Page last updated: 2024-11-04

trifluralin

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Description

Trifluralin: A microtubule-disrupting pre-emergence herbicide. [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

trifluralin : A substituted aniline that is N,N-dipropylaniline substituted by a nitro groups at positions 2 and 6 and a trifluoromethyl group at position 4. It is an agrochemical used as a pre-emergence herbicide. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Cross-References

ID SourceID
PubMed CID5569
CHEMBL ID31970
CHEBI ID35027
SCHEMBL ID21994
MeSH IDM0021963

Synonyms (146)

Synonym
BIDD:ER0382
BIDD:PXR0025
2,6-dinitro-n,n-dipropyl-4-(trifluoromethyl)benzenamine
DIVK1C_006536
KBIO1_001480
trifluralin, technical grade
SPECTRUM_001839
p-toluidine, .alpha.,.alpha.,.alpha.-trifluoro-2,6-dinitro-n,n-dipropyl-
BSPBIO_002359
2,6-dinitro-n,n-dipropyl-4-trifluoromethylaniline
NCGC00091301-01
treficon
treflanocide elancolan
trefanocide
4-(di-n-propylamino)-3,5-dinitro-1-trifluoromethylbenzene
super-treflan
hsdb 1003
olitref
brn 1893555
agriflan 24
su seguro carpidor
tri-4
n,n-di-n-propyl-2,6-dinitro-4-trifluoromethylaniline
trifluralina 600
caswell no. 889
n,n-dipropyl-2,6-dinitro-4-trifluoromethylaniline
l-36352
2,6-dinitro-4-trifluormethyl-n,n-dipropylanilin [german]
nci-c00442
digermin
2,6-dinitro-6-trifluormethyl-n,n-dipropylanilin [german]
synfloran
epa pesticide chemical code 036101
trifurex
einecs 216-428-8
trifluraline
p-toluidine, alpha,alpha,alpha-trifluoro-2,6-dinitro-n,n-dipropyl-
treflam
ccris 607
trifluralin [ansi:bsi:iso]
alpha,alpha,alpha-trifluoro-2,6-dinitro-n,n-dipropyl-p-toluidine
trikepin
tristar
2,6-dinitro-n,n-di-n-propyl-alpha,alpha,alpha-trifluoro-p-toluidine
treflan (trifluralin)
n,n-dipropyl-2,6-dinitro-4-trifluormethylanilin [german]
elancolan
treflan ec
4-(trifluoromethyl)-2,6-dinitro-n,n-dipropylaniline
ai3-28203
n,n-dipropyl-4-trifluoromethyl-2,6-dinitroaniline
trifluraline [iso-french]
lilly 36,352
ipersan
1582-09-8
nitran k
benzenamine, 2,6-dinitro-n,n-dipropyl-4-(trifluoromethyl)-
triflurex
treflan
crisalina
trifluralin
crisalin
agreflan
nitran
2,6-dinitro-n,n-dipropyl-4-(trifluoromethyl)aniline
trifluralin, analytical standard
NCGC00091301-03
NCGC00091301-04
NCGC00091301-02
KBIO2_004909
KBIOGR_001079
KBIO2_002341
KBIO3_001859
KBIO2_007477
KBIOSS_002344
SPECTRUM2_001888
SPECTRUM3_000830
SPECPLUS_000440
SPBIO_001796
SPECTRUM4_000670
SPECTRUM330038
SPECTRUM5_001972
trifluralin2,6-dinitro-n,n-dipropyl-4-(trifluoromethyl)aniline
NCGC00091301-05
NCGC00091301-06
CHEMBL31970
chebi:35027 ,
trifuraline
smr000778097
MLS002454453
A809905
AKOS005608916
NCGC00091301-07
NCGC00091301-08
STK792949
EN300-67184
unii-c8bx46ql7k
2,6-dinitro-6-trifluormethyl-n,n-dipropylanilin
n,n-dipropyl-2,6-dinitro-4-trifluormethylanilin
2,6-dinitro-4-trifluormethyl-n,n-dipropylanilin
c8bx46ql7k ,
tox21_300918
dtxsid4021395 ,
cas-1582-09-8
NCGC00258904-01
NCGC00254821-01
dtxcid401395
tox21_201352
CCG-39426
FT-0603564
premerlin
.alpha.,.alpha.,.alpha.-trifluoro-2,6-dinitro-n,n-dipropyl-p-toluidine
trifluralin [hsdb]
trifluralin [mi]
trifluralin [iarc]
trifluralin [iso]
SCHEMBL21994
HY-B2050
CS-5200
n,n-di-n-propyl-2,6-dinitro-4-(trifluoromethyl)aniline
4-(di-n-propylamino)-3,5-dinitro-1-(trifluoromethyl)benzene
agriphlan 24
2,6-dinitro-n,n-dipropyl-4-(trifluoromethyl)benzeneamine
benzeneamine, 2,6-dinitro-n,n-dipropyl-4-(trifluoromethyl)-
brassix
trimaran (salt/mix)
2,6-dinitro-n,n-di-n-propyl-.alpha.,.alpha.,.alpha.-trifluoro-p-toluidine
2,6-dinitro-n,n-dipropyl-4-(trifluoromethyl)aniline #
zeltoxone
sinflouran
trilin
trifloran
nci c00443
KS-5357
mfcd00055241
trifluralin, pestanal(r), analytical standard
trifluralin 10 microg/ml in cyclohexane
J-009482
trifluralin-d14 (di-n-propyl-d14)
trifluralin;2,6-dinitro-n,n-dipropyl-4-(trifluoromethyl)-benzamine; 4-(di-n-propylamino)-3,5-dinitro-1-trifluoromethylbenzene; alpha,alpha,alpha-trifluoro-2,6-dinitro-n,n-dipropyl-p-toluidine; agrefla
Q418247
T3999
trifluralin 1000 microg/ml in acetone
2,6-dinitro-n,n-dipropyl-4-(tri fluoromethyl)benzenamine
Z57117646
AKOS040742778

Research Excerpts

Overview

Trifluralin (TFL) is a widely used dinitroaniline herbicide, which can persist in the environment and has substantial ecotoxicity, especially to aquatic organisms. It is a herbicide capable of interfering in mitotic cell division due to either microtubule depolymerization or alteration in the concentration of calcium ions.

ExcerptReferenceRelevance
"Trifluralin (TFL) is a highly persistent with a strong adsorption capacity on soil particles herbicide. "( Bioremediation of a trifluralin contaminated soil using bioaugmentation with novel isolated bacterial strains and cyclodextrin.
Lara-Moreno, A; Madrid, F; Merchán, F; Morillo, E; Villaverde, J, 2022
)
2.49
"Trifluralin is a widely used dinitroaniline herbicide, which can persist in the environment and has substantial ecotoxicity, especially to aquatic organisms. "( Biodegradation and Abiotic Degradation of Trifluralin: A Commonly Used Herbicide with a Poorly Understood Environmental Fate.
Coleman, NV; Maggi, F; Rich, DJ; Tang, FHM; Vervoort, RW, 2020
)
2.27
"Trifluralin is a widely used dinitroaniline herbicide in cotton fields of China but is highly persistent in the environment and can act as a biotoxin and cause genotoxicity to terrestrial organisms, including humans. "( Trifluralin residues in soils from main cotton fields of China and associated ecological risk.
Li, B; Li, C; Li, Y; Ma, Z, 2021
)
3.51
"Trifluralin is a herbicide capable of interfering in mitotic cell division due to either microtubule depolymerization or alteration in the concentration of calcium ions within the cell. "( Origin of nuclear and chromosomal alterations derived from the action of an aneugenic agent--Trifluralin herbicide.
Fernandes, TC; Marin-Morales, MA; Mazzeo, DE, 2009
)
2.02
"Trifluralin is a widely used dinitroaniline herbicide throughout the world. "( Application of random amplified polymorphic DNA (RAPD) to detect genotoxic effect of trifluralin on maize (Zea mays).
Aksakal, O; Bozari, S, 2013
)
2.06
"Trifluralin is a widely used herbicide for the control of broad leaf weeds in a variety of crops. "( Using 19F NMR spectroscopy to determine trifluralin binding to soil.
Benesi, A; Bollag, JM; Dec, J; Fry, RA; Jones, AD; Strynar, M, 2004
)
2.03
"Trifluralin is a dinitroaniline with proved anti-Leishmania activity in vitro."( Efficacy of the liposome trifluralin in the treatment of experimental canine leishmaniosis.
Carvalheiro, M; Cruz, ME; Jorge, J; Marques, C; Pereira, MA; Santos-Gomes, GM, 2008
)
1.37

Effects

Trifluralin has low water solubility and is strongly bound to soil components. Mean Koc values range from 4,000 to 13,000.

ExcerptReferenceRelevance
"The trifluralin residues have been determined through GC-ECD, according to different cultivation phases for two entire production cycles: with 30% of leaf covering, at the moment of flowering and maturation, during production and at the harvest ending, on soil, leaves and maturation, during the production and, at the harvest ending, on fruits."( Subsurface drip irrigation with micro-encapsulated trifluralin. Trifluralin residues in soils and cultivations.
Rosati, S; Rossi, E; Scicchitano, S; Spera, G, 2006
)
1.07
"Trifluralin has low water solubility and is strongly bound to soil components; mean Koc values range from 4,000 to 13,000."( Environmental fate of trifluralin.
Cessna, AJ; Grover, R; Schiefer, HB; Wolt, JD, 1997
)
1.33

Actions

Trifluralin displays anti-Trypanosoma cruzi activity and a potential therapeutic effect for the treatment of Chagas disease. TrifLuralin at lower concentrations from 0.5 mg microg(-1) dry soil to lower than 10.0mg microg (-1), stimulate the growth of soil bacteria, actinomycetes, mould, and the pure cultures of Br.

ExcerptReferenceRelevance
"Trifluralin displays anti-Trypanosoma cruzi activity and a potential therapeutic effect for the treatment of Chagas disease. "( Pharmacokinetics of trifluralin in blood and heart tissue of mice.
Marra, C; Rule, R; Villagra, S; Zaidenberg, A, 2009
)
2.12
"Trifluralin at lower concentrations from 0.5 mg microg(-1) dry soil to lower than 10.0 mg microg(-1) dry soil appeared to stimulate the growth of soil bacteria, actinomycetes, mould, and the pure cultures of Br."( Effects of trifluralin on soil microbial populations and the nitrogen fixation activities.
Hang, M; Meichi, C; Yuhua, Z; Zhongyun, C, 2001
)
1.42

Treatment

Trifluralin treatment led to disassembly of the well ordered subpellicular microtubules. In Trifolium repens, root tips increased in diameter and decreased in length. Cell elongation was decreased, cell wall deposition was abnormal, root hairs were deformed.

ExcerptReferenceRelevance
"Trifluralin treatment increased bile flow, caused a 3.2-fold increase in biliary elimination of conjugated T4 and 63% increase in conjugated T3."( Mechanism of trifluralin-induced thyroid tumors in rats.
Bartels, MJ; Brzak, KA; Charles, GD; Clark, AJ; Dryzga, MD; Kan, LH; Saghir, SA, 2008
)
1.44
"Trifluralin treatment led to disassembly of the well ordered subpellicular microtubules, whereas it had no effect on microtubules of human platelets or of rat neuronal cells in vitro."( Effect and localization of trifluralin in Plasmodium falciparum gametocytes: an electron microscopic study.
Aikawa, M; Fujioka, H; Kaidoh, T; Nath, J; Okoye, V,
)
1.15
"In trifluralin treated seedlings of Trifolium repens, root tips increased in diameter and decreased in length, cell elongation was decreased, cell wall deposition was abnormal, root hairs were deformed, and a marked reduction was seen in the number of infection threads induced by the bacterial symbionts."( Inhibitory effects of the herbicide trifluralin on the establishment of the clover root nodule symbiosis.
De Rosa, F; Haber, D; Margulis, L; Williams, C, 1978
)
1.05
"Trifluralin treatment also inhibited the binding of [3H]BP to liver and lung DNA, as well as to protein in the liver."( Protective effects of trifluralin on benzo(a)pyrene-induced tumors in A/J mice.
Kratky, M; Lang, WR; Simpson, JB; Triano, EA; Triolo, AJ, 1985
)
1.31

Toxicity

ExcerptReferenceRelevance
" The discussion includes a detailed analysis of apparently relevant metabolic pathways and associated modes of toxic action of nitroaromatics."( Quantitative structure-activity analysis of the algae toxicity of nitroaromatic compounds.
Altenburger, R; Jastorff, B; Schmitt, H; Schüürmann, G, 2000
)
0.31
" Acute toxic effects were assayed by administration of 50 or 200 mg/kg body weight daily for 30 days, and chronic effects by administration of 200 mg/kg body weight once a week for 90 days (n = 20)."( Trifluralin toxicity in a Chagas disease mouse model.
Drut, R; Gómez, P; Luong, T; Marra, C; Milani, L; Villagra, S; Zaidenberg, A, 2007
)
1.78
"The aim of this study was to use the diplopod Rhinocricus padbergi as test organism to verify the possible toxic effects of the herbicide trifluralin in a representative of the edaphic fauna."( Toxicity of trifluralin herbicide in a representative of the edaphic fauna: histopathology of the midgut of Rhinocricus padbergi (Diplopoda).
Fontanetti, CS; Marin-Morales, MA; Merlini, VV; Nogarol, LR, 2012
)
0.96
"The herbicide itself and the degradation products are highly toxic on biological systems."( The effects of resveratrol against trifluralin toxicity in the urinary tract of rats.
Denek, Z; Erbil, G; Micili, SC; Ozbal, S; Ozogul, C, 2016
)
0.71
" They are considered extremely safe agrochemicals because they act specifically on tubulin proteins and inhibit shoot and root growth of plants."( Dinitroaniline herbicides: a comprehensive review of toxicity and side effects on animal non-target organisms.
Giglio, A; Vommaro, ML, 2022
)
0.72

Compound-Compound Interactions

ExcerptReferenceRelevance
"The oxidation of bromoxynil and trifluralin was investigated using ozone (O(3)) and O(3) combined with hydrogen peroxide (H(2)O(2)) in natural waters using batch reactors."( Oxidation kinetics of two pesticides in natural waters by ozonation and ozone combined with hydrogen peroxide.
Adams, CD; Chelme-Ayala, P; El-Din, MG; Smith, DW, 2011
)
0.65

Bioavailability

ExcerptReferenceRelevance
" By assessing the type of bonding involved between pesticide and plants or soil, some assessment of the bioavailability of these bound residues to the environment can be made."( Incorporation of foreign compound metabolites into plant and soil constituents.
Adler, IR; Boka, G; Honeycutt, RC; Secrest, WL; Simoneaux, BJ; Sumner, DD,
)
0.13
" To show the importance of physicochemical properties, the classic QSAR and CoMFA of neonicotinoids and prediction of bioavailability of pesticides in terms of membrane permeability in comparison with drugs are described."( Importance of physicochemical properties for the design of new pesticides.
Akamatsu, M, 2011
)
0.37
"We evaluated wheat straw biochar produced at 450°C for its ability to influence bioavailability and persistence of two commonly used herbicides (atrazine and trifluralin) with different modes of action (photosynthesis versus root tip mitosis inhibitors) in two contrasting soils."( Poor efficacy of herbicides in biochar-amended soils as affected by their chemistry and mode of action.
Gill, G; Kookana, R; Krull, E; Macdonald, LM; Nag, SK; Smith, L, 2011
)
0.57
" These techniques consisted of: i) biostimulation, using a nutrients solution (NS); ii) bioaugmentation, using a natural microbial consortium (NMC), seven individual bacterial strains isolated from NMC, and an artificial bacterial consortium formed by the seven TFL-degrading bacterial strains (ABC); iii) bioavailability enhancement, using a biodegradable compound, a randomly methylated cyclodextrin, RAMEB."( Bioremediation of a trifluralin contaminated soil using bioaugmentation with novel isolated bacterial strains and cyclodextrin.
Lara-Moreno, A; Madrid, F; Merchán, F; Morillo, E; Villaverde, J, 2022
)
1.04

