Page last updated: 2024-12-07

methoxyfenozide

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

Description

Methoxyfenozide is a synthetic insecticide that belongs to the phenylpyrazole class. It is a potent and selective insecticide that acts by disrupting the nervous system of insects. The compound is typically used in agriculture and public health for controlling a variety of insect pests, including mosquitoes, flies, and cockroaches. Methoxyfenozide is considered to be relatively safe for humans and the environment compared to other insecticides, due to its specific target site and rapid degradation in the environment. However, research is ongoing to assess its potential ecological impacts and understand its long-term effects. The compound is studied to develop new and sustainable insect control strategies that minimize the use of broad-spectrum insecticides and reduce the risk of resistance development.'

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

methoxyfenozide : A carbohydrazide that is hydrazine in which the amino hydrogens have been replaced by 3-methoxy-2-methylbenzoyl, 3,5-dimethylbenzoyl, and tert-butyl groups respectively. [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 CID105010
CHEMBL ID55772
CHEBI ID38449
SCHEMBL ID27595
MeSH IDM0360846

Synonyms (61)

Synonym
methoxyfenozide
CHEBI:38449 ,
161050-58-4
n-tert-butyl-n'-(3-methoxy-o-toluoyl)-3,5-xylohydrazide
3-methoxy-2-methylbenzoic acid 2-(3,5-dimethylbenzoyl)-2-(1,1-dimethylethyl)hydrazide
n'-tert-butyl-n'-(3,5-dimethylbenzoyl)-3-methoxy-2-methylbenzohydrazide
n'-(tert-butyl)-n'-(3,5-dimethylbenzoyl)-3-methoxy-2-methylbenzohydrazide
methoxyfenozide [iso:ansi:bsi]
benzoic acid, 3-methoxy-2-methyl-, 2-(3,5-dimethylbenzoyl)-2-(1,1-dimethylethyl)hydrazide
NCGC00163951-01
NCGC00163951-02
n''-tert-butyl-n''-(3,5-dimethylbenzoyl)-3-methoxy-2-methylbenzohydrazide
bdbm50128305
n-tert-butyl-n''-(3-methoxy-o-toluoyl)-3,5-xylohydrazide
n''-(tert-butyl)-n''-(3,5-dimethylbenzoyl)-3-methoxy-2-methylbenzohydrazide
CHEMBL55772 ,
A20844
3-methoxymethylbenzoic acid 2-(3,5-dimethylbenzoyl)-2-(1,1-dimethylethyl)hydrazide
NCGC00163951-03
C18525
tox21_301100
cas-161050-58-4
NCGC00255000-01
dtxsid3032628 ,
dtxcid1012628
n'-(tert-butyl )-n'-(3,5-dimethylbenzoyl)-3-methoxy-2-methylbenzohydrazide
rg 102398
62a22651zx ,
runner
hsdb 7936
rh 2485
unii-62a22651zx
rh-2485
rh 112485
methoxyphenozide
intrepid (pesticide)
intrepid
3-methoxy-2-methylbenzoic acid 2-(3,5-dimethylbenzoyl)-2-tert-butylhydrazide
FT-0631190
AKOS015895784
prodigy
rh-112485
methoxyfenozide [mi]
methoxyfenozide [iso]
SCHEMBL27595
QCAWEPFNJXQPAN-UHFFFAOYSA-N
n-(3-methoxy-2-methylbenzoyl)-n'-(3,5-dimethylbenzoyl)-n'-tert-butylhydrazine
n-(3-methoxy-2-methylbenzoyl)-n'(3,5-dimethylbenzoyl)-n'-tert-butylhydrazine
163442-56-6
mfcd03792750
methoxyfenozide, pestanal(r), analytical standard
methoxyfenozide 10 microg/ml in acetonitrile
J-009776
DS-16494
rg 102398; rh 112485; rh 2485
BCP10196
Q15632812
C73059
CS-0065614
HY-117386
benzoic acid, 3-methoxy-2-methyl-, 2-(3,5-dimethyl-benzoyl)-2-(1,1-dimethylethyl)hydrazide

Research Excerpts

Overview

Methoxyfenozide is a lepidopteran-specific insecticide. It belongs to a new group of insecticides, the non-steroidal ecdysteroid agonists. Its impact on honey bees in not fully understood.

ExcerptReferenceRelevance
"Methoxyfenozide is an insect growth regulator (IGR) commonly used in agriculture to simultaneously control pests and preserve beneficial insect populations; however, its impact on honey bees in not fully understood. "( Exposure to sublethal concentrations of methoxyfenozide disrupts honey bee colony activity and thermoregulation.
Beren, E; Brown, N; Carroll, MJ; Corby-Harris, V; Meador, CAD; Meikle, WG; Snyder, LA; Weiss, M, 2019
)
2.22
"Methoxyfenozide is a bio-rational insecticide having many environmentally friendly attributes that make it compatible with integrated pest management programs."( Assessment of resistance risk in Musca domestica L. (Diptera: Muscidae) to methoxyfenozide.
Abbas, N; Shad, SA; Shah, RM, 2015
)
1.37
"Methoxyfenozide is a lepidopteran-specific insecticide that belongs to a new group of insecticides, the non-steroidal ecdysteroid agonists, also called moulting accelerating compounds (MACs). "( Biochemical mechanisms of methoxyfenozide resistance in the cotton leafworm Spodoptera littoralis.
Mosallanejad, H; Smagghe, G, 2009
)
2.1
"Methoxyfenozide is an ecdysone agonist, the most new class of insect growth regulators. "( Effects of larval exposure to sublethal concentrations of methoxyfenozide in Spodoptera frugiperda (J.E. Smith).
Diaz, O; Figueroa, JI; Martínez, AM; Pineda, S; Schneider, MI; Smagghe, G; Zarate, N, 2009
)
2.04
"Methoxyfenozide (RH-2485) is a non-steroidal ecdysteroid agonist with a dibenzoylhydrazine structure, representing a group used as novel biorational insecticides in the control of insect pests. "( Ecdysone signaling and transcript signature in Drosophila cells resistant against methoxyfenozide.
Badisco, L; Knapen, D; Mosallanejad, H; Smagghe, G; Soin, T; Swevers, L; Vanden Broeck, J, 2010
)
2.03

Treatment

ExcerptReferenceRelevance
"Oral treatment with methoxyfenozide reduced the fecundity and fertility of G(7) adults, confirming sublethal effects on reproduction."( Monitoring of beet armyworm resistance to spinosad and methoxyfenozide in Mexico.
Avilés, MC; Corrales, JL; Díaz, O; Martínez, AM; Osorio, A; Pineda, S; Schneider, MI; Smagghe, G, 2008
)
0.91

Toxicity

ExcerptReferenceRelevance
" Methoxyfenozide was the most toxic followed by tebufenozide, halofenozide, and RH-5849."( Significance of absorption, oxidation, and binding to toxicity of four ecdysone agonists in multi-resistant cotton leafworm.
Carton, B; Decombel, L; Smagghe, G; Tirry, L, 2001
)
1.22
" While two of the bisacylhydrazines (coded as RH-5992 and RH-2485) are predominantly toxic to lepidopteran pests, RH-5849, which has not been commercialized, has a broader spectrum of toxicity."( Comparative toxicity and ecdysone receptor affinity of non-steroidal ecdysone agonists and 20-hydroxyecdysone in Chironomus tentans.
Dhadialla, TS; Lezzi, M; Smagghe, G, 2002
)
0.31
"5-fold less toxic in terms of LD50 values against last-instar larvae of a greenhouse-selected strain of the beet armyworm Spodoptera exigua (Hübner) that was collected in July 2001 in an experimental greenhouse for resistance at Murcia in southern Spain, in comparison with a laboratory susceptible strain."( Toxicity and kinetics of methoxyfenozide in greenhouse-selected Spodoptera exigua (Lepidoptera: Noctuidae).
Budia, F; Carton, B; Del Estal, P; Pineda, S; Smagghe, G; Viñuela, E, 2003
)
0.62
" Endosulfan and cypermethrin were highly toxic towards eggs and larvae with mortality rates ranging from 80% to 100%."( Side effects of conventional and non-conventional insecticides on eggs and larvae of Chrysoperla externa (Hagen) (Neuroptera: Chrysopidae) in Argentine.
Pineda, P; Schneider, MI; Smagghe, G, 2006
)
0.33
"The new analytical method using Quick, Easy, Cheap, Effective, Rugged, and Safe (QuEChERS) procedure for simultaneous determination of diacylhydrazine insecticide residues in fruits and vegetables was developed using ultra-performance liquid chromatography coupled with tandem mass spectrometry (UPLC-MS/MS)."( Residue analysis of four diacylhydrazine insecticides in fruits and vegetables by Quick, Easy, Cheap, Effective, Rugged, and Safe (QuEChERS) method using ultra-performance liquid chromatography coupled to tandem mass spectrometry.
Dong, F; Li, Y; Liu, X; Song, W; Xu, J; Zheng, Y, 2011
)
0.37
", fungi that produce toxic aflatoxins."( Effects of a naturally occurring and a synthetic synergist on toxicity of three insecticides and a phytochemical to navel orangeworm (Lepidoptera: Pyralidae).
Berenbaum, MR; Lawrance, A; Niu, G; Pollock, HS; Siegel, JP, 2012
)
0.38
" Chlorfenapyr was the most toxic adulticide among all the tested insecticides."( Toxicity of 25 synthetic insecticides to the field population of Culex quinquefasciatus Say.
Ahmad, D; Alam, M; Ali, Q; Binyamin, M; Shad, SA; Shah, RM; Waqas, M, 2016
)
0.43
" The evaluation of the chorion of the eggshell in this study has clarified the toxic effect of methomyl and cartap hydrochloride on eggs."( Insecticide toxicity to the borer Neoleucinodes elegantalis (Guenée) (Lepidoptera: Crambidae): developmental and egg-laying effects.
Arcanjo, LP; Costa, ÁH; Ferreira, DO; Martins, JC; Picanço, MC; Serrão, JE; Silva, RS; Soares, JRS, 2018
)
0.48
" littoralis larvae, and the same concentrations were used to assess the toxic impact of their combination on susceptible (SUS) and M-selected (MS) strains."( Toxicity and biochemical impact of methoxyfenozide/spinetoram mixture on susceptible and methoxyfenozide-selected strains of Spodoptera littoralis (Lepidoptera: Noctuidae).
Ahmed, FS; Helmy, WS; Helmy, YS, 2022
)
1

