Chemical Structure
Z-Leu-Leu-Leu-B(OH)2 [MG-262] [179324-22-2]
AG-CP3-0024
Overview
- SupplierAdipoGen Life Sciences
- Product NameZ-Leu-Leu-Leu-B(OH)2 [MG-262]
- Delivery Days Customer10
- CAS Number179324-22-2
- CertificationResearch Use Only
- Estimated Purity>95%
- Molecular FormulaC25H42BN3O6
- Molecular Weight491.4
- Scientific DescriptionChemical. CAS: 179324-22-2. Formula: C25H42BN3O6. MW: 491.4. Highly potent and selective cell permeable inhibitor of the proteasome. Inhibits the chymotrypsin-like and caspase-like peptidase activity of the proteasome. Calpain and cathepsin inhibitor. Autophagy activator. Similar structure as MG-132 (AG-CP3-0011) but much higher potency. - Highly potent and selective cell permeable inhibitor of the proteasome. Inhibits the chymotrypsin-like and caspase-like peptidase activity of the proteasome. Calpain and cathepsin inhibitor. Autophagy activator. Similar structure as MG-132 (AG-CP3-0011) but much higher potency.
- SMILESCC(C)C[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)OCC1=CC=CC=C1)B(O)O
- Storage Instruction-20°C,2°C to 8°C
- UNSPSC51202000
References
- Down-regulation of Flt-1 gene expression by the proteasome inhibitor MG262: J. Mezquita, et al.; J. Cell. Biochem. 89, 1138 (2003)
- Importance of the different proteolytic sites of the proteasome and the efficacy of inhibitors varies with the protein substrate: A.F. Kisselev, et al.; J. Biol. Chem. 281, 8582 (2006)
- Identification of the proteasome inhibitor MG262 as a potent ATP-dependent inhibitor of the Salmonella enterica serovar Typhimurium Lon protease: H. Frase, et al.; Biochemistry 45, 8264 (2006)
- Characterization of the Physiological Turnover of Native and Inactivated Cytochromes P450 3A in Cultured Rat Hepatocytes: A Role for the Cytosolic AAA ATPase p97?: S. Faouzi, et al.; Biochemistry 46, 7793 (2007)
- Proteasome activity and autophagosome content in liver are reciprocally regulated by ethanol treatment: P.G. Thomes, et al.; BBRC 417, 262 (2012)