Dosage Studied

ExcerptRelevanceReference
" Pregnant rats and rabbits were dosed once daily by gavage on Gestation Days 6-15 and 6-18, respectively."( Developmental toxicity of dinitroaniline herbicides in rats and rabbits. I. Trifluralin.
Byrd, RA; Emmerson, JL; Markham, JK, 1995
)
0.52
" Poisson regression was used to examine internal dose-response relationships, while controlling for important lifestyle factors and other agricultural exposures."( Cancer incidence among pesticide applicators exposed to trifluralin in the Agricultural Health Study.
Alavanja, M; Beane-Freeman, L; Blair, A; Coble, J; Dosemeci, M; Hoppin, JA; Kang, D; Knott, CE; Lubin, J; Lynch, CF; Park, SK; Sandler, DP, 2008
)
0.59
"0% (w/w) and the herbicides were applied to those soil-biochar mixes at nil, half, full, two times, and four times, the recommended dosage (H(4))."( Poor efficacy of herbicides in biochar-amended soils as affected by their chemistry and mode of action.
Gill, G; Kookana, R; Krull, E; Macdonald, LM; Nag, SK; Smith, L, 2011
)
0.37
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (4)

RoleDescription
environmental contaminantAny minor or unwanted substance introduced into the environment that can have undesired effects.
xenobioticA xenobiotic (Greek, xenos "foreign"; bios "life") is a compound that is foreign to a living organism. Principal xenobiotics include: drugs, carcinogens and various compounds that have been introduced into the environment by artificial means.
herbicideA substance used to destroy plant pests.
agrochemicalAn agrochemical is a substance that is used in agriculture or horticulture.
[role information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Drug Classes (3)

ClassDescription
C-nitro compoundA nitro compound having the nitro group (-NO2) attached to a carbon atom.
(trifluoromethyl)benzenesAn organofluorine compound that is (trifluoromethyl)benzene and derivatives arising from substitution of one or more of the phenyl hydrogens.
substituted aniline
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Protein Targets (38)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Chain A, MAJOR APURINIC/APYRIMIDINIC ENDONUCLEASEHomo sapiens (human)Potency35.48130.003245.467312,589.2998AID2517
Chain A, TYROSYL-DNA PHOSPHODIESTERASEHomo sapiens (human)Potency39.47230.004023.8416100.0000AID485290
pregnane X receptorRattus norvegicus (Norway rat)Potency50.11870.025127.9203501.1870AID651751
hypoxia-inducible factor 1 alpha subunitHomo sapiens (human)Potency0.19493.189029.884159.4836AID1224846
USP1 protein, partialHomo sapiens (human)Potency28.18380.031637.5844354.8130AID504865
AR proteinHomo sapiens (human)Potency35.48130.000221.22318,912.5098AID588516
thyroid stimulating hormone receptorHomo sapiens (human)Potency12.58930.001318.074339.8107AID926
nuclear receptor subfamily 1, group I, member 3Homo sapiens (human)Potency34.30630.001022.650876.6163AID1224839
retinoid X nuclear receptor alphaHomo sapiens (human)Potency34.60610.000817.505159.3239AID1159531
estrogen-related nuclear receptor alphaHomo sapiens (human)Potency30.88800.001530.607315,848.9004AID1224841; AID1224849
farnesoid X nuclear receptorHomo sapiens (human)Potency25.02810.375827.485161.6524AID588527; AID743217
pregnane X nuclear receptorHomo sapiens (human)Potency27.86690.005428.02631,258.9301AID1346982; AID720659
estrogen nuclear receptor alphaHomo sapiens (human)Potency38.79630.000229.305416,493.5996AID743069; AID743075; AID743079
peroxisome proliferator-activated receptor deltaHomo sapiens (human)Potency0.63100.001024.504861.6448AID588535
thyroid stimulating hormone receptorHomo sapiens (human)Potency8.77090.001628.015177.1139AID1224843; AID1224895
potassium voltage-gated channel subfamily H member 2 isoform dHomo sapiens (human)Potency14.12540.01789.637444.6684AID588834
thyroid hormone receptor beta isoform 2Rattus norvegicus (Norway rat)Potency68.51990.000323.4451159.6830AID743065; AID743067
mitogen-activated protein kinase 1Homo sapiens (human)Potency11.89610.039816.784239.8107AID1454; AID995
nuclear factor erythroid 2-related factor 2 isoform 1Homo sapiens (human)Potency74.97800.000627.21521,122.0200AID651741
cytochrome P450 3A4 isoform 1Homo sapiens (human)Potency15.84890.031610.279239.8107AID884; AID885
lethal factor (plasmid)Bacillus anthracis str. A2012Potency5.01190.020010.786931.6228AID912
Gamma-aminobutyric acid receptor subunit piRattus norvegicus (Norway rat)Potency15.84891.000012.224831.6228AID885
Cellular tumor antigen p53Homo sapiens (human)Potency17.19390.002319.595674.0614AID651631
Gamma-aminobutyric acid receptor subunit beta-1Rattus norvegicus (Norway rat)Potency15.84891.000012.224831.6228AID885
Gamma-aminobutyric acid receptor subunit deltaRattus norvegicus (Norway rat)Potency15.84891.000012.224831.6228AID885
Gamma-aminobutyric acid receptor subunit gamma-2Rattus norvegicus (Norway rat)Potency15.84891.000012.224831.6228AID885
Gamma-aminobutyric acid receptor subunit alpha-5Rattus norvegicus (Norway rat)Potency15.84891.000012.224831.6228AID885
Gamma-aminobutyric acid receptor subunit alpha-3Rattus norvegicus (Norway rat)Potency15.84891.000012.224831.6228AID885
Gamma-aminobutyric acid receptor subunit gamma-1Rattus norvegicus (Norway rat)Potency15.84891.000012.224831.6228AID885
Gamma-aminobutyric acid receptor subunit alpha-2Rattus norvegicus (Norway rat)Potency15.84891.000012.224831.6228AID885
Gamma-aminobutyric acid receptor subunit alpha-4Rattus norvegicus (Norway rat)Potency15.84891.000012.224831.6228AID885
Gamma-aminobutyric acid receptor subunit gamma-3Rattus norvegicus (Norway rat)Potency15.84891.000012.224831.6228AID885
Gamma-aminobutyric acid receptor subunit alpha-6Rattus norvegicus (Norway rat)Potency15.84891.000012.224831.6228AID885
Gamma-aminobutyric acid receptor subunit alpha-1Rattus norvegicus (Norway rat)Potency15.84891.000012.224831.6228AID885
Gamma-aminobutyric acid receptor subunit beta-3Rattus norvegicus (Norway rat)Potency15.84891.000012.224831.6228AID885
Gamma-aminobutyric acid receptor subunit beta-2Rattus norvegicus (Norway rat)Potency15.84891.000012.224831.6228AID885
GABA theta subunitRattus norvegicus (Norway rat)Potency15.84891.000012.224831.6228AID885
Gamma-aminobutyric acid receptor subunit epsilonRattus norvegicus (Norway rat)Potency15.84891.000012.224831.6228AID885
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Biological Processes (124)

Processvia Protein(s)Taxonomy
negative regulation of cell population proliferationCellular tumor antigen p53Homo sapiens (human)
regulation of cell cycleCellular tumor antigen p53Homo sapiens (human)
regulation of cell cycle G2/M phase transitionCellular tumor antigen p53Homo sapiens (human)
DNA damage responseCellular tumor antigen p53Homo sapiens (human)
ER overload responseCellular tumor antigen p53Homo sapiens (human)
cellular response to glucose starvationCellular tumor antigen p53Homo sapiens (human)
intrinsic apoptotic signaling pathway in response to DNA damage by p53 class mediatorCellular tumor antigen p53Homo sapiens (human)
regulation of apoptotic processCellular tumor antigen p53Homo sapiens (human)
positive regulation of transcription by RNA polymerase IICellular tumor antigen p53Homo sapiens (human)
positive regulation of miRNA transcriptionCellular tumor antigen p53Homo sapiens (human)
negative regulation of transcription by RNA polymerase IICellular tumor antigen p53Homo sapiens (human)
mitophagyCellular tumor antigen p53Homo sapiens (human)
in utero embryonic developmentCellular tumor antigen p53Homo sapiens (human)
somitogenesisCellular tumor antigen p53Homo sapiens (human)
release of cytochrome c from mitochondriaCellular tumor antigen p53Homo sapiens (human)
hematopoietic progenitor cell differentiationCellular tumor antigen p53Homo sapiens (human)
T cell proliferation involved in immune responseCellular tumor antigen p53Homo sapiens (human)
B cell lineage commitmentCellular tumor antigen p53Homo sapiens (human)
T cell lineage commitmentCellular tumor antigen p53Homo sapiens (human)
response to ischemiaCellular tumor antigen p53Homo sapiens (human)
nucleotide-excision repairCellular tumor antigen p53Homo sapiens (human)
double-strand break repairCellular tumor antigen p53Homo sapiens (human)
regulation of DNA-templated transcriptionCellular tumor antigen p53Homo sapiens (human)
regulation of transcription by RNA polymerase IICellular tumor antigen p53Homo sapiens (human)
protein import into nucleusCellular tumor antigen p53Homo sapiens (human)
autophagyCellular tumor antigen p53Homo sapiens (human)
DNA damage responseCellular tumor antigen p53Homo sapiens (human)
DNA damage response, signal transduction by p53 class mediator resulting in cell cycle arrestCellular tumor antigen p53Homo sapiens (human)
DNA damage response, signal transduction by p53 class mediator resulting in transcription of p21 class mediatorCellular tumor antigen p53Homo sapiens (human)
transforming growth factor beta receptor signaling pathwayCellular tumor antigen p53Homo sapiens (human)
Ras protein signal transductionCellular tumor antigen p53Homo sapiens (human)
gastrulationCellular tumor antigen p53Homo sapiens (human)
neuroblast proliferationCellular tumor antigen p53Homo sapiens (human)
negative regulation of neuroblast proliferationCellular tumor antigen p53Homo sapiens (human)
protein localizationCellular tumor antigen p53Homo sapiens (human)
negative regulation of DNA replicationCellular tumor antigen p53Homo sapiens (human)
negative regulation of cell population proliferationCellular tumor antigen p53Homo sapiens (human)
determination of adult lifespanCellular tumor antigen p53Homo sapiens (human)
mRNA transcriptionCellular tumor antigen p53Homo sapiens (human)
rRNA transcriptionCellular tumor antigen p53Homo sapiens (human)
response to salt stressCellular tumor antigen p53Homo sapiens (human)
response to inorganic substanceCellular tumor antigen p53Homo sapiens (human)
response to X-rayCellular tumor antigen p53Homo sapiens (human)
response to gamma radiationCellular tumor antigen p53Homo sapiens (human)
positive regulation of gene expressionCellular tumor antigen p53Homo sapiens (human)
cardiac muscle cell apoptotic processCellular tumor antigen p53Homo sapiens (human)
positive regulation of cardiac muscle cell apoptotic processCellular tumor antigen p53Homo sapiens (human)
glial cell proliferationCellular tumor antigen p53Homo sapiens (human)
viral processCellular tumor antigen p53Homo sapiens (human)
glucose catabolic process to lactate via pyruvateCellular tumor antigen p53Homo sapiens (human)
cerebellum developmentCellular tumor antigen p53Homo sapiens (human)
negative regulation of cell growthCellular tumor antigen p53Homo sapiens (human)
DNA damage response, signal transduction by p53 class mediatorCellular tumor antigen p53Homo sapiens (human)
negative regulation of transforming growth factor beta receptor signaling pathwayCellular tumor antigen p53Homo sapiens (human)
mitotic G1 DNA damage checkpoint signalingCellular tumor antigen p53Homo sapiens (human)
negative regulation of telomere maintenance via telomeraseCellular tumor antigen p53Homo sapiens (human)
T cell differentiation in thymusCellular tumor antigen p53Homo sapiens (human)
tumor necrosis factor-mediated signaling pathwayCellular tumor antigen p53Homo sapiens (human)
regulation of tissue remodelingCellular tumor antigen p53Homo sapiens (human)
cellular response to UVCellular tumor antigen p53Homo sapiens (human)
multicellular organism growthCellular tumor antigen p53Homo sapiens (human)
positive regulation of mitochondrial membrane permeabilityCellular tumor antigen p53Homo sapiens (human)
cellular response to glucose starvationCellular tumor antigen p53Homo sapiens (human)
intrinsic apoptotic signaling pathway in response to DNA damage by p53 class mediatorCellular tumor antigen p53Homo sapiens (human)
positive regulation of apoptotic processCellular tumor antigen p53Homo sapiens (human)
negative regulation of apoptotic processCellular tumor antigen p53Homo sapiens (human)
entrainment of circadian clock by photoperiodCellular tumor antigen p53Homo sapiens (human)
mitochondrial DNA repairCellular tumor antigen p53Homo sapiens (human)
regulation of DNA damage response, signal transduction by p53 class mediatorCellular tumor antigen p53Homo sapiens (human)
positive regulation of neuron apoptotic processCellular tumor antigen p53Homo sapiens (human)
transcription initiation-coupled chromatin remodelingCellular tumor antigen p53Homo sapiens (human)
negative regulation of proteolysisCellular tumor antigen p53Homo sapiens (human)
negative regulation of DNA-templated transcriptionCellular tumor antigen p53Homo sapiens (human)
positive regulation of DNA-templated transcriptionCellular tumor antigen p53Homo sapiens (human)
positive regulation of RNA polymerase II transcription preinitiation complex assemblyCellular tumor antigen p53Homo sapiens (human)
positive regulation of transcription by RNA polymerase IICellular tumor antigen p53Homo sapiens (human)
response to antibioticCellular tumor antigen p53Homo sapiens (human)
fibroblast proliferationCellular tumor antigen p53Homo sapiens (human)
negative regulation of fibroblast proliferationCellular tumor antigen p53Homo sapiens (human)
circadian behaviorCellular tumor antigen p53Homo sapiens (human)
bone marrow developmentCellular tumor antigen p53Homo sapiens (human)
embryonic organ developmentCellular tumor antigen p53Homo sapiens (human)
positive regulation of peptidyl-tyrosine phosphorylationCellular tumor antigen p53Homo sapiens (human)
protein stabilizationCellular tumor antigen p53Homo sapiens (human)
negative regulation of helicase activityCellular tumor antigen p53Homo sapiens (human)
protein tetramerizationCellular tumor antigen p53Homo sapiens (human)
chromosome organizationCellular tumor antigen p53Homo sapiens (human)
neuron apoptotic processCellular tumor antigen p53Homo sapiens (human)
regulation of cell cycleCellular tumor antigen p53Homo sapiens (human)
hematopoietic stem cell differentiationCellular tumor antigen p53Homo sapiens (human)
negative regulation of glial cell proliferationCellular tumor antigen p53Homo sapiens (human)
type II interferon-mediated signaling pathwayCellular tumor antigen p53Homo sapiens (human)
cardiac septum morphogenesisCellular tumor antigen p53Homo sapiens (human)
positive regulation of programmed necrotic cell deathCellular tumor antigen p53Homo sapiens (human)
protein-containing complex assemblyCellular tumor antigen p53Homo sapiens (human)
intrinsic apoptotic signaling pathway in response to endoplasmic reticulum stressCellular tumor antigen p53Homo sapiens (human)
thymocyte apoptotic processCellular tumor antigen p53Homo sapiens (human)
positive regulation of thymocyte apoptotic processCellular tumor antigen p53Homo sapiens (human)
necroptotic processCellular tumor antigen p53Homo sapiens (human)
cellular response to hypoxiaCellular tumor antigen p53Homo sapiens (human)
cellular response to xenobiotic stimulusCellular tumor antigen p53Homo sapiens (human)
cellular response to ionizing radiationCellular tumor antigen p53Homo sapiens (human)
cellular response to gamma radiationCellular tumor antigen p53Homo sapiens (human)
cellular response to UV-CCellular tumor antigen p53Homo sapiens (human)
stem cell proliferationCellular tumor antigen p53Homo sapiens (human)
signal transduction by p53 class mediatorCellular tumor antigen p53Homo sapiens (human)
intrinsic apoptotic signaling pathway by p53 class mediatorCellular tumor antigen p53Homo sapiens (human)
reactive oxygen species metabolic processCellular tumor antigen p53Homo sapiens (human)
cellular response to actinomycin DCellular tumor antigen p53Homo sapiens (human)
positive regulation of release of cytochrome c from mitochondriaCellular tumor antigen p53Homo sapiens (human)
cellular senescenceCellular tumor antigen p53Homo sapiens (human)
replicative senescenceCellular tumor antigen p53Homo sapiens (human)
oxidative stress-induced premature senescenceCellular tumor antigen p53Homo sapiens (human)
intrinsic apoptotic signaling pathwayCellular tumor antigen p53Homo sapiens (human)
oligodendrocyte apoptotic processCellular tumor antigen p53Homo sapiens (human)
positive regulation of execution phase of apoptosisCellular tumor antigen p53Homo sapiens (human)
negative regulation of mitophagyCellular tumor antigen p53Homo sapiens (human)
regulation of mitochondrial membrane permeability involved in apoptotic processCellular tumor antigen p53Homo sapiens (human)
regulation of intrinsic apoptotic signaling pathway by p53 class mediatorCellular tumor antigen p53Homo sapiens (human)
positive regulation of miRNA transcriptionCellular tumor antigen p53Homo sapiens (human)
negative regulation of G1 to G0 transitionCellular tumor antigen p53Homo sapiens (human)
negative regulation of miRNA processingCellular tumor antigen p53Homo sapiens (human)
negative regulation of glucose catabolic process to lactate via pyruvateCellular tumor antigen p53Homo sapiens (human)
negative regulation of pentose-phosphate shuntCellular tumor antigen p53Homo sapiens (human)
intrinsic apoptotic signaling pathway in response to hypoxiaCellular tumor antigen p53Homo sapiens (human)
regulation of fibroblast apoptotic processCellular tumor antigen p53Homo sapiens (human)
negative regulation of reactive oxygen species metabolic processCellular tumor antigen p53Homo sapiens (human)
positive regulation of reactive oxygen species metabolic processCellular tumor antigen p53Homo sapiens (human)
negative regulation of stem cell proliferationCellular tumor antigen p53Homo sapiens (human)
positive regulation of cellular senescenceCellular tumor antigen p53Homo sapiens (human)
positive regulation of intrinsic apoptotic signaling pathwayCellular tumor antigen p53Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Molecular Functions (34)

Processvia Protein(s)Taxonomy
transcription cis-regulatory region bindingCellular tumor antigen p53Homo sapiens (human)
RNA polymerase II cis-regulatory region sequence-specific DNA bindingCellular tumor antigen p53Homo sapiens (human)
DNA-binding transcription factor activity, RNA polymerase II-specificCellular tumor antigen p53Homo sapiens (human)
cis-regulatory region sequence-specific DNA bindingCellular tumor antigen p53Homo sapiens (human)
core promoter sequence-specific DNA bindingCellular tumor antigen p53Homo sapiens (human)
TFIID-class transcription factor complex bindingCellular tumor antigen p53Homo sapiens (human)
DNA-binding transcription repressor activity, RNA polymerase II-specificCellular tumor antigen p53Homo sapiens (human)
DNA-binding transcription activator activity, RNA polymerase II-specificCellular tumor antigen p53Homo sapiens (human)
protease bindingCellular tumor antigen p53Homo sapiens (human)
p53 bindingCellular tumor antigen p53Homo sapiens (human)
DNA bindingCellular tumor antigen p53Homo sapiens (human)
chromatin bindingCellular tumor antigen p53Homo sapiens (human)
DNA-binding transcription factor activityCellular tumor antigen p53Homo sapiens (human)
mRNA 3'-UTR bindingCellular tumor antigen p53Homo sapiens (human)
copper ion bindingCellular tumor antigen p53Homo sapiens (human)
protein bindingCellular tumor antigen p53Homo sapiens (human)
zinc ion bindingCellular tumor antigen p53Homo sapiens (human)
enzyme bindingCellular tumor antigen p53Homo sapiens (human)
receptor tyrosine kinase bindingCellular tumor antigen p53Homo sapiens (human)
ubiquitin protein ligase bindingCellular tumor antigen p53Homo sapiens (human)
histone deacetylase regulator activityCellular tumor antigen p53Homo sapiens (human)
ATP-dependent DNA/DNA annealing activityCellular tumor antigen p53Homo sapiens (human)
identical protein bindingCellular tumor antigen p53Homo sapiens (human)
histone deacetylase bindingCellular tumor antigen p53Homo sapiens (human)
protein heterodimerization activityCellular tumor antigen p53Homo sapiens (human)
protein-folding chaperone bindingCellular tumor antigen p53Homo sapiens (human)
protein phosphatase 2A bindingCellular tumor antigen p53Homo sapiens (human)
RNA polymerase II-specific DNA-binding transcription factor bindingCellular tumor antigen p53Homo sapiens (human)
14-3-3 protein bindingCellular tumor antigen p53Homo sapiens (human)
MDM2/MDM4 family protein bindingCellular tumor antigen p53Homo sapiens (human)
disordered domain specific bindingCellular tumor antigen p53Homo sapiens (human)
general transcription initiation factor bindingCellular tumor antigen p53Homo sapiens (human)
molecular function activator activityCellular tumor antigen p53Homo sapiens (human)
promoter-specific chromatin bindingCellular tumor antigen p53Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Ceullar Components (20)

Processvia Protein(s)Taxonomy
nuclear bodyCellular tumor antigen p53Homo sapiens (human)
nucleusCellular tumor antigen p53Homo sapiens (human)
nucleoplasmCellular tumor antigen p53Homo sapiens (human)
replication forkCellular tumor antigen p53Homo sapiens (human)
nucleolusCellular tumor antigen p53Homo sapiens (human)
cytoplasmCellular tumor antigen p53Homo sapiens (human)
mitochondrionCellular tumor antigen p53Homo sapiens (human)
mitochondrial matrixCellular tumor antigen p53Homo sapiens (human)
endoplasmic reticulumCellular tumor antigen p53Homo sapiens (human)
centrosomeCellular tumor antigen p53Homo sapiens (human)
cytosolCellular tumor antigen p53Homo sapiens (human)
nuclear matrixCellular tumor antigen p53Homo sapiens (human)
PML bodyCellular tumor antigen p53Homo sapiens (human)
transcription repressor complexCellular tumor antigen p53Homo sapiens (human)
site of double-strand breakCellular tumor antigen p53Homo sapiens (human)
germ cell nucleusCellular tumor antigen p53Homo sapiens (human)
chromatinCellular tumor antigen p53Homo sapiens (human)
transcription regulator complexCellular tumor antigen p53Homo sapiens (human)
protein-containing complexCellular tumor antigen p53Homo sapiens (human)
plasma membraneGamma-aminobutyric acid receptor subunit gamma-2Rattus norvegicus (Norway rat)
plasma membraneGamma-aminobutyric acid receptor subunit alpha-1Rattus norvegicus (Norway rat)
plasma membraneGamma-aminobutyric acid receptor subunit beta-2Rattus norvegicus (Norway rat)
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (73)

