Compounds > cafenstrole
Page last updated: 2024-12-08

cafenstrole

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

Description

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

Cross-References

ID SourceID
PubMed CID195429
CHEMBL ID2252191
CHEBI ID81787
SCHEMBL ID54625
MeSH IDM0411827

Synonyms (29)

Synonym
cafenstrole
125306-83-4
n,n-diethyl-3-mesitylsulfonyl-1h-1,2,4-triazole-1-carboxamide
n,n-diethyl-3-(mesitylsulfonyl)-1h-1,2,4-triazole-1-carboxamide
n,n-diethyl-3-(2,4,6-trimethylphenyl)sulfonyl-1,2,4-triazole-1-carboxamide
C18497
unii-ii8jp4ly7a
1h-1,2,4-triazole-1-carboxamide, n,n-diethyl-3-mesitylsulfonyl-
ii8jp4ly7a ,
cafenstrole [iso]
himeadow
ch-900
1h-1,2,4-triazole-1-carboxamide, n,n-diethyl-3-((2,4,6-trimethylphenyl)sulfonyl)-
grachitor
SCHEMBL54625
CHEMBL2252191
chebi:81787 ,
DTXSID7057949
AC-22340
AKOS025401572
J-523228
n,n-diethyl-3-[(2,4,6-trimethylphenyl)sulfonyl]-1h-1,2,4-triazole-1-carboxamide
cafenstrole, pestanal(r), analytical standard
cafenstrole 100 microg/ml in acetonitrile
Q22807103
AMY10973
1h-1,2,4-triazole-1-carboxamide, n,n-diethyl-3-[(2,4,6-trimethylphenyl)sulfonyl]-
mfcd01631150
CS-0443660
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (3)

RoleDescription
antimitoticAny compound that inhibits cell division (mitosis).
herbicideA substance used to destroy plant pests.
agrochemicalAn agrochemical is a substance that is used in agriculture or horticulture.
[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
benzenesAny benzenoid aromatic compound consisting of the benzene skeleton and its substituted derivatives.
sulfoneAn organosulfur compound having the structure RS(=O)2R (R =/= H).
triazolesAn azole in which the five-membered heterocyclic aromatic skeleton contains three N atoms and two C atoms.
[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 (2)

Inhibition Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
3-ketoacyl-CoA synthase 18Arabidopsis thaliana (thale cress)IC50 (µMol)0.19950.10000.14980.1995AID1090122
3-ketoacyl-CoA synthase 20Arabidopsis thaliana (thale cress)IC50 (µMol)0.39810.39810.39810.3981AID1090121
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (49)

