Page last updated: 2024-11-11

kresoxim-methyl

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Description

kresoxim-methyl: strobilurin analogue; an industrial fungicide [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

kresoxim-methyl : A carboxylic ester that is the methyl ester of (2E)-(methoxyimino){2-[(2-methylphenoxy)methyl]phenyl}acetic acid. A fungicide for the control of scab on apples and pears and other fungal diseases on a wide range of crops. [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 CID6112114
CHEMBL ID203191
CHEBI ID2962
SCHEMBL ID18664
MeSH IDM0443487

Synonyms (52)

Synonym
kresoxim-methyl [iso]
hsdb 7020
einecs annex i index 607-310-00-0
bas 490f
methyl (e)-alpha-(methoxyimino)-2-((2-methylphenoxy)methyl)benzeneacetate
benzeneacetic acid, alpha-(methoxyimino)-2-((2-methylphenoxy)methyl)-, methyl ester, (e)-
bas 490 f
143390-89-0
kresoxim-methyl
NCGC00163896-01
CHEMBL203191
chebi:2962 ,
stroby
candit
methyl (2e)-2-methoxyimino-2-[2-[(2-methylphenoxy)methyl]phenyl]acetate
methyl 2-methoxyimino-2-[2-[(2-methylphenoxy)methyl]phenyl]acetate
methyl (2e)-2-methoxyimino-2-[2-[(2-methylphenoxy)methyl]phenyl]ethanoate
A808064
(2e)-2-methoxyimino-2-[2-[(2-methylphenoxy)methyl]phenyl]acetic acid methyl ester
0lxz062ttb ,
unii-0lxz062ttb
cas-143390-89-0
NCGC00255374-01
dtxsid2032558 ,
tox21_302251
dtxcid0012558
AKOS015995142
kresoxim-methyl [mi]
kresoxim-methyl [hsdb]
(.alpha.e)-.alpha.-(methoxyimino)-2-((2-methylphenoxy)methyl)benzeneacetic acid methyl ester
sovran
methyl (e)-methoxyimino(.alpha.-(o-tolyloxy)-o-tolyl)acetate
kresoxim methyl ester
bas-490-02f
bas-490 f
methyl (.alpha.e)-.alpha.-(methoxyimino)-2-((2-methylphenoxy)methyl)benzeneacetate
SCHEMBL18664
methyl (e)-methoxyimino[alpha-(o-tolyloxy)-o-tolyl]acetate
methyl (alphae)-alpha-(methoxyimino)-2-[(2-methylphenoxy)methyl]benzeneacetate
methyl (2e)-(methoxyimino){2-[(2-methylphenoxy)methyl]phenyl}acetate
kresoxim-methyl, pestanal(r), analytical standard
bdbm50487140
kresoxim-methyl 10 microg/ml in cyclohexane
J-007806
kresoxim methyl
methyl 2(e)-methoxyimino-2-[2-(2-methylphenoxymethyl)phenyl]acetate
kresoxim-methyl 1000 microg/ml in acetone
mfcd00871777
HY-125776
AS-13058
CS-0099295
AMY6566

Research Excerpts

Toxicity

ExcerptReferenceRelevance
"Strobilurins have been reported highly toxic to non-target aquatic organisms but few illustrated how they cause toxic effects on algae."( Acute toxicity and associated mechanisms of four strobilurins in algae.
Chen, H; Li, X; Liu, X; Pang, S; Wang, C; Wang, Y; Zhang, J, 2018
)
0.48
"Studies have shown that kresoxim-methyl (KM) and other strobilurin fungicides have toxic effects on aquatic organisms."( Histology and metabonomics reveal the toxic effects of kresoxim-methyl on adult zebrafish.
Fang, N; Hu, H; Jiang, J; Li, Y; Wang, X; Zhang, C; Zhao, X, 2022
)
1.28

Compound-Compound Interactions

ExcerptReferenceRelevance
" A simple and sensitive liquid chromatography-ultraviolet detection (LC-UV) method combined with the 'Quick Easy Cheap Effective Rugged and Safe' (QuEChERS) protocol was developed to quantify the levels of kresoxim-methyl and trifloxystrobin residues in citrus."( Simultaneous detection and degradation patterns of kresoxim-methyl and trifloxystrobin residues in citrus fruits by HPLC combined with QuEChERS.
Dai, XJ; Fang, JJ; Zhu, HM; Zhu, J, 2013
)
0.83

Dosage Studied

ExcerptRelevanceReference
" The preliminary bioassay showed that some of the chalcone analogues exhibited good in vivo fungicidal activities against Pseudoperoniospora cubensis and Sphaerotheca fuliginea at the dosage of 200 microg mL(-1)."( Synthesis and fungicidal evaluation of novel chalcone-based strobilurin analogues.
Huang, W; Liu, CL; Wang, YZ; Yang, GF; Zhao, PL, 2007
)
0.34
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (4)

RoleDescription
mitochondrial cytochrome-bc1 complex inhibitornull
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 (4)

ClassDescription
oxime O-etherO-organyl oximes R2C=NOR' (R' =/= H).
aromatic etherAny ether in which the oxygen is attached to at least one aryl substituent.
methyl esterAny carboxylic ester resulting from the formal condensation of a carboxy group with methanol.
methoxyiminoacetate strobilurin antifungal agent
[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 (24)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
pregnane X receptorRattus norvegicus (Norway rat)Potency10.00000.025127.9203501.1870AID651751
RAR-related orphan receptor gammaMus musculus (house mouse)Potency2.53630.006038.004119,952.5996AID1159521; AID1159523
SMAD family member 2Homo sapiens (human)Potency19.49380.173734.304761.8120AID1346859
SMAD family member 3Homo sapiens (human)Potency19.49380.173734.304761.8120AID1346859
GLI family zinc finger 3Homo sapiens (human)Potency3.47780.000714.592883.7951AID1259369; AID1259392
AR proteinHomo sapiens (human)Potency18.54870.000221.22318,912.5098AID1259243; AID1259247; AID588515; AID588516; AID743035; AID743036; AID743042; AID743053; AID743054; AID743063
estrogen receptor 2 (ER beta)Homo sapiens (human)Potency17.68760.000657.913322,387.1992AID1259377; AID1259378
nuclear receptor subfamily 1, group I, member 3Homo sapiens (human)Potency7.69590.001022.650876.6163AID1224839
progesterone receptorHomo sapiens (human)Potency61.13060.000417.946075.1148AID1346795
glucocorticoid receptor [Homo sapiens]Homo sapiens (human)Potency19.49380.000214.376460.0339AID720692
retinoic acid nuclear receptor alpha variant 1Homo sapiens (human)Potency6.78940.003041.611522,387.1992AID1159552; AID1159555
retinoid X nuclear receptor alphaHomo sapiens (human)Potency10.96220.000817.505159.3239AID1159527
estrogen-related nuclear receptor alphaHomo sapiens (human)Potency2.77390.001530.607315,848.9004AID1224841; AID1224842; AID1224848; AID1224849; AID1259401; AID1259403
farnesoid X nuclear receptorHomo sapiens (human)Potency31.62280.375827.485161.6524AID588526
pregnane X nuclear receptorHomo sapiens (human)Potency8.63490.005428.02631,258.9301AID1346982
estrogen nuclear receptor alphaHomo sapiens (human)Potency19.24480.000229.305416,493.5996AID588513; AID743069; AID743075; AID743077; AID743078
peroxisome proliferator-activated receptor deltaHomo sapiens (human)Potency35.98640.001024.504861.6448AID588534; AID588535; AID743212; AID743215
peroxisome proliferator activated receptor gammaHomo sapiens (human)Potency21.16200.001019.414170.9645AID588536; AID743191
vitamin D (1,25- dihydroxyvitamin D3) receptorHomo sapiens (human)Potency25.11890.023723.228263.5986AID588541
cytochrome P450, family 19, subfamily A, polypeptide 1, isoform CRA_aHomo sapiens (human)Potency34.37620.001723.839378.1014AID743083
thyroid hormone receptor beta isoform 2Rattus norvegicus (Norway rat)Potency3.06380.000323.4451159.6830AID743065; AID743067
nuclear factor erythroid 2-related factor 2 isoform 1Homo sapiens (human)Potency14.13300.000627.21521,122.0200AID651741; AID743202; AID743219
Cellular tumor antigen p53Homo sapiens (human)Potency55.45410.002319.595674.0614AID651631; AID651743; AID720552
[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)
Cytochrome bSus scrofa (pig)Ki0.15960.00330.15350.2976AID1091872
[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 (19)

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)
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (67)

Assay IDTitleYearJournalArticle
AID1091636In vivo fungicidal activity against Podosphaera fuliginea infected cucumber plants assessed as inhibition of disease symptoms at 200 ug/ml treated one day prior to fungal spore inoculation measured after one week2008Journal of agricultural and food chemistry, Nov-26, Volume: 56, Issue:22
Synthesis, fungicidal, and insecticidal activities of beta-Methoxyacrylate-containing N-acetyl pyrazoline derivatives.
AID1090702Antifungal activity against Pseudoperonospora cubensis in cucumber plants under greenhouse conditions assessed as fungicidal activity at 100 mg/mL by in vivo assay2007Journal of agricultural and food chemistry, Jul-11, Volume: 55, Issue:14
Synthesis and fungicidal evaluation of novel chalcone-based strobilurin analogues.
AID1111112Antifungal activity against Magnaporthe oryzae infected 12 day old rice plant assessed as disease control at 400 mg/l after 6 days relative to control2010Pest management science, Jan, Volume: 66, Issue:1
Design, synthesis and biological activities of new strobilurin derivatives containing substituted pyrazoles.
AID1080370Fungicidal activity against Colletotrichum lagenaria infected in compound pre-treated cucumber plants assessed as inhibition of fungal growth at 6.25 mg/ml measured 3 days post compound treatment2008Journal of agricultural and food chemistry, Jul-09, Volume: 56, Issue:13
Synthesis and fungicidal activities of novel indene-substituted oxime ether strobilurins.
AID263761Antifungal activity against Botrytis cinereapers at 50 ug/ml2006Bioorganic & medicinal chemistry letters, Apr-15, Volume: 16, Issue:8
Stereoselective synthesis and fungicidal activities of (E)-alpha-(methoxyimino)-benzeneacetate derivatives containing 1,3,4-oxadiazole ring.
AID1090701Antifungal activity against Pseudoperonospora cubensis in cucumber plants under greenhouse conditions assessed as fungicidal activity at 50 mg/mL by in vivo assay2007Journal of agricultural and food chemistry, Jul-11, Volume: 55, Issue:14
Synthesis and fungicidal evaluation of novel chalcone-based strobilurin analogues.
AID1090623Antifungal activity against Rhizoctonia solani assessed as inhibition rate at 50 ug/mL2007Journal of agricultural and food chemistry, Apr-18, Volume: 55, Issue:8
Design, synthesis, and fungicidal activities of new strobilurin derivatives.
AID1111108Antifungal activity against Pseudoperonospora cubensis infected cucumber leaves assessed as disease control at 6.25 mg/l after 5 days relative to control2010Pest management science, Jan, Volume: 66, Issue:1
Design, synthesis and biological activities of new strobilurin derivatives containing substituted pyrazoles.
AID1081032Antifungal activity against Blumeria graminis assessed as inhibition at 1.56 mg/L relative to control2010Journal of agricultural and food chemistry, Mar-10, Volume: 58, Issue:5
Synthesis and biological activity of new (E)-alpha-(Methoxyimino)benzeneacetate derivatives containing a substituted pyrazole ring.
AID1111104Antifungal activity against Blumeria graminis f. sp. tritici infected seven-day-old wheat seedlings assessed as disease control at 1.56 mg/l after 7 days relative to control2010Pest management science, Jan, Volume: 66, Issue:1
Design, synthesis and biological activities of new strobilurin derivatives containing substituted pyrazoles.
AID1112536Antifungal activity against Botryotinia fuckeliana SAS405 assessed as inhibition of colony growth2012Pest management science, Sep, Volume: 68, Issue:9
Genetic analysis and molecular characterisation of laboratory and field mutants of Botryotinia fuckeliana (Botrytis cinerea) resistant to QoI fungicides.
AID1090617Antifungal activity against Podosphaera fuliginea inoculated in inoculated in cucumber plant assessed as preventive fungicidal activity at 25 ug/mL measured after 7 days2007Journal of agricultural and food chemistry, Apr-18, Volume: 55, Issue:8
Design, synthesis, and fungicidal activities of new strobilurin derivatives.
AID1111613Fungicidal activity against Pseudoperonospora cubensis at 25 mg/L relative to untreated control2011Pest management science, Jun, Volume: 67, Issue:6
Design, synthesis and structure-activity relationship of novel coumarin derivatives.
AID1081036Antifungal activity against Pseudoperonospora cubensis assessed as inhibition at 25 mg/L relative to control2010Journal of agricultural and food chemistry, Mar-10, Volume: 58, Issue:5
Synthesis and biological activity of new (E)-alpha-(Methoxyimino)benzeneacetate derivatives containing a substituted pyrazole ring.
AID1090700Antifungal activity against Pseudoperonospora cubensis in cucumber plants under greenhouse conditions assessed as fungicidal activity at 25 mg/mL by in vivo assay2007Journal of agricultural and food chemistry, Jul-11, Volume: 55, Issue:14
Synthesis and fungicidal evaluation of novel chalcone-based strobilurin analogues.
AID1090616Antifungal activity against Podosphaera fuliginea inoculated in inoculated in cucumber plant assessed as preventive fungicidal activity measured after 7 days2007Journal of agricultural and food chemistry, Apr-18, Volume: 55, Issue:8
Design, synthesis, and fungicidal activities of new strobilurin derivatives.
AID1112534Antifungal activity against Botryotinia fuckeliana SAS56 assessed as complete inhibition of colony growth at 3 mg/ml2012Pest management science, Sep, Volume: 68, Issue:9
Genetic analysis and molecular characterisation of laboratory and field mutants of Botryotinia fuckeliana (Botrytis cinerea) resistant to QoI fungicides.
AID1081034Antifungal activity against Pseudoperonospora cubensis assessed as inhibition at 6.25 mg/L relative to control2010Journal of agricultural and food chemistry, Mar-10, Volume: 58, Issue:5
Synthesis and biological activity of new (E)-alpha-(Methoxyimino)benzeneacetate derivatives containing a substituted pyrazole ring.
AID1090612Antifungal activity against Pseudoperonospora cubensis inoculated in inoculated in cucumber plant assessed as preventive fungicidal activity measured after 7 days2007Journal of agricultural and food chemistry, Apr-18, Volume: 55, Issue:8
Design, synthesis, and fungicidal activities of new strobilurin derivatives.
AID1080375Fungicidal activity against Magnaporthe oryzae assessed as inhibition of mycelial growth at 25 mg/ml measured after 48 hr2008Journal of agricultural and food chemistry, Jul-09, Volume: 56, Issue:13
Synthesis and fungicidal activities of novel indene-substituted oxime ether strobilurins.
AID1091676Fungicidal activity against Botryotinia fuckeliana assessed as inhibition of mycelial elongation at 50 ug/mL incubated for 48 hr2006Journal of agricultural and food chemistry, May-17, Volume: 54, Issue:10
Stereoselective synthesis and antifungal activities of (E)-alpha-(methoxyimino)benzeneacetate derivatives containing 1,3,5-substituted pyrazole ring.
AID1091632In vivo fungicidal activity against Podosphaera fuliginea infected cucumber plants assessed as inhibition of disease symptoms treated one day prior to fungal spore inoculation measured after one week2008Journal of agricultural and food chemistry, Nov-26, Volume: 56, Issue:22
Synthesis, fungicidal, and insecticidal activities of beta-Methoxyacrylate-containing N-acetyl pyrazoline derivatives.
AID1091872Inhibition of Sus scrofa (pig) heart cytochrome bc1 complex using DBH2 as substrate by spectrophotometric analysis2010Journal of the American Chemical Society, Jan-13, Volume: 132, Issue:1
Subnanomolar inhibitor of cytochrome bc1 complex designed by optimizing interaction with conformationally flexible residues.
AID1111614Fungicidal activity against Pseudoperonospora cubensis at 6.25 mg/L relative to untreated control2011Pest management science, Jun, Volume: 67, Issue:6
Design, synthesis and structure-activity relationship of novel coumarin derivatives.
AID1080371Fungicidal activity against Blumeria graminis grown on compound pre-treated wheat seedlings assessed as inhibition of fungal growth at 6.25 mg/ml measured 7 days post fungal inoculation2008Journal of agricultural and food chemistry, Jul-09, Volume: 56, Issue:13
Synthesis and fungicidal activities of novel indene-substituted oxime ether strobilurins.
AID1090625Antifungal activity against Fusarium oxysporum assessed as inhibition rate at 50 ug/mL2007Journal of agricultural and food chemistry, Apr-18, Volume: 55, Issue:8
Design, synthesis, and fungicidal activities of new strobilurin derivatives.
AID1090705Antifungal activity against Podosphaera fuliginea in cucumber plants under greenhouse conditions assessed as fungicidal activity at 50 mg/mL by in vivo assay2007Journal of agricultural and food chemistry, Jul-11, Volume: 55, Issue:14
Synthesis and fungicidal evaluation of novel chalcone-based strobilurin analogues.
AID1090621Antifungal activity against Dothiorella gregaria assessed as inhibition rate at 50 ug/mL2007Journal of agricultural and food chemistry, Apr-18, Volume: 55, Issue:8
Design, synthesis, and fungicidal activities of new strobilurin derivatives.
AID1090618Antifungal activity against Podosphaera fuliginea inoculated in inoculated in cucumber plant assessed as preventive fungicidal activity at 50 ug/mL measured after 7 days2007Journal of agricultural and food chemistry, Apr-18, Volume: 55, Issue:8
Design, synthesis, and fungicidal activities of new strobilurin derivatives.
AID1090710Antifungal activity against Pseudoperonospora cubensis assessed as fungicidal activity at 200 mg/L (beneficial crop - cucumber)2007Journal of agricultural and food chemistry, Jul-11, Volume: 55, Issue:14
Synthesis and fungicidal evaluation of novel chalcone-based strobilurin analogues.
AID1111111Antifungal activity against Botryotinia fuckeliana infected cucumber leaves assessed as disease control at 400 mg/l after 4 days relative to control2010Pest management science, Jan, Volume: 66, Issue:1
Design, synthesis and biological activities of new strobilurin derivatives containing substituted pyrazoles.
AID1081035Antifungal activity against Blumeria graminis assessed as inhibition at 400 mg/L relative to control2010Journal of agricultural and food chemistry, Mar-10, Volume: 58, Issue:5
Synthesis and biological activity of new (E)-alpha-(Methoxyimino)benzeneacetate derivatives containing a substituted pyrazole ring.
AID263764Antifungal activity against Bipolaris maydis at 50 ug/ml2006Bioorganic & medicinal chemistry letters, Apr-15, Volume: 16, Issue:8
Stereoselective synthesis and fungicidal activities of (E)-alpha-(methoxyimino)-benzeneacetate derivatives containing 1,3,4-oxadiazole ring.
AID1091677Fungicidal activity against Rhizoctonia solani assessed as inhibition of mycelial elongation at 50 ug/mL incubated for 48 hr2006Journal of agricultural and food chemistry, May-17, Volume: 54, Issue:10
Stereoselective synthesis and antifungal activities of (E)-alpha-(methoxyimino)benzeneacetate derivatives containing 1,3,5-substituted pyrazole ring.
AID399185Antifungal activity against Pyricularia grisea assessed as inhibition of germ-tube development by microdilution method2004Journal of natural products, Jan, Volume: 67, Issue:1
Antifungal 3-butylisocoumarins from Asteraceae-Anthemideae.
AID1112537Antifungal activity against Botryotinia fuckeliana SAS56 assessed as inhibition of colony growth2012Pest management science, Sep, Volume: 68, Issue:9
Genetic analysis and molecular characterisation of laboratory and field mutants of Botryotinia fuckeliana (Botrytis cinerea) resistant to QoI fungicides.
AID1091633In vivo fungicidal activity against Pseudoperonospora cubensis infected in cucumber plants assessed as inhibition of disease symptoms treated one day prior to fungal spore inoculation measured after one week2008Journal of agricultural and food chemistry, Nov-26, Volume: 56, Issue:22
Synthesis, fungicidal, and insecticidal activities of beta-Methoxyacrylate-containing N-acetyl pyrazoline derivatives.
AID1090704Antifungal activity against Podosphaera fuliginea in cucumber plants under greenhouse conditions assessed as fungicidal activity at 25 mg/mL by in vivo assay2007Journal of agricultural and food chemistry, Jul-11, Volume: 55, Issue:14
Synthesis and fungicidal evaluation of novel chalcone-based strobilurin analogues.
AID1091637In vivo fungicidal activity against Pseudoperonospora cubensis infected in cucumber plants assessed as inhibition of disease symptoms at 200 ug/ml treated one day prior to fungal spore inoculation measured after one week2008Journal of agricultural and food chemistry, Nov-26, Volume: 56, Issue:22
Synthesis, fungicidal, and insecticidal activities of beta-Methoxyacrylate-containing N-acetyl pyrazoline derivatives.
AID1080373Fungicidal activity against Botryotinia fuckeliana assessed as inhibition of mycelial growth at 25 mg/ml measured after 48 hr2008Journal of agricultural and food chemistry, Jul-09, Volume: 56, Issue:13
Synthesis and fungicidal activities of novel indene-substituted oxime ether strobilurins.
AID1111106Antifungal activity against Blumeria graminis f. sp. tritici infected seven-day-old wheat seedlings assessed as disease control at 400 mg/l after 7 days relative to control2010Pest management science, Jan, Volume: 66, Issue:1
Design, synthesis and biological activities of new strobilurin derivatives containing substituted pyrazoles.
AID1081039Antifungal activity against Phytophthora infestans assessed as inhibition at 25 mg/L relative to control2010Journal of agricultural and food chemistry, Mar-10, Volume: 58, Issue:5
Synthesis and biological activity of new (E)-alpha-(Methoxyimino)benzeneacetate derivatives containing a substituted pyrazole ring.
AID1111107Antifungal activity against Pseudoperonospora cubensis infected cucumber leaves assessed as disease control at 3.12 mg/l after 5 days relative to control2010Pest management science, Jan, Volume: 66, Issue:1
Design, synthesis and biological activities of new strobilurin derivatives containing substituted pyrazoles.
AID263762Antifungal activity against Gibberella zeae at 50 ug/ml2006Bioorganic & medicinal chemistry letters, Apr-15, Volume: 16, Issue:8
Stereoselective synthesis and fungicidal activities of (E)-alpha-(methoxyimino)-benzeneacetate derivatives containing 1,3,4-oxadiazole ring.
AID263763Antifungal activity against Physalospora piricola at 50 ug/ml2006Bioorganic & medicinal chemistry letters, Apr-15, Volume: 16, Issue:8
Stereoselective synthesis and fungicidal activities of (E)-alpha-(methoxyimino)-benzeneacetate derivatives containing 1,3,4-oxadiazole ring.
AID1090620Antifungal activity against Colletotrichum gossypii assessed as inhibition rate at 50 ug/mL2007Journal of agricultural and food chemistry, Apr-18, Volume: 55, Issue:8
Design, synthesis, and fungicidal activities of new strobilurin derivatives.
AID399186Antifungal activity against Cladosporium herbarum assessed as inhibition zone in mycelial layer assessed per spot by TLC bioautography assay2004Journal of natural products, Jan, Volume: 67, Issue:1
Antifungal 3-butylisocoumarins from Asteraceae-Anthemideae.
AID1111109Antifungal activity against Pseudoperonospora cubensis infected cucumber leaves assessed as disease control at 25 mg/l after 5 days relative to control2010Pest management science, Jan, Volume: 66, Issue:1
Design, synthesis and biological activities of new strobilurin derivatives containing substituted pyrazoles.
AID263760Antifungal activity against Rhizoctonia solani at 50 ug/ml2006Bioorganic & medicinal chemistry letters, Apr-15, Volume: 16, Issue:8
Stereoselective synthesis and fungicidal activities of (E)-alpha-(methoxyimino)-benzeneacetate derivatives containing 1,3,4-oxadiazole ring.
AID1090703Antifungal activity against Podosphaera fuliginea in cucumber plants under greenhouse conditions assessed as fungicidal activity by in vivo assay2007Journal of agricultural and food chemistry, Jul-11, Volume: 55, Issue:14
Synthesis and fungicidal evaluation of novel chalcone-based strobilurin analogues.
AID1090622Antifungal activity against Fusarium graminearum assessed as inhibition rate at 50 ug/mL2007Journal of agricultural and food chemistry, Apr-18, Volume: 55, Issue:8
Design, synthesis, and fungicidal activities of new strobilurin derivatives.
AID1080372Fungicidal activity against Pseudoperonospora cubensis grown on compound pre-treated cucumber leaves assessed as inhibition of fungal growth at 6.25 mg/ml measured 5 days post compound treatment2008Journal of agricultural and food chemistry, Jul-09, Volume: 56, Issue:13
Synthesis and fungicidal activities of novel indene-substituted oxime ether strobilurins.
AID1111110Antifungal activity against Pseudoperonospora cubensis infected cucumber leaves assessed as disease control at 400 mg/l after 5 days relative to control2010Pest management science, Jan, Volume: 66, Issue:1
Design, synthesis and biological activities of new strobilurin derivatives containing substituted pyrazoles.
AID1090613Antifungal activity against Pseudoperonospora cubensis inoculated in inoculated in cucumber plant assessed as preventive fungicidal activity at 25 ug/mL measured after 7 days2007Journal of agricultural and food chemistry, Apr-18, Volume: 55, Issue:8
Design, synthesis, and fungicidal activities of new strobilurin derivatives.
AID1081041Antifungal activity against Magnaporthe oryzae assessed as inhibition at 25 mg/L relative to control2010Journal of agricultural and food chemistry, Mar-10, Volume: 58, Issue:5
Synthesis and biological activity of new (E)-alpha-(Methoxyimino)benzeneacetate derivatives containing a substituted pyrazole ring.
AID1090699Antifungal activity against Pseudoperonospora cubensis in cucumber plants under greenhouse conditions assessed as fungicidal activity by in vivo assay2007Journal of agricultural and food chemistry, Jul-11, Volume: 55, Issue:14
Synthesis and fungicidal evaluation of novel chalcone-based strobilurin analogues.
AID1090624Antifungal activity against Botrytis cinereapers assessed as inhibition rate at 50 ug/mL2007Journal of agricultural and food chemistry, Apr-18, Volume: 55, Issue:8
Design, synthesis, and fungicidal activities of new strobilurin derivatives.
AID1091675Fungicidal activity against Fusarium graminearum assessed as inhibition of mycelial elongation at 50 ug/mL incubated for 48 hr2006Journal of agricultural and food chemistry, May-17, Volume: 54, Issue:10
Stereoselective synthesis and antifungal activities of (E)-alpha-(methoxyimino)benzeneacetate derivatives containing 1,3,5-substituted pyrazole ring.
AID1081033Antifungal activity against Blumeria graminis assessed as inhibition at 6.25 mg/L relative to control2010Journal of agricultural and food chemistry, Mar-10, Volume: 58, Issue:5
Synthesis and biological activity of new (E)-alpha-(Methoxyimino)benzeneacetate derivatives containing a substituted pyrazole ring.
AID1090619Antifungal activity against Podosphaera fuliginea inoculated in inoculated in cucumber plant assessed as preventive fungicidal activity at 100 ug/mL measured after 7 days2007Journal of agricultural and food chemistry, Apr-18, Volume: 55, Issue:8
Design, synthesis, and fungicidal activities of new strobilurin derivatives.
AID1111105Antifungal activity against Blumeria graminis f. sp. tritici infected seven-day-old wheat seedlings assessed as disease control at 12.5 mg/l after 7 days relative to control2010Pest management science, Jan, Volume: 66, Issue:1
Design, synthesis and biological activities of new strobilurin derivatives containing substituted pyrazoles.
AID1090709Antifungal activity against Podosphaera fuliginea assessed as fungicidal activity at 200 mg/L (beneficial crop - cucumber)2007Journal of agricultural and food chemistry, Jul-11, Volume: 55, Issue:14
Synthesis and fungicidal evaluation of novel chalcone-based strobilurin analogues.
AID1090615Antifungal activity against Pseudoperonospora cubensis inoculated in inoculated in cucumber plant assessed as preventive fungicidal activity at 100 ug/mL measured after 7 days2007Journal of agricultural and food chemistry, Apr-18, Volume: 55, Issue:8
Design, synthesis, and fungicidal activities of new strobilurin derivatives.
AID1090614Antifungal activity against Pseudoperonospora cubensis inoculated in inoculated in cucumber plant assessed as preventive fungicidal activity at 50 ug/mL measured after 7 days2007Journal of agricultural and food chemistry, Apr-18, Volume: 55, Issue:8
Design, synthesis, and fungicidal activities of new strobilurin derivatives.
AID1091674Fungicidal activity against Botryosphaeria berengeriana assessed as inhibition of mycelial elongation at 50 ug/mL incubated for 48 hr2006Journal of agricultural and food chemistry, May-17, Volume: 54, Issue:10
Stereoselective synthesis and antifungal activities of (E)-alpha-(methoxyimino)benzeneacetate derivatives containing 1,3,5-substituted pyrazole ring.
AID1091673Fungicidal activity against Cochliobolus heterostrophus assessed as inhibition of mycelial elongation at 50 ug/mL incubated for 48 hr2006Journal of agricultural and food chemistry, May-17, Volume: 54, Issue:10
Stereoselective synthesis and antifungal activities of (E)-alpha-(methoxyimino)benzeneacetate derivatives containing 1,3,5-substituted pyrazole ring.
AID1090706Antifungal activity against Podosphaera fuliginea in cucumber plants under greenhouse conditions assessed as fungicidal activity at 100 mg/mL by in vivo assay2007Journal of agricultural and food chemistry, Jul-11, Volume: 55, Issue:14
Synthesis and fungicidal evaluation of novel chalcone-based strobilurin analogues.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (99)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's3 (3.03)18.2507
2000's24 (24.24)29.6817
2010's60 (60.61)24.3611
2020's12 (12.12)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 37.41

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 Index37.41 (24.57)
Research Supply Index4.62 (2.92)
Research Growth Index5.56 (4.65)
Search Engine Demand Index72.27 (26.88)
Search Engine Supply Index2.85 (0.95)

This Compound (37.41)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other100 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]