Page last updated: 2024-11-06

hexafluoron

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

Description

hexafluoron: insect growth regulator against mosquito larva; the active agent in Sonet, a Russian product, is hexaflumuron [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

hexaflumuron : An N-acylurea that is urea in which a hydrogen attached to one of the nitrogens is replaced by a 2,6-difluorobenzoyl group, while a hycrogen attached to the other nitorgen is replaced by a 3,5-dichloro-4-(1,1,2,2-tetrafluoroethoxy)phenyl group. [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 CID91741
CHEMBL ID1892746
CHEBI ID39383
SCHEMBL ID26793
MeSH IDM0162071

Synonyms (56)

Synonym
AC-12560
epa pesticide chemical code 118202
hexafluoron
hsdb 7049
xrd 473
hexafluron
naf-46
oms 3031
benzamide, n-(((3,5-dichloro-4-(1,1,2,2-tetrafluoroethoxy)phenyl)amino)carbonyl)-2,6-difluoro-
sentricon
recruit
ai3-29832
hexaflumuron [iso]
1-(3,5-dichloro-4-(1,1,2,2-tetrafluoroethoxy)phenyl)-3-(2,6-difluorobenzoyl)urea (iupac)
1-(3,5-dichloro-4-(1,1,2,2-tetrafluoroethoxy)phenyl)-3-(2,6-difluorobenzoyl)urea
n-({[3,5-dichloro-4-(1,1,2,2-tetrafluoroethoxy)phenyl]amino}carbonyl)-2,6-difluorobenzamide
86479-06-3
CHEBI:39383 ,
hexaflumuron
NCGC00095089-03
FT-0657502
n-[[3,5-dichloro-4-(1,1,2,2-tetrafluoroethoxy)phenyl]carbamoyl]-2,6-difluorobenzamide
n-[[3,5-bis(chloranyl)-4-[1,1,2,2-tetrakis(fluoranyl)ethoxy]phenyl]carbamoyl]-2,6-bis(fluoranyl)benzamide
n-[[3,5-dichloro-4-(1,1,2,2-tetrafluoroethoxy)anilino]-oxomethyl]-2,6-difluorobenzamide
A841678
NCGC00248023-01
C18861
xrd-473
n-(((3,5-dichloro-4-(1,1,2,2-tetrafluoroethoxy)phenyl)amino)carbonyl)-2,6-difluorobenzamide
cas-86479-06-3
tox21_300411
dtxcid1012620
dtxsid3032620 ,
NCGC00254327-01
sonet
unii-4gw50r449t
4gw50r449t ,
ec 401-400-1
AKOS015895485
1-(3,5-dichloro-4-(1,1,2,2-tetrafluoroethoxy) phenyl)-3-(2,6-difluorobenzoyl)urea
hexaflumuron [mi]
de-473
hexaflumuron [hsdb]
n-((3,5-dichloro-4-(1,1,2,2-tetrafluoroethoxy)phenyl)carbamoyl)-2,6-difluorobenzamide
SCHEMBL26793
CHEMBL1892746
benzamide, n-[[[3,5-dichloro-4-(1,1,2,2-tetrafluoroethoxy)phenyl]amino]carbonyl]-2,6-difluoro-
Q2717971
hexaflumuron, pestanal(r), analytical standard
pesticide3_hexaflumuron_c16h8cl2f6n2o3_
n-(3,5-dichloro-4-(1,1,2,2-tetrafluoroethoxy)phenylcarbamoyl)-2,6-difluorobenzamide
mfcd01743935
AS-15486
A12898
CS-0013916
HY-B1848