Assay IDTitleYearJournalArticle
AID1104550Inhibition of fatty acid synthesis in Hordeum vulgare (barley) using [14C]acetate assessed as [14C]-labeled 16C fatty acid level at 7 uM after 3 hr by liquid scintillation counting (Rvb = 30.6 +/- 0.2%)2010Pest management science, Jul, Volume: 66, Issue:7
The action of herbicides on fatty acid biosynthesis and elongation in barley and cucumber.
AID1090126Inhibition of Arbidopsis thaliana C-terminal His-tagged CER60 expressed in Saccharomyces cerevisiae INVSc1 at 100 uM after 18 to 20 hr by GC/MS analysis2004Proceedings of the National Academy of Sciences of the United States of America, Aug-10, Volume: 101, Issue:32
Specific and differential inhibition of very-long-chain fatty acid elongases from Arabidopsis thaliana by different herbicides.
AID1090120Growth inhibition of Saccharomyces cerevisiae INVSc1 at 100 uM after 18 to 20 hr2004Proceedings of the National Academy of Sciences of the United States of America, Aug-10, Volume: 101, Issue:32
Specific and differential inhibition of very-long-chain fatty acid elongases from Arabidopsis thaliana by different herbicides.
AID1090524Herbicidal activity against semen euphorbiae assessed as inhibition of weed growth at at 3.75 ug/mL measured 15 days post compound treatment by pot-culture method2006Journal of agricultural and food chemistry, Oct-04, Volume: 54, Issue:20
Synthesis and herbicidal activity of N,N-diethyl-3-(arylselenonyl)-1H-1,2,4-triazole-1-carboxamide.
AID1090535Herbicidal activity against Cucumis sativus jinyou 15 (cucumber) assessed as inhibition of weed growth at 500 ug/mL measured 15 days post compound treatment by pot-culture method2006Journal of agricultural and food chemistry, Oct-04, Volume: 54, Issue:20
Synthesis and herbicidal activity of N,N-diethyl-3-(arylselenonyl)-1H-1,2,4-triazole-1-carboxamide.
AID1090119Inhibition of Saccharomyces cerevisiae INVSc1 ELO at 100 uM after 18 to 20 hr by GC/MS analysis2004Proceedings of the National Academy of Sciences of the United States of America, Aug-10, Volume: 101, Issue:32
Specific and differential inhibition of very-long-chain fatty acid elongases from Arabidopsis thaliana by different herbicides.
AID1104518Inhibition of fatty acid synthesis in Hordeum vulgare (barley) using [14C]malonate assessed as reduction in [14C]-labeled 20C fatty acid level at 70 uM after 3 hr by liquid scintillation counting relative to control2010Pest management science, Jul, Volume: 66, Issue:7
The action of herbicides on fatty acid biosynthesis and elongation in barley and cucumber.
AID1090124Inhibition of Arbidopsis thaliana C-terminal His-tagged At5g43760 expressed in Saccharomyces cerevisiae INVSc1 at 100 uM after 18 to 20 hr by GC/MS analysis2004Proceedings of the National Academy of Sciences of the United States of America, Aug-10, Volume: 101, Issue:32
Specific and differential inhibition of very-long-chain fatty acid elongases from Arabidopsis thaliana by different herbicides.
AID1090129Inhibition of Arbidopsis thaliana C-terminal His-tagged FAE1 expressed in Saccharomyces cerevisiae INVSc1 at 100 uM after 18 to 20 hr by GC/MS analysis2004Proceedings of the National Academy of Sciences of the United States of America, Aug-10, Volume: 101, Issue:32
Specific and differential inhibition of very-long-chain fatty acid elongases from Arabidopsis thaliana by different herbicides.
AID1104546Inhibition of fatty acid synthesis in Hordeum vulgare (barley) using [14C]acetate assessed as [14C]-labeled 18C fatty acid level at 7 uM after 3 hr by liquid scintillation counting (Rvb = 57 +/- 0.9%)2010Pest management science, Jul, Volume: 66, Issue:7
The action of herbicides on fatty acid biosynthesis and elongation in barley and cucumber.
AID1104528Inhibition of fatty acid synthesis in Cucumis sativus (cucumber) assessed as inhibition of [14C]malonate incoporation in total fatty acids at 70 uM measured as total disintegration per g of fresh weight after 3 hr by liquid scintillation counting (Rvb = 12010Pest management science, Jul, Volume: 66, Issue:7
The action of herbicides on fatty acid biosynthesis and elongation in barley and cucumber.
AID1104524Inhibition of fatty acid synthesis in Cucumis sativus (cucumber) using [14C]malonate assessed as [14C]-labeled 16C fatty acid level at 70 uM after 3 hr by liquid scintillation counting (Rvb = 5.1 +/- 0.9%)2010Pest management science, Jul, Volume: 66, Issue:7
The action of herbicides on fatty acid biosynthesis and elongation in barley and cucumber.
