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Details

Stereochemistry ABSOLUTE
Molecular Formula C8H11N3O3.H2O
Molecular Weight 215.2065
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of N-ACETYLHISTIDINE MONOHYDRATE

SMILES

O.CC(=O)N[C@@H](CC1=CNC=N1)C(O)=O

InChI

InChIKey=PSWSDQRXCOJSFC-FJXQXJEOSA-N
InChI=1S/C8H11N3O3.H2O/c1-5(12)11-7(8(13)14)2-6-3-9-4-10-6;/h3-4,7H,2H2,1H3,(H,9,10)(H,11,12)(H,13,14);1H2/t7-;/m0./s1

HIDE SMILES / InChI

Molecular Formula C8H11N3O3
Molecular Weight 197.1912
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Molecular Formula H2O
Molecular Weight 18.0153
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Ultraviolet spectrophotometric characterization of copper(II) complexes with imidazole N-methyl derivatives of L-histidine in aqueous solution.
2003 Jan 1
Histidine nutrition and genotype affect cataract development in Atlantic salmon, Salmo salar L.
2005 Jun
Kinetic analysis of the role of histidine chloramines in hypochlorous acid mediated protein oxidation.
2005 May 17
Solution interactions between the uranyl cation [UO2(2+)] and histidine, N-acetyl-histidine, tyrosine, and N-acetyl-tyrosine.
2009 Jan
Prostate cancer-targeted imaging using magnetofluorescent polymeric nanoparticles functionalized with bombesin.
2010 Apr
Influence of histidine on the release of all-trans retinoic acid from self-assembled glycol chitosan nanoparticles.
2010 Jul
Ability of hypochlorous acid and N-chloramines to chlorinate DNA and its constituents.
2010 Jul 19
Tumor targeting efficiency of bare nanoparticles does not mean the efficacy of loaded anticancer drugs: importance of radionuclide imaging for optimization of highly selective tumor targeting polymeric nanoparticles with or without drug.
2010 Oct 15
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 01:04:42 GMT 2023
Edited
by admin
on Sat Dec 16 01:04:42 GMT 2023
Record UNII
PQ2TC3X11O
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
N-ACETYLHISTIDINE MONOHYDRATE
Common Name English
N-ACETYL-L-HISTIDINE HYDRATE
Brand Name English
L-N-ACETYLHISTIDINE MONOHYDRATE
Systematic Name English
ACETYL HISTIDINE
INCI  
INCI  
Official Name English
ACETYL HISTIDINE [INCI]
Common Name English
L-HISTIDINE, N-ACETYL-, HYDRATE (1:1)
Systematic Name English
L-HISTIDINE, N-ACETYL-, MONOHYDRATE
Systematic Name English
Code System Code Type Description
PUBCHEM
2724380
Created by admin on Sat Dec 16 01:04:42 GMT 2023 , Edited by admin on Sat Dec 16 01:04:42 GMT 2023
PRIMARY
EPA CompTox
DTXSID901021292
Created by admin on Sat Dec 16 01:04:42 GMT 2023 , Edited by admin on Sat Dec 16 01:04:42 GMT 2023
PRIMARY
SMS_ID
300000023531
Created by admin on Sat Dec 16 01:04:42 GMT 2023 , Edited by admin on Sat Dec 16 01:04:42 GMT 2023
PRIMARY
CAS
39145-52-3
Created by admin on Sat Dec 16 01:04:42 GMT 2023 , Edited by admin on Sat Dec 16 01:04:42 GMT 2023
PRIMARY
FDA UNII
PQ2TC3X11O
Created by admin on Sat Dec 16 01:04:42 GMT 2023 , Edited by admin on Sat Dec 16 01:04:42 GMT 2023
PRIMARY
Related Record Type Details
ANHYDROUS->SOLVATE
PARENT -> SALT/SOLVATE