Research Excerpts

Toxicity

ExcerptReferenceRelevance
"Studying the toxic risk of pesticide exposure to ladybird beetles is important from an agronomical and ecological perspective since larval and adult ladybirds are dominant predators of herbivorous pest insects (e."( Toxic effects of hexaflumuron on the development of Coccinella septempunctata.
Brock, TC; Fu, M; Jiang, H; Lin, R; Yongquan, L; Yu, C; Zhang, Y, 2014
)
0.4
"The use of surfactants in the development of a suitable formulation for insecticides should improve the solubility behavior, the permeability and the efficiency against pests meanwhile decrease the toxic risks of insecticides on human health."( Synergistic effect of non-ionic surfactants Tween 80 and PEG6000 on cytotoxicity of insecticides.
Huang, Q; Li, D; Tao, L; Wu, X; Yu, X, 2015
)
0.42
" Taken together, piericidin A was the most toxic and imidacloprid was the least toxic to hemocytes, and the alterations in hemocyte functions compromised immunity."( The immunotoxicity of ten insecticides against insect hemocyte cells in vitro.
Chen, Y; Huang, Q; Xu, J; Yan, D, 2022
)
0.72

Pharmacokinetics

ExcerptReferenceRelevance
" Noviflumuron was cleared from termites in a first order process with a half-life of approximately 29 d, whereas the half-life of hexaflumuron was much shorter (8-9 d)."( Laboratory performance and pharmacokinetics of the benzoylphenylurea noviflumuron in eastern subterranean termites (Isoptera: Rhinotermitidae).
Dripps, JE; Karr, LL; King, JE; Sheets, JJ, 2004
)
0.32
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (6)

ClassDescription
benzoylurea insecticide
organofluorine insecticide
organochlorine insecticideAny organochlorine pesticide that has been used as an insecticide.
dichlorobenzeneAny member of the class of chlorobenzenes carrying two chloro groups at unspecified positions.
N-acylureaA member of the class of ureas that has the general formula R-CO-NH-CO-NH2 or R-CO-NH-CO-NH-CO-R', formally derived by the acylation of one or both of the nitrogens of a urea moiety.
aromatic etherAny ether in which the oxygen is attached to at least one aryl substituent.
[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 (17)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
RAR-related orphan receptor gammaMus musculus (house mouse)Potency4.69390.006038.004119,952.5996AID1159521; AID1159523
AR proteinHomo sapiens (human)Potency25.18450.000221.22318,912.5098AID1259243; AID588516; AID743036; AID743042; AID743053; AID743054
nuclear receptor subfamily 1, group I, member 3Homo sapiens (human)Potency2.37110.001022.650876.6163AID1224838; AID1224839; AID1224893
glucocorticoid receptor [Homo sapiens]Homo sapiens (human)Potency49.29110.000214.376460.0339AID720691; AID720719
retinoic acid nuclear receptor alpha variant 1Homo sapiens (human)Potency1.89740.003041.611522,387.1992AID1159552; AID1159553; AID1159555
retinoid X nuclear receptor alphaHomo sapiens (human)Potency15.48450.000817.505159.3239AID1159531
estrogen-related nuclear receptor alphaHomo sapiens (human)Potency6.02990.001530.607315,848.9004AID1224841; AID1224842; AID1259401; AID1259403
pregnane X nuclear receptorHomo sapiens (human)Potency25.11890.005428.02631,258.9301AID720659
estrogen nuclear receptor alphaHomo sapiens (human)Potency5.93360.000229.305416,493.5996AID1259244; AID1259248; AID588513; AID743079; AID743080; AID743091
vitamin D (1,25- dihydroxyvitamin D3) receptorHomo sapiens (human)Potency43.93070.023723.228263.5986AID743222; AID743241
aryl hydrocarbon receptorHomo sapiens (human)Potency0.11160.000723.06741,258.9301AID743085; AID743122
cytochrome P450, family 19, subfamily A, polypeptide 1, isoform CRA_aHomo sapiens (human)Potency1.36850.001723.839378.1014AID743083
nuclear factor of kappa light polypeptide gene enhancer in B-cells 1 (p105), isoform CRA_aHomo sapiens (human)Potency5.494119.739145.978464.9432AID1159509
thyroid hormone receptor beta isoform 2Rattus norvegicus (Norway rat)Potency27.30600.000323.4451159.6830AID743066
nuclear factor erythroid 2-related factor 2 isoform 1Homo sapiens (human)Potency24.03080.000627.21521,122.0200AID651741; AID743202
Voltage-dependent calcium channel gamma-2 subunitMus musculus (house mouse)Potency2.73060.001557.789015,848.9004AID1259244
Glutamate receptor 2Rattus norvegicus (Norway rat)Potency2.73060.001551.739315,848.9004AID1259244
[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]

