bis(4-nitrophenyl)phosphate and paraoxon

bis(4-nitrophenyl)phosphate has been researched along with paraoxon in 9 studies

Research

Studies (9)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's6 (66.67)18.2507
2000's3 (33.33)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Monteith, DK; Strom, SC1
Hanna, PE; Wick, MJ1
Jakoby, WB; Kim, DH; Yang, YS1
Hemingway, J; Jayawardena, KG; Karunaratne, SH; Ketterman, AJ1
Heymann, E; Hoppe, W; Krüsselmann, A; Tschoetschel, C1
Pavković, E; Radić, Z; Reiner, E; Simeon, V1
Nagy, A; Plonowski, A; Schally, AV1
Ghanem, E; Li, Y; Raushel, FM; Xu, C1
Ackermann, C; Fate, G; Jewell, C; Payne, NA; Voorman, R; Williams, FM1

Other Studies

9 other study(ies) available for bis(4-nitrophenyl)phosphate and paraoxon

ArticleYear
A comparison of the inhibition of deacetylase in primary cultures of rat and human hepatocytes effecting metabolism and DNA-binding of 2-acetylaminofluorene.
    Cell biology and toxicology, 1990, Volume: 6, Issue:3

    Topics: 2-Acetylaminofluorene; Adult; Aged; Amidohydrolases; Animals; Cell Survival; Cells, Cultured; DNA; Female; Humans; Liver; Male; Nitrophenols; Paraoxon; Rats; Species Specificity

1990
Bioactivation of N-arylhydroxamic acids by rat hepatic N-acetyltransferase. Detection of multiple enzyme forms by mechanism-based inactivation.
    Biochemical pharmacology, 1990, Mar-15, Volume: 39, Issue:6

    Topics: Acetyltransferases; Animals; Arylamine N-Acetyltransferase; Biotransformation; Enzyme Activation; Hydroxamic Acids; Hydroxyacetylaminofluorene; Isoenzymes; Liver; Nitrophenols; Paraoxon; Protein Binding; Rats; Substrate Specificity

1990
Aspirin hydrolyzing esterases from rat liver cytosol.
    Biochemical pharmacology, 1990, Aug-01, Volume: 40, Issue:3

    Topics: Animals; Aspirin; Chromatography, DEAE-Cellulose; Chromatography, Gel; Cytosol; Esterases; Hydrogen-Ion Concentration; Hydrolysis; Isoenzymes; Liver; Molecular Weight; Nitrophenols; Paraoxon; Rats; Substrate Specificity

1990
The function of esterases in insecticide resistance in Culex quinquefasciatus mosquitoes from Sri Lanka.
    Biochemical Society transactions, 1993, Volume: 21, Issue:4

    Topics: Animals; Carboxylic Ester Hydrolases; Chromatography; Chromatography, Ion Exchange; Culex; Durapatite; Edetic Acid; Insecticide Resistance; Insecticides; Kinetics; Molecular Weight; Nitrophenols; Paraoxon; Physostigmine; Serine Endopeptidases; Sri Lanka

1993
Organophosphate sensitive and insensitive carboxylesterases in human skin.
    Chemico-biological interactions, 1993, Volume: 87, Issue:1-3

    Topics: Carboxylic Ester Hydrolases; Chromatography; Female; Humans; Isoelectric Focusing; Kinetics; Male; Nitrophenols; Paraoxon; Sensitivity and Specificity; Skin

1993
Differentiation of esterases reacting with organophosphorus compounds.
    Chemico-biological interactions, 1993, Volume: 87, Issue:1-3

    Topics: Adolescent; Adult; Aged; Aged, 80 and over; Aryldialkylphosphatase; Cholinesterase Inhibitors; Cholinesterases; Edetic Acid; Esterases; Female; Humans; Hydrolysis; Kinetics; Male; Middle Aged; Naphthaleneacetic Acids; Nitrophenols; Organophosphates; Organophosphorus Compounds; Paraoxon; Phenylacetates; Phosphoric Monoester Hydrolases; Physostigmine; Sensitivity and Specificity; Substrate Specificity; Tetraisopropylpyrophosphamide; Thiocholine

1993
Stability of cytotoxic luteinizing hormone-releasing hormone conjugate (AN-152) containing doxorubicin 14-O-hemiglutarate in mouse and human serum in vitro: implications for the design of preclinical studies.
    Proceedings of the National Academy of Sciences of the United States of America, 2000, Jan-18, Volume: 97, Issue:2

    Topics: Adult; Animals; Antineoplastic Agents; Bombesin; Carboxylesterase; Carboxylic Ester Hydrolases; Cholinesterase Inhibitors; Dose-Response Relationship, Drug; Doxorubicin; Drug Evaluation, Preclinical; Drug Interactions; Drug Stability; Gonadotropin-Releasing Hormone; Half-Life; Humans; Hydrolysis; Isoflurophate; Male; Mice; Mice, Nude; Nitrophenols; Paraoxon; Pyrroles; Weight Loss

2000
Characterization of a phosphodiesterase capable of hydrolyzing EA 2192, the most toxic degradation product of the nerve agent VX.
    Biochemistry, 2007, Aug-07, Volume: 46, Issue:31

    Topics: Chemical Warfare Agents; Cholinesterase Inhibitors; Disulfoton; Enterobacter aerogenes; Kinetics; Microbial Viability; Molecular Structure; Mutation; Nitrophenols; Organophosphates; Organophosphonates; Organothiophosphorus Compounds; Paraoxon; Phenols; Phosphoric Diester Hydrolases; Phosphoric Triester Hydrolases; Recombinant Proteins; Substrate Specificity

2007
Specificity of procaine and ester hydrolysis by human, minipig, and rat skin and liver.
    Drug metabolism and disposition: the biological fate of chemicals, 2007, Volume: 35, Issue:11

    Topics: Animals; Enzyme Inhibitors; Esterases; Esters; Female; Humans; Hydrolysis; Liver; Loperamide; Male; Microsomes, Liver; Molecular Structure; Nitrophenols; Paraoxon; Pentanoic Acids; Phenylacetates; Phenylmethylsulfonyl Fluoride; Procaine; Rats; Rats, Wistar; Skin; Swine; Swine, Miniature; Umbelliferones

2007