Pharmacokinetics

ExcerptReferenceRelevance
" In a second part, pharmacokinetic studies using a (14)C isotope of each IGR showed similar patterns of penetration through the cuticle, but different absorption and distribution rates inside the insect body."( The ecological impact of four IGR insecticides in adults of Hyposoter didymator (Hym., Ichneumonidae): pharmacokinetics approach.
Pineda, S; Schneider, M; Smagghe, G; Viñuela, E, 2008
)
0.35

Bioavailability

ExcerptReferenceRelevance
" To show the importance of physicochemical properties, the classic QSAR and CoMFA of neonicotinoids and prediction of bioavailability of pesticides in terms of membrane permeability in comparison with drugs are described."( Importance of physicochemical properties for the design of new pesticides.
Akamatsu, M, 2011
)
0.37

Dosage Studied

ExcerptRelevanceReference
" Dose-response regression lines for tebufenozide were parallel across populations, suggesting that the resistance mechanism(s) were quantitatively, but not qualitatively, different."( Resistance and cross-resistance to four insecticides in populations of obliquebanded leafroller (Lepidoptera: Tortricidae).
Lowery, DT; Smirle, MJ; Zurowski, CL, 2002
)
0.31
" Dose-response relationships were determined for the three agonists; RH-2485 was found to be the most effective endocrine disruptor against all three species."( Comparative larvicidal toxicities of three ecdysone agonists on the mosquitoes Aedes aegypti, Culex quinquefasciatus, and Anopheles gambiae.
Beckage, NE; Marion, KM; Tan, FF; Walton, WE; Wirth, MC, 2004
)
0.32
" A drastic effect was observed on spermatozoon production, with a dose-response relationship."( Proteomic investigation of male Gammarus fossarum, a freshwater crustacean, in response to endocrine disruptors.
Abbaci, K; Armengaud, J; Chaumot, A; Gaillard, JC; Geffard, O; Habtoul, Y; Pible, O; Trapp, J, 2015
)
0.42
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (3)

RoleDescription
environmental contaminantAny minor or unwanted substance introduced into the environment that can have undesired effects.
xenobioticA xenobiotic (Greek, xenos "foreign"; bios "life") is a compound that is foreign to a living organism. Principal xenobiotics include: drugs, carcinogens and various compounds that have been introduced into the environment by artificial means.
insecticideStrictly, a substance intended to kill members of the class Insecta. In common usage, any substance used for preventing, destroying, repelling or controlling insects.
[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 (2)

ClassDescription
carbohydrazideA hydrazide consisting of hydrazine carrying one or more carboacyl groups.
monomethoxybenzeneCompounds containing a benzene skeleton substituted with one methoxy group.
[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 (16)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
pregnane X receptorRattus norvegicus (Norway rat)Potency3.16230.025127.9203501.1870AID651751
RAR-related orphan receptor gammaMus musculus (house mouse)Potency3.37320.006038.004119,952.5996AID1159521; AID1159523
AR proteinHomo sapiens (human)Potency36.79420.000221.22318,912.5098AID1259243; AID743035; AID743054; AID743063
estrogen-related nuclear receptor alphaHomo sapiens (human)Potency29.07340.001530.607315,848.9004AID1224848; AID1224849; AID1259403
farnesoid X nuclear receptorHomo sapiens (human)Potency54.94100.375827.485161.6524AID743217
pregnane X nuclear receptorHomo sapiens (human)Potency7.94330.005428.02631,258.9301AID720659
vitamin D (1,25- dihydroxyvitamin D3) receptorHomo sapiens (human)Potency44.66840.023723.228263.5986AID588543
aryl hydrocarbon receptorHomo sapiens (human)Potency27.48720.000723.06741,258.9301AID743085; AID743122
thyroid hormone receptor beta isoform 2Rattus norvegicus (Norway rat)Potency41.77050.000323.4451159.6830AID743065; AID743067
nuclear factor erythroid 2-related factor 2 isoform 1Homo sapiens (human)Potency76.95880.000627.21521,122.0200AID651741
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Inhibition Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
ATP-dependent translocase ABCB1Homo sapiens (human)IC50 (µMol)44.30000.00022.318510.0000AID1306283
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Activation Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
20-hydroxy-ecdysone receptor Spodoptera littoralis (African cotton leafworm)EC50 (µMol)0.00600.00220.35121.2882AID1111388
20-hydroxy-ecdysone receptor Choristoneura fumiferana (eastern spruce budworm)EC50 (µMol)0.28000.28000.28000.2800AID68294
Protein ultraspiracleDrosophila melanogaster (fruit fly)EC50 (µMol)16.59590.52484.17857.7625AID1111606
Ecdysone receptorDrosophila melanogaster (fruit fly)EC50 (µMol)16.59590.52484.17857.7625AID1111606
Ecdysone receptorBombyx mori (domestic silkworm)EC50 (µMol)0.03650.00100.11410.4365AID1111391; AID1111600; AID68292
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Biological Processes (17)

