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Atomfair Histidylglycine His-Gly C8H12N4O3

Description Histidylglycine (CAS: 2657-93-4) is a high-purity dipeptide composed of L-histidine and glycine, with the molecular formula C8H12N4O3. This biologically active compound is widely utilized in biochemical research, peptide synthesis, and pharmaceutical development. Its IUPAC name, 2-[[(2S)-2-amino-3-(1H-imidazol-5-yl)propanoyl]amino]acetic acid , reflects its precise chiral configuration and functional groups. Our product is rigorously tested via HPLC and mass spectrometry to ensure ??98% purity, making it ideal for sensitive applications. Supplied as a lyophilized powder with batch-specific certificates of analysis, it is stable at recommended storage conditions (-20??C). Suitable for cell culture studies, enzyme-substrate interactions, and as a building block for complex peptides.

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Description

Description

Histidylglycine (CAS: 2657-93-4) is a high-purity dipeptide composed of L-histidine and glycine, with the molecular formula C8H12N4O3. This biologically active compound is widely utilized in biochemical research, peptide synthesis, and pharmaceutical development. Its IUPAC name, 2-[[(2S)-2-amino-3-(1H-imidazol-5-yl)propanoyl]amino]acetic acid, reflects its precise chiral configuration and functional groups. Our product is rigorously tested via HPLC and mass spectrometry to ensure ??98% purity, making it ideal for sensitive applications. Supplied as a lyophilized powder with batch-specific certificates of analysis, it is stable at recommended storage conditions (-20??C). Suitable for cell culture studies, enzyme-substrate interactions, and as a building block for complex peptides.

  • CAS No: 2657-93-4
  • Molecular Formula: C8H12N4O3
  • Molecular Weight: 212.21
  • Exact Mass: 212.09094026
  • Monoisotopic Mass: 212.09094026
  • IUPAC Name: 2-[[(2S)-2-amino-3-(1H-imidazol-5-yl)propanoyl]amino]acetic acid
  • SMILES: C1=C(NC=N1)C[C@@H](C(=O)NCC(=O)O)N
  • Synonyms: 2578-58-7, Histidylglycine, His-Gly, L-Histidyl-glycine, histidyl-glycine

Application

Histidylglycine serves as a crucial intermediate in peptide synthesis, particularly for studying histidine-containing motifs in proteins. Researchers employ it to investigate metal-binding properties due to the imidazole moiety’s chelation capacity. It’s also used in metabolic pathway studies and as a reference standard in analytical chemistry. The dipeptide’s structural features make it valuable for probing enzyme specificity in proteolysis research.

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