Assay IDTitleYearJournalArticle
AID522819Antimicrobial activity against Cryptosporidium parvum by short-term in vitro culture assay2010Antimicrobial agents and chemotherapy, Apr, Volume: 54, Issue:4
Dinitroaniline activity in Toxoplasma gondii expressing wild-type or mutant alpha-tubulin.
AID1090439Inhibition of Spinacia oleracea (spinach) chloroplast electron transport chain-mediated DAD-induced cyclic phosphorylation at 200 uM by polarographically1977Plant physiology, Dec, Volume: 60, Issue:6
Inhibition of chloroplast electron transport reactions by trifluralin and diallate.
AID977602Inhibition of sodium fluorescein uptake in OATP1B3-transfected CHO cells at an equimolar substrate-inhibitor concentration of 10 uM2013Molecular pharmacology, Jun, Volume: 83, Issue:6
Structure-based identification of OATP1B1/3 inhibitors.
AID456126Ratio of miltefosine HC50 to compound HC50 for human RBC2010Bioorganic & medicinal chemistry, Jan-01, Volume: 18, Issue:1
Synthesis and biological evaluation of trifluralin analogues as antileishmanial agents.
AID456120Cytotoxicity against human RBC assessed as hemolysis after 1 hr by microplate reader method2010Bioorganic & medicinal chemistry, Jan-01, Volume: 18, Issue:1
Synthesis and biological evaluation of trifluralin analogues as antileishmanial agents.
AID1090428Inhibition of Spinacia oleracea (spinach) chloroplast electron transport chain-mediated sulfhydryl-induced ATP-Pi exchange assessed as inorganic phosphate release at 200 uM treated during incubation stage1977Plant physiology, Dec, Volume: 60, Issue:6
Inhibition of chloroplast electron transport reactions by trifluralin and diallate.
AID522812Antimicrobial activity against Toxoplasma gondii RH containing alpha1-tubulin I235T mutation infected in HFF cells by plaque assay2010Antimicrobial agents and chemotherapy, Apr, Volume: 54, Issue:4
Dinitroaniline activity in Toxoplasma gondii expressing wild-type or mutant alpha-tubulin.
AID1090446Inhibition of Spinacia oleracea (spinach) chloroplast electron transport chain-mediated PMS-induced cyclic phosphorylation at 50 uM by polarographically1977Plant physiology, Dec, Volume: 60, Issue:6
Inhibition of chloroplast electron transport reactions by trifluralin and diallate.
AID522814Antimicrobial activity against Toxoplasma gondii RH containing alpha1-tubulin T239I mutation infected in HFF cells by plaque assay2010Antimicrobial agents and chemotherapy, Apr, Volume: 54, Issue:4
Dinitroaniline activity in Toxoplasma gondii expressing wild-type or mutant alpha-tubulin.
AID1090424Inhibition of Spinacia oleracea (spinach) chloroplast electron transport chain-mediated rate of oxygen evolution per mg of chloroplast at 62.5 uM preincubated with DTT in dark condition for 5 min presence of 0.31 mM DTT1977Plant physiology, Dec, Volume: 60, Issue:6
Inhibition of chloroplast electron transport reactions by trifluralin and diallate.
AID1090452Inhibition of Spinacia oleracea (spinach) photosystem I mediated noncyclic photophosphorylation assessed as 32P-orthophosphate incorporation into ATP up to 300 uM by polarographically1977Plant physiology, Dec, Volume: 60, Issue:6
Inhibition of chloroplast electron transport reactions by trifluralin and diallate.
AID456122Antileishmanial activity against Leishmania infantum MHOM/TN/80/IPT1/LEM 235 promastigotes after 72 hrs by propidium iodide and SYBR14 satining-base flow cytometry2010Bioorganic & medicinal chemistry, Jan-01, Volume: 18, Issue:1
Synthesis and biological evaluation of trifluralin analogues as antileishmanial agents.
AID522815Antimicrobial activity against Toxoplasma gondii RH containing alpha1-tubulin R243C mutation infected in HFF cells by plaque assay2010Antimicrobial agents and chemotherapy, Apr, Volume: 54, Issue:4
Dinitroaniline activity in Toxoplasma gondii expressing wild-type or mutant alpha-tubulin.
AID1090451Inhibition of Spinacia oleracea (spinach) photosystem II mediated noncyclic photophosphorylation assessed as 32P-orthophosphate incorporation into ATP up to 300 uM by polarographically1977Plant physiology, Dec, Volume: 60, Issue:6
Inhibition of chloroplast electron transport reactions by trifluralin and diallate.
AID1090427Inhibition of Spinacia oleracea (spinach) chloroplast electron transport chain-mediated sulfhydryl-induced ATP-Pi exchange assessed as inorganic phosphate release at 200 uM treated during activation stage1977Plant physiology, Dec, Volume: 60, Issue:6
Inhibition of chloroplast electron transport reactions by trifluralin and diallate.
AID1090460Inhibition of Spinacia oleracea (spinach) photosystem I assessed as electron flow from ascorbate/DAD to methylviologen at >200 uM after 1 hr by polarographically1977Plant physiology, Dec, Volume: 60, Issue:6
Inhibition of chloroplast electron transport reactions by trifluralin and diallate.
AID1090461Inhibition of Spinacia oleracea (spinach) chloroplast electron transport chain assessed as residual activity of noncyclic electron flow using methylviologen as acceptor up to 300 uM by polarographically relative to control1977Plant physiology, Dec, Volume: 60, Issue:6
Inhibition of chloroplast electron transport reactions by trifluralin and diallate.
AID289346Octanol-air partition coefficient, log KOA of the compound2007Science (New York, N.Y.), Jul-13, Volume: 317, Issue:5835
Food web-specific biomagnification of persistent organic pollutants.
AID622162Antimicrobial activity against Plasmodium falciparum2011Bioorganic & medicinal chemistry letters, Oct-15, Volume: 21, Issue:20
Synthesis and evaluation of phosphoramidate and phosphorothioamidate analogues of amiprophos methyl as potential antimalarial agents.
AID502117Antimicrobial activity against Toxoplasma gondii infected in HFF after 8 days by plaque assay2010Bioorganic & medicinal chemistry letters, Sep-01, Volume: 20, Issue:17
Synthesis and evaluation of oryzalin analogs against Toxoplasma gondii.
AID1090445Inhibition of Spinacia oleracea (spinach) chloroplast electron transport chain-mediated PMS-induced cyclic phosphorylation at 100 uM by polarographically1977Plant physiology, Dec, Volume: 60, Issue:6
Inhibition of chloroplast electron transport reactions by trifluralin and diallate.
AID1090464Inhibition of Spinacia oleracea (spinach) chloroplast electron transport chain assessed as residual electron flow from water to ferricyanide up to 300 uM by polarographically relative to control1977Plant physiology, Dec, Volume: 60, Issue:6
Inhibition of chloroplast electron transport reactions by trifluralin and diallate.
AID1090443Inhibition of Spinacia oleracea (spinach) chloroplast electron transport chain-mediated DAD-induced cyclic phosphorylation at 10 uM by polarographically1977Plant physiology, Dec, Volume: 60, Issue:6
Inhibition of chloroplast electron transport reactions by trifluralin and diallate.
AID522807Antimicrobial activity against Toxoplasma gondii RH containing alpha1-tubulin S6I mutation infected in HFF cells by plaque assay2010Antimicrobial agents and chemotherapy, Apr, Volume: 54, Issue:4
Dinitroaniline activity in Toxoplasma gondii expressing wild-type or mutant alpha-tubulin.
AID1090437Inhibition of Spinacia oleracea (spinach) chloroplast electron transport chain-mediated DAD-induced cyclic phosphorylation up to 200 uM by polarographically in absence of DCMU in red light1977Plant physiology, Dec, Volume: 60, Issue:6
