U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry RACEMIC
Molecular Formula C6H9N3O2
Molecular Weight 155.1546
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of HISTIDINE, DL-

SMILES

NC(CC1=CNC=N1)C(O)=O

InChI

InChIKey=HNDVDQJCIGZPNO-UHFFFAOYSA-N
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)

HIDE SMILES / InChI

Molecular Formula C6H9N3O2
Molecular Weight 155.1546
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Histidine racemate is a mixture of naturally occurring essential amino acid L-histidine and its enantiomer D-histidine. D-histidine is less readily utilized than the natural isomer. It is not metabolized by histidase and is not readily oxidized by D-amino acid oxidase. Some fungi incorporate D-histidine into proteins as a measure of protection against hydrolases and to enhance antimicrobial activity.

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 14:58:20 GMT 2023
Edited
by admin
on Fri Dec 15 14:58:20 GMT 2023
Record UNII
QU6SDF3Q03
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
HISTIDINE, DL-
Systematic Name English
1H-IMIDAZOLE-4-ALANINE
Common Name English
DL-2-AMINO-3-(4-IMIDAZOLYL)PROPIONSAEURE
Common Name English
(±)-HISTIDINE
Systematic Name English
DL-HISTIDINE
Systematic Name English
Classification Tree Code System Code
CFR 21 CFR 862.1375
Created by admin on Fri Dec 15 14:58:21 GMT 2023 , Edited by admin on Fri Dec 15 14:58:21 GMT 2023
Code System Code Type Description
PUBCHEM
773
Created by admin on Fri Dec 15 14:58:21 GMT 2023 , Edited by admin on Fri Dec 15 14:58:21 GMT 2023
PRIMARY
CAS
4998-57-6
Created by admin on Fri Dec 15 14:58:21 GMT 2023 , Edited by admin on Fri Dec 15 14:58:21 GMT 2023
PRIMARY
EPA CompTox
DTXSID00901785
Created by admin on Fri Dec 15 14:58:21 GMT 2023 , Edited by admin on Fri Dec 15 14:58:21 GMT 2023
PRIMARY
ECHA (EC/EINECS)
225-660-9
Created by admin on Fri Dec 15 14:58:21 GMT 2023 , Edited by admin on Fri Dec 15 14:58:21 GMT 2023
PRIMARY
CHEBI
27570
Created by admin on Fri Dec 15 14:58:21 GMT 2023 , Edited by admin on Fri Dec 15 14:58:21 GMT 2023
PRIMARY
FDA UNII
QU6SDF3Q03
Created by admin on Fri Dec 15 14:58:21 GMT 2023 , Edited by admin on Fri Dec 15 14:58:21 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE