||
| MG-101 is a potent inhibitor of cysteine proteases including calpain I (Ki = 190 nM), calpain II (Ki = 220 nM), cathepsin B (Ki = 150 nM), and cathepsin L (Ki = 500 pM). IC50 value: 150 nM (Ki) | ||
| M7764 | PD150606 | Proteasome |
| PD150606 is a selective, cellular permeable non-peptide calpain inhibitor with Ki of 0.21 μ m and 0.37 μ m on μ-calpains and M-calpains, respectively, and has neuroprotective activity. | ||
| 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. | ||
| M8329 | PD 151746 | Calpain |
| PD151746 | ||
| PD151746 is a calpain inhibitor that selectively inhibits U-calpain (Ki = 0.26 ± 0.03 μM) 20 times more than m-calpain (Ki = 5.33 ± 0.77μM). | ||
| M11294 | Alicapistat | Proteasome |
| ABT-957 | ||
| Alicapistat (ABT-957) is an orally active, selective inhibitor of human calpains 1 and 2 that can be used in alzheimer's disease (AD) studies. | ||
| M13366 | (R)-MG-132 | Proteasome |
| Z-Leu-Leu-Leu-al | ||
| (R)-MG-132 (Z-LEu-LEu-Al) is a cellular permeable proteasome and Calpain inhibitor with IC50 of 100 nM and 1.2 μM, respectively. | ||
| M14192 | CALP3 | Calcium Channel |
| CALP3, a Ca2+-like peptide, is a potent Ca2+ channel blocker that activates EF hand motifs of Ca2+-binding proteins. | ||
| M27985 | Pirepemat | Others |
| IRL752 | ||
| Pirepemat (IRL752) is a corticalpreferring catecholamine- and cognition-promoting agent. Pirepemat (IRL752) is used for the study of Parkinson's disease. | ||
| M28912 | (Rac)-Calpain Inhibitor XII | Proteasome |
| (Rac)-Calpain Inhibitor XII is a reversible and selective inhibitor of calpain I (μ-calpain, Ki=19 nM). (Rac)-Calpain Inhibitor XII has lower affinities for calpain II (m-calpain, Ki=120 nM) and cathepsin B (Ki=750 nM). | ||
| M29365 | Dazcapistat | Proteasome |
| Dazcapistat is a potent calpain inhibitor, with IC50s of <3 μM for calpain 1, calpain 2 and calpain 9, respectively. | ||
| M53076 | CALP1 | GluR |
| CALP1 is a calmodulin (CaM) agonist (Kd of 88 µM) with binding to the CaM EF-hand/Ca2+-binding site. | ||
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