Date published: 2025-12-16

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L-β-Imidazolelactic acid (CAS 14403-45-3)

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Alternate Names:
2-Hydroxy-3-(4-Imidazolyl)propanoic acid
Application:
L-β-Imidazolelactic acid is used in the study and characterization of histidine proteins
CAS Number:
14403-45-3
Molecular Weight:
156.14
Molecular Formula:
C6H8N2O3
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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L-β-Imidazolelactic acid is a unique organic compound featuring an imidazole ring linked to a lactic acid structure, making it an intriguing subject in the realm of biochemical research. The imidazole component, a five-membered ring containing two nitrogen atoms at non-adjacent positions, offers critical functionality that influences the chemical′s biological interactions. This structure is notably similar to metabolites involved in histidine degradation, positioning L-β-Imidazolelactic acid as a potential tool for studying metabolic pathways related to amino acid catabolism. In research settings, this compound can be utilized to explore enzyme kinetics and mechanisms, particularly those processes involving histidine derivatives. It might act as a competitive inhibitor or a substrate mimic, aiding in the elucidation of enzyme specificity and action. Beyond enzymatic studies, L-β-Imidazolelactic acid is also valuable in synthetic chemistry for the creation of complex biochemical compounds or as a foundational element in peptide construction. Its inherent properties may further allow it to serve as a pH buffer or a chelating agent in various biochemical assays, enhancing its utility across multiple scientific investigations that delve into biological and chemical phenomena.


L-β-Imidazolelactic acid (CAS 14403-45-3) References

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  2. Synthesis of all nineteen appropriately protected chiral alpha-hydroxy acid equivalents of the alpha-amino acids for Boc solid-phase depsi-peptide synthesis.  |  Deechongkit, S., et al. 2004. Org Lett. 6: 497-500. PMID: 14961607
  3. Effects of histidine and imidazolelactic acid on various parameters of the oxidative stress in cerebral cortex of young rats.  |  Tansini, CM., et al. 2004. Int J Dev Neurosci. 22: 67-72. PMID: 15036381
  4. Anti-crosslinking properties of carnosine: significance of histidine.  |  Hobart, LJ., et al. 2004. Life Sci. 75: 1379-89. PMID: 15234195
  5. Nitrogen K-edge XANES - an overview of reference compounds used to identify unknown organic nitrogen in environmental samples.  |  Leinweber, P., et al. 2007. J Synchrotron Radiat. 14: 500-11. PMID: 17960033
  6. Bis [2-hydroxy-3-(1H-imidazol-4-yl) propionato] nickel (II)[J].  |  Odoko M, Adachi Y, Okabe N. 2002,. Acta Crystallographica Section E: Structure Reports Online,. 58(1):: m7-m9.
  7. Nitrogen compounds in dissolved and solid environmental samples[M]  |  Leinweber P, Kruse J, Walley F. 2010,. Developments in Soil Science. Elsevier,. 34:: 255-288.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

L-β-Imidazolelactic acid, 100 mg

sc-286037
100 mg
$200.00

L-β-Imidazolelactic acid, 1 g

sc-286037A
1 g
$400.00