Inhibition of chloroplast electron transport reactions by trifluralin and diallate.
AID1090440Inhibition of Spinacia oleracea (spinach) chloroplast electron transport chain-mediated DAD-induced cyclic phosphorylation at 100 uM by polarographically1977Plant physiology, Dec, Volume: 60, Issue:6
Inhibition of chloroplast electron transport reactions by trifluralin and diallate.
AID433903Hepatotoxicity in mouse assessed as carcinogenic potency2009European journal of medicinal chemistry, Sep, Volume: 44, Issue:9
Development of QSAR models for predicting hepatocarcinogenic toxicity of chemicals.
AID318681Anticarcinogenic activity in rat assessed as induction of tumors per day2008Bioorganic & medicinal chemistry, Mar-15, Volume: 16, Issue:6
QSAR modeling of the rodent carcinogenicity of nitrocompounds.
AID456121Cytotoxicity against human RBC assessed as hemolysis at 100 uM after 1 hr by microplate reader method2010Bioorganic & medicinal chemistry, Jan-01, Volume: 18, Issue:1
Synthesis and biological evaluation of trifluralin analogues as antileishmanial agents.
AID1090430Inhibition of Spinacia oleracea (spinach) chloroplast electron transport chain-mediated light-induced ATP-Pi exchange assessed as inorganic phosphate release at 200 uM treated during incubation stage1977Plant physiology, Dec, Volume: 60, Issue:6
Inhibition of chloroplast electron transport reactions by trifluralin and diallate.
AID456123Antileishmanial activity against Leishmania donovani MHOM/IN/80/DD8/LEM 703 promastigotes after 72 hrs by propidium iodide and SYBR14 satining-base flow cytometry2010Bioorganic & medicinal chemistry, Jan-01, Volume: 18, Issue:1
Synthesis and biological evaluation of trifluralin analogues as antileishmanial agents.
AID522816Antimicrobial activity against Toxoplasma gondii RH containing alpha1-tubulin R243S mutation infected in HFF cells by plaque assay2010Antimicrobial agents and chemotherapy, Apr, Volume: 54, Issue:4
Dinitroaniline activity in Toxoplasma gondii expressing wild-type or mutant alpha-tubulin.
AID1090436Inhibition of Spinacia oleracea (spinach) chloroplast electron transport chain-mediated DAD-induced cyclic phosphorylation up to 200 uM by polarographically in presence of ascorbate in red light1977Plant physiology, Dec, Volume: 60, Issue:6
Inhibition of chloroplast electron transport reactions by trifluralin and diallate.
AID522806Antimicrobial activity against Toxoplasma gondii RH containing alpha1-tubulin V4L mutation infected in HFF cells by plaque assay2010Antimicrobial agents and chemotherapy, Apr, Volume: 54, Issue:4
Dinitroaniline activity in Toxoplasma gondii expressing wild-type or mutant alpha-tubulin.
AID1090459Inhibition of Spinacia oleracea (spinach) photosystem II assessed as electron flow from H20 to PDOX at 300 uM after 1 hr by polarographically1977Plant physiology, Dec, Volume: 60, Issue:6
Inhibition of chloroplast electron transport reactions by trifluralin and diallate.
AID977599Inhibition of sodium fluorescein uptake in OATP1B1-transfected CHO cells at an equimolar substrate-inhibitor concentration of 10 uM2013Molecular pharmacology, Jun, Volume: 83, Issue:6
Structure-based identification of OATP1B1/3 inhibitors.
AID522809Antimicrobial activity against Toxoplasma gondii RH containing alpha1-tubulin H28Q mutation infected in HFF cells by plaque assay2010Antimicrobial agents and chemotherapy, Apr, Volume: 54, Issue:4
Dinitroaniline activity in Toxoplasma gondii expressing wild-type or mutant alpha-tubulin.
AID1090429Inhibition of Spinacia oleracea (spinach) chloroplast electron transport chain-mediated Mg2+-ATPase activity assessed as inorganic phosphate release1977Plant physiology, Dec, Volume: 60, Issue:6
Inhibition of chloroplast electron transport reactions by trifluralin and diallate.
AID1090425Inhibition of Spinacia oleracea (spinach) chloroplast electron transport chain-mediated rate of oxygen evolution per mg of chloroplast at 62.5 uM1977Plant physiology, Dec, Volume: 60, Issue:6
Inhibition of chloroplast electron transport reactions by trifluralin and diallate.
AID1090441Inhibition of Spinacia oleracea (spinach) chloroplast electron transport chain-mediated DAD-induced cyclic phosphorylation at 50 uM by polarographically1977Plant physiology, Dec, Volume: 60, Issue:6
Inhibition of chloroplast electron transport reactions by trifluralin and diallate.
AID456118Aqueous solubility in water by NMR spectrophotometry2010Bioorganic & medicinal chemistry, Jan-01, Volume: 18, Issue:1
Synthesis and biological evaluation of trifluralin analogues as antileishmanial agents.
AID1090435Inhibition of Spinacia oleracea (spinach) chloroplast electron transport chain-mediated light-induced ATP-Pi exchange assessed as inorganic phosphate release1977Plant physiology, Dec, Volume: 60, Issue:6
Inhibition of chloroplast electron transport reactions by trifluralin and diallate.
AID1090426Inhibition of Spinacia oleracea (spinach) chloroplast electron transport chain-mediated rate of oxygen evolution per mg of chloroplast at 62.5 uM in presence of 0.31 mM DTT1977Plant physiology, Dec, Volume: 60, Issue:6
Inhibition of chloroplast electron transport reactions by trifluralin and diallate.
AID522813Antimicrobial activity against Toxoplasma gondii RH containing alpha1-tubulin I235V mutation infected in HFF cells by plaque assay2010Antimicrobial agents and chemotherapy, Apr, Volume: 54, Issue:4
Dinitroaniline activity in Toxoplasma gondii expressing wild-type or mutant alpha-tubulin.
AID289345Octanol-water partition coefficient, log KOW of the compound2007Science (New York, N.Y.), Jul-13, Volume: 317, Issue:5835
Food web-specific biomagnification of persistent organic pollutants.
AID1090463Inhibition of Spinacia oleracea (spinach) chloroplast electron transport chain assessed as electron flow from water to ferricyanide by polarographically1977Plant physiology, Dec, Volume: 60, Issue:6
Inhibition of chloroplast electron transport reactions by trifluralin and diallate.
AID1090448Inhibition of Spinacia oleracea (spinach) chloroplast electron transport chain-mediated PMS-induced cyclic phosphorylation at 10 uM by polarographically1977Plant physiology, Dec, Volume: 60, Issue:6
Inhibition of chloroplast electron transport reactions by trifluralin and diallate.
AID1090434Inhibition of Spinacia oleracea (spinach) chloroplast electron transport chain-mediated sulfhydryl-induced ATP-Pi exchange assessed as inorganic phosphate release1977Plant physiology, Dec, Volume: 60, Issue:6
Inhibition of chloroplast electron transport reactions by trifluralin and diallate.
AID1090431Inhibition of Spinacia oleracea (spinach) chloroplast electron transport chain-mediated light-induced ATP-Pi exchange assessed as inorganic phosphate release at 200 uM treated during activation stage1977Plant physiology, Dec, Volume: 60, Issue:6
Inhibition of chloroplast electron transport reactions by trifluralin and diallate.
AID1090444Inhibition of Spinacia oleracea (spinach) chloroplast electron transport chain-mediated PMS-induced cyclic phosphorylation at 200 uM by polarographically1977Plant physiology, Dec, Volume: 60, Issue:6
Inhibition of chloroplast electron transport reactions by trifluralin and diallate.