Processvia Protein(s)Taxonomy
G2/M transition of mitotic cell cycleATP-dependent translocase ABCB1Homo sapiens (human)
xenobiotic metabolic processATP-dependent translocase ABCB1Homo sapiens (human)
response to xenobiotic stimulusATP-dependent translocase ABCB1Homo sapiens (human)
phospholipid translocationATP-dependent translocase ABCB1Homo sapiens (human)
terpenoid transportATP-dependent translocase ABCB1Homo sapiens (human)
regulation of response to osmotic stressATP-dependent translocase ABCB1Homo sapiens (human)
transmembrane transportATP-dependent translocase ABCB1Homo sapiens (human)
transepithelial transportATP-dependent translocase ABCB1Homo sapiens (human)
stem cell proliferationATP-dependent translocase ABCB1Homo sapiens (human)
ceramide translocationATP-dependent translocase ABCB1Homo sapiens (human)
export across plasma membraneATP-dependent translocase ABCB1Homo sapiens (human)
transport across blood-brain barrierATP-dependent translocase ABCB1Homo sapiens (human)
positive regulation of anion channel activityATP-dependent translocase ABCB1Homo sapiens (human)
carboxylic acid transmembrane transportATP-dependent translocase ABCB1Homo sapiens (human)
xenobiotic detoxification by transmembrane export across the plasma membraneATP-dependent translocase ABCB1Homo sapiens (human)
xenobiotic transport across blood-brain barrierATP-dependent translocase ABCB1Homo sapiens (human)
regulation of chloride transportATP-dependent translocase ABCB1Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Molecular Functions (14)

Processvia Protein(s)Taxonomy
protein bindingATP-dependent translocase ABCB1Homo sapiens (human)
ATP bindingATP-dependent translocase ABCB1Homo sapiens (human)
ABC-type xenobiotic transporter activityATP-dependent translocase ABCB1Homo sapiens (human)
efflux transmembrane transporter activityATP-dependent translocase ABCB1Homo sapiens (human)
ATP hydrolysis activityATP-dependent translocase ABCB1Homo sapiens (human)
transmembrane transporter activityATP-dependent translocase ABCB1Homo sapiens (human)
ubiquitin protein ligase bindingATP-dependent translocase ABCB1Homo sapiens (human)
ATPase-coupled transmembrane transporter activityATP-dependent translocase ABCB1Homo sapiens (human)
xenobiotic transmembrane transporter activityATP-dependent translocase ABCB1Homo sapiens (human)
carboxylic acid transmembrane transporter activityATP-dependent translocase ABCB1Homo sapiens (human)
phosphatidylcholine floppase activityATP-dependent translocase ABCB1Homo sapiens (human)
phosphatidylethanolamine flippase activityATP-dependent translocase ABCB1Homo sapiens (human)
ceramide floppase activityATP-dependent translocase ABCB1Homo sapiens (human)
floppase activityATP-dependent translocase ABCB1Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Ceullar Components (7)

Processvia Protein(s)Taxonomy
cytoplasmATP-dependent translocase ABCB1Homo sapiens (human)
plasma membraneATP-dependent translocase ABCB1Homo sapiens (human)
cell surfaceATP-dependent translocase ABCB1Homo sapiens (human)
membraneATP-dependent translocase ABCB1Homo sapiens (human)
apical plasma membraneATP-dependent translocase ABCB1Homo sapiens (human)
extracellular exosomeATP-dependent translocase ABCB1Homo sapiens (human)
external side of apical plasma membraneATP-dependent translocase ABCB1Homo sapiens (human)
plasma membraneATP-dependent translocase ABCB1Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (94)

