Date published: 2025-10-19

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Z-L-Abu-CONH-ethyl

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Alternate Names:
Z-Leu-Abu-CONHC2H5; AK275
Application:
Z-L-Abu-CONH-ethyl is cell-permeable dipeptidyl α-ketoamide showing potent, reversible inhibition of calpain-1 and -2
Purity:
≥95%
Molecular Weight:
405.48
Molecular Formula:
C21H31N3O5
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Z-L-Abu-CONH-ethyl, or Benzyloxycarbonyl-L-α-aminobutyric acid ethylamide, is a synthetic peptide derivative extensively utilized in biochemical research to explore protease activity and enzyme kinetics. This compound features an L-α-aminobutyric acid moiety linked to an ethylamide group, enhancing its stability and utility in experimental settings. The benzyloxycarbonyl (Z) group serves as a protective element, commonly employed in peptide synthesis to shield the amino group, thus preventing non-specific reactions and degradation during lab procedures. Z-L-Abu-CONH-ethyl is particularly valuable for probing the specificity and action mechanisms of proteases, enzymes critical for protein processing and regulation in biological systems. By serving as both a substrate and an inhibitor in enzymatic assays, this chemical helps delineate protease preferences for substrates, their catalytic actions, and potential regulatory roles in processes like apoptosis and cell signaling. Its role in facilitating the understanding of enzyme behavior and the synthesis of complex peptides makes Z-L-Abu-CONH-ethyl a pivotal tool in advancing fundamental research in protein chemistry and enzyme functionality, thereby aiding in the development of sophisticated biochemical techniques without direct clinical or therapeutic implications.


Z-L-Abu-CONH-ethyl References

  1. Amyloid beta-mediated cell death of cultured hippocampal neurons reveals extensive Tau fragmentation without increased full-length tau phosphorylation.  |  Reifert, J., et al. 2011. J Biol Chem. 286: 20797-811. PMID: 21482827
  2. Neuroprotective strategies against calpain-mediated neurodegeneration.  |  Yildiz-Unal, A., et al. 2015. Neuropsychiatr Dis Treat. 11: 297-310. PMID: 25709452
  3. Bispecific repurposed medicines targeting the viral and immunological arms of COVID-19.  |  Redhead, MA., et al. 2021. Sci Rep. 11: 13208. PMID: 34168183
  4. Postischemic administration of AK275, a calpain inhibitor, provides substantial protection against focal ischemic brain damage.  |  Bartus, RT., et al. 1994. J Cereb Blood Flow Metab. 14: 537-44. PMID: 8014200
  5. Peptide alpha-keto ester, alpha-keto amide, and alpha-keto acid inhibitors of calpains and other cysteine proteases.  |  Li, Z., et al. 1993. J Med Chem. 36: 3472-80. PMID: 8230139
  6. New inhibitors of calpain prevent degradation of cytoskeletal and myelin proteins in spinal cord in vitro.  |  James, T., et al. 1998. J Neurosci Res. 51: 218-22. PMID: 9469575

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Z-L-Abu-CONH-ethyl, 1 mg

sc-301995
1 mg
$120.00

Z-L-Abu-CONH-ethyl, 5 mg

sc-301995A
5 mg
$471.00