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Details

Stereochemistry ACHIRAL
Molecular Formula C7H9N2O.I
Molecular Weight 264.0636
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0
Stereo Comments Assumed E-isomer (MM2 minimum energy for E and Z isomers of moieties are 9.9968 and 13.3275 kcal/mol)

SHOW SMILES / InChI
Structure of PRALIDOXIME IODIDE

SMILES

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

InChI

InChIKey=QNBVYCDYFJUNLO-UHFFFAOYSA-N
InChI=1S/C7H8N2O.HI/c1-9-5-3-2-4-7(9)6-8-10;/h2-6H,1H3;1H

HIDE SMILES / InChI

Molecular Formula HI
Molecular Weight 127.9124
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

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

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:49:11 UTC 2023
Edited
by admin
on Fri Dec 15 15:49:11 UTC 2023
Record UNII
7H254VC0NT
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PRALIDOXIME IODIDE
INN   JAN   MART.   USAN   WHO-DD  
USAN   INN  
Official Name English
2-Formyl-1-methylpyridinium iodide oxime
Systematic Name English
PRALIDOXIME IODIDE [JAN]
Common Name English
1-METHYL-2-HYDROXYIMINOETHYLPYRIDINIUM IODIDE
Systematic Name English
NSC-7760
Code English
NSC-40164
Code English
Pralidoxime iodide [WHO-DD]
Common Name English
PRALIDOXIME IODIDE [MART.]
Common Name English
PRALIDOXIME IODIDE [USAN]
Common Name English
PRALIDOXIME IODIDE [MI]
Common Name English
pralidoxime iodide [INN]
Common Name English
PAM
Brand Name English
Classification Tree Code System Code
NCI_THESAURUS C47796
Created by admin on Fri Dec 15 15:49:11 UTC 2023 , Edited by admin on Fri Dec 15 15:49:11 UTC 2023
Code System Code Type Description
FDA UNII
7H254VC0NT
Created by admin on Fri Dec 15 15:49:11 UTC 2023 , Edited by admin on Fri Dec 15 15:49:11 UTC 2023
PRIMARY
NCI_THESAURUS
C73847
Created by admin on Fri Dec 15 15:49:11 UTC 2023 , Edited by admin on Fri Dec 15 15:49:11 UTC 2023
PRIMARY
NSC
40164
Created by admin on Fri Dec 15 15:49:11 UTC 2023 , Edited by admin on Fri Dec 15 15:49:11 UTC 2023
PRIMARY
CHEBI
32038
Created by admin on Fri Dec 15 15:49:11 UTC 2023 , Edited by admin on Fri Dec 15 15:49:11 UTC 2023
PRIMARY
INN
851
Created by admin on Fri Dec 15 15:49:11 UTC 2023 , Edited by admin on Fri Dec 15 15:49:11 UTC 2023
PRIMARY
SMS_ID
100000081393
Created by admin on Fri Dec 15 15:49:11 UTC 2023 , Edited by admin on Fri Dec 15 15:49:11 UTC 2023
PRIMARY
ChEMBL
CHEMBL1420
Created by admin on Fri Dec 15 15:49:11 UTC 2023 , Edited by admin on Fri Dec 15 15:49:11 UTC 2023
PRIMARY
CAS
74070-01-2
Created by admin on Fri Dec 15 15:49:11 UTC 2023 , Edited by admin on Fri Dec 15 15:49:11 UTC 2023
ALTERNATIVE
PUBCHEM
65342
Created by admin on Fri Dec 15 15:49:11 UTC 2023 , Edited by admin on Fri Dec 15 15:49:11 UTC 2023
PRIMARY
ECHA (EC/EINECS)
202-349-6
Created by admin on Fri Dec 15 15:49:11 UTC 2023 , Edited by admin on Fri Dec 15 15:49:11 UTC 2023
PRIMARY
NSC
7760
Created by admin on Fri Dec 15 15:49:11 UTC 2023 , Edited by admin on Fri Dec 15 15:49:11 UTC 2023
PRIMARY
RXCUI
55052
Created by admin on Fri Dec 15 15:49:11 UTC 2023 , Edited by admin on Fri Dec 15 15:49:11 UTC 2023
PRIMARY RxNorm
EVMPD
SUB09988MIG
Created by admin on Fri Dec 15 15:49:11 UTC 2023 , Edited by admin on Fri Dec 15 15:49:11 UTC 2023
PRIMARY
MESH
C028797
Created by admin on Fri Dec 15 15:49:11 UTC 2023 , Edited by admin on Fri Dec 15 15:49:11 UTC 2023
PRIMARY
EPA CompTox
DTXSID80916716
Created by admin on Fri Dec 15 15:49:11 UTC 2023 , Edited by admin on Fri Dec 15 15:49:11 UTC 2023
PRIMARY
CAS
94-63-3
Created by admin on Fri Dec 15 15:49:11 UTC 2023 , Edited by admin on Fri Dec 15 15:49:11 UTC 2023
NON-SPECIFIC STEREOCHEMISTRY
MERCK INDEX
m9092
Created by admin on Fri Dec 15 15:49:11 UTC 2023 , Edited by admin on Fri Dec 15 15:49:11 UTC 2023
PRIMARY Merck Index
Related Record Type Details
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY