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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
Structure of MIPAFOX

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)

HIDE SMILES / InChI

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

PubMed

TitleDatePubMed
Resolving pathways of interaction of mipafox and a sarin analog with human acetylcholinesterase by kinetics, mass spectrometry and molecular modeling approaches.
2016-03
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.
2014-01-09
Motor neuron disease due to neuropathy target esterase mutation: enzyme analysis of fibroblasts from human subjects yields insights into pathogenesis.
2010-11-10
Constructs of human neuropathy target esterase catalytic domain containing mutations related to motor neuron disease have altered enzymatic properties.
2010-07-01
Effect of inhibition of neuropathy target esterase in mouse nervous tissues in vitro on phosphatidylcholine and lysophosphatidylcholine homeostasis.
2009-07-22
Mechanism of aging of mipafox-inhibited butyrylcholinesterase.
2007-03
Degradation of organophosphorus neurotoxicity in SY5Y neuroblastoma cells by organophosphorus hydrolase (OPH).
2006-08
Aging of mipafox-inhibited human acetylcholinesterase proceeds by displacement of both isopropylamine groups to yield a phosphate adduct.
2006-02
Weak inhibitors protect cholinesterases from strong inhibitors (paraoxon): in vitro effect of tiapride.
2005-09-30
In vitro protection of plasma cholinesterases by metoclopramide from inhibition by mipafox.
2004-03-31
The mipafox-inhibited catalytic domain of human neuropathy target esterase ages by reversible proton loss.
2004-03-30
In vitro protection of red blood cell acetylcholinesterase by metoclopramide from inhibition by organophosphates (paraoxon and mipafox).
2003-11-25
Biosensor detection of neuropathy target esterase in whole blood as a biomarker of exposure to neuropathic organophosphorus compounds.
2003-04-11
Inhibition of carboxylesterases in SH-SY5Y human and NB41A3 mouse neuroblastoma cells by organophosphorus esters.
1998-03-13
Acetylcholinesterase and neuropathy target esterase inhibitions in neuroblastoma cells to distinguish organophosphorus compounds causing acute and delayed neurotoxicity.
1997-07
Comparison of the relative inhibition of acetylcholinesterase and neuropathy target esterase in rats and hens given cholinesterase inhibitors.
1995-01
Interactions between neuropathy target esterase and its inhibitors and the development of polyneuropathy.
1993-10
Biochemical properties and possible toxicological significance of various forms of NTE.
1993-06
Delayed neurotoxic effect of sarin in mice after repeated inhalation exposure.
1993-03-01
Comparative dose-response studies of organophosphorus ester-induced delayed neuropathy in rats and hens administered mipafox.
1992
Comparative evolution of mipafox-induced delayed neuropathy in rats and hens.
1992
Age sensitivity to organophosphate-induced delayed polyneuropathy. Biochemical and toxicological studies in developing chicks.
1991-05-15
The correlation between neurotoxic esterase inhibition and mipafox-induced neuropathic damage in rats.
1986
Phenylmethylsulfonyl fluoride protects rats from Mipafox-induced delayed neuropathy.
1985-11
Striatal neurochemical changes and motor dysfunction in mipafox-treated animals.
1985-02
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 19:20:02 GMT 2025
Edited
by admin
on Mon Mar 31 19:20:02 GMT 2025
Record UNII
24MJP5H3YN
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MIPAFOX
HSDB   ISO   MI  
Common Name English
NSC-8924
Preferred Name English
N,N'-DIISOPROPYLPHOSPHORODIAMIDIC FLUORIDE
Systematic Name English
MIPAFOX [MI]
Common Name English
N,N'-BIS(1-METHYLETHYL)PHOSPHORODIAMIDIC FLUORIDE
Systematic Name English
MIPAFOX [HSDB]
Common Name English
MIPAFOX [ISO]
Common Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 356300
Created by admin on Mon Mar 31 19:20:02 GMT 2025 , Edited by admin on Mon Mar 31 19:20:02 GMT 2025
Code System Code Type Description
FDA UNII
24MJP5H3YN
Created by admin on Mon Mar 31 19:20:02 GMT 2025 , Edited by admin on Mon Mar 31 19:20:02 GMT 2025
PRIMARY
ECHA (EC/EINECS)
206-742-3
Created by admin on Mon Mar 31 19:20:02 GMT 2025 , Edited by admin on Mon Mar 31 19:20:02 GMT 2025
PRIMARY
EPA CompTox
DTXSID5042160
Created by admin on Mon Mar 31 19:20:02 GMT 2025 , Edited by admin on Mon Mar 31 19:20:02 GMT 2025
PRIMARY
MERCK INDEX
m7557
Created by admin on Mon Mar 31 19:20:02 GMT 2025 , Edited by admin on Mon Mar 31 19:20:02 GMT 2025
PRIMARY Merck Index
HSDB
1585
Created by admin on Mon Mar 31 19:20:02 GMT 2025 , Edited by admin on Mon Mar 31 19:20:02 GMT 2025
PRIMARY
MESH
C005238
Created by admin on Mon Mar 31 19:20:02 GMT 2025 , Edited by admin on Mon Mar 31 19:20:02 GMT 2025
PRIMARY
ALANWOOD
mipafox
Created by admin on Mon Mar 31 19:20:02 GMT 2025 , Edited by admin on Mon Mar 31 19:20:02 GMT 2025
PRIMARY
PUBCHEM
9738
Created by admin on Mon Mar 31 19:20:02 GMT 2025 , Edited by admin on Mon Mar 31 19:20:02 GMT 2025
PRIMARY
CAS
371-86-8
Created by admin on Mon Mar 31 19:20:02 GMT 2025 , Edited by admin on Mon Mar 31 19:20:02 GMT 2025
PRIMARY
NSC
8924
Created by admin on Mon Mar 31 19:20:02 GMT 2025 , Edited by admin on Mon Mar 31 19:20:02 GMT 2025
PRIMARY
WIKIPEDIA
Mipafox
Created by admin on Mon Mar 31 19:20:02 GMT 2025 , Edited by admin on Mon Mar 31 19:20:02 GMT 2025
PRIMARY