Assay IDTitleYearJournalArticle
AID1111386Agonist activity at ecdysone receptor in Spodoptera littoralis Sl2 cells after 24 hr by luciferase reporter gene assay relative to tebufenozide2010Pest management science, May, Volume: 66, Issue:5
Assessment of species specificity of moulting accelerating compounds in Lepidoptera: comparison of activity between Bombyx mori and Spodoptera littoralis by in vitro reporter and in vivo toxicity assays.
AID1111591Agonist activity at ecdysone receptor in Drosophila melanogaster S2 cells treated with ouabain for 24 hr prior to compound addition measured after 24 hr by luciferase reporter gene assay2010Pest management science, Nov, Volume: 66, Issue:11
Comparison of the activity of non-steroidal ecdysone agonists between dipteran and lepidopteran insects, using cell-based EcR reporter assays.
AID288192Partition coefficient, log P of the compound2007Bioorganic & medicinal chemistry, Jun-01, Volume: 15, Issue:11
QSAR study on permeability of hydrophobic compounds with artificial membranes.
AID1112686Insecticidal activity against Bactrocera oleae assessed as insect mortality at 96 mg Ai/L applied through oral ingestion measured after 15 days (Rvb = 2.5 +/- 2.5%)2013Pest management science, Jan, Volume: 69, Issue:1
Insect growth regulators as potential insecticides to control olive fruit fly (Bactrocera oleae Rossi): insect toxicity bioassays and molecular docking approach.
AID1112202Insecticidal activity against po dosed Cydia pomonella (codling moth) Clear Creek abandoned neonate measured after 4 days2012Pest management science, Jun, Volume: 68, Issue:6
Development of a rapid resistance monitoring bioassay for codling moth larvae.
AID1081866Stomach toxicity against third-instar Ostrinia nubilalis (European corn borer) in compound treated fresh corn leaves assessed as insecticidal activity at 200 mg/L measured after 4 days by leaf-dip method2011Journal of agricultural and food chemistry, Jan-26, Volume: 59, Issue:2
Synthesis, crystal structures, insecticidal activities, and structure--activity relationships of novel N'-tert-Butyl-N'-substituted-benzoyl-N-[di(octa)hydro]benzofuran{(2,3-dihydro)benzo[1,3]([1,4])dioxine}carbohydrazide derivatives.
AID229584Ratio of maximum level of gene expression (ecdysone receptor and luciferase gene) of compound to maximum level of gene expression with GSTM-E expressed as RMFI2003Bioorganic & medicinal chemistry letters, Jun-02, Volume: 13, Issue:11
Optimization of alpha-acylaminoketone ecdysone agonists for control of gene expression.
AID1112188Insecticidal activity against po dosed 11 day-old larvae of spinetoram-selected Cydia pomonella (codling moth) reared on apple assessed as mortality measured after 4 days2012Pest management science, Jun, Volume: 68, Issue:6
Development of a rapid resistance monitoring bioassay for codling moth larvae.
AID1111389Agonist activity at ecdysone receptor in Bombyx mori Bm5 cells after 24 hr by luciferase reporter gene assay relative to tebufenozide2010Pest management science, May, Volume: 66, Issue:5
Assessment of species specificity of moulting accelerating compounds in Lepidoptera: comparison of activity between Bombyx mori and Spodoptera littoralis by in vitro reporter and in vivo toxicity assays.
AID1111595Cytotoxicity against Drosophila melanogaster S2 cells at 10 to 100 uM after 24 hr by CellTiter assay2010Pest management science, Nov, Volume: 66, Issue:11
Comparison of the activity of non-steroidal ecdysone agonists between dipteran and lepidopteran insects, using cell-based EcR reporter assays.
AID1081854Stomach toxicity against third-instar Mythimna separata (Oriental armyworm) in compound treated fresh corn leaves assessed as insecticidal activity at 200 mg/L measured after 4 days by leaf-dip method2011Journal of agricultural and food chemistry, Jan-26, Volume: 59, Issue:2
Synthesis, crystal structures, insecticidal activities, and structure--activity relationships of novel N'-tert-Butyl-N'-substituted-benzoyl-N-[di(octa)hydro]benzofuran{(2,3-dihydro)benzo[1,3]([1,4])dioxine}carbohydrazide derivatives.
AID1112684Insecticidal activity against Bactrocera oleae assessed as insect survival lifespan at 96 mg Ai/L applied through oral ingestion (Rvb = 79.7 +/- 12.2 days)2013Pest management science, Jan, Volume: 69, Issue:1
Insect growth regulators as potential insecticides to control olive fruit fly (Bactrocera oleae Rossi): insect toxicity bioassays and molecular docking approach.
AID1103862Toxicity against Metaseiulus occidentalis adults in bean leaf disk infested with two-spotted spider mites assessed as repellency at 0.3767 g AI/L treated using worst-case laboratory exposure procedure measured after 48 hr (Rvb = 13.6%)2009Pest management science, Jun, Volume: 65, Issue:6
Effect of seven new orchard pesticides on Galendromus occidentalis in laboratory studies.
AID1112205Insecticidal activity against po dosed fourth-instar larvae of Cydia pomonella (codling moth) lab-s measured after 4 days2012Pest management science, Jun, Volume: 68, Issue:6
Development of a rapid resistance monitoring bioassay for codling moth larvae.
AID1112190Insecticidal activity against po dosed 15 day-old larvae of Cydia pomonella (codling moth) lab-s reared on apple assessed as mortality measured after 4 days2012Pest management science, Jun, Volume: 68, Issue:6
Development of a rapid resistance monitoring bioassay for codling moth larvae.
AID1112199Insecticidal activity against po dosed fourth-instar larvae of Cydia pomonella (codling moth) Holt measured after 4 days2012Pest management science, Jun, Volume: 68, Issue:6
Development of a rapid resistance monitoring bioassay for codling moth larvae.