AID1104530Inhibition of fatty acid synthesis in Hordeum vulgare (barley) assessed as inhibition of [14C]malonate incoporation in total fatty acids at 70 uM measured as total disintegration per g of fresh weight after 3 hr by liquid scintillation counting (Rvb = 5.22010Pest management science, Jul, Volume: 66, Issue:7
The action of herbicides on fatty acid biosynthesis and elongation in barley and cucumber.
AID1104514Inhibition of fatty acid synthesis in Hordeum vulgare (barley) using [14C]malonate assessed as [14C]-labeled 22C fatty acid level at 70 uM after 3 hr by liquid scintillation counting (Rvb = 34.7 +/- 2.4%)2010Pest management science, Jul, Volume: 66, Issue:7
The action of herbicides on fatty acid biosynthesis and elongation in barley and cucumber.
AID1090121Inhibition of Arbidopsis thaliana C-terminal His-tagged At5g43760 expressed in Saccharomyces cerevisiae INVSc1 after 18 to 20 hr by GC/MS analysis2004Proceedings of the National Academy of Sciences of the United States of America, Aug-10, Volume: 101, Issue:32
Specific and differential inhibition of very-long-chain fatty acid elongases from Arabidopsis thaliana by different herbicides.
AID1090128Inhibition of Arbidopsis thaliana C-terminal His-tagged KCS1 expressed in Saccharomyces cerevisiae INVSc1 at 100 uM after 18 to 20 hr by GC/MS analysis2004Proceedings of the National Academy of Sciences of the United States of America, Aug-10, Volume: 101, Issue:32
Specific and differential inhibition of very-long-chain fatty acid elongases from Arabidopsis thaliana by different herbicides.
AID1090525Herbicidal activity against semen euphorbiae assessed as inhibition of weed growth at at 1.875 ug/mL measured 15 days post compound treatment by pot-culture method2006Journal of agricultural and food chemistry, Oct-04, Volume: 54, Issue:20
Synthesis and herbicidal activity of N,N-diethyl-3-(arylselenonyl)-1H-1,2,4-triazole-1-carboxamide.
AID1104512Inhibition of fatty acid synthesis in Cucumis sativus (cucumber) using [14C]malonate assessed as reduction in [14C]-labeled 22C fatty acid level at 70 uM after 3 hr by liquid scintillation counting relative to control2010Pest management science, Jul, Volume: 66, Issue:7
The action of herbicides on fatty acid biosynthesis and elongation in barley and cucumber.
AID1090531Toxicity against Oryza sativa xiuanyou 63 (rice) assessed as growth inhibition at 1.875 ug/mL measured 15 days post compound treatment by pot-culture method2006Journal of agricultural and food chemistry, Oct-04, Volume: 54, Issue:20
Synthesis and herbicidal activity of N,N-diethyl-3-(arylselenonyl)-1H-1,2,4-triazole-1-carboxamide.
AID1104536Inhibition of fatty acid synthesis in wheat using [14C]acetate assessed as reduction in [14C]-labeled 22C fatty acid level at 7 uM after 3 hr by liquid scintillation counting2010Pest management science, Jul, Volume: 66, Issue:7
The action of herbicides on fatty acid biosynthesis and elongation in barley and cucumber.
AID1090528Toxicity against Oryza sativa xiuanyou 63 (rice) assessed as growth inhibition at 3.75 ug/mL measured 15 days post compound treatment by pot-culture method2006Journal of agricultural and food chemistry, Oct-04, Volume: 54, Issue:20
Synthesis and herbicidal activity of N,N-diethyl-3-(arylselenonyl)-1H-1,2,4-triazole-1-carboxamide.
AID1104544Inhibition of fatty acid synthesis in Cucumis sativus (cucumber) using [14C]acetate assessed as [14C]-labeled 18C fatty acid level at 7 uM after 3 hr by liquid scintillation counting (Rvb = 33.5 +/- 1.5%)2010Pest management science, Jul, Volume: 66, Issue:7
The action of herbicides on fatty acid biosynthesis and elongation in barley and cucumber.
AID1104520Inhibition of fatty acid synthesis in Cucumis sativus (cucumber) using [14C]malonate assessed as [14C]-labeled 18C fatty acid level at 70 uM after 3 hr by liquid scintillation counting (Rvb = 14.3 +/- 2%)2010Pest management science, Jul, Volume: 66, Issue:7
The action of herbicides on fatty acid biosynthesis and elongation in barley and cucumber.
AID1104506Inhibition of fatty acid synthesis in Hordeum vulgare (barley) using [14C]malonate assessed as reduction in [14C]-labeled 26C fatty acid level at 70 uM after 3 hr by liquid scintillation counting relative to control2010Pest management science, Jul, Volume: 66, Issue:7
The action of herbicides on fatty acid biosynthesis and elongation in barley and cucumber.
AID1104522Inhibition of fatty acid synthesis in Hordeum vulgare (barley) using [14C]malonate assessed as [14C]-labeled 18C fatty acid level at 70 uM after 3 hr by liquid scintillation counting (Rvb = 14.4 +/- 6.3%)2010Pest management science, Jul, Volume: 66, Issue:7
