Page last updated: 2024-12-07

mepanipyrim

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

Description

Mepanipyrim is a systemic fungicide that belongs to the pyrimidinyl-amino-pyrimidine class. It is used to control a wide range of fungal diseases in various crops, including wheat, barley, rice, and potatoes. Mepanipyrim acts by inhibiting the biosynthesis of ergosterol, an essential component of fungal cell membranes. Its mode of action differs from other fungicides, making it effective against resistant fungal strains. Mepanipyrim is known for its long-lasting protective and curative activity. Its importance lies in its ability to control important fungal diseases, such as powdery mildew, Septoria tritici blotch, and rust. Mepanipyrim is studied to understand its efficacy, environmental impact, and potential for resistance development. Its unique mechanism of action and effectiveness against resistant strains make it a valuable tool for disease management in agriculture.'

mepanipyrim : A member of the class of aminopyrimidines that is N-phenylpyrimidin-2-amine carrying additional methyl and 1-propynyl substituents at positions 4 and 6 respectively. A fungicide used to control a wide range of diseases including grey mould on strawberries, tomatoes and cucumabers, and scab on apples and pears. [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 CID86296
CHEMBL ID2269513
CHEBI ID6751
SCHEMBL ID22040
MeSH IDM0271972

Synonyms (35)

Synonym
mepanipyrim [iso]
2-pyrimidinamine, 4-methyl-n-phenyl-6-(1-propynyl)-
4-methyl-n-phenyl-6-(1-propynyl)-2-pyrimidinamine
n-(4-methyl-6-prop-1-ynylpyrimidin-2-yl)aniline (iupac)
110235-47-7
mepanipyrim
4-methyl-n-phenyl-6-prop-1-ynylpyrimidin-2-amine
NCGC00248117-01
4-methyl-n-phenyl-6-(prop-1-ynyl)pyrimidin-2-amine
b150x76ojy ,
unii-b150x76ojy
dtxsid4042121 ,
NCGC00254251-01
cas-110235-47-7
dtxcid2022121
tox21_300635
AKOS015916777
kif-3535
kuf-6201
mepanipyrim [mi]
n-(4-methyl-6-prop-1-ynylpyrimidin-2-yl)aniline
2-anilino-4-methyl-6-(1-propynyl)pyrimidine
frupica
SCHEMBL22040
chebi:6751 ,
CHEMBL2269513
2-anilino-4-methyl-6-(1-propynyl)-pyrimidine
2-anilino-4-methyl-6(1-propynyl)pyrimidine
4-methyl-n-phenyl-6-prop-1-ynyl-pyrimidin-2-amine
J-002408
mepanipyrim, pestanal(r), analytical standard
mepanipyrim 10 microg/ml in cyclohexane
FT-0759386
Q15632906
4-methyl-n-phenyl-6-(prop-1-yn-1-yl)pyrimidin-2-amine

Research Excerpts

Overview

Mepanipyrim is an anilinopyrimidine fungicide. It is used worldwide for crop protection.

ExcerptReferenceRelevance
"Mepanipyrim is an anilinopyrimidine fungicide used worldwide for crop protection. "( Mepanipyrim haptens and antibodies with nanomolar affinity.
Abad-Fuentes, A; Abad-Somovilla, A; Agulló, C; Esteve-Turrillas, FA; Mercader, JV, 2013
)
3.28
"Mepanipyrim is a fungicide against several plant pathogens. "( Metabolism of a fungicide mepanipyrim by soil fungus Cunninghamella elegans ATCC36112.
Keum, YS; Kim, JH; Lee, H; Park, H; Yang, L; Zhu, YZ, 2010
)
2.1

Toxicity

ExcerptReferenceRelevance
" Our data will help explain the toxic effects of mepanipyrim on organisms and provide new insight into the AhR agonistic activity pesticide-induced cardiotoxicity."( Mepanipyrim induces cardiotoxicity of zebrafish (Danio rerio) larvae via promoting AhR-regulated COX expression pathway.
He, C; He, J; Shen, C; Yang, C; Yu, Y; Zheng, N; Zhu, K; Zuo, Z, 2023
)
2.61
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (3)

RoleDescription
aryl hydrocarbon receptor agonistAn agonist that binds to and activates aryl hydrocarbon receptors (AhRs).
hepatotoxic agentA role played by a chemical compound exihibiting itself through the ability to induce damage to the liver in animals.
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
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.
acetylenic compoundAny organic molecule containing a C#C bond.
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 (18)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
LuciferasePhotinus pyralis (common eastern firefly)Potency39.88240.007215.758889.3584AID1224835
RAR-related orphan receptor gammaMus musculus (house mouse)Potency13.25940.006038.004119,952.5996AID1159521; AID1159523
GLI family zinc finger 3Homo sapiens (human)Potency55.49810.000714.592883.7951AID1259368; AID1259369; AID1259392
AR proteinHomo sapiens (human)Potency55.19290.000221.22318,912.5098AID1259243; AID1259247; AID743035; AID743063
nuclear receptor subfamily 1, group I, member 3Homo sapiens (human)Potency16.79500.001022.650876.6163AID1224838; AID1224839; AID1224893
progesterone receptorHomo sapiens (human)Potency24.31180.000417.946075.1148AID1346795
glucocorticoid receptor [Homo sapiens]Homo sapiens (human)Potency54.88050.000214.376460.0339AID720692
retinoic acid nuclear receptor alpha variant 1Homo sapiens (human)Potency12.49280.003041.611522,387.1992AID1159552; AID1159553; AID1159555
estrogen-related nuclear receptor alphaHomo sapiens (human)Potency4.72130.001530.607315,848.9004AID1224841; AID1224848; AID1224849; AID1259401; AID1259403
pregnane X nuclear receptorHomo sapiens (human)Potency30.60670.005428.02631,258.9301AID1346982
estrogen nuclear receptor alphaHomo sapiens (human)Potency10.76670.000229.305416,493.5996AID1259244; AID1259248; AID743079; AID743080; AID743091
aryl hydrocarbon receptorHomo sapiens (human)Potency20.73320.000723.06741,258.9301AID743085; AID743122
cytochrome P450, family 19, subfamily A, polypeptide 1, isoform CRA_aHomo sapiens (human)Potency5.44270.001723.839378.1014AID743083
thyroid hormone receptor beta isoform 2Rattus norvegicus (Norway rat)Potency54.42730.000323.4451159.6830AID743067
histone deacetylase 9 isoform 3Homo sapiens (human)Potency61.06840.037617.082361.1927AID1259364
nuclear factor erythroid 2-related factor 2 isoform 1Homo sapiens (human)Potency40.51170.000627.21521,122.0200AID743202; AID743219
Voltage-dependent calcium channel gamma-2 subunitMus musculus (house mouse)Potency4.85080.001557.789015,848.9004AID1259244
Glutamate receptor 2Rattus norvegicus (Norway rat)Potency4.85080.001551.739315,848.9004AID1259244
[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]

Research

Studies (25)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's5 (20.00)18.2507
2000's5 (20.00)29.6817
2010's10 (40.00)24.3611
2020's5 (20.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 24.63

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 moderate demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index24.63 (24.57)
Research Supply Index3.30 (2.92)
Research Growth Index4.80 (4.65)
Search Engine Demand Index45.89 (26.88)
Search Engine Supply Index4.00 (0.95)

This Compound (24.63)

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%
Other26 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]