Page last updated: 2024-12-04

2,4,5-trichlorophenoxyacetic acid

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

2,4,5-Trichlorophenoxyacetic Acid: An herbicide with strong irritant properties. Use of this compound on rice fields, orchards, sugarcane, rangeland, and other noncrop sites was terminated by the EPA in 1985. (From Merck Index, 11th ed) [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

(2,4,5-trichlorophenoxy)acetic acid : A chlorophenoxyacetic acid that is phenoxyacetic acid in which the ring hydrogens at postions 2, 4 and 5 are substituted by chlorines. [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 CID1480
CHEMBL ID194458
CHEBI ID27903
SCHEMBL ID117704
MeSH IDM0023202

Synonyms (165)

Synonym
BIDD:ER0673
BRD-K92860374-001-02-5
(2,4,5-trichlorophenoxy)acetic acid
acetic acid, (2,4,5-trichlorophenoxy)-
DIVK1C_006564
KBIO1_001508
tippon
brushtox
visko rhap low volatile ester
farmco fence rider
SPECTRUM_001857
2,4,5-(trichlorophenoxy)acetic acid
brush tox
2-(2,4,5-trichlorophenoxy)acetic acid
brush killer
crossbow
BSPBIO_002387
OPREA1_711288
acide 2,4,5-trichloro phenoxyacetique [french]
t-nox
ai3-14656
debroussaillant concentre
caswell no. 881
hsdb 1145
rcra waste number u232
(2,4,5-trichlor-phenoxy)-essigsaeure [german]
einecs 202-273-3
visko rhap
kwas 2,4,5-trojchlorofenoksyoctowy [polish]
cido (2,4,5-tricloro-fenossi)-acetico [italian]
nsc 430
(2,4,5-trichloor-fenoxy)-azijnzuur [dutch]
ccris 1466
brn 2055620
arbokan
epa pesticide chemical code 082001
debroussaillant super concentre
rcra waste no. u232
2,4,5-t [bsi:iso]
acido (2,4,5-tricloro-fenossi)-acetico [italian]
lo-vol
2,4,5-t [chlorophenoxy herbicides]
ded-weed brush killer
nsc-430
decamine 4t
veon
inverton 245
phortox
(2,5-trichlor-phenoxy)-essigsaeure
reddon
envert-t
(2,5-trichlorophenoxy)acetic acid
ded-weed lv-6 brush kil and t-5 brush kil
2,5-t
acetic acid,4,5-trichlorophenoxy)-
verton 2-t
fruitone a
forst u 46
forron
brush-off 445 low volatile brush killer
weedone 2,5-t
tippontormona
esteron 245
93-76-5
C07100
brush rhap
2,4,5-trichlorophenoxyacetic acid
acido (2,5-tricloro-fenossi)-acetico
nsc430
wln: qv1or bg dg eg
2,4,5-t
fence rider
acide 2,5-trichloro phenoxyacetique
bcf-bushkiller
(2,5-trichloor-fenoxy)-azijnzuur
2,5-trichlorophenoxyacetic acid
verton 2t
veon 245
estercide t-2 and t-245
trioxon
reddox
fortex
line rider
inchi=1/c8h5cl3o3/c9-4-1-6(11)7(2-5(4)10)14-3-8(12)13/h1-2h,3h2,(h,12,13
2,4,5-trichlorophenoxyacetic acid, plant cell culture tested, bioreagent, >=95%, crystalline
AJ-087/13205219
(2,4,5-trichlorphenoxy)essigsaeure
CHEBI:27903 ,
2,4,5-trichlorphenoxyessigsaeure
NCGC00094533-03
NCGC00094533-01
NCGC00094533-02
KBIOGR_001107
KBIOSS_002374
KBIO2_004938
KBIO2_002370
KBIO2_007506
KBIO3_001887
SPECPLUS_000468
SPBIO_001068
SPECTRUM4_000674
SPECTRUM2_001224
SPECTRUM3_000834
SPECTRUM330042
SPECTRUM5_001982
NCGC00094533-04
smr001294708
MLS002207208
CHEMBL194458 ,
BMSE000640
AKOS000120113
NCGC00094533-05
STL119782
(2,4,5-trichloro-phenoxy)-acetic acid
NCGC00256364-01
tox21_302882
dtxsid5021388 ,
dtxcid301388
cas-93-76-5
tox21_201605
NCGC00259154-01
BBL009513
acetic acid, (2,4,5(or 2,4,6)-trichlorophenoxy)-
35915-18-5
(2,4,5(or 2,4,6)-trichlorophenoxy)acetic acid
CCG-39137
bdbm50410519
FT-0675447
(2,4,5-trichloor-fenoxy)-azijnzuur
cido (2,4,5-tricloro-fenossi)-acetico
(2,4,5-trichlor-phenoxy)-essigsaeure
acetic acid, 2-(2,4,5-trichlorophenoxy)-
acide 2,4,5-trichloro phenoxyacetique
4-06-00-00973 (beilstein handbook reference)
kwas 2,4,5-trojchlorofenoksyoctowy
9q963s4ymx ,
acido (2,4,5-tricloro-fenossi)-acetico
unii-9q963s4ymx
2,4,5-t [iso]
2,4,5-t [mi]
2,4,5-t [hsdb]
trichlorophenoxyacetic acid [mart.]
SCHEMBL117704
sr-01000060853
SR-01000060853-1
2,4,5-trichloro-phenoxy acetic acid
2,4,5-t-d4
esteron brush killer (salt/mix)
acetic acid, 2,4,5-trichlorophenoxy-
na 2765
mfcd00004301
2,4,5-t, pestanal(r), analytical standard
Z57048946
2,4,5-t 10 microg/ml in acetonitrile
2,4,5-t 100 microg/ml in acetonitrile
(2,4,5-trichlorophenoxy)acetic acid - 2,2',2''-nitrilotriethanol (1:1)
2-[2,4,5-tris(chloranyl)phenoxy]ethanoic acid
F52 ,
VS-02095
(2,4,5-trichlorophenoxy)ethanoic acid
Q209188
AMY25118
BRD-K92860374-001-03-3
EN300-17847
2,4,5-trichlorophenoxyaceticacid-13c6

Research Excerpts

Toxicity

ExcerptReferenceRelevance
"The hypothesis that chemically induced overt maternal toxicity induces a characteristic syndrome of adverse developmental effects in the rat was investigated."( Effects of chemically induced maternal toxicity on prenatal development in the rat.
Chernoff, N; Miller, DB; Rogers, JM; Rosen, MB; Setzer, RW, 1990
)
0.28
"The potential toxic and mutagenic action of 2,4-dichlorophenoxyacetic acid has been studied in different test systems, and the obtained results range from increased chromosomal damage to no effect at all."( Genotoxic effect of substituted phenoxyacetic acids.
Alexieva, V; Georgieva, M; Karanov, E; Topashka-Ancheva, M; Venkov, P, 2000
)
0.31
"Developmental neurotoxicity concerns the adverse health effects of exogenous agents acting on neurodevelopment."( Quantitative risk assessment for developmental neurotoxic effects.
Kodell, R; Razzaghi, M, 2004
)
0.32

Pharmacokinetics

The pharmacokinetic profile of the herbicide 2,4,5-T PGBE ester was examined in rats given a single dermal application of 5 mg/kg.

ExcerptReferenceRelevance
"A pharmacokinetic study was conducted in CD-1 mice with the herbicide 2,4,5-trichlorophenoxyacetic acid (2,4,5-T) as a function of dose (15, 30, 60, and 90 mg/kg, iv) and gestational status (nonpregnant, day 6, 10, 13, and 17 of gestation, and postpartum)."( Pharmacokinetics of 2,4,5-T in mice as a function of dose and gestational status.
Bazare, JJ; Nelson, CJ; Young, JF, 1990
)
0.51
" While a single-animal, multiple-sample design requires the availability of microanalytical methods, it has many economic and practical advantages and results in a more accurate pharmacokinetic profile of the chemical in mice."( Sampling methods for pharmacokinetic studies in the mouse.
Bazare, J; Leamons, ML; Young, JF, 1981
)
0.26
"The pharmacokinetic profile of the herbicide 2,4,5-T PGBE ester (propylene glycol butyl ether esters of 2,4,5-trichlorophenoxyacetic acid) 14C-labeled in the ring was examined in rats given a single dermal application of 5 mg/kg."( Pharmacokinetics of 2,4,5-T PGBE ester applied dermally to rats.
Braun, WH; Ramsey, JC; Young, JD, 1981
)
0.48

Bioavailability

ExcerptReferenceRelevance
" Analysis of liver samples demonstrated low bioavailability of TCDD from this soil."( Bioavailability of dioxin in soil from a 2,4,5-T manufacturing site.
Gallo, MA; Hesse, EJ; Umbreit, TH, 1986
)
0.27
" The rate of absorption of the ester through the skin was lower than the rate of hydrolysis to 2,4,5-T acid and the rate of excretion of 2,4,5-T in the urine."( Pharmacokinetics of 2,4,5-T PGBE ester applied dermally to rats.
Braun, WH; Ramsey, JC; Young, JD, 1981
)
0.26
" Specifically, the mechanisms of dissipation and degradation as they relate to environmental distribution and bioavailability are addressed."( Environmental fate and bioavailability of Agent Orange and its associated dioxin during the Vietnam War.
Giesy, JP; Jones, PD; Newton, M; Young, AL, 2004
)
0.32
" Photochemical degradation of TCDD and limited bioavailability of any residual TCDD present in soil or on vegetation suggest that dioxin concentrations in ground troops who served in Vietnam would have been small and indistinguishable from background levels even if they had been in recently treated areas."( Environmental fate and bioavailability of Agent Orange and its associated dioxin during the Vietnam War.
Giesy, JP; Jones, PD; Newton, M; Young, AL, 2004
)
0.32
"Serum dioxin studies of Vietnam (VN) veterans, military historical records of tactical herbicide use in Vietnam, and the compelling evidence of the photodegradation of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) and other aspects of environmental fate and low bioavailability of TCDD are consistent with few, if any, ground troop veterans being exposed to Agent Orange."( Agent Orange exposure and attributed health effects in Vietnam veterans.
Cecil, PF; Young, AL, 2011
)
0.37

Dosage Studied

ExcerptRelevanceReference
"A large scale replicated dose-response teratology study of 2,4,5-T was done in mice."( Statistical analysis of teratologic data: problems and advancements.
Holson, JF; Nelson, CJ,
)
0.13
" On days corresponding to days 6 through 14 of pregnancy, groups of pregnant and nonpregnant CD-1 mice and male and nonpregnant female dihybrid cross F2 mice received by gavage 2,4,5-trichlorophenoxyacetic acid (2,4,5-T) ranging in dosage from 30 to 140 mg/kg."( Strain differences in histopathologic, hematologic, and blood chemistry changes induced in mice by a technical and a purified preparation of 2,4,5-trichlorphenoxyacetic acid.
Gaines, TB; Haley, TJ; Highman, B; Schumacher, HJ, 1976
)
0.45
"The problem of developing biologically-based dose-response models is addressed for predicting the prevalence of birth defects at low doses of toxic chemicals administered during pregnancy."( Process of building biologically based dose-response models for developmental defects.
Gaylor, DW; Razzaghi, M, 1992
)
0.28
" For corticosterone determinations, mice were dosed on GD 10, and blood was collected at 1, 4, 24, or 48 hr after dosing."( The effect of teratogens on maternal corticosterone levels and cleft incidence in A/J mice.
Hansen, DK; Holson, RR; Sheehan, DM; Sullivan-Jones, P,
)
0.13
" Regression and/or probit analyses were conducted to determine whether a dose-response relationship existed."( Developmental toxicity of 2,4,5-trichlorophenoxyacetic acid (2,4,5-T). I. Multireplicated dose-response studies in four inbred strains and one outbred stock of mice.
Gaines, TB; Gaylor, DW; Holson, JF; LaBorde, JB; Nelson, CJ; Sheehan, DM; Young, JF, 1992
)
0.58
" Both the outcross and outbred mice exhibited a dose-response relationship with each of the above endpoints and the dose-response curves were parallel."( Developmental toxicity of 2,4,5-trichlorophenoxyacetic acid (2,4,5-T). II. Multireplicated dose-response studies with technical and analytical grades of 2,4,5-T in four-way outcross mice.
Gaines, TB; Holson, JF; LaBorde, JB; McCallum, WF; Nelson, CJ; Sheehan, DM; Wolff, GL; Young, JF, 1992
)
0.58
" Pregnant animals (Sprague-Dawley strain) were dosed by oral gavage with one of a series of compounds on days 6-15 of gestation."( Effects of chemically induced maternal toxicity on prenatal development in the rat.
Chernoff, N; Miller, DB; Rogers, JM; Rosen, MB; Setzer, RW, 1990
)
0.28
" 2,4-D/2,4,5-T was behaviorally teratogenic at all dosage levels."( Behavioral and developmental effects in rats following in utero exposure to 2,4-D/2,4,5-t mixture.
Mohammad, FK; St Omer, VE,
)
0.13
" Cytogenetic analysis of the spermatogonia of male Chinese hamsters orally dosed five times at 24-hr intervals with 2,4,5-T at levels of up to and including 100 mg/kg did not provide any indication of 2,4,5-T having chromosome-damaging effects."( Mutagenicity studies with 2,4,5-T on bacteria and mammalian germ cells.
Herbold, BA; Machemer, L; Röhrborn, G, 1982
)
0.26
"05) dose-response relationships."( Testing of 2,4,5-T-amino acid conjugates for mutagenic activity in Salmonella typhimurium strains.
Babish, JG; Mumma, RO; Rashid, KA, 1984
)
0.27
" At the conclusion of an 8-wk dosing period, treated males cohabited with untreated virgin C57BL/6 female mice."( Development and viability of offspring of male mice treated with chlorinated phenoxy acids and 2,3,7,8-tetrachlorodibenzo-p-dioxin.
Haseman, JK; Lamb, JC; Marks, TA; Moore, JA,
)
0.13
" This note addresses issues in the interpretation of statistical variability in fitting dose-response models and estimating exposures associated with a low (or at least specified) level of risk."( Statistical variability: what does it mean in risk assessment?
Catalano, P; Weller, E,
)
0.13
" The positive response of yeast and transformed hematopoietic cells was verified in kinetics and dose-response experiments."( Genotoxic effect of substituted phenoxyacetic acids.
Alexieva, V; Georgieva, M; Karanov, E; Topashka-Ancheva, M; Venkov, P, 2000
)
0.31
"Modeling of developmental toxicity studies often requires simple parametric analyses of the dose-response relationship between exposure and probability of a birth defect but poses challenges because of nonstandard distributions of birth defects for a fixed level of exposure."( Bayesian semiparametric analysis of developmental toxicology data.
Dominici, F; Parmigiani, G, 2001
)
0.31
" Using a two-stage hierarchical normal dose-response model, upper confidence limits on the excess risk due to a given level of added exposure are derived."( Quantitative risk assessment for developmental neurotoxic effects.
Kodell, R; Razzaghi, M, 2004
)
0.32
" For the same dose-response relationship, the fit based on the shared response distribution is superior to that based on the beta-binomial, and comparable to that based on the recently proposed q-power distribution (Kuk, 2004, Applied Statistics53, 369-386)."( A shared response model for clustered binary data in developmental toxicity studies.
Kuk, AY; Pang, Z, 2005
)
0.33
" From the fraction of TCDD in AO, absorbed dosage of the manufacturing contaminant was estimated."( Exposure to TCDD from base perimeter application of Agent Orange in Vietnam.
Armitage, J; Ginevan, ME; Hewitt, A; Ross, JH; Solomon, K; Watkins, DK, 2015
)
0.42
" Data for children conceived after the start of Vietnam War service for participants with measured dioxin values were used to estimate dose-response curves for the effect of dioxin exposure on the occurrence of each of the eight general categories of birth defects and developmental disabilities."( An analysis of birth defects and developmental disabilities for children of participants of the Air Force Health Study.
Knafl, GJ, 2023
)
0.91
" Data for conceptions after the start of Vietnam War service for participants with measured dioxin values were used to estimate dose-response curves for the effect of dioxin exposure on the occurrence of each of the three non-sparsely occurring outcomes."( An analysis of reproductive outcomes for conceptions of participants of the Air Force Health Study.
Knafl, GJ, 2023
)
0.91
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (3)

RoleDescription
defoliantA herbicide which when sprayed or dusted on plants causes its leaves to fall off.
synthetic auxinA synthetic compound exhibiting auxin activity.
phenoxy herbicideAny member of the class of herbicides whose members contain a phenoxy or substituted phenoxy group.
[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 (2)

ClassDescription
chlorophenoxyacetic acidA monocarboxylic acid that is phenoxyacetic acid in which at least one of the phenyl hydrogens is replaced by chlorine.
trichlorobenzeneAny member of the class of chlorobenzenes carrying three chloro substituents at unspecified positions.
[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 (16)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Chain A, Putative fructose-1,6-bisphosphate aldolaseGiardia intestinalisPotency17.74070.140911.194039.8107AID2451
SMAD family member 2Homo sapiens (human)Potency32.78480.173734.304761.8120AID1346859
SMAD family member 3Homo sapiens (human)Potency32.78480.173734.304761.8120AID1346859
AR proteinHomo sapiens (human)Potency21.88710.000221.22318,912.5098AID743036
retinoid X nuclear receptor alphaHomo sapiens (human)Potency34.10890.000817.505159.3239AID1159527
estrogen-related nuclear receptor alphaHomo sapiens (human)Potency48.55770.001530.607315,848.9004AID1224849
farnesoid X nuclear receptorHomo sapiens (human)Potency21.87510.375827.485161.6524AID743220
pregnane X nuclear receptorHomo sapiens (human)Potency70.79460.005428.02631,258.9301AID720659
estrogen nuclear receptor alphaHomo sapiens (human)Potency20.27440.000229.305416,493.5996AID743069; AID743075
peroxisome proliferator-activated receptor deltaHomo sapiens (human)Potency39.81070.001024.504861.6448AID588534
peroxisome proliferator activated receptor gammaHomo sapiens (human)Potency41.72860.001019.414170.9645AID588536; AID743191
vitamin D (1,25- dihydroxyvitamin D3) receptorHomo sapiens (human)Potency5.49480.023723.228263.5986AID743223
thyroid hormone receptor beta isoform aHomo sapiens (human)Potency0.01260.010039.53711,122.0200AID588545
thyroid hormone receptor beta isoform 2Rattus norvegicus (Norway rat)Potency49.47870.000323.4451159.6830AID743065; AID743067
nuclear factor erythroid 2-related factor 2 isoform 1Homo sapiens (human)Potency40.52730.000627.21521,122.0200AID651741; AID743202; AID743219
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Inhibition Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Androgen receptorRattus norvegicus (Norway rat)IC50 (µMol)457.08800.00101.979414.1600AID255211
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (16)

Assay IDTitleYearJournalArticle
AID588499High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set2010Current protocols in cytometry, Oct, Volume: Chapter 13Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening.
AID588499High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set2006Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5
Microsphere-based protease assays and screening application for lethal factor and factor Xa.
AID588499High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set2010Assay and drug development technologies, Feb, Volume: 8, Issue:1
High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors.
AID588497High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set2010Current protocols in cytometry, Oct, Volume: Chapter 13Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening.
AID588497High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set2006Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5
Microsphere-based protease assays and screening application for lethal factor and factor Xa.
AID588497High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set2010Assay and drug development technologies, Feb, Volume: 8, Issue:1
High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors.
AID588501High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set2010Current protocols in cytometry, Oct, Volume: Chapter 13Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening.
AID588501High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set2006Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5
Microsphere-based protease assays and screening application for lethal factor and factor Xa.
AID588501High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set2010Assay and drug development technologies, Feb, Volume: 8, Issue:1
High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors.
AID255211Inhibitory concentration against recombinant rat androgen receptor expressed in Escherichia coli using [3H]methyltrienolone (R 1881)2005Journal of medicinal chemistry, Sep-08, Volume: 48, Issue:18
Impact of induced fit on ligand binding to the androgen receptor: a multidimensional QSAR study to predict endocrine-disrupting effects of environmental chemicals.
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.
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.
AID679055TP_TRANSPORTER: Western in vivo, liver of CF I mouse1999The Biochemical journal, Jul-01, Volume: 341 ( Pt 1)Induction of the multispecific organic anion transporter (cMoat/mrp2) gene and biliary glutathione secretion by the herbicide 2,4,5-trichlorophenoxyacetic acid in the mouse liver.
AID679180TP_TRANSPORTER: Northern blot in vivo, liver of CF I mouse1999The Biochemical journal, Jul-01, Volume: 341 ( Pt 1)Induction of the multispecific organic anion transporter (cMoat/mrp2) gene and biliary glutathione secretion by the herbicide 2,4,5-trichlorophenoxyacetic acid in the mouse liver.
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.
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.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (769)

TimeframeStudies, This Drug (%)All Drugs %
pre-1990427 (55.53)18.7374
1990's104 (13.52)18.2507
2000's125 (16.25)29.6817
2010's103 (13.39)24.3611
2020's10 (1.30)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 61.25

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 very strong demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index61.25 (24.57)
Research Supply Index6.74 (2.92)
Research Growth Index4.36 (4.65)
Search Engine Demand Index103.50 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (61.25)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials4 (0.48%)5.53%
Reviews57 (6.77%)6.00%
Case Studies23 (2.73%)4.05%
Observational0 (0.00%)0.25%
Other758 (90.02%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]