The action of herbicides on fatty acid biosynthesis and elongation in barley and cucumber.
AID1104552Inhibition of fatty acid synthesis in Cucumis sativus (cucumber) assessed as inhibition of [14C]acetate incoporation in total fatty acids at 7 uM measured as total disintegration per g of fresh weight after 3 hr by liquid scintillation counting (Rvb = 4.42010Pest management science, Jul, Volume: 66, Issue:7
The action of herbicides on fatty acid biosynthesis and elongation in barley and cucumber.
AID1104508Inhibition of fatty acid synthesis in Cucumis sativus (cucumber) using [14C]malonate assessed as reduction in [14C]-labeled 24C fatty acid level at 70 uM after 3 hr by liquid scintillation counting relative to control2010Pest management science, Jul, Volume: 66, Issue:7
The action of herbicides on fatty acid biosynthesis and elongation in barley and cucumber.
AID1090529Toxicity against Oryza sativa xiuanyou 63 (rice) assessed as growth inhibition at 7.5 ug/mL measured 15 days post compound treatment by pot-culture method2006Journal of agricultural and food chemistry, Oct-04, Volume: 54, Issue:20
Synthesis and herbicidal activity of N,N-diethyl-3-(arylselenonyl)-1H-1,2,4-triazole-1-carboxamide.
AID1090125Inhibition of Arbidopsis thaliana C-terminal His-tagged At1g04220 expressed in Saccharomyces cerevisiae INVSc1 at 100 uM after 18 to 20 hr by GC/MS analysis2004Proceedings of the National Academy of Sciences of the United States of America, Aug-10, Volume: 101, Issue:32
Specific and differential inhibition of very-long-chain fatty acid elongases from Arabidopsis thaliana by different herbicides.
AID1090527Toxicity against Oryza sativa xiuanyou 63 (rice) assessed as growth inhibition at 15 ug/mL measured 15 days post compound treatment by pot-culture method2006Journal of agricultural and food chemistry, Oct-04, Volume: 54, Issue:20
Synthesis and herbicidal activity of N,N-diethyl-3-(arylselenonyl)-1H-1,2,4-triazole-1-carboxamide.
AID1104526Inhibition of fatty acid synthesis in Hordeum vulgare (barley) using [14C]malonate assessed as [14C]-labeled 16C fatty acid level at 70 uM after 3 hr by liquid scintillation counting (Rvb = 3.3 +/- 0.9%)2010Pest management science, Jul, Volume: 66, Issue:7
The action of herbicides on fatty acid biosynthesis and elongation in barley and cucumber.
AID1090523Herbicidal activity against semen euphorbiae assessed as inhibition of weed growth at at 7.5 ug/mL measured 15 days post compound treatment by pot-culture method2006Journal of agricultural and food chemistry, Oct-04, Volume: 54, Issue:20
Synthesis and herbicidal activity of N,N-diethyl-3-(arylselenonyl)-1H-1,2,4-triazole-1-carboxamide.
AID1104532Inhibition of fatty acid synthesis in wheat using [14C]acetate assessed as reduction in [14C]-labeled 24C fatty acid level at 7 uM after 3 hr by liquid scintillation counting2010Pest management science, Jul, Volume: 66, Issue:7
The action of herbicides on fatty acid biosynthesis and elongation in barley and cucumber.
AID1090123Herbicidal activity against Arabidopsis thaliana assessed as apperance of fiddle head phenotype2004Proceedings of the National Academy of Sciences of the United States of America, Aug-10, Volume: 101, Issue:32
Specific and differential inhibition of very-long-chain fatty acid elongases from Arabidopsis thaliana by different herbicides.
AID1090530Toxicity against Oryza sativa xiuanyou 63 (rice) assessed as growth inhibition at 0.9375 ug/mL measured 15 days post compound treatment by pot-culture method2006Journal of agricultural and food chemistry, Oct-04, Volume: 54, Issue:20
Synthesis and herbicidal activity of N,N-diethyl-3-(arylselenonyl)-1H-1,2,4-triazole-1-carboxamide.
AID1104547Inhibition of fatty acid synthesis in Cucumis sativus (cucumber) using [14C]acetate assessed as [14C]-labeled 16C fatty acid level at 7 uM after 3 hr by liquid scintillation counting (Rvb = 27.6 +/- 5.1%)2010Pest management science, Jul, Volume: 66, Issue:7
The action of herbicides on fatty acid biosynthesis and elongation in barley and cucumber.
AID1090526Herbicidal activity against semen euphorbiae assessed as inhibition of weed growth at at 0.9375 ug/mL measured 15 days post compound treatment by pot-culture method2006Journal of agricultural and food chemistry, Oct-04, Volume: 54, Issue:20
Synthesis and herbicidal activity of N,N-diethyl-3-(arylselenonyl)-1H-1,2,4-triazole-1-carboxamide.
AID1090534Herbicidal activity against semen euphorbiae assessed as inhibition of weed growth at 500 ug/mL measured 15 days post compound treatment by pot-culture method2006Journal of agricultural and food chemistry, Oct-04, Volume: 54, Issue:20
Synthesis and herbicidal activity of N,N-diethyl-3-(arylselenonyl)-1H-1,2,4-triazole-1-carboxamide.
AID1104516Inhibition of fatty acid synthesis in Cucumis sativus (cucumber) using [14C]malonate assessed as [14C]-labeled 20C fatty acid level at 70 uM after 3 hr by liquid scintillation counting (Rvb = 11.7 +/- 2%)2010Pest management science, Jul, Volume: 66, Issue:7
The action of herbicides on fatty acid biosynthesis and elongation in barley and cucumber.
AID1104543Inhibition of fatty acid synthesis in Hordeum vulgare (barley) using [14C]acetate assessed as [14C]-labeled 20C fatty acid level at 7 uM after 3 hr by liquid scintillation counting (Rvb = 2.1 +/- 0.4%)2010Pest management science, Jul, Volume: 66, Issue:7
The action of herbicides on fatty acid biosynthesis and elongation in barley and cucumber.
AID1104510Inhibition of fatty acid synthesis in Hordeum vulgare (barley) using [14C]malonate assessed as reduction in [14C]-labeled 24C fatty acid level at 70 uM after 3 hr by liquid scintillation counting relative to control2010Pest management science, Jul, Volume: 66, Issue:7
The action of herbicides on fatty acid biosynthesis and elongation in barley and cucumber.
AID1104534Inhibition of fatty acid synthesis in Hordeum vulgare (barley) using [14C]acetate assessed as reduction in [14C]-labeled 24C fatty acid level at 7 uM after 3 hr by liquid scintillation counting2010Pest management science, Jul, Volume: 66, Issue:7
The action of herbicides on fatty acid biosynthesis and elongation in barley and cucumber.
AID1090522Herbicidal activity against semen euphorbiae assessed as inhibition of weed growth at at 15 ug/mL measured 15 days post compound treatment by pot-culture method2006Journal of agricultural and food chemistry, Oct-04, Volume: 54, Issue:20
Synthesis and herbicidal activity of N,N-diethyl-3-(arylselenonyl)-1H-1,2,4-triazole-1-carboxamide.
AID1104554Inhibition of fatty acid synthesis in Hordeum vulgare (barley) assessed as inhibition of [14C]acetate incoporation in total fatty acids at 7 uM measured as total disintegration per g of fresh weight after 3 hr by liquid scintillation counting (Rvb = 5.8 +2010Pest management science, Jul, Volume: 66, Issue:7
The action of herbicides on fatty acid biosynthesis and elongation in barley and cucumber.
AID1104540Inhibition of fatty acid synthesis in Cucumis sativus (cucumber) using [14C]acetate assessed as reduction in [14C]-labeled 20C fatty acid level at 7 uM after 3 hr by liquid scintillation counting relative to control2010Pest management science, Jul, Volume: 66, Issue:7
The action of herbicides on fatty acid biosynthesis and elongation in barley and cucumber.
AID1090122Inhibition of Arbidopsis thaliana C-terminal His-tagged FAE1 expressed in Saccharomyces cerevisiae INVSc1 after 18 to 20 hr by GC/MS analysis2004Proceedings of the National Academy of Sciences of the United States of America, Aug-10, Volume: 101, Issue:32
Specific and differential inhibition of very-long-chain fatty acid elongases from Arabidopsis thaliana by different herbicides.
AID1090532Herbicidal activity against Cucumis sativus jinyou 15 (cucumber) assessed as inhibition of weed growth at 0.9357 ug/mL measured 15 days post compound treatment by pot-culture method2006Journal of agricultural and food chemistry, Oct-04, Volume: 54, Issue:20
Synthesis and herbicidal activity of N,N-diethyl-3-(arylselenonyl)-1H-1,2,4-triazole-1-carboxamide.
AID1104539Inhibition of fatty acid synthesis in Hordeum vulgare (barley) using [14C]acetate assessed as reduction in [14C]-labeled 22C fatty acid level at 7 uM after 3 hr by liquid scintillation counting2010Pest management science, Jul, Volume: 66, Issue:7
The action of herbicides on fatty acid biosynthesis and elongation in barley and cucumber.
AID1090127Inhibition of Arbidopsis thaliana C-terminal His-tagged KCS2 expressed in Saccharomyces cerevisiae INVSc1 at 100 uM after 18 to 20 hr by GC/MS analysis2004Proceedings of the National Academy of Sciences of the United States of America, Aug-10, Volume: 101, Issue:32
Specific and differential inhibition of very-long-chain fatty acid elongases from Arabidopsis thaliana by different herbicides.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (8)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's3 (37.50)29.6817
2010's4 (50.00)24.3611
2020's1 (12.50)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 21.55

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 Index21.55 (24.57)
Research Supply Index2.30 (2.92)
Research Growth Index4.56 (4.65)
Search Engine Demand Index18.60 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (21.55)

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%
Other9 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]
SubstanceRelationship StrengthStudiesTrialsClassesRoles
alachlor
alachlor : An aromatic amide that is N-(2,6-diethylphenyl)acetamide substituted by a methoxymethyl group at at the nitrogen atom while one of the hydrogens of the methyl group has been replaced by a chlorine atom.		2.0210aromatic amide;
monocarboxylic acid amide;
organochlorine compound		environmental contaminant;
herbicide;
xenobiotic
triallate
Triallate: A pre-emergence, selective herbicide for the control of wild oats in various crops.		2.0210tertiary amine
bensulide
[no description available]		2.0210benzenes
diphenamid
diphenamid: do not confuse with anti-inflammatory agent difenpiramide; structure		2.4420diarylmethane
devrinol
devrinol: structure. napropamide : A racemate composed of equimolar amounts of (S)- and (R)-napropamide.. N,N-diethyl-2-(naphthalen-1-yloxy)propanamide : A monocarboxylic acid amide that is propanamide substituted by two ethyl groups at the nitrogen atom and a naphthalen-1-yloxy group at position 2.		2.4420aromatic ether;
monocarboxylic acid amide;
naphthalenes
ethofumesate
ethofumesate: structure in first source. ethofumesate : A racemate comprising of equimolar amounts of (S)- and (R)-ethofumesate.. 2-ethoxy-3,3-dimethyl-2,3-dihydro-1-benzofuran-5-yl methanesulfonate : A methanesulfonate ester that is methanesulfonic acid in which the hydrogen of the hydroxy group has been replaced by a 2-ethoxy-3,3-dimethyl-2,3-dihydro-1-benzofuran-5-yl group.		2.02101-benzofurans;
ether;
methanesulfonate ester
triazoles
Triazoles: Heterocyclic compounds containing a five-membered ring with two carbon atoms and three nitrogen atoms with the molecular formula C2H3N3.. triazoles : An azole in which the five-membered heterocyclic aromatic skeleton contains three N atoms and two C atoms.		3.16501,2,3-triazole
foe 5043
FOE 5043: an oxyacetamide with herbicidal activity; structure given in first source. flufenacet : An aromatic amide that is acetamide in which the amino hydrogens have been replaced by a propan-2-yl and 4-fluorophenyl groups while the methyl hydrogen is replaced by a [5-(trifluoromethyl)-1,3,4-thiadiazol-2-yl]oxy group.		2.0210aromatic amide;
monofluorobenzenes;
thiadiazoles		environmental contaminant;
herbicide;
xenobiotic
bitertanol
bitertanol: a triazole fungicide; structure given in first source. bitertanol : A diastereoisomeric mixture composed of the enantiomeric pair (1R,2S)- and (1S,2R)-bitertanol in a 4:1 ratio with the enantiomeric pair (1R,2R)- and (1S,2S)-bitertanol. A fungicide used to control a range of diseases including scab, powder mildew, rusts and blackspot. It is moderately toxic to most animal and insect species but is non-toxic to honeybees.. 1-(biphenyl-4-yloxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)butan-2-ol : A member of the class of triazoles that is 3,3-dimethyl-1-(1,2,4-triazol-1-yl)butane-1,2-diol substituted at position O-1 by a biphenyl-4-yl group.		2.610aromatic ether;
biphenyls;
secondary alcohol;
triazoles
ConditionIndicatedRelationship StrengthStudiesTrials
Sensitivity and Specificity
Binary classification measures to assess test results. Sensitivity or recall rate is the proportion of true positives. Specificity is the probability of correctly determining the absence of a condition. (From Last, Dictionary of Epidemiology, 2d ed)		02.0410