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

Details

Stereochemistry ACHIRAL
Molecular Formula C14H16N4O3
Molecular Weight 288.3018
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 2
Charge 2

SHOW SMILES / InChI
Structure of OBIDOXIME

SMILES

O\N=C\C1=CC=[N+](COC[N+]2=CC=C(C=C2)\C=N\O)C=C1

InChI

InChIKey=HIGRLDNHDGYWQJ-UHFFFAOYSA-P
InChI=1S/C14H14N4O3/c19-15-9-13-1-5-17(6-2-13)11-21-12-18-7-3-14(4-8-18)10-16-20/h1-10H,11-12H2/p+2

HIDE SMILES / InChI

Molecular Formula C14H14N4O3
Molecular Weight 286.286
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Obidoxime is an antidote for organophosphorous nerve agent poisoning including chlorosarin, cyclosarin (GF), R-33 (VR), R-VX, sarin (GB), tabun (GA), VX, chlorosoman, soman (GD), and organophosphorous pesticides. It acts as an acetylcholinesterase (AChE) reactivator. In combination with atropine obidoxime can be used to treat super toxic organophosphate poisoning by relieving the symptoms of skeletal neuromuscular blocking that occurs during a cholinergic crisis.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: P22303|||Q53F46
Gene ID: 43.0
Gene Symbol: ACHE
Target Organism: Homo sapiens (Human)
Patents

Patents

Substance Class Chemical
Created
by admin
on Fri Dec 15 17:31:25 GMT 2023
Edited
by admin
on Fri Dec 15 17:31:25 GMT 2023
Record UNII
N6KNE1QA9O
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
OBIDOXIME
WHO-DD  
Common Name English
PIPERIDINIUM, 1,1'-(OXYBIS(METHYLENE))BIS(4-((HYDROXYIMINO)METHYL)-
Common Name English
1,1'-(OXYDIMETHYLENE)BIS(4-FORMYLPYRIDINIUM) DIOXIME
Systematic Name English
Obidoxime [WHO-DD]
Common Name English
PYRIDINIUM, 1,1'-(OXYBIS(METHYLENE))BIS(4-(HYDROXYIMINO)METHYL)-
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C66880
Created by admin on Fri Dec 15 17:31:25 GMT 2023 , Edited by admin on Fri Dec 15 17:31:25 GMT 2023
WHO-VATC QV03AB13
Created by admin on Fri Dec 15 17:31:25 GMT 2023 , Edited by admin on Fri Dec 15 17:31:25 GMT 2023
WHO-ATC V03AB13
Created by admin on Fri Dec 15 17:31:25 GMT 2023 , Edited by admin on Fri Dec 15 17:31:25 GMT 2023
Code System Code Type Description
EVMPD
SUB14676MIG
Created by admin on Fri Dec 15 17:31:25 GMT 2023 , Edited by admin on Fri Dec 15 17:31:25 GMT 2023
PRIMARY
WIKIPEDIA
OBIDOXIME
Created by admin on Fri Dec 15 17:31:25 GMT 2023 , Edited by admin on Fri Dec 15 17:31:25 GMT 2023
PRIMARY
DRUG BANK
DB13750
Created by admin on Fri Dec 15 17:31:25 GMT 2023 , Edited by admin on Fri Dec 15 17:31:25 GMT 2023
PRIMARY
CAS
7683-36-5
Created by admin on Fri Dec 15 17:31:25 GMT 2023 , Edited by admin on Fri Dec 15 17:31:25 GMT 2023
PRIMARY
EPA CompTox
DTXSID50227649
Created by admin on Fri Dec 15 17:31:25 GMT 2023 , Edited by admin on Fri Dec 15 17:31:25 GMT 2023
PRIMARY
SMS_ID
100000080007
Created by admin on Fri Dec 15 17:31:25 GMT 2023 , Edited by admin on Fri Dec 15 17:31:25 GMT 2023
PRIMARY
DRUG CENTRAL
4676
Created by admin on Fri Dec 15 17:31:25 GMT 2023 , Edited by admin on Fri Dec 15 17:31:25 GMT 2023
PRIMARY
PUBCHEM
8251
Created by admin on Fri Dec 15 17:31:25 GMT 2023 , Edited by admin on Fri Dec 15 17:31:25 GMT 2023
PRIMARY
FDA UNII
N6KNE1QA9O
Created by admin on Fri Dec 15 17:31:25 GMT 2023 , Edited by admin on Fri Dec 15 17:31:25 GMT 2023
PRIMARY
NCI_THESAURUS
C84023
Created by admin on Fri Dec 15 17:31:25 GMT 2023 , Edited by admin on Fri Dec 15 17:31:25 GMT 2023
PRIMARY
RXCUI
42826
Created by admin on Fri Dec 15 17:31:25 GMT 2023 , Edited by admin on Fri Dec 15 17:31:25 GMT 2023
PRIMARY RxNorm
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY