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N-Acetyl-L-histidine (CAS 39145-52-3)

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Alternate Names:
N-Acetylhistidine; N-α-Acetyl-L-histidine; N2-Acetylhistidine
CAS Number:
39145-52-3
Molecular Weight:
197.19
Molecular Formula:
C8H11N3O3
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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N-Acetyl-L-histidine is a derivative of the essential amino acid histidine, characterized by the acetylation of the amino group. This modification imparts unique properties to the molecule, distinguishing it from its parent amino acid. In biochemical research, N-Acetyl-L-histidine plays a significant role as a model compound to study acetylation reactions, which are critical in the post-translational modification of proteins, affecting their function, localization, and interaction with other molecules. Furthermore, it serves as a tool in enzymology studies, especially in understanding the specificity and mechanism of action of histidine acetyltransferases and deacetylases. This compound also finds utility in the synthesis of complex peptides and proteins, where the acetyl group can protect the amino group during peptide bond formation, later to be removed enzymatically or chemically, revealing the native amine for further modifications or functional studies. Its stability and reactive properties make N-Acetyl-L-histidine an indispensable reagent in the elucidation of biochemical pathways and the investigation of histidine-related metabolism and enzymatic activities.


N-Acetyl-L-histidine (CAS 39145-52-3) References

  1. Interaction of copper(II) with imidazole pyridine nitrogen-containing ligands in aqueous medium: a spectroscopic study.  |  Prenesti, E. and Berto, S. 2002. J Inorg Biochem. 88: 37-43. PMID: 11750023
  2. Differential expression of carnosine, homocarnosine and N-acetyl-L-histidine hydrolytic activities in cultured rat macroglial cells.  |  Baslow, MH., et al. 2001. J Mol Neurosci. 17: 351-9. PMID: 11859931
  3. Ultraviolet spectrophotometric characterization of copper(II) complexes with imidazole N-methyl derivatives of L-histidine in aqueous solution.  |  Prenesti, E., et al. 2003. Spectrochim Acta A Mol Biomol Spectrosc. 59: 201-7. PMID: 12509160
  4. Calcium sensitizing action of carnosine and other endogenous imidazoles in chemically skinned striated muscle.  |  Lamont, C. and Miller, DJ. 1992. J Physiol. 454: 421-34. PMID: 1474497
  5. Purification and characterization of a novel aminoacylase from Streptomyces mobaraensis.  |  Koreishi, M., et al. 2005. Biosci Biotechnol Biochem. 69: 1914-22. PMID: 16244442
  6. Reduction of chronic graft injury with a new HTK-based preservation solution in a murine heart transplantation model.  |  Türk, TR., et al. 2012. Cryobiology. 64: 273-8. PMID: 22406211
  7. N-acetyl-L-histidine, a Prominent Biomolecule in Brain and Eye of Poikilothermic Vertebrates.  |  Baslow, MH. and Guilfoyle, DN. 2015. Biomolecules. 5: 635-46. PMID: 25919898
  8. Novel 125I-labeled nortriptyline derivatives and their use in liquid-phase or magnetizable solid-phase second-antibody radioimmunoassays.  |  Kamel, RS., et al. 1979. Clin Chem. 25: 1997-2002. PMID: 41648
  9. N-acetylhistidine isolated from frog heart.  |  Kuroda, Y. and Ikoma, T. 1966. Science. 152: 1241-2. PMID: 5949241
  10. N -acetyl-L-histidine synthetase activity from the brain of the killifish.  |  Baslow, MH. 1966. Brain Res. 3: 210-3. PMID: 5971525
  11. N-acetyl-L-histidine metabolism in the fish eye: evidence for ocular fluid--lens L-histidine recycling.  |  Baslow, MH. 1967. Exp Eye Res. 6: 336-42. PMID: 6060545
  12. A review of phylogenetic and metabolic relationships between the acylamino acids, N-acetyl-L-aspartic acid and N-acetyl-L-histidine, in the vertebrate nervous system.  |  Baslow, MH. 1997. J Neurochem. 68: 1335-44. PMID: 9084403
  13. Function of the N-acetyl-L-histidine system in the vertebrate eye. Evidence in support of a role as a molecular water pump.  |  Baslow, MH. 1998. J Mol Neurosci. 10: 193-208. PMID: 9770642

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

N-Acetyl-L-histidine, 5 mg

sc-488146
5 mg
$311.00