H9000
His-Gly
Sinonimo/i:
histidylglycine
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About This Item
Formula empirica (notazione di Hill):
C8H12N4O3
Numero CAS:
Peso molecolare:
212.21
Numero MDL:
Codice UNSPSC:
12352200
ID PubChem:
Prodotti consigliati
Temperatura di conservazione
−20°C
Stringa SMILE
NC(Cc1cnc[nH]1)C(=O)NCC(O)=O
Azioni biochim/fisiol
Histidylleucine (His-Leu); histidylglycine (His-Gly) and histidylserine (His-Ser) are N-terminal imidazole containing dipeptides used to study binding of metals such as copper, nickel and zinc.
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
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Brandon I Macdonald et al.
Rapid communications in mass spectrometry : RCM, 22(18), 2946-2954 (2008-08-30)
Pathways for proton transfer in the histidylglycine cation are examined in the gas-phase environment with the goal of understanding the mechanism by which protons may become mobile in proteins with basic amino acid residues. An extensive search of the potential
Brandon J Green et al.
Inorganic chemistry, 43(4), 1463-1471 (2004-02-18)
Self-decomposition of the nickel(III) doubly deprotonated peptide complex of Gly2HisGly occurs by base-assisted oxidation of the peptide. At < or =p[H+] 7.0, the major pathway is a four-electron oxidation (via 4 Ni(III) complexes) at the alpha carbon of the N-terminal
Terézia Szabó-Plánka et al.
Inorganic chemistry, 41(13), 3483-3490 (2002-06-25)
Twelve ESR-active (and one inactive) copper(II) complexes of L-histidylglycine (HL) were characterized via their formation (micro)constants and ESR parameters obtained by two-dimensional ESR spectroscopic evaluation in aqueous solution. In strongly acidic media, the ligand is coordinated through its N-terminal donor
M A Hefford et al.
Biochimica et biophysica acta, 998(3), 267-270 (1989-10-19)
Secretin has a single histidine residue located at the amino terminus which plays a crucial role in its biological activity. The chemical properties, viz. pK and reactivity, of the alpha-amino and imidazole groups of this residue were determined at a
G Kilian et al.
Die Pharmazie, 68(3), 207-211 (2013-04-06)
Cyclic dipeptides have been well characterized for their biological activity, including antimicrobial and anticancer activities. Cyclo(His-Gly) and cyclo(His-Ala) have also recently demonstrated significant anticancer activity against a range of cell lines, however, as a result of their physicochemistry, namely high
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