Details
Stereochemistry | ACHIRAL |
Molecular Formula | C6H16FN2OP |
Molecular Weight | 182.1762 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)NP(F)(=O)NC(C)C
InChI
InChIKey=UOSHUBFBCPGQAY-UHFFFAOYSA-N
InChI=1S/C6H16FN2OP/c1-5(2)8-11(7,10)9-6(3)4/h5-6H,1-4H3,(H2,8,9,10)
Molecular Formula | C6H16FN2OP |
Molecular Weight | 182.1762 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Approval Year
PubMed
Title | Date | PubMed |
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Striatal neurochemical changes and motor dysfunction in mipafox-treated animals. | 1985 Feb |
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Phenylmethylsulfonyl fluoride protects rats from Mipafox-induced delayed neuropathy. | 1985 Nov |
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The correlation between neurotoxic esterase inhibition and mipafox-induced neuropathic damage in rats. | 1986 Spring |
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Age sensitivity to organophosphate-induced delayed polyneuropathy. Biochemical and toxicological studies in developing chicks. | 1991 May 15 |
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Comparative dose-response studies of organophosphorus ester-induced delayed neuropathy in rats and hens administered mipafox. | 1992 Winter |
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Comparative evolution of mipafox-induced delayed neuropathy in rats and hens. | 1992 Winter |
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Biochemical properties and possible toxicological significance of various forms of NTE. | 1993 Jun |
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Delayed neurotoxic effect of sarin in mice after repeated inhalation exposure. | 1993 Mar-Apr |
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Interactions between neuropathy target esterase and its inhibitors and the development of polyneuropathy. | 1993 Oct |
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Comparison of the relative inhibition of acetylcholinesterase and neuropathy target esterase in rats and hens given cholinesterase inhibitors. | 1995 Jan |
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Acetylcholinesterase and neuropathy target esterase inhibitions in neuroblastoma cells to distinguish organophosphorus compounds causing acute and delayed neurotoxicity. | 1997 Jul |
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Inhibition of carboxylesterases in SH-SY5Y human and NB41A3 mouse neuroblastoma cells by organophosphorus esters. | 1998 Mar 13 |
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Biosensor detection of neuropathy target esterase in whole blood as a biomarker of exposure to neuropathic organophosphorus compounds. | 2003 Apr 11 |
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In vitro protection of red blood cell acetylcholinesterase by metoclopramide from inhibition by organophosphates (paraoxon and mipafox). | 2003 Nov-Dec |
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The mipafox-inhibited catalytic domain of human neuropathy target esterase ages by reversible proton loss. | 2004 Mar 30 |
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In vitro protection of plasma cholinesterases by metoclopramide from inhibition by mipafox. | 2004 Mar-Apr |
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Weak inhibitors protect cholinesterases from strong inhibitors (paraoxon): in vitro effect of tiapride. | 2005 Nov-Dec |
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Degradation of organophosphorus neurotoxicity in SY5Y neuroblastoma cells by organophosphorus hydrolase (OPH). | 2006 Aug |
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Aging of mipafox-inhibited human acetylcholinesterase proceeds by displacement of both isopropylamine groups to yield a phosphate adduct. | 2006 Feb |
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Mechanism of aging of mipafox-inhibited butyrylcholinesterase. | 2007 Mar |
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Effect of inhibition of neuropathy target esterase in mouse nervous tissues in vitro on phosphatidylcholine and lysophosphatidylcholine homeostasis. | 2009 Sep-Oct |
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Constructs of human neuropathy target esterase catalytic domain containing mutations related to motor neuron disease have altered enzymatic properties. | 2010 Jul 1 |
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Motor neuron disease due to neuropathy target esterase mutation: enzyme analysis of fibroblasts from human subjects yields insights into pathogenesis. | 2010 Nov 10 |
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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. | 2014 Jan 9 |
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Resolving pathways of interaction of mipafox and a sarin analog with human acetylcholinesterase by kinetics, mass spectrometry and molecular modeling approaches. | 2016 Mar |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 18:44:48 GMT 2023
by
admin
on
Fri Dec 15 18:44:48 GMT 2023
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Record UNII |
24MJP5H3YN
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Record Status |
Validated (UNII)
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Record Version |
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EPA PESTICIDE CODE |
356300
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24MJP5H3YN
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206-742-3
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DTXSID5042160
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m7557
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1585
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C005238
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mipafox
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371-86-8
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8924
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Mipafox
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