Page last updated: 2024-11-06

pyrimethanil

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

Description

Pyrimethanil is a systemic fungicide used to control a wide range of fungal diseases in various crops, including fruits, vegetables, and ornamentals. Its mechanism of action involves inhibiting the biosynthesis of ergosterol, an essential component of fungal cell membranes, leading to cell disruption and death. Pyrimethanil exhibits both preventative and curative properties, meaning it can protect plants from infection and also treat existing infections. It is often used in combination with other fungicides for broader spectrum control and reduced resistance development. Research on pyrimethanil focuses on understanding its efficacy, environmental impact, and potential risks to human health. Studies have investigated its degradation in soil and water, its effects on non-target organisms, and its potential for residues in food products.'

pyrimethanil: structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

pyrimethanil : A member of the class of aminopyrimidines that is N-phenylpyrimidin-2-amine carrying two additional methyl substituents at positions 4 and 6. A fungicide used to control grey mould on fruit, vegetables and ornamentals as well as leaf scab on pome fruit. Also commonly employed to control Botrytis cinerea throughout the winemaking process in grapes, must, fermenting must and wine. [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 CID91650
CHEMBL ID540677
CHEBI ID8674
SCHEMBL ID20817
MeSH IDM0281475

Synonyms (55)

Synonym
AC-12527
53112-28-0
pyrimethanil
NCGC00164307-01
hsdb 6916
2-pyrimidinamine, 4,6-dimethyl-n-phenyl-
pyrimethanil [iso]
PEAKDALE1_000145
4,6-dimethyl-n-phenylpyrimidin-2-amine
NCGC00164307-02
HMS518G13
CHEMBL540677
chebi:8674 ,
AKOS005604858
NCGC00164307-03
STK693289
dtxsid8034877 ,
dtxcid6014877
NCGC00254712-01
cas-53112-28-0
tox21_300808
A829404
4,6-dimethyl-n-phenyl-2-pyrimidinamine
unii-6ia5hp6c8z
6ia5hp6c8z ,
FT-0630658
AM20060659
2-anilino-4,6-dimethylpyrimidine
pyrimethanil [hsdb]
sn 100309
sn-100309
pyrimethanil [mi]
scala
n-(4,6-dimethylpyrimidin-2-yl)aniline
SCHEMBL20817
12B-067
4,6-dimethyl-n-phenyl-pyrimidin-2-amine
DS-0891
mfcd00172113
pyrimethanil, pestanal(r), analytical standard
4,6-dimethyl-~{n}-phenyl-pyrimidin-2-amine
MUK ,
pyrimethanil 100 microg/ml in methanol
pyrimethanil 10 microg/ml in cyclohexane
zk 100309
pyrimethanil, bsi
mythos
CS-0014128
bariumselenate
Q7263600
O11144
pyrimethanil 1000 microg/ml in toluene
HY-B2033
EN300-651703
Z285675722

Research Excerpts

Overview

Pyrimethanil is a broad-spectrum fungicide commonly used in the prevention and treatment of Botrytis cinerea. It is an anilinopyrimidine bactericide with poor water solubility, which limits its applications.

ExcerptReferenceRelevance
"Pyrimethanil (PMT) is an anilinopyrimidine bactericide with poor water solubility, which limits its applications. "( Fabrication and Characterization of Antifungal Hydroxypropyl-β-Cyclodextrin/Pyrimethanil Inclusion Compound Nanofibers Based on Electrospinning.
Feng, W; Fu, Y; Gao, S; Li, X; Sun, H; Ye, F; Zhao, L; Zong, L, 2022
)
2.39
"Pyrimethanil is a broad-spectrum fungicide commonly used in the prevention and treatment of Botrytis cinerea. "( Exposure to pyrimethanil induces developmental toxicity and cardiotoxicity in zebrafish.
Cao, Z; Chen, S; Huang, Y; Liao, X; Lu, H; Ma, J; Meng, Y; Tang, L; Wei, Y; Wu, J; Xiao, J; Zhong, K, 2020
)
2.38
"Pyrimethanil (PYM) is a fungicide used pre- and post-harvest on many crops. "( Biomarkers of Exposure to Pyrimethanil After Controlled Human Experiments.
Ekman, E; Faniband, M; Larsson, E; Lindh, CH; Littorin, M; Maxe, M, 2019
)
2.26
"Pyrimethanil is a fungicide mostly applied in vineyards. "( Potential mechanisms underlying response to effects of the fungicide pyrimethanil from gene expression profiling in Saccharomyces cerevisiae.
Becker, JD; Gil, FN; Viegas, CA, 2014
)
2.08

Actions

ExcerptReferenceRelevance
"A pyrimethanil-induced increase of total mortality was buffered by the strongly related increase of the general reproductive capacity, while population growth was stronger influenced by temperature than by the fungicide."( Aquatic ecotoxicity of the fungicide pyrimethanil: effect profile under optimal and thermal stress conditions.
Müller, R; Oehlmann, J; Seeland, A, 2012
)
1.21

Toxicity

ExcerptReferenceRelevance
"The present study is aimed at evaluating whether a gene expression assay with the microbial eukaryotic model Saccharomyces cerevisiae could be used as a suitable warning tool for the rapid preliminary screening of potential toxic effects on organisms due to scenarios of soil and water contamination with pyrimethanil."( Suitability of a Saccharomyces cerevisiae-based assay to assess the toxicity of pyrimethanil sprayed soils via surface runoff: comparison with standard aquatic and soil toxicity assays.
Chelinho, S; Feliciano, JR; Gil, FN; Leitão, JH; Moreira-Santos, M; Pereira, C; Ribeiro, R; Sousa, JP; Viegas, CA, 2015
)
0.82

Compound-Compound Interactions

ExcerptReferenceRelevance
"The postinfection activity of azoxystrobin (AZX), fludioxonil (FLU), and pyrimethanil (PYR), applied alone or in combination with imazalil (IMZ), in controlling postharvest green mold in 'Salustiana' oranges inoculated with Penicillium digitatum was studied."( Postinfection activity, residue levels, and persistence of azoxystrobin, fludioxonil, and pyrimethanil applied alone or in combination with heat and imazalil for green mold control on inoculated oranges.
Angioni, A; Barberis, A; Cabras, P; D'Aquino, S; Garau, VL; Palma, A; Schirra, M, 2010
)
0.81
" Effects of pesticides, especially in agricultural areas, may interact with environmental factors, such as soil moisture fluctuation caused by global climate change."( A TME study with the fungicide pyrimethanil combined with different moisture regimes: effects on enchytraeids.
Bandow, C; Ng, EL; Römbke, J; Schmelz, RM; Sousa, JP, 2016
)
0.72

Dosage Studied

ExcerptRelevanceReference
" It was shown that the pyrimethanil-loaded mesoporous silica nanoparticles might be more conducive to acropetal, rather than basipetal, uptake, and the dosage had almost no effect on the distribution and dissipation rate in cucumber plants."( Synthesis of Pyrimethanil-Loaded Mesoporous Silica Nanoparticles and Its Distribution and Dissipation in Cucumber Plants.
Cao, L; Huang, Q; Ma, D; Pan, C; Zhao, P; Zhou, Z, 2017
)
1.14
" Adding the methylated vegetable oil adjuvant to fungicides would result in unprolonging half-life and acceptably low dietary exposure risk on strawberries, but lower dosage of fungicides were used."( Positive effects of an oil adjuvant on efficacy, dissipation and safety of pyrimethanil and boscalid on greenhouse strawberry.
Cang, T; Qi, P; Wang, Q; Wang, X; Wang, Z; Wu, S; Xu, X; Zhao, X, 2018
)
0.71
" In short, the fabrication HPβCD/PMT-IC-NF inhibited improved solubility and thermostability of PMT, thus promoting the development of pesticide dosage form to water-based and low-pollution direction."( Fabrication and Characterization of Antifungal Hydroxypropyl-β-Cyclodextrin/Pyrimethanil Inclusion Compound Nanofibers Based on Electrospinning.
Feng, W; Fu, Y; Gao, S; Li, X; Sun, H; Ye, F; Zhao, L; Zong, L, 2022
)
0.95
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Occurs in Manufacturing (48 Items)

ItemProcessFrequency
Fruitscore-ingredient22
Agrumescore-ingredient13
Fruits et produits dérivéscore-ingredient13
Aliments à base de fruits et de légumescore-ingredient13
Aliments d'origine végétalecore-ingredient13
Aliments et boissons à base de végétauxcore-ingredient13
Fruits fraiscore-ingredient12
Orangescore-ingredient11
Fruits based foodscore-ingredient9
Fruits and vegetables based foodscore-ingredient9
Plant-based foodscore-ingredient9
Plant-based foods and beveragescore-ingredient9
Citruscore-ingredient8
Oranges fraîchescore-ingredient8
Mandarin orangescore-ingredient4
Fresh fruitscore-ingredient4
Mandarinescore-ingredient4
Fresh orangescore-ingredient3
Mandarines fraîchescore-ingredient3
Clementinescore-ingredient2
Pflanzliche Lebensmittelcore-ingredient2
Fruchtbasierte Lebensmittelcore-ingredient2
Frucht- und gemüsebasierte Lebensmittelcore-ingredient2
Früchtecore-ingredient2
Pflanzliche Lebensmittel und Getränkecore-ingredient2
Oranges-a-juscore-ingredient1
Clémentines fraîchescore-ingredient1
Surgeléscore-ingredient1
en:lemonscore-ingredient1
Tangerinescore-ingredient1
Citronscore-ingredient1
Verse mandarijnencore-ingredient1
Mandarijnencore-ingredient1
Vers fruitcore-ingredient1
Citrusvruchtencore-ingredient1
Fruitcore-ingredient1
Fruit en afgeleide productencore-ingredient1
Voedsel op basis van fruit en groentencore-ingredient1
Plantaardige levensmiddelencore-ingredient1
Plantaardige levensmiddelen en drankencore-ingredient1
Clementinestrace-ingredient1
Mandarin orangestrace-ingredient1
Citrustrace-ingredient1
Fruitstrace-ingredient1
Fruits based foodstrace-ingredient1
Fruits and vegetables based foodstrace-ingredient1
Plant-based foodstrace-ingredient1
Plant-based foods and beveragestrace-ingredient1

Roles (4)

RoleDescription
aryl hydrocarbon receptor agonistAn agonist that binds to and activates aryl hydrocarbon receptors (AhRs).
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.
antifungal agrochemicalAny substance used in acriculture, horticulture, forestry, etc. for its fungicidal properties.
[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
aminopyrimidineA member of the class of pyrimidines that is pyrimidine substituted by at least one amino group and its derivatives.
secondary amino compoundA compound formally derived from ammonia by replacing two hydrogen atoms by organyl groups.
anilinopyrimidine fungicideAny pyrimidine fungicide in which the pyrimidine ring is substituted by the nitrogen of an aniline moiety.
[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 (14)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
RAR-related orphan receptor gammaMus musculus (house mouse)Potency0.10870.006038.004119,952.5996AID1159521
AR proteinHomo sapiens (human)Potency48.50590.000221.22318,912.5098AID1259243; AID1259247; AID743042; AID743054
nuclear receptor subfamily 1, group I, member 3Homo sapiens (human)Potency40.04760.001022.650876.6163AID1224838; AID1224839; AID1224893
retinoic acid nuclear receptor alpha variant 1Homo sapiens (human)Potency31.60300.003041.611522,387.1992AID1159552; AID1159553; AID1159555
estrogen-related nuclear receptor alphaHomo sapiens (human)Potency37.49530.001530.607315,848.9004AID1224848; AID1224849; AID1259403
farnesoid X nuclear receptorHomo sapiens (human)Potency44.66840.375827.485161.6524AID588526
pregnane X nuclear receptorHomo sapiens (human)Potency76.95880.005428.02631,258.9301AID1346982
estrogen nuclear receptor alphaHomo sapiens (human)Potency36.12650.000229.305416,493.5996AID1259244; AID1259248; AID743080; AID743091
aryl hydrocarbon receptorHomo sapiens (human)Potency48.55770.000723.06741,258.9301AID743085; AID743122
cytochrome P450, family 19, subfamily A, polypeptide 1, isoform CRA_aHomo sapiens (human)Potency34.37620.001723.839378.1014AID743083
histone deacetylase 9 isoform 3Homo sapiens (human)Potency35.74740.037617.082361.1927AID1259364; AID1259388
nuclear factor erythroid 2-related factor 2 isoform 1Homo sapiens (human)Potency57.80670.000627.21521,122.0200AID651741; AID720636
Voltage-dependent calcium channel gamma-2 subunitMus musculus (house mouse)Potency34.37620.001557.789015,848.9004AID1259244
Glutamate receptor 2Rattus norvegicus (Norway rat)Potency34.37620.001551.739315,848.9004AID1259244
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Ceullar Components (1)

Processvia Protein(s)Taxonomy
plasma membraneGlutamate receptor 2Rattus norvegicus (Norway rat)
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (44)

Assay IDTitleYearJournalArticle
AID1101688Drug degradation in Solanum lycopersicum (tomato) plant fruits at 300 g/L treated under green house condition measured after 10 days relative to initial level2002Journal of agricultural and food chemistry, Feb-27, Volume: 50, Issue:5
Disappearance of pyrimethanil residues on tomato plants.
AID1112880Resistance index, ratio of EC50 for sterol 14alpha-demethylation inhibitor-resistant Oculimacula yallundae TriR2 to EC50 for wild type Oculimacula yallundae TriS by germ tube elongation assay2013Pest management science, Jan, Volume: 69, Issue:1
Fungicide resistance status in French populations of the wheat eyespot fungi Oculimacula acuformis and Oculimacula yallundae.
AID1081375Fungicidal activity against Botryotinia fuckeliana assessed as inhibition of spore germination at 25 degC after 6 hr by microscopic analysis2010Journal of agricultural and food chemistry, Mar-10, Volume: 58, Issue:5
Synthesis of 1-acyl-3-isopropenylbenzimidazolone derivatives and their activity against Botrytis cinerea.
AID1081391Fungicidal activity Fusarium oxysporum assessed as inhibition of mycelium growth at 50 mg/L at 24 degC measured after 2 days2010Journal of agricultural and food chemistry, Mar-10, Volume: 58, Issue:5
Synthesis and fungicidal activity of aryl carbamic acid-5-aryl-2-furanmethyl ester.
AID1081276Antifungal activity against Phomopsis asparagi by mycelium growth rate test2010Journal of agricultural and food chemistry, Mar-10, Volume: 58, Issue:5
Synthesis, fungicidal activity, and structure-activity relationship of spiro-compounds containing macrolactam (macrolactone) and thiadiazoline rings.
AID1112877Resistance index, ratio of EC50 for sterol 14alpha-demethylation inhibitor-resistant Oculimacula yallundae MDR to EC50 for sterol 14alpha-demethylation inhibitor-resistant Oculimacula yallundae TriR1 by germ tube elongation assay2013Pest management science, Jan, Volume: 69, Issue:1
Fungicide resistance status in French populations of the wheat eyespot fungi Oculimacula acuformis and Oculimacula yallundae.
AID1081280Antifungal activity against Botryotinia fuckeliana by mycelium growth rate test2010Journal of agricultural and food chemistry, Mar-10, Volume: 58, Issue:5
Synthesis, fungicidal activity, and structure-activity relationship of spiro-compounds containing macrolactam (macrolactone) and thiadiazoline rings.
AID1101705Drug recovery in Solanum lycopersicum (tomato) plant fruits at 0.14 ug/g of spiking level2002Journal of agricultural and food chemistry, Feb-27, Volume: 50, Issue:5
Disappearance of pyrimethanil residues on tomato plants.
AID1101691Drug degradation in Solanum lycopersicum (tomato) plant fruits at 300 g/L treated under green house condition measured after 5 days relative to initial level2002Journal of agricultural and food chemistry, Feb-27, Volume: 50, Issue:5
Disappearance of pyrimethanil residues on tomato plants.
AID1112881Resistance index, ratio of EC50 for sterol 14alpha-demethylation inhibitor-resistant Oculimacula yallundae TriR1 to EC50 for wild type Oculimacula yallundae TriS by germ tube elongation assay2013Pest management science, Jan, Volume: 69, Issue:1
Fungicide resistance status in French populations of the wheat eyespot fungi Oculimacula acuformis and Oculimacula yallundae.
AID1101701Drug degradation in Solanum lycopersicum (tomato) plant fruits at 300 g/L treated under green house condition measured after 8 days relative to initial level2002Journal of agricultural and food chemistry, Feb-27, Volume: 50, Issue:5
Disappearance of pyrimethanil residues on tomato plants.
AID1101681Drug degradation in Solanum lycopersicum (tomato) plant fruits at 300 g/L treated under green house condition measured after 11 days relative to initial level2002Journal of agricultural and food chemistry, Feb-27, Volume: 50, Issue:5
Disappearance of pyrimethanil residues on tomato plants.
AID1101689Drug degradation in Solanum lycopersicum (tomato) plant fruits at 300 g/L treated under green house condition measured after 7 days relative to initial level2002Journal of agricultural and food chemistry, Feb-27, Volume: 50, Issue:5
Disappearance of pyrimethanil residues on tomato plants.
AID1112879Resistance index, ratio of EC50 for sterol 14alpha-demethylation inhibitor-resistant Oculimacula yallundae TriR2 to EC50 for sterol 14alpha-demethylation inhibitor-resistant Oculimacula yallundae TriR1 by germ tube elongation assay2013Pest management science, Jan, Volume: 69, Issue:1
Fungicide resistance status in French populations of the wheat eyespot fungi Oculimacula acuformis and Oculimacula yallundae.
AID426461Antifungal activity against Botrytis cinerea at 500 ug/ml relative to control2009European journal of medicinal chemistry, Jul, Volume: 44, Issue:7
Synthesis, antifungal activities and 3D-QSAR study of N-(5-substituted-1,3,4-thiadiazol-2-yl)cyclopropanecarboxamides.
AID1081277Antifungal activity against Magnaporthe oryzae by mycelium growth rate test2010Journal of agricultural and food chemistry, Mar-10, Volume: 58, Issue:5
Synthesis, fungicidal activity, and structure-activity relationship of spiro-compounds containing macrolactam (macrolactone) and thiadiazoline rings.
AID1081758Fungicidal activity against Botryotinia fuckeliana grown on compound pre-treated cucumber leaves assessed as control efficiency against gray mold disease on leaves at 500 ug/mL2010Journal of agricultural and food chemistry, Nov-10, Volume: 58, Issue:21
Synthesis, fungicidal activity, and structure-activity relationship of 2-oxo- and 2-hydroxycycloalkylsulfonamides.
AID1101683Drug degradation in Solanum lycopersicum (tomato) plant fruits at 300 g/L treated under green house condition measured after 6 days relative to initial level2002Journal of agricultural and food chemistry, Feb-27, Volume: 50, Issue:5
Disappearance of pyrimethanil residues on tomato plants.
AID1101686Drug degradation in Solanum lycopersicum (tomato) plant leaves at 300 g/L treated under green house condition measured after 10 days relative to initial level2002Journal of agricultural and food chemistry, Feb-27, Volume: 50, Issue:5
Disappearance of pyrimethanil residues on tomato plants.
AID1112878Resistance index, ratio of EC50 for sterol 14alpha-demethylation inhibitor-resistant Oculimacula yallundae MDR to EC50 for wild type Oculimacula yallundae TriS by germ tube elongation assay2013Pest management science, Jan, Volume: 69, Issue:1
Fungicide resistance status in French populations of the wheat eyespot fungi Oculimacula acuformis and Oculimacula yallundae.
AID1101703Drug degradation in Solanum lycopersicum (tomato) plant fruits at 300 g/L treated under green house condition measured after 1 day relative to initial level2002Journal of agricultural and food chemistry, Feb-27, Volume: 50, Issue:5
Disappearance of pyrimethanil residues on tomato plants.
AID1101690Drug degradation in Solanum lycopersicum (tomato) plant leaves at 300 g/L treated under green house condition measured after 5 days relative to initial level2002Journal of agricultural and food chemistry, Feb-27, Volume: 50, Issue:5
Disappearance of pyrimethanil residues on tomato plants.
AID1101696Drug degradation in Solanum lycopersicum (tomato) plant leaves at 300 g/L treated under green house condition measured after 22 days relative to initial level2002Journal of agricultural and food chemistry, Feb-27, Volume: 50, Issue:5
Disappearance of pyrimethanil residues on tomato plants.
AID1081757Fungicidal activity against Botryotinia fuckeliana grown on compound pre-treated cucumber leaves assessed as control efficiency against gray mold disease on leaves at 125 ug/mL2010Journal of agricultural and food chemistry, Nov-10, Volume: 58, Issue:21
Synthesis, fungicidal activity, and structure-activity relationship of 2-oxo- and 2-hydroxycycloalkylsulfonamides.
AID1101695Half life in Solanum lycopersicum (tomato) plant fruits at 300 g/L treated under green house condition2002Journal of agricultural and food chemistry, Feb-27, Volume: 50, Issue:5
Disappearance of pyrimethanil residues on tomato plants.
AID1101702Drug degradation in Solanum lycopersicum (tomato) plant fruits at 300 g/L treated under green house condition measured after 15 days relative to initial level2002Journal of agricultural and food chemistry, Feb-27, Volume: 50, Issue:5
Disappearance of pyrimethanil residues on tomato plants.
AID1101682Drug degradation in Solanum lycopersicum (tomato) plant leaves at 300 g/L treated under green house condition measured after 6 days relative to initial level2002Journal of agricultural and food chemistry, Feb-27, Volume: 50, Issue:5
Disappearance of pyrimethanil residues on tomato plants.
AID1101693Drug degradation in Solanum lycopersicum (tomato) plant leaves at 300 g/L treated under green house condition measured after 3 days relative to initial level2002Journal of agricultural and food chemistry, Feb-27, Volume: 50, Issue:5
Disappearance of pyrimethanil residues on tomato plants.
AID1101692Drug degradation in Solanum lycopersicum (tomato) plant fruits at 300 g/L treated under green house condition measured after 3 days relative to initial level2002Journal of agricultural and food chemistry, Feb-27, Volume: 50, Issue:5
Disappearance of pyrimethanil residues on tomato plants.
AID1101699Drug degradation in Solanum lycopersicum (tomato) plant leaves at 300 g/L treated under green house condition measured after 8 days relative to initial level2002Journal of agricultural and food chemistry, Feb-27, Volume: 50, Issue:5
Disappearance of pyrimethanil residues on tomato plants.
AID1081279Antifungal activity against Sclerotinia sclerotiorum by mycelium growth rate test2010Journal of agricultural and food chemistry, Mar-10, Volume: 58, Issue:5
Synthesis, fungicidal activity, and structure-activity relationship of spiro-compounds containing macrolactam (macrolactone) and thiadiazoline rings.
AID1101684Drug degradation in Solanum lycopersicum (tomato) plant leaves at 300 g/L treated under green house condition measured after 4 days relative to initial level2002Journal of agricultural and food chemistry, Feb-27, Volume: 50, Issue:5
Disappearance of pyrimethanil residues on tomato plants.
AID1101697Drug degradation in Solanum lycopersicum (tomato) plant leaves at 300 g/L treated under green house condition measured after 15 days relative to initial level2002Journal of agricultural and food chemistry, Feb-27, Volume: 50, Issue:5
Disappearance of pyrimethanil residues on tomato plants.
AID1081756Fungicidal activity against Botryotinia fuckeliana grown on compound pre-treated cucumber leaves assessed as control efficiency against gray mold disease on leaves at 31.25 ug/mL2010Journal of agricultural and food chemistry, Nov-10, Volume: 58, Issue:21
Synthesis, fungicidal activity, and structure-activity relationship of 2-oxo- and 2-hydroxycycloalkylsulfonamides.
AID1101680Drug degradation in Solanum lycopersicum (tomato) plant leaves at 300 g/L treated under green house condition measured after 11 days relative to initial level2002Journal of agricultural and food chemistry, Feb-27, Volume: 50, Issue:5
Disappearance of pyrimethanil residues on tomato plants.
AID1112891Fungicidal activity against Oculimacula yallundae assessed as inhibition of germ tube elongation incubated at 19 degC in dark for 48 hr2013Pest management science, Jan, Volume: 69, Issue:1
Fungicide resistance status in French populations of the wheat eyespot fungi Oculimacula acuformis and Oculimacula yallundae.
AID1083139Fungicidal activity against Botryotinia fuckeliana infected in drug-pretreated cucumber two seeded leaves assessed as decrease in disease index at 40% SC formulation (acetone Rvb = 1.53 +/-0.21%)2012Journal of agricultural and food chemistry, Nov-28, Volume: 60, Issue:47
Synthesis and fungicidal activity of novel 2,5-disubstituted-1,3,4-oxadiazole derivatives.
AID1101700Drug degradation in Solanum lycopersicum (tomato) plant fruits at 300 g/L treated under green house condition measured after 22 days relative to initial level2002Journal of agricultural and food chemistry, Feb-27, Volume: 50, Issue:5
Disappearance of pyrimethanil residues on tomato plants.
AID1101687Drug degradation in Solanum lycopersicum (tomato) plant leaves at 300 g/L treated under green house condition measured after 7 days relative to initial level2002Journal of agricultural and food chemistry, Feb-27, Volume: 50, Issue:5
Disappearance of pyrimethanil residues on tomato plants.
AID1101694Half life in Solanum lycopersicum (tomato) plant leaves at 300 g/L treated under green house condition2002Journal of agricultural and food chemistry, Feb-27, Volume: 50, Issue:5
Disappearance of pyrimethanil residues on tomato plants.
AID1081278Antifungal activity against Rhizoctonia solani Kuhn by mycelium growth rate test2010Journal of agricultural and food chemistry, Mar-10, Volume: 58, Issue:5
Synthesis, fungicidal activity, and structure-activity relationship of spiro-compounds containing macrolactam (macrolactone) and thiadiazoline rings.
AID1101704Drug recovery in Solanum lycopersicum (tomato) plant leaves at 1.83 ug/cm'2 of spiking level2002Journal of agricultural and food chemistry, Feb-27, Volume: 50, Issue:5
Disappearance of pyrimethanil residues on tomato plants.
AID1101698Drug degradation in Solanum lycopersicum (tomato) plant leaves at 300 g/L treated under green house condition measured after 1 day relative to initial level2002Journal of agricultural and food chemistry, Feb-27, Volume: 50, Issue:5
Disappearance of pyrimethanil residues on tomato plants.
AID1101685Drug degradation in Solanum lycopersicum (tomato) plant fruits at 300 g/L treated under green house condition measured after 4 days relative to initial level2002Journal of agricultural and food chemistry, Feb-27, Volume: 50, Issue:5
Disappearance of pyrimethanil residues on tomato plants.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (129)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's1 (0.78)18.2507
2000's37 (28.68)29.6817
2010's77 (59.69)24.3611
2020's14 (10.85)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 55.18

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 Index55.18 (24.57)
Research Supply Index4.88 (2.92)
Research Growth Index6.75 (4.65)
Search Engine Demand Index88.13 (26.88)
Search Engine Supply Index2.11 (0.95)

This Compound (55.18)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews2 (1.53%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other129 (98.47%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]