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Histidinol The penultimate step in the pathway of histidine biosynthesis. Oxidation of the alcohol group on the side chain gives the acid group forming histidine. Histidinol has also been used as an inhibitor of protein synthesis.
[1. The alcohol analogue of histidine (–COOH becomes –CH2OH).
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Molecular Formula:
C6H11N3O
InChI: InChI=1/C6H11N3O/c7-5(3-10)1-6-2-8-4-9-6/h2,4-5,10H,1,3,7H2,(H,8,9)/f/h9H
InChIKey: InChIKey=ZQISRDCJNBUVMM-BGGKNDAXCW
SMILES: C1=C(NC=N1)CC(CO)N
Names:
histidinol
L-histidinol
2-amino-3-(3H-imidazol-4-yl)propan-1-ol
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Registries:
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PubChem CID 776
PubChem ID 10363789
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