Page last updated: 2024-12-05

etridiazol

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

Description

Etridiazol is a fungicide that is used to control a wide range of fungal diseases in crops. It is a broad-spectrum fungicide, meaning that it is effective against a wide variety of fungal species. Etridiazol is typically applied as a seed treatment, a foliar spray, or a soil drench. The compound is thought to work by inhibiting the biosynthesis of ergosterol, a vital component of fungal cell membranes. Etridiazol has been shown to be effective in controlling fungal diseases in a variety of crops, including cereals, vegetables, fruits, and ornamental plants. It has also been used to control fungal diseases in turfgrass. Etridiazol is a synthetic compound that is manufactured through a multi-step process. The synthesis of etridiazol begins with the reaction of 2-chloro-4-nitroaniline with 2-methyl-2-propanol. This reaction produces 2-(2-chloro-4-nitrophenylamino)-2-methylpropan-1-ol. This compound is then reacted with 2-methyl-2-propanol to produce etridiazol. The compound is known to be toxic to aquatic organisms, and it is important to apply it in a way that minimizes the risk of environmental contamination. Etridiazol is an important fungicide for crop protection. It has been shown to be effective in controlling a wide range of fungal diseases and it is an important tool for farmers to help them protect their crops from disease.'

etridiazol: structure [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

etridiazole : A member of the class of thiadiazoles that is 1,2,4-thiadiazole which is substituted at positions 3 and 5 by trichloromethyl and ethoxy groups, respectively. A fungicide, it has been used particularly for the control of Phytophthora and Pythium species in soils. [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 CID17432
CHEMBL ID3183350
CHEBI ID81761
SCHEMBL ID20227
MeSH IDM0063124

Synonyms (78)

Synonym
1,2,4-thiadiazole, 5-ethoxy-3-(trichloromethyl)-
wln: t5ns dnj co2 exggg
banrot
terracoat
olin mathieson 2,424
ethazol
terracoat l21
etmt
terrachlor-super x
5-ethoxy-3-(trichloromethyl)-1,4-thiadiazole
3-(trichloromethyl)-5-ethoxy-1,4-thiadiazole
ethazole (fungicide)
aaterra
nsc524929
om 2424
terrazole
truban
etridiazol
om 2425
1,4-thiadiazole, 5-ethoxy-3-(trichloromethyl)-
nsc-524929
2593-15-9
etridiazole
etcmtb
5-aethoxy-3-trichlormethyl-1,4-thiadiazol
echlomezole
echlomezol
koban
etridiazole, analytical standard
NCGC00163854-01
mf-344
pansoil
einecs 219-991-8
terraflo
ethyl 3-trichloromethyl-1,2,4-thiadiazol-5-yl ether
brn 1074817
dwell
5-aethoxy-3-trichlormethyl-1,2,4-thiadiazol [german]
hsdb 1709
etridiazole [bsi:iso]
ai3-29280
5-ethoxy-3-trichloromethyl-1,2,4-thiadiazole
caswell no. 428
epa pesticide chemical code 084701
nsc 524929
planvate
3-(trichloromethyl)-5-ethoxy-1,2,4-thiadiazole
5-ethoxy-3-(trichloromethyl)-1,2,4-thiadiazole
NCGC00163854-02
NCGC00163854-03
C18460
9f8237i875 ,
unii-9f8237i875
5-aethoxy-3-trichlormethyl-1,2,4-thiadiazol
dtxsid3032547 ,
tox21_300924
cas-2593-15-9
NCGC00254826-01
dtxcid1012547
BP-10210
FT-0603613
AKOS015898229
om-2424
sanyard
etridiazole [iso]
etridiazole [hsdb]
SCHEMBL20227
CHEBI:81761 ,
3-trichloromethyl-5-ethoxy-1,2,4-thiadiazole
ethyl 3-(trichloromethyl)-1,2,4-thiadiazol-5-yl ether #
etridazole
5-ethoxy-3-trichloromethyl-1,2,4-thiadiazol
CHEMBL3183350
etridiazole, pestanal(r), analytical standard
etridiazole 10 microg/ml in cyclohexane
J-016188
Q1371667
CAA59315

Research Excerpts

Overview

Etridiazole (EDZ) is a thiadiazole-containing fungicide commonly used to control  fungi.

ExcerptReferenceRelevance
"Etridiazole (EDZ) is a thiadiazole-containing fungicide commonly used to control "( Transcriptome Profiling of Etridiazole-Exposed Zebrafish (
Choi, JY; Chon, K; Hwang, S; Kim, J; Park, KH; Vasamsetti, BMK; Yoon, CY, 2023
)
2.65

Compound-Compound Interactions

ExcerptReferenceRelevance
"Continuous flow microextraction (CFME) combined with high-performance liquid chromatography-ultraviolet (HPLC-UV) detection has been applied to the analysis of five widely used pesticides, simazine, fensulfothion, etridiazole, mepronil and bensulide, present at trace levels in water samples."( Continuous flow microextraction combined with high-performance liquid chromatography for the analysis of pesticides in natural waters.
He, Y; Lee, HK, 2006
)
0.52
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (2)

RoleDescription
antifungal agrochemicalAny substance used in acriculture, horticulture, forestry, etc. for its fungicidal properties.
nitrification inhibitorAny inhibitor added to nitrogen fertilizers which can reduce the rate at which ammonium is converted to nitrate. Under appropriate conditions, this can help reduce nitrogen losses through denitrification and leaching.
[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
aromatic etherAny ether in which the oxygen is attached to at least one aryl substituent.
thiadiazoles
organochlorine compoundAn organochlorine compound is a compound containing at least one carbon-chlorine bond.
thiadiazole antifungal agentA compound that has significant antifungal properties whose structure contains a thiadiazole 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 (4)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
acetylcholinesteraseHomo sapiens (human)Potency89.35840.002541.796015,848.9004AID1347398
AR proteinHomo sapiens (human)Potency61.13060.000221.22318,912.5098AID1259243
estrogen-related nuclear receptor alphaHomo sapiens (human)Potency3.06380.001530.607315,848.9004AID1224848; AID1224849
nuclear factor erythroid 2-related factor 2 isoform 1Homo sapiens (human)Potency1.53550.000627.21521,122.0200AID720636
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (9)

TimeframeStudies, This Drug (%)All Drugs %
pre-19904 (44.44)18.7374
1990's1 (11.11)18.2507
2000's2 (22.22)29.6817
2010's0 (0.00)24.3611
2020's2 (22.22)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 24.39

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 Index24.39 (24.57)
Research Supply Index2.64 (2.92)
Research Growth Index4.40 (4.65)
Search Engine Demand Index50.49 (26.88)
Search Engine Supply Index4.00 (0.95)

This Compound (24.39)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies1 (7.69%)4.05%
Observational0 (0.00%)0.25%
Other12 (92.31%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]