AID1081858Stomach toxicity against third-instar Mythimna separata (Oriental armyworm) in compound treated fresh corn leaves assessed as insecticidal activity at 10 mg/L measured after 4 days by leaf-dip method2011Journal of agricultural and food chemistry, Jan-26, Volume: 59, Issue:2
Synthesis, crystal structures, insecticidal activities, and structure--activity relationships of novel N'-tert-Butyl-N'-substituted-benzoyl-N-[di(octa)hydro]benzofuran{(2,3-dihydro)benzo[1,3]([1,4])dioxine}carbohydrazide derivatives.
AID1112206Insecticidal activity against po dosed Cydia pomonella (codling moth) lab-s neonate measured after 4 days2012Pest management science, Jun, Volume: 68, Issue:6
Development of a rapid resistance monitoring bioassay for codling moth larvae.
AID1112201Insecticidal activity against po dosed fourth-instar larvae of Cydia pomonella (codling moth) Clear Creek abandoned measured after 4 days2012Pest management science, Jun, Volume: 68, Issue:6
Development of a rapid resistance monitoring bioassay for codling moth larvae.
AID1103868Toxicity against Metaseiulus occidentalis adults in bean leaf disk infested with two-spotted spider mites assessed as repellency at 0.3767 g AI/L treated using worst-case laboratory exposure procedure measured after 24 hr (Rvb = 3.6%)2009Pest management science, Jun, Volume: 65, Issue:6
Effect of seven new orchard pesticides on Galendromus occidentalis in laboratory studies.
AID1111378Larvicidal activity against Bombyx mori assessed as mortality applied topically after 1 week2010Pest management science, May, Volume: 66, Issue:5
Assessment of species specificity of moulting accelerating compounds in Lepidoptera: comparison of activity between Bombyx mori and Spodoptera littoralis by in vitro reporter and in vivo toxicity assays.
AID1091956Apparent hydrophobicity, log D of the compound in Octanol-buffer2011Journal of agricultural and food chemistry, Apr-13, Volume: 59, Issue:7
Importance of physicochemical properties for the design of new pesticides.
AID1112194Resistant ratio of LC50 for Cydia pomonella (codling moth) Holt neonate to Cydia pomonella (codling moth) Glibert neonate2012Pest management science, Jun, Volume: 68, Issue:6
Development of a rapid resistance monitoring bioassay for codling moth larvae.
AID1081862Stomach toxicity against third-instar Spodoptera exigua in compound treated fresh cabbage leaves assessed as insecticidal activity at 10 mg/L measured after 3 days by leaf-dip method2011Journal of agricultural and food chemistry, Jan-26, Volume: 59, Issue:2
Synthesis, crystal structures, insecticidal activities, and structure--activity relationships of novel N'-tert-Butyl-N'-substituted-benzoyl-N-[di(octa)hydro]benzofuran{(2,3-dihydro)benzo[1,3]([1,4])dioxine}carbohydrazide derivatives.
AID1112197Insecticidal activity against po dosed fourth-instar larvae of Cydia pomonella (codling moth) Gilbert measured after 4 days2012Pest management science, Jun, Volume: 68, Issue:6
Development of a rapid resistance monitoring bioassay for codling moth larvae.
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).
AID1081859Stomach toxicity against third-instar Spodoptera exigua in compound treated fresh cabbage leaves assessed as insecticidal activity at 200 mg/L measured after 3 days by leaf-dip method2011Journal of agricultural and food chemistry, Jan-26, Volume: 59, Issue:2
Synthesis, crystal structures, insecticidal activities, and structure--activity relationships of novel N'-tert-Butyl-N'-substituted-benzoyl-N-[di(octa)hydro]benzofuran{(2,3-dihydro)benzo[1,3]([1,4])dioxine}carbohydrazide derivatives.
AID1112198Insecticidal activity against po dosed Cydia pomonella (codling moth) Gilbert neonate measured after 4 days2012Pest management science, Jun, Volume: 68, Issue:6
Development of a rapid resistance monitoring bioassay for codling moth larvae.
AID1112195Resistant ratio of LC50 for fourth-instar larvae of Cydia pomonella (codling moth) lab-s to fourth-instar larvae of Cydia pomonella (codling moth) Glibert2012Pest management science, Jun, Volume: 68, Issue:6
Development of a rapid resistance monitoring bioassay for codling moth larvae.
AID1110956Antifeedant activity against third-instar larval stage of Plutella xylostella (diamondback moth) infested compound-treated leaf assessed as time required to stop feeding at 467 mg a.i/L after 48 hr by leaf disk assay (Rvb = > 2880 min)2009Pest management science, Sep, Volume: 65, Issue:9
Feeding cessation effects of chlorantraniliprole, a new anthranilic diamide insecticide, in comparison with several insecticides in distinct chemical classes and mode-of-action groups.
AID1103886Toxicity against Metaseiulus occidentalis adults in bean leaf disk infested with two-spotted spider mites assessed as average number of eggs laid (fecundity) at 0.3767 g AI/L treated using worst-case laboratory exposure procedure measured after 24 hr (Rvb2009Pest management science, Jun, Volume: 65, Issue:6
Effect of seven new orchard pesticides on Galendromus occidentalis in laboratory studies.
AID1112186Insecticidal activity against po dosed 10 day-old larvae of Cydia pomonella (codling moth) Owensby reared on apple assessed as mortality measured after 4 days2012Pest management science, Jun, Volume: 68, Issue:6
Development of a rapid resistance monitoring bioassay for codling moth larvae.
AID1112185Insecticidal activity against po dosed 15 day-old larvae of Cydia pomonella (codling moth) reared on apple assessed as mortality measured after 4 days2012Pest management science, Jun, Volume: 68, Issue:6
Development of a rapid resistance monitoring bioassay for codling moth larvae.
