H-Gly-Gly-His-OH centers its biochemical utility on histidine’s metal-binding and protonation properties. Glycine residues allow extensive conformational freedom. Structural behavior aids analysis of catalytic and folding pathways. Applications include coordination chemistry and enzymatic modeling.
CAT No: C5407
CAS No:7451-76-5
Synonyms/Alias:H-Gly-Gly-His-OH;7451-76-5;Diglycyl-histidine;Gly-gly-his;Glycylglycyl-L-histidine;(S)-2-(2-(2-Aminoacetamido)acetamido)-3-(1H-imidazol-4-yl)propanoic acid;(2S)-2-[[2-[(2-aminoacetyl)amino]acetyl]amino]-3-(1H-imidazol-5-yl)propanoic acid;(2S)-2-[2-(2-AMINOACETAMIDO)ACETAMIDO]-3-(1H-IMIDAZOL-4-YL)PROPANOIC ACID;glycyl-glycyl-l-histidine;MFCD00079323;SCHEMBL483987;H-Gly-Gly-His-OH, AldrichCPR;CHEBI:163695;PDAWDNVHMUKWJR-ZETCQYMHSA-N;AKOS010420476;AKOS040744581;CS-W014586;HY-W013870;AS-57022;FG108997;
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