AID1090433Inhibition of Spinacia oleracea (spinach) chloroplast electron transport chain-mediated light-induced ATP-Pi exchange assessed as inorganic phosphate release at 200 uM1977Plant physiology, Dec, Volume: 60, Issue:6
Inhibition of chloroplast electron transport reactions by trifluralin and diallate.
AID1090442Inhibition of Spinacia oleracea (spinach) chloroplast electron transport chain-mediated DAD-induced cyclic phosphorylation at 25 uM by polarographically1977Plant physiology, Dec, Volume: 60, Issue:6
Inhibition of chloroplast electron transport reactions by trifluralin and diallate.
AID1090462Inhibition of Spinacia oleracea (spinach) chloroplast electron transport chain-mediated noncyclic electron flow using methylviologen as acceptor by polarographically1977Plant physiology, Dec, Volume: 60, Issue:6
Inhibition of chloroplast electron transport reactions by trifluralin and diallate.
AID522805Antimicrobial activity against Toxoplasma gondii RH infected in HFF cells by plaque assay2010Antimicrobial agents and chemotherapy, Apr, Volume: 54, Issue:4
Dinitroaniline activity in Toxoplasma gondii expressing wild-type or mutant alpha-tubulin.
AID522810Antimicrobial activity against Toxoplasma gondii RH containing alpha1-tubulin L136F mutation infected in HFF cells by plaque assay2010Antimicrobial agents and chemotherapy, Apr, Volume: 54, Issue:4
Dinitroaniline activity in Toxoplasma gondii expressing wild-type or mutant alpha-tubulin.
AID522811Antimicrobial activity against Toxoplasma gondii RH containing alpha1-tubulin I235L mutation infected in HFF cells by plaque assay2010Antimicrobial agents and chemotherapy, Apr, Volume: 54, Issue:4
Dinitroaniline activity in Toxoplasma gondii expressing wild-type or mutant alpha-tubulin.
AID456124Antileishmanial activity against Leishmania infantum A1 amastigotes infected in human THP1 cells assessed as reduction in intracellular parasite load after 48 hrs by Giemsa staining2010Bioorganic & medicinal chemistry, Jan-01, Volume: 18, Issue:1
Synthesis and biological evaluation of trifluralin analogues as antileishmanial agents.
AID522808Antimicrobial activity against Toxoplasma gondii RH containing alpha1-tubulin F24H mutation infected in HFF cells by plaque assay2010Antimicrobial agents and chemotherapy, Apr, Volume: 54, Issue:4
Dinitroaniline activity in Toxoplasma gondii expressing wild-type or mutant alpha-tubulin.
AID289348Biomagnification factors in human2007Science (New York, N.Y.), Jul-13, Volume: 317, Issue:5835
Food web-specific biomagnification of persistent organic pollutants.
AID289347Biomagnification factors in Diporeia2007Science (New York, N.Y.), Jul-13, Volume: 317, Issue:5835
Food web-specific biomagnification of persistent organic pollutants.
AID1090456Inhibition of Spinacia oleracea (spinach) photosystem II assessed as light-induced re-reduction of Cyt-f at 200 uM added prior to illumination by dual wavelength spectrophotometer analysis1977Plant physiology, Dec, Volume: 60, Issue:6
Inhibition of chloroplast electron transport reactions by trifluralin and diallate.
AID1090453Inhibition of Spinacia oleracea (spinach) chloroplast electron transport chain-mediated noncyclic photophosphorylation assessed as 32P-orthophosphate incorporation into ATP by polarographically1977Plant physiology, Dec, Volume: 60, Issue:6
Inhibition of chloroplast electron transport reactions by trifluralin and diallate.
AID1090447Inhibition of Spinacia oleracea (spinach) chloroplast electron transport chain-mediated PMS-induced cyclic phosphorylation at 25 uM by polarographically1977Plant physiology, Dec, Volume: 60, Issue:6
Inhibition of chloroplast electron transport reactions by trifluralin and diallate.
AID1091958Hydrophobicity, log P of the compound in octanol-water by shaking-flask method2011Journal of agricultural and food chemistry, Apr-13, Volume: 59, Issue:7
Importance of physicochemical properties for the design of new pesticides.
AID1090438Inhibition of Spinacia oleracea (spinach) chloroplast electron transport chain-mediated DAD-induced cyclic phosphorylation up to 200 uM by polarographically in absence of DCMU in white light1977Plant physiology, Dec, Volume: 60, Issue:6
Inhibition of chloroplast electron transport reactions by trifluralin and diallate.
AID456119Cytotoxicity against human THP1 cells after 48 hrs by propidium iodide and SYBR14 satining-base flow cytometry2010Bioorganic & medicinal chemistry, Jan-01, Volume: 18, Issue:1
Synthesis and biological evaluation of trifluralin analogues as antileishmanial agents.
AID1090432Inhibition of Spinacia oleracea (spinach) chloroplast electron transport chain-mediated sulfhydryl-induced ATP-Pi exchange assessed as inorganic phosphate release at 200 uM1977Plant physiology, Dec, Volume: 60, Issue:6
Inhibition of chloroplast electron transport reactions by trifluralin and diallate.
AID1090457Inhibition of Spinacia oleracea (spinach) photosystem I assessed as light-induced oxidation of Cyt-f at 200 uM added prior to illumination by dual wavelength spectrophotometer analysis1977Plant physiology, Dec, Volume: 60, Issue:6
Inhibition of chloroplast electron transport reactions by trifluralin and diallate.
AID622161Antimicrobial activity against Cryptosporidium parvum infected in HCT8 cells assessed as parasite count after 72 to 120 hrs2011Bioorganic & medicinal chemistry letters, Oct-15, Volume: 21, Issue:20
Synthesis and evaluation of phosphoramidate and phosphorothioamidate analogues of amiprophos methyl as potential antimalarial agents.
AID1159607Screen for inhibitors of RMI FANCM (MM2) intereaction2016Journal of biomolecular screening, Jul, Volume: 21, Issue:6
A High-Throughput Screening Strategy to Identify Protein-Protein Interaction Inhibitors That Block the Fanconi Anemia DNA Repair Pathway.
AID1794808Fluorescence-based screening to identify small molecule inhibitors of Plasmodium falciparum apicoplast DNA polymerase (Pf-apPOL).2014Journal of biomolecular screening, Jul, Volume: 19, Issue:6
A High-Throughput Assay to Identify Inhibitors of the Apicoplast DNA Polymerase from Plasmodium falciparum.
AID1794808Fluorescence-based screening to identify small molecule inhibitors of Plasmodium falciparum apicoplast DNA polymerase (Pf-apPOL).
AID1159550Human Phosphogluconate dehydrogenase (6PGD) Inhibitor Screening2015Nature cell biology, Nov, Volume: 17, Issue:11
6-Phosphogluconate dehydrogenase links oxidative PPP, lipogenesis and tumour growth by inhibiting LKB1-AMPK signalling.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (296)

TimeframeStudies, This Drug (%)All Drugs %
pre-199061 (20.61)18.7374
1990's39 (13.18)18.2507
2000's93 (31.42)29.6817
2010's76 (25.68)24.3611
2020's27 (9.12)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 35.88

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be strong demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index35.88 (24.57)
Research Supply Index5.78 (2.92)
Research Growth Index4.66 (4.65)
Search Engine Demand Index85.19 (26.88)
Search Engine Supply Index3.24 (0.95)

This Compound (35.88)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials1 (0.31%)5.53%
Reviews9 (2.79%)6.00%
Case Studies1 (0.31%)4.05%
Observational0 (0.00%)0.25%
Other312 (96.59%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]