Bioassays (8)

Assay IDTitleYearJournalArticle
AID1112038Insecticidal activity against third-instar larvae of fufenozide-susceptible Plutella xylostella (diamondback moth) assessed as mortality by leaf-dip bioassay method2012Pest management science, Feb, Volume: 68, Issue:2
Cross-resistance patterns and fitness in fufenozide-resistant diamondback moth, Plutella xylostella (Lepidoptera: Plutellidae).
AID1112039Insecticidal activity against third-instar larvae of fufenozide-resistant Plutella xylostella (diamondback moth) assessed as mortality by leaf-dip bioassay method2012Pest management science, Feb, Volume: 68, Issue:2
Cross-resistance patterns and fitness in fufenozide-resistant diamondback moth, Plutella xylostella (Lepidoptera: Plutellidae).
AID1091642Larvicidal activity against fourth-instar larval stage of Mythimna separata (Oriental armyworm) in compound-pretreated corn leaves assessed as mortality at 25 +/-1 degC after 4 days2008Journal of agricultural and food chemistry, Dec-10, Volume: 56, Issue:23
Design, synthesis, bioactivity, and structure-activity relationship (SAR) studies of novel benzoylphenylureas containing oxime ether group.
AID1081994Insecticidal activity against fourth-instar larval stage of Mythimna separata (Oriental armyworm) infested drug-pretreated corn leaves assessed as mortality at 10 mg/l at 25 +/-1 degC after 4 days2011Journal of agricultural and food chemistry, Mar-23, Volume: 59, Issue:6
Design and synthesis of benzoylphenylureas with fluorinated substituents on the aniline ring as insect growth regulators.
AID1081983Insecticidal activity against fourth-instar larval stage of Culex pipiens pallens (mosquito) assessed as mortality at 0.25 mg/l at 25 +/-1 degC after 8 days2011Journal of agricultural and food chemistry, Mar-23, Volume: 59, Issue:6
Design and synthesis of benzoylphenylureas with fluorinated substituents on the aniline ring as insect growth regulators.
AID1080743Larvicidal activity against fourth-instar larval stage of Culex pipiens pallens (mosquito) assessed as mortality at 0.25 mg/l at 25 +/-1 degC measured after 8 days2009Journal of agricultural and food chemistry, Jul-22, Volume: 57, Issue:14
Design, synthesis, and bioactivity study of novel benzoylpyridazyl ureas.
AID1112037Resistance ratio, ratio of LC50 for third-instar larvae of fufenozide-resistant Plutella xylostella (diamondback moth) to LC50 for third-instar larvae of fufenozide-susceptible Plutella xylostella2012Pest management science, Feb, Volume: 68, Issue:2
Cross-resistance patterns and fitness in fufenozide-resistant diamondback moth, Plutella xylostella (Lepidoptera: Plutellidae).
AID1080746Larvicidal activity against fourth-instar larval stage of Mythimna separata (Oriental armyworm) in compound pretreated corn leaves assessed as mortality at 10 mg/l at 25 +/-1 degC measured after 4 days2009Journal of agricultural and food chemistry, Jul-22, Volume: 57, Issue:14
Design, synthesis, and bioactivity study of novel benzoylpyridazyl ureas.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (58)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901 (1.72)18.7374
1990's9 (15.52)18.2507
2000's21 (36.21)29.6817
2010's21 (36.21)24.3611
2020's6 (10.34)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 11.60

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

MetricThis Compound (vs All)
Research Demand Index11.60 (24.57)
Research Supply Index4.13 (2.92)
Research Growth Index5.73 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (11.60)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews2 (3.28%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other59 (96.72%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]