His

Esters []
Histidine benzoate

Molecular structure via molpic
Conformer structure via 3Dmol.js
Molecular formula	C6H9N3O2[1]
Molecular mass	155.15 g/mol[1]
Predicted LogP	-3.2[1]
Chirality	racemic[2]

Identifiers []
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

Histidine

(Redirected from L-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 []
D-Histidine L-Histidine DL-Histidine

See also

• Substituted amino acids
• Anodyne

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)