His | |
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Esters [] | |
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Histidine benzoate | |
Molecular structure via molpic | |
Conformer structure via 3Dmol.js | |
Molecular formula | C6H9N3O2[1] |
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Molecular mass | 155.15 g/mol[1] |
Predicted LogP | -3.2[1] |
Chirality | racemic[2] |
Identifiers [] | |
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IUPAC name | 2-amino-3-(1H-imidazol-5-yl)propanoic acid[1] |
SMILES | C1=C(NC=N1)CC(C(=O)O)N[1] |
InChI | InChI=1S/C6H9N3O2/c7-5(6(10)11)1-4-2-8-3-9-4/h2-3,5H,1,7H2,(H,8,9)(H,10,11)[1] |
InChIKey | HNDVDQJCIGZPNO-UHFFFAOYSA-N[1] |
Dosing |
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Histidine
Histidine (also known as Dl-histidine, 26062-48-6, DL-2-Amino-3-(4-imidazolyl)propionsaeure, 1H-imidazole-4-alanine, 2-azaniumyl-3-(1h-imidazol-5-yl)propanoate, 225-660-9, dl2amino3(4imidazolyl)propionsaeure, dtxcid40196658, histidine, dl or l-histidine, homopolymer) is a substance of the amino acid class.
Chemistry
Histidine is typically found in the form of its benzoate ester.
Stereochemistry
DL-Histidine is a racemic mixture of the logical stereoisomers:
Stereoisomers [] |
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See also
External links
- Histidine (Wikipedia)
- Histidine / D-Histidine / L-Histidine (Wikidata)
- Histidine / D-Histidine / L-Histidine (PubChem)
- Histidine / D-Histidine / L-Histidine (Common Chemistry)
- Histidine / L-Histidine (HMDB)
- Histidine / D-Histidine / L-Histidine (KEGG)
- Histidine / D-Histidine / L-Histidine (UNII)
- Histidine / D-Histidine / L-Histidine (EPA DSSTox)