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Substance Name: 1H-Imidazole-4-propanol, beta-amino-, dihydrochloride, (S)- (9CI)
RN: 1596-64-1
InChIKey: FRCAFNBBXRWXQA-XRIGFGBMSA-N

Note

  • 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.

Classification Code

  • Mutation Data

Molecular Formulas

  • C6-H11-H3-O.2Cl-H
  • C6-H11-N3-O.2Cl-H

Molecular Weight

  • 214.095
 
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Names and Synonyms

Synonyms

  • beta-Aminoimidazole-4-propanol dihydrochloride
  • EINECS 216-482-2
  • L-Histidinol dihydrochloride

Systematic Names

  • (S)-beta-Amino-1H-imidazole-4-propanol dihydrochloride
  • 1H-Imidazole-4-propanol, beta-amino-, dihydrochloride, (S)- (9CI)
  • Imidazole-4-propanol, beta-amino-, dihydrochloride

Registry Numbers

CAS Registry Number

  • 1596-64-1

System Generated Number

  • 0001596641

Molecular Formulas

Molecular Formulas

  • C6-H11-H3-O.2Cl-H
  • C6-H11-N3-O.2Cl-H

Molecular Formula Fragments

  • C6-H11-H3-O
  • C6-H11-N3-O
  • Cl-H
  • COMPONENT

Structure Descriptors

InChI

1S/C6H11N3O.2ClH/c7-5(3-10)1-6-2-8-4-9-6;;/h2,4-5,10H,1,3,7H2,(H,8,9);2*1H/t5-;;/m0../s1

InChIKey

FRCAFNBBXRWXQA-XRIGFGBMSA-N

Smiles

[nH]1cncc1C[C@H](N)CO.Cl.Cl