AID1112196Resistant ratio of LC50 for Cydia pomonella (codling moth) lab-s neonate to Cydia pomonella (codling moth) Glibert neonate2012Pest management science, Jun, Volume: 68, Issue:6
Development of a rapid resistance monitoring bioassay for codling moth larvae.
AID1111388Agonist activity at ecdysone receptor in Spodoptera littoralis Sl2 cells after 24 hr by luciferase reporter gene assay2010Pest management science, May, Volume: 66, Issue:5
Assessment of species specificity of moulting accelerating compounds in Lepidoptera: comparison of activity between Bombyx mori and Spodoptera littoralis by in vitro reporter and in vivo toxicity assays.
AID1112678Insecticidal activity against Bactrocera oleae assessed as insect mortality at 96 mg Ai/L applied through residual contact on glass surfaces measured after 15 days (Rvb = 45.8 +/- 16.3%)2013Pest management science, Jan, Volume: 69, Issue:1
Insect growth regulators as potential insecticides to control olive fruit fly (Bactrocera oleae Rossi): insect toxicity bioassays and molecular docking approach.
AID1103856Toxicity against Metaseiulus occidentalis adults in bean leaf disk infested with two-spotted spider mites assessed as repellency at 0.3767 g AI/L treated using worst-case laboratory exposure procedure measured after 72 hr (Rvb = 16.1%)2009Pest management science, Jun, Volume: 65, Issue:6
Effect of seven new orchard pesticides on Galendromus occidentalis in laboratory studies.
AID288184Permeability coefficient through artificial membrane in presence of unstirred water layer by PAMPA2007Bioorganic & medicinal chemistry, Jun-01, Volume: 15, Issue:11
QSAR study on permeability of hydrophobic compounds with artificial membranes.
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).
AID1091958Hydrophobicity, log P of the compound in octanol-water by shaking-flask method2011Journal of agricultural and food chemistry, Apr-13, Volume: 59, Issue:7
Importance of physicochemical properties for the design of new pesticides.
AID68294Dose affording 50% of maximum transactivation for ecdysone receptor from Choristoneura fumiferana (CfEcR) and a luciferase reporter gene in CHO cells2003Bioorganic & medicinal chemistry letters, Jun-02, Volume: 13, Issue:11
Optimization of alpha-acylaminoketone ecdysone agonists for control of gene expression.
AID1081857Stomach toxicity against third-instar Mythimna separata (Oriental armyworm) in compound treated fresh corn leaves assessed as insecticidal activity at 25 mg/L measured after 4 days by leaf-dip method2011Journal of agricultural and food chemistry, Jan-26, Volume: 59, Issue:2
Synthesis, crystal structures, insecticidal activities, and structure--activity relationships of novel N'-tert-Butyl-N'-substituted-benzoyl-N-[di(octa)hydro]benzofuran{(2,3-dihydro)benzo[1,3]([1,4])dioxine}carbohydrazide derivatives.
AID1306283Inhibition of human P-glycoprotein transfected in pig LLC-GA5-COL150 cells assessed as quinidine transport from apical to basolateral side preincubated for 30 mins followed by quinidine addition to apical side measured after 60 mins2016Bioorganic & medicinal chemistry, 07-15, Volume: 24, Issue:14
Structure-activity relationships of dibenzoylhydrazines for the inhibition of P-glycoprotein-mediated quinidine transport.
AID1112191Insecticidal activity against po dosed 10 day-old larvae of Cydia pomonella (codling moth) lab-s reared on apple assessed as mortality measured after 4 days2012Pest management science, Jun, Volume: 68, Issue:6
Development of a rapid resistance monitoring bioassay for codling moth larvae.
AID1110989Antifeedant activity against third-instar larval stage of Spodoptera exigua infested compound-treated leaf assessed as reduction in feeding damage at 467 mg a.i/L after 48 hr by leaf disk assay relative to untreated control2009Pest management science, Sep, Volume: 65, Issue:9
Feeding cessation effects of chlorantraniliprole, a new anthranilic diamide insecticide, in comparison with several insecticides in distinct chemical classes and mode-of-action groups.
AID1306285Lipophilicity logP of the compound2016Bioorganic & medicinal chemistry, 07-15, Volume: 24, Issue:14
Structure-activity relationships of dibenzoylhydrazines for the inhibition of P-glycoprotein-mediated quinidine transport.
AID1111606Agonist activity at ecdysone receptor in Drosophila melanogaster S2 cells after 24 hr by luciferase reporter gene assay2010Pest management science, Nov, Volume: 66, Issue:11
Comparison of the activity of non-steroidal ecdysone agonists between dipteran and lepidopteran insects, using cell-based EcR reporter assays.
AID1112200Insecticidal activity against po dosed Cydia pomonella (codling moth) Holt neonate measured after 4 days2012Pest management science, Jun, Volume: 68, Issue:6
Development of a rapid resistance monitoring bioassay for codling moth larvae.
AID1111590Agonist activity at ecdysone receptor in Drosophila melanogaster S2 cells after 24 hr by luciferase reporter gene assay in presence of ouabain2010Pest management science, Nov, Volume: 66, Issue:11
Comparison of the activity of non-steroidal ecdysone agonists between dipteran and lepidopteran insects, using cell-based EcR reporter assays.
AID68292Dose affording 50% of maximum transactivation for ecdysone receptor from Bombyx mori (BmEcR) and a beta-galactosidase reporter gene in HEK293 cell-line2003Bioorganic & medicinal chemistry letters, Jun-02, Volume: 13, Issue:11
Optimization of alpha-acylaminoketone ecdysone agonists for control of gene expression.
AID288191Membrane retention in permeability experiment with artificial membrane2007Bioorganic & medicinal chemistry, Jun-01, Volume: 15, Issue:11
