Kinetics of substrate hydrolysis and inhibition by mipafox of paraoxon-preinhibited hen brain esterase activityChanges in LD 50 of parathion and hepatachlor following turpentine pretreatment.Triphenyl phosphite-induced ultrastructural changes in bovine adrenomedullary chromaffin cells.Serum paraoxonase and its influence on paraoxon and chlorpyrifos-oxon toxicity in rats.Parathion and diisopropylfluorophosphate (DFP) toxicity in partially hepatectomized rats.A personal air sampler for pesticidesPreliminary Results from a Regional Comparison of Insecticide DecayOccupational exposure of fieldworkers to organophosphate pesticide residues: environmental correlates of hazardParathion residues on citrus foliage. Decay and composition as related to worker hazard.Differential effects of triphenylphosphite and diisopropyl phosphorofluoridate on catecholamine secretion from bovine adrenomedullary chromaffin cellsSpecies Differences in Serum Paraoxonase Correlate with Sensitivity to Paraoxon ToxicityHealth hazard evaluation report: HETA-82-248-1472, Pesticide Applicators, Fresno, CaliforniaRole of κ→λ light-chain constant-domain switch in the structure and functionality of A17 reactibodyOccupational exposure to organophosphorus compoundsNeurotoxic esterase and neurotoxicityWestern blot analysis of organophosphate exposureOxidative stress resulting from exposure of a human salivary gland cells to paraoxon: an in vitro model for organophosphate oral exposure.Genomic and phenotypic alterations of the neuronal-like cells derived from human embryonal carcinoma stem cells (NT2) caused by exposure to organophosphorus compounds paraoxon and mipafox.Blood glutamate scavenging as a novel neuroprotective treatment for paraoxon intoxication.Protection against paraoxon toxicity by an intravenous pretreatment with polyethylene-glycol-conjugated recombinant butyrylcholinesterase in macaques.Synthesis of silver nanocubes as a SERS substrate for the determination of pesticide paraoxon and thiram.Biophysical aspects of cyclodextrin interaction with paraoxon.
P921
Q23910655-8F5C39CD-F49B-462F-8C7B-17D463BE0E8AQ23912895-C2435183-B27C-4FF7-B275-295C85EAD2E7Q23914441-3AB3E7E2-874A-45C1-89E9-8F5E51D38D4BQ23917151-00EC49FE-9B1D-4E33-A511-E3B9B92CF683Q23919447-F9159BB8-F09D-4DFB-9127-3CFB3CA5B244Q23920288-E59107F8-2787-4576-B00D-EF4A4F473857Q26324491-B0564F51-C30F-469B-9A22-6A17702E8120Q26330117-B39385FA-D28A-498B-9E62-F9DD18BC8035Q26340596-C7B246B5-9D33-4FE7-A066-372734014E9AQ26341944-B7899498-6E1C-4760-962C-85B2D1177FA5Q26345274-0CBC55A2-8D35-4C09-9F89-4CBE2C70697EQ26353166-272E6DB0-6DBF-4B03-AEF0-6965AEC5DF4CQ27681993-81680420-99BF-4BB0-A5BC-4DD918F22DE1Q29007599-DC551C6D-F97C-410A-A342-B0E4C1A241D5Q29008234-E5CCA4D3-B8A4-4C25-A7D7-D27E1331C13DQ29008799-3136B719-42B7-4671-AA15-C195827D8B40Q33723705-7C3935F7-AB5C-4BD5-AC0E-D9733C6216FEQ37535553-B8DC58F2-37B0-4559-9481-30C3A22A9FBFQ39327872-875A7609-FAE1-40D9-BC44-188FCE48C457Q42216415-A22960DE-1243-4CA7-A4F8-1EF7F04DFB0FQ52762292-7F1A497E-39A6-486F-9432-D4670DE65C13Q52764409-EA89F100-C7F9-45B8-87C8-025050EA0597
P921
description
chemesch Verbindung
@lb
chemical compound
@en
chemical compound
@en-ca
chemical compound
@en-gb
chemická sloučenina
@cs
chemická zlúčenina
@sk
chemiese verbinding
@af
chemische Verbindung
@de
chemische Verbindung
@de-ch
chemische verbinding
@nl
name
Paraokson
@sh
Paraokson
@sr
Paraoxon
@cs
Paraoxon
@de
Paraoxon
@hu
Paraoxon
@nl
Paraoxon
@vi
Paraoxone
@fr
Paraoxón
@es
paraoxon
@en
type
label
Paraokson
@sh
Paraokson
@sr
Paraoxon
@cs
Paraoxon
@de
Paraoxon
@hu
Paraoxon
@nl
Paraoxon
@vi
Paraoxone
@fr
Paraoxón
@es
paraoxon
@en
altLabel
311-45-5
@fr
O,O-diethyl O-p-nitrophenyl phosphate
@en
Paraoxon
@es
Paraoxon
@zh
diethyl p-nitrophenyl phosphate
@en
diethyl paraoxon
@en
ethyl paraoxon
@en
p-nitrophenyl diethyl phosphate
@en
phosphacol
@en
phosphoric acid diethyl 4-nitrophenyl ester
@en
prefLabel
Paraokson
@sh
Paraokson
@sr
Paraoxon
@cs
Paraoxon
@de
Paraoxon
@hu
Paraoxon
@nl
Paraoxon
@vi
Paraoxone
@fr
Paraoxón
@es
paraoxon
@en
P486
P592
P6366
P646
P661
P662
P665
P683
P1578
P1579
P2067
P231
P232
P233
CCOP(=O)(OCC)OC1=CC=C(C=C1)[N+](=O)[O-]