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Details

Stereochemistry ACHIRAL
Molecular Formula C7H9N2O
Molecular Weight 137.1592
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 1
Stereo Comments Assumed E-isomer as in USP/NF chloride salt record

SHOW SMILES / InChI
Structure of PRALIDOXIME

SMILES

C[N+]1=C(\C=N\O)C=CC=C1

InChI

InChIKey=JBKPUQTUERUYQE-UHFFFAOYSA-O
InChI=1S/C7H8N2O/c1-9-5-3-2-4-7(9)6-8-10/h2-6H,1H3/p+1

HIDE SMILES / InChI
Molecular Formula C7H8N2O
Molecular Weight 136.1512
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

Approval Year

Unknown
86413
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:55:27 UTC 2023
Edited
by admin
on Fri Dec 15 15:55:27 UTC 2023
Record UNII
P7MU9UTP52
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PRALIDOXIME
MART.   VANDF   WHO-DD  
Common Name English
PRALIDOXIME [VANDF]
Common Name English
PRALIDOXIME ION
Common Name English
PRALIDOXIME [MART.]
Common Name English
Pralidoxime [WHO-DD]
Common Name English
PRALIDOXIME CATION
Common Name English
Classification Tree Code System Code
NDF-RT N0000175742
Created by admin on Fri Dec 15 15:55:27 UTC 2023 , Edited by admin on Fri Dec 15 15:55:27 UTC 2023
WHO-ATC V03AB04
Created by admin on Fri Dec 15 15:55:27 UTC 2023 , Edited by admin on Fri Dec 15 15:55:27 UTC 2023
WHO-VATC QV03AB04
Created by admin on Fri Dec 15 15:55:27 UTC 2023 , Edited by admin on Fri Dec 15 15:55:27 UTC 2023
NDF-RT N0000000080
Created by admin on Fri Dec 15 15:55:27 UTC 2023 , Edited by admin on Fri Dec 15 15:55:27 UTC 2023
NCI_THESAURUS C47796
Created by admin on Fri Dec 15 15:55:27 UTC 2023 , Edited by admin on Fri Dec 15 15:55:27 UTC 2023
Code System Code Type Description
EPA CompTox
DTXSID1044144
Created by admin on Fri Dec 15 15:55:27 UTC 2023 , Edited by admin on Fri Dec 15 15:55:27 UTC 2023
PRIMARY
NCI_THESAURUS
C78131
Created by admin on Fri Dec 15 15:55:27 UTC 2023 , Edited by admin on Fri Dec 15 15:55:27 UTC 2023
PRIMARY
DRUG CENTRAL
2231
Created by admin on Fri Dec 15 15:55:27 UTC 2023 , Edited by admin on Fri Dec 15 15:55:27 UTC 2023
PRIMARY
CAS
6735-59-7
Created by admin on Fri Dec 15 15:55:27 UTC 2023 , Edited by admin on Fri Dec 15 15:55:27 UTC 2023
NON-SPECIFIC STEREOCHEMISTRY
ECHA (EC/EINECS)
229-787-0
Created by admin on Fri Dec 15 15:55:27 UTC 2023 , Edited by admin on Fri Dec 15 15:55:27 UTC 2023
PRIMARY
CHEBI
8354
Created by admin on Fri Dec 15 15:55:27 UTC 2023 , Edited by admin on Fri Dec 15 15:55:27 UTC 2023
PRIMARY
EVMPD
SUB04002MIG
Created by admin on Fri Dec 15 15:55:27 UTC 2023 , Edited by admin on Fri Dec 15 15:55:27 UTC 2023
PRIMARY
IUPHAR
7597
Created by admin on Fri Dec 15 15:55:27 UTC 2023 , Edited by admin on Fri Dec 15 15:55:27 UTC 2023
PRIMARY
DAILYMED
P7MU9UTP52
Created by admin on Fri Dec 15 15:55:27 UTC 2023 , Edited by admin on Fri Dec 15 15:55:27 UTC 2023
PRIMARY
PUBCHEM
4884
Created by admin on Fri Dec 15 15:55:27 UTC 2023 , Edited by admin on Fri Dec 15 15:55:27 UTC 2023
PRIMARY
ChEMBL
CHEMBL1420
Created by admin on Fri Dec 15 15:55:27 UTC 2023 , Edited by admin on Fri Dec 15 15:55:27 UTC 2023
PRIMARY
SMS_ID
100000085479
Created by admin on Fri Dec 15 15:55:27 UTC 2023 , Edited by admin on Fri Dec 15 15:55:27 UTC 2023
PRIMARY
RXCUI
34345
Created by admin on Fri Dec 15 15:55:27 UTC 2023 , Edited by admin on Fri Dec 15 15:55:27 UTC 2023
ALTERNATIVE
CAS
25615-00-3
Created by admin on Fri Dec 15 15:55:27 UTC 2023 , Edited by admin on Fri Dec 15 15:55:27 UTC 2023
PRIMARY
DRUG BANK
DB00733
Created by admin on Fri Dec 15 15:55:27 UTC 2023 , Edited by admin on Fri Dec 15 15:55:27 UTC 2023
PRIMARY
WIKIPEDIA
PRALIDOXIME
Created by admin on Fri Dec 15 15:55:27 UTC 2023 , Edited by admin on Fri Dec 15 15:55:27 UTC 2023
PRIMARY
RXCUI
1546365
Created by admin on Fri Dec 15 15:55:27 UTC 2023 , Edited by admin on Fri Dec 15 15:55:27 UTC 2023
PRIMARY
FDA UNII
P7MU9UTP52
Created by admin on Fri Dec 15 15:55:27 UTC 2023 , Edited by admin on Fri Dec 15 15:55:27 UTC 2023
PRIMARY
MESH
C028797
Created by admin on Fri Dec 15 15:55:27 UTC 2023 , Edited by admin on Fri Dec 15 15:55:27 UTC 2023
PRIMARY
Related Record Type Details
Structure of PRALIDOXIME METHYL SULFATE
SALT/SOLVATE -> PARENT
Structure of PRALIDOXIME CHLORIDE
SALT/SOLVATE -> PARENT
Structure of PRALIDOXIME IODIDE
SALT/SOLVATE -> PARENT
Structure of PRALIDOXIME BROMIDE
SALT/SOLVATE -> PARENT
Structure of PRALIDOXIME MESYLATE
SALT/SOLVATE -> PARENT
Related Record Type Details
Structure of 2-CYANO-N-METHYLPYRIDINIUM
METABOLITE -> PARENT
Pralidoxime is largely excreted unchanged in urine
Related Record Type Details
Structure of PRALIDOXIME
ACTIVE MOIETY
Name Property Type Amount Referenced Substance Defining Parameters References
Biological Half-life PHARMACOKINETIC
NIH
NCATS
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