Page last updated: 2024-11-12

fluensulfone

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

Description

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

fluensulfone : A member of the class of 1,3-thiazoles carrying 3,4,4-trifluorobut-3-ene-1-sulfonyl and chloro substituents at positions 2 and 5 respectively. A nematicide that is effective against a number of plant parasitic nematodes in a range of agricultural and horticultural 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 CID11534927
CHEBI ID131597
SCHEMBL ID174908
MeSH IDM0573490

Synonyms (34)

Synonym
5-chloro-2-(3,4,4-trifluorobut-3-enylsulfonyl)-1,3-thiazole
FT-0668570
5-chloro-1,3-thiazol-2-yl 3,4,4-trifluorobut-3-en-1-yl sulfone
5-chloro-2-(3,4,4-trifluorobut-3-en-1-ylsulfonyl)-1,3-thiazole
fluensulfone
318290-98-1
5-chloro-2-(3,4,4-trifluorobut-3-ene-1-sulfonyl)-1,3-thiazole
CHEBI:131597
fluensulfone [iso]
unii-i7v6200877
i7v6200877 ,
5-chloro-2-[(3,4,4-trifluoro-3-buten-1-yl)sulfonyl]thiazole
5-chloro-2-[(3,4,4-trifluorobut-3-en-1-yl)sulfonyl]-1,3-thiazole
SCHEMBL174908
5-chloro-2-((3,4,4-trifluoro-3-buten-1-yl)sulfonyl)thiazole
DTXSID1058054
AC-35258
CS-7957
HY-107771
mcw-2
thiazole, 5-chloro-2-[(3,4,4-trifluoro-3-butenyl)sulfonyl]-
AKOS027439950
mfcd29047086
thiazole, 5-chloro-2-[(3,4,4-trifluoro-3-butenyl)sulfonyl]- (9ci); 5-chloro-2-[(3,4,4-trifluorobut-3-en-1-yl)sulfonyl]-1,3-thiazole; fluensulfone; mcw 2; thiazole, 5-chloro-2-[(3,4,4-trifluoro-3-buten-1-yl)sulfonyl]-
fluensulfone 100 microg/ml in acetonitrile
BCP16864
mcw-2;mcw 2;mcw2
5-chloro-2-((3,4,4-trifluorobut-3-en-1-yl)sulfonyl)thiazole
AS-49857
Q27225210
N11430
A902682
xsnmwapkhugzgq-uhfffaoysa-n
thiazole, 5-chloro-2-[(3,4,4-trifluoro-3-buten-1-yl)sulfonyl]-

Research Excerpts

Overview

Fluensulfone is a fluoroalkenyl chemical with activity against multiple genera of plant-parasitic nematodes. It is a potent inhibitor of hatching and impacts on the viability of the J2 s emerging from the cysts.

ExcerptReferenceRelevance
"Fluensulfone is a nematicide with a novel mode of action against plant parasitic nematodes. "( The distinct profiles of the inhibitory effects of fluensulfone, abamectin, aldicarb and fluopyram on Globodera pallida hatching.
Feist, E; Gaihre, Y; Holden-Dye, L; Kearn, J; O'Connor, V, 2020
)
2.25
"Fluensulfone is a potent inhibitor of hatching and impacts on the viability of the J2 s emerging from the cysts."( The distinct profiles of the inhibitory effects of fluensulfone, abamectin, aldicarb and fluopyram on Globodera pallida hatching.
Feist, E; Gaihre, Y; Holden-Dye, L; Kearn, J; O'Connor, V, 2020
)
1.53
"Fluensulfone is a fluoroalkenyl chemical with activity against multiple genera of plant-parasitic nematodes. "( Fluensulfone sorption and mobility as affected by soil type.
Davis, RF; Grey, TL; Langston, DB; Li, X; Morris, KA; Timper, P, 2018
)
3.37
"Fluensulfone is a new nematicide with an excellent profile of selective toxicity against plant parasitic nematodes. "( Progressive metabolic impairment underlies the novel nematicidal action of fluensulfone on the potato cyst nematode Globodera pallida.
Holden-Dye, L; Kearn, J; Lilley, C; O'Connor, V; Urwin, P, 2017
)
2.13
"Fluensulfone is a new nematicide of the fluoroalkenyl thioether group that has significantly reduced environmental impact with low toxicity to non-target insects and mammals."( Fluensulfone is a nematicide with a mode of action distinct from anticholinesterases and macrocyclic lactones.
Dillon, J; Holden-Dye, L; Kearn, J; Ludlow, E; O'Connor, V, 2014
)
2.57
"Fluensulfone is a nematicide for agricultural use. "( Relationship of Metabolism and Cell Proliferation to the Mode of Action of Fluensulfone-Induced Mouse Lung Tumors. II: Additional Mechanistic Studies.
Bomann, W; Cohen, SM; Strupp, C; Weber, K, 2016
)
2.11

Effects

ExcerptReferenceRelevance
"Fluensulfone has shown an increased incidence of lung adenomas in mice, but not in rats, at high doses."( Relationship of metabolism and cell proliferation to the mode of action of fluensulfone-induced mouse lung tumors: analysis of their human relevance using the IPCS framework.
Banas, DA; Cohen, SM; Gordon, EB; Jaeger, M; Strupp, C; Weber, K, 2012
)
1.33

Treatment

ExcerptReferenceRelevance
"The fluensulfone treatments at the full rate had more consistent effects than the lower rates, and there were no greater effects for the treatments higher than this full rate."( Field evaluation of the nematicide fluensulfone for control of the potato cyst nematode Globodera pallida.
Back, MA; Grove, IG; Norshie, PM, 2016
)
1.19
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (2)

RoleDescription
nematicideA substance used to destroy pests of the phylum Nematoda (roundworms).
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 (5)

ClassDescription
1,3-thiazoles
organochlorine pesticideAny organochlorine compound that has been used as a pesticide.
sulfoneAn organosulfur compound having the structure RS(=O)2R (R =/= H).
organofluorine pesticide
olefinic compoundAny organic molecular entity that contains at least one C=C bond.
[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]

Research

Studies (18)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's11 (61.11)24.3611
2020's7 (38.89)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 32.79

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 Index32.79 (24.57)
Research Supply Index2.94 (2.92)
Research Growth Index4.63 (4.65)
Search Engine Demand Index57.70 (26.88)
Search Engine Supply Index2.94 (0.95)

This Compound (32.79)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews1 (5.56%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other17 (94.44%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]