QSAR study on permeability of hydrophobic compounds with artificial membranes.
AID1103902Toxicity against Metaseiulus occidentalis adults in bean leaf disk infested with two-spotted spider mites assessed as corrected mortality at 0.3767 g AI/L treated using worst-case laboratory exposure procedure measured after 72 hr2009Pest management science, Jun, Volume: 65, Issue:6
Effect of seven new orchard pesticides on Galendromus occidentalis in laboratory studies.
AID1110949Antifeedant activity against third-instar larval stage of Plutella xylostella (diamondback moth) infested compound-treated leaf assessed as reduction in feeding damage at 467 mg a.i/L after 48 hr by leaf disk assay relative to untreated control2009Pest management science, Sep, Volume: 65, Issue:9
Feeding cessation effects of chlorantraniliprole, a new anthranilic diamide insecticide, in comparison with several insecticides in distinct chemical classes and mode-of-action groups.
AID1112193Resistant ratio of LC50 for fourth-instar larvae of Cydia pomonella (codling moth) Holt to fourth-instar larvae of Cydia pomonella (codling moth) Glibert2012Pest management science, Jun, Volume: 68, Issue:6
Development of a rapid resistance monitoring bioassay for codling moth larvae.
AID1112184Insecticidal activity against po dosed 20 day-old larvae of Cydia pomonella (codling moth) reared on apple assessed as mortality measured after 4 days2012Pest management science, Jun, Volume: 68, Issue:6
Development of a rapid resistance monitoring bioassay for codling moth larvae.
AID1103913Ovicidal activity against Metaseiulus occidentalis eggs in bean leaf disk infested with two-spotted spider mites assessed as corrected cumulative mortality at 240 g/L SC formulation treated using worst-case laboratory exposure procedure measured after 1442009Pest management science, Jun, Volume: 65, Issue:6
Effect of seven new orchard pesticides on Galendromus occidentalis in laboratory studies.
AID506691Toxicity in zebrafish AB embryos assessed as induction of patterning deffects at 10 uM dosed every 24 hrs measured 72 hrs post fertilization2007Nature chemical biology, Mar, Volume: 3, Issue:3
Small-molecule regulation of zebrafish gene expression.
AID1081864Stomach toxicity against third-instar Plutella xylostella (diamondback moth) in compound treated fresh cabbage leaves assessed as insecticidal activity at 100 mg/L measured after 3 days by leaf-dip method2011Journal of agricultural and food chemistry, Jan-26, Volume: 59, Issue:2
Synthesis, crystal structures, insecticidal activities, and structure--activity relationships of novel N'-tert-Butyl-N'-substituted-benzoyl-N-[di(octa)hydro]benzofuran{(2,3-dihydro)benzo[1,3]([1,4])dioxine}carbohydrazide derivatives.
AID1111377Larvicidal activity against Spodoptera littoralis assessed as mortality applied topically after 1 week2010Pest management science, May, Volume: 66, Issue:5
Assessment of species specificity of moulting accelerating compounds in Lepidoptera: comparison of activity between Bombyx mori and Spodoptera littoralis by in vitro reporter and in vivo toxicity assays.
AID1081855Stomach toxicity against third-instar Mythimna separata (Oriental armyworm) in compound treated fresh corn leaves assessed as insecticidal activity at 100 mg/L measured after 4 days by leaf-dip method2011Journal of agricultural and food chemistry, Jan-26, Volume: 59, Issue:2
Synthesis, crystal structures, insecticidal activities, and structure--activity relationships of novel N'-tert-Butyl-N'-substituted-benzoyl-N-[di(octa)hydro]benzofuran{(2,3-dihydro)benzo[1,3]([1,4])dioxine}carbohydrazide derivatives.
AID1112682Insecticidal activity against Bactrocera oleae assessed as insect mortality at 96 mg Ai/L applied through residual contact on glass surfaces measured after 24 hr (Rvb = 2.0 +/- 2.0%)2013Pest management science, Jan, Volume: 69, Issue:1
Insect growth regulators as potential insecticides to control olive fruit fly (Bactrocera oleae Rossi): insect toxicity bioassays and molecular docking approach.
AID1306282Inhibition of human P-glycoprotein transfected in pig LLC-GA5-COL150 cells assessed as quinidine transport from apical to basolateral side at 30 uM preincubated for 30 mins followed by quinidine addition to apical side measured after 60 mins2016Bioorganic & medicinal chemistry, 07-15, Volume: 24, Issue:14
Structure-activity relationships of dibenzoylhydrazines for the inhibition of P-glycoprotein-mediated quinidine transport.
AID288188Permeability from apical to basolateral side of the Caco-2 cell membrane2007Bioorganic & medicinal chemistry, Jun-01, Volume: 15, Issue:11
QSAR study on permeability of hydrophobic compounds with artificial membranes.
AID1091173Stomach toxicity against Mythimna separata (Oriental armyworm) fourth-instar larvae reared on compound pre-treated corn leaves assessed as insect mortality at 5 mg/kg measured 4 days post compound treatment2008Journal of agricultural and food chemistry, Jul-09, Volume: 56, Issue:13
Synthesis and insecticidal activities of novel N-sulfenyl-N'-tert-butyl-N,N'-diacylhydrazines. 2. N-substituted phenoxysulfenate derivatives.
AID1111376Ratio of LD50 for Spodoptera littoralis to LD50 for Bombyx mori2010Pest management science, May, Volume: 66, Issue:5
Assessment of species specificity of moulting accelerating compounds in Lepidoptera: comparison of activity between Bombyx mori and Spodoptera littoralis by in vitro reporter and in vivo toxicity assays.
AID1112189Insecticidal activity against po dosed 10 day-old larvae of Chlorantraniliprole-selected Cydia pomonella (codling moth) reared on apple assessed as