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Details

Stereochemistry ACHIRAL
Molecular Formula C12H21N2O4P
Molecular Weight 288.2799
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DIAZOXON

SMILES

CCOP(=O)(OCC)OC1=CC(C)=NC(=N1)C(C)C

InChI

InChIKey=VBLJFQYCTRKKKF-UHFFFAOYSA-N
InChI=1S/C12H21N2O4P/c1-6-16-19(15,17-7-2)18-11-8-10(5)13-12(14-11)9(3)4/h8-9H,6-7H2,1-5H3

HIDE SMILES / InChI

Molecular Formula C12H21N2O4P
Molecular Weight 288.2799
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
In vitro evaluation of neurotoxicity potential and oxidative stress responses of diazinon and its degradation products in rat brain synaptosomes.
2015-02-17
Assessing protection against OP pesticides and nerve agents provided by wild-type HuPON1 purified from Trichoplusia ni larvae or induced via adenoviral infection.
2013-03-25
Pyridostigmine bromide protection against acetylcholinesterase inhibition by pesticides.
2012-01
Environmental impact on vascular development predicted by high-throughput screening.
2011-11
Adenovirus-mediated human paraoxonase1 gene transfer to provide protection against the toxicity of the organophosphorus pesticide toxicant diazoxon.
2011-03
Serum albumins and detoxication of anti-cholinesterase agents.
2010-09-06
Engineering human PON1 in an E. coli expression system.
2010
Relationship between human paraoxonase-1 activity and PON1 polymorphisms in Mexican workers exposed to organophosphate pesticides.
2009-07-24
Paraoxonase 1 (PON1) modulates the toxicity of mixed organophosphorus compounds.
2009-04-15
Paraoxonase 1 (PON1) status and substrate hydrolysis.
2009-02-15
Age-related brain cholinesterase inhibition kinetics following in vitro incubation with chlorpyrifos-oxon and diazinon-oxon.
2007-01
Serine hydrolase KIAA1363: toxicological and structural features with emphasis on organophosphate interactions.
2006-09
Degradation and by-product formation of diazinon in water during UV and UV/H(2)O(2) treatment.
2006-08-25
Each lipase has a unique sensitivity profile for organophosphorus inhibitors.
2006-05
Albumin, a new biomarker of organophosphorus toxicant exposure, identified by mass spectrometry.
2005-02
Paraoxonase 1 status in the Thai population.
2005
Paraoxonase and susceptibility to organophosphorus poisoning in farmers dipping sheep.
2003-02
Cannabinoid CB1 receptor as a target for chlorpyrifos oxon and other organophosphorus pesticides.
2002-09-05
Differential toxicities of organophosphate and carbamate insecticides in the nestling European starling (Sturnus vulgaris).
2000-08
Analysis of paraoxonase (PON1) L55M status requires both genotype and phenotype.
2000-07
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:11:40 GMT 2025
Edited
by admin
on Mon Mar 31 19:11:40 GMT 2025
Record UNII
9FX08D2L1U
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DIAZINON OXYGEN ANALOG
Preferred Name English
DIAZOXON
Common Name English
PHOSPHORIC ACID, DIETHYL 6-METHYL-2-(1-METHYLETHYL)-4-PYRIMIDINYL ESTER
Common Name English
DIETHYL (6-METHYL-2-PROPAN-2-YLPYRIMIDIN-4-YL) PHOSPHATE
Systematic Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 657802
Created by admin on Mon Mar 31 19:11:40 GMT 2025 , Edited by admin on Mon Mar 31 19:11:40 GMT 2025
Code System Code Type Description
EPA CompTox
DTXSID5037523
Created by admin on Mon Mar 31 19:11:40 GMT 2025 , Edited by admin on Mon Mar 31 19:11:40 GMT 2025
PRIMARY
CAS
962-58-3
Created by admin on Mon Mar 31 19:11:40 GMT 2025 , Edited by admin on Mon Mar 31 19:11:40 GMT 2025
PRIMARY
FDA UNII
9FX08D2L1U
Created by admin on Mon Mar 31 19:11:40 GMT 2025 , Edited by admin on Mon Mar 31 19:11:40 GMT 2025
PRIMARY
PUBCHEM
13754
Created by admin on Mon Mar 31 19:11:40 GMT 2025 , Edited by admin on Mon Mar 31 19:11:40 GMT 2025
PRIMARY
MESH
C000912
Created by admin on Mon Mar 31 19:11:40 GMT 2025 , Edited by admin on Mon Mar 31 19:11:40 GMT 2025
PRIMARY