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Details

Stereochemistry ABSOLUTE
Molecular Formula C6H9N3O2.ClH
Molecular Weight 191.616
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of HISTIDINE MONOHYDROCHLORIDE

SMILES

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

InChI

InChIKey=QZNNVYOVQUKYSC-JEDNCBNOSA-N
InChI=1S/C6H9N3O2.ClH/c7-5(6(10)11)1-4-2-8-3-9-4;/h2-3,5H,1,7H2,(H,8,9)(H,10,11);1H/t5-;/m0./s1

HIDE SMILES / InChI

Molecular Formula C6H9N3O2
Molecular Weight 155.1546
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 16:07:34 UTC 2023
Edited
by admin
on Fri Dec 15 16:07:34 UTC 2023
Record UNII
1D5Q932XM6
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
HISTIDINE MONOHYDROCHLORIDE
Systematic Name English
HISTIDINE HYDROCHLORIDE
WHO-DD  
Systematic Name English
SUNACTYL LS 9610
Brand Name English
L-HISTIDINE, HYDROCHLORIDE (1:1)
Systematic Name English
OSMHYDRAN LS 8453
Brand Name English
PHOTONYL
Brand Name English
L-HISTIDINE HYDROCHLORIDE
Systematic Name English
HISTIDINE, L-, MONOHYDROCHLORIDE
Common Name English
HISTIDINE HCL [INCI]
Common Name English
HISTIDINE MONOHYDROCHLORIDE ANHYDROUS
Common Name English
L-HISTIDINE MONOHYDROCHLORIDE
JAN  
Systematic Name English
P.P.A.A.
Brand Name English
HISTIDINE HCL
INCI  
INCI  
Official Name English
NSC-257867
Code English
Histidine hydrochloride [WHO-DD]
Common Name English
HISTIDINE HYDROCHLORIDE, L-
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C68442
Created by admin on Fri Dec 15 16:07:34 UTC 2023 , Edited by admin on Fri Dec 15 16:07:34 UTC 2023
Code System Code Type Description
DAILYMED
1D5Q932XM6
Created by admin on Fri Dec 15 16:07:34 UTC 2023 , Edited by admin on Fri Dec 15 16:07:34 UTC 2023
PRIMARY
CAS
645-35-2
Created by admin on Fri Dec 15 16:07:34 UTC 2023 , Edited by admin on Fri Dec 15 16:07:34 UTC 2023
PRIMARY
ChEMBL
CHEMBL17962
Created by admin on Fri Dec 15 16:07:34 UTC 2023 , Edited by admin on Fri Dec 15 16:07:34 UTC 2023
PRIMARY
EVMPD
SUB14110MIG
Created by admin on Fri Dec 15 16:07:34 UTC 2023 , Edited by admin on Fri Dec 15 16:07:34 UTC 2023
PRIMARY
PUBCHEM
66091
Created by admin on Fri Dec 15 16:07:34 UTC 2023 , Edited by admin on Fri Dec 15 16:07:34 UTC 2023
PRIMARY
SMS_ID
100000078312
Created by admin on Fri Dec 15 16:07:34 UTC 2023 , Edited by admin on Fri Dec 15 16:07:34 UTC 2023
PRIMARY
NCI_THESAURUS
C87704
Created by admin on Fri Dec 15 16:07:34 UTC 2023 , Edited by admin on Fri Dec 15 16:07:34 UTC 2023
PRIMARY
EPA CompTox
DTXSID3020700
Created by admin on Fri Dec 15 16:07:34 UTC 2023 , Edited by admin on Fri Dec 15 16:07:34 UTC 2023
PRIMARY
ECHA (EC/EINECS)
211-438-9
Created by admin on Fri Dec 15 16:07:34 UTC 2023 , Edited by admin on Fri Dec 15 16:07:34 UTC 2023
PRIMARY
NSC
257867
Created by admin on Fri Dec 15 16:07:34 UTC 2023 , Edited by admin on Fri Dec 15 16:07:34 UTC 2023
PRIMARY
EVMPD
SUB20035
Created by admin on Fri Dec 15 16:07:34 UTC 2023 , Edited by admin on Fri Dec 15 16:07:34 UTC 2023
PRIMARY
FDA UNII
1D5Q932XM6
Created by admin on Fri Dec 15 16:07:34 UTC 2023 , Edited by admin on Fri Dec 15 16:07:34 UTC 2023
PRIMARY
RXCUI
1309689
Created by admin on Fri Dec 15 16:07:34 UTC 2023 , Edited by admin on Fri Dec 15 16:07:34 UTC 2023
PRIMARY RxNorm
Related Record Type Details
SOLVATE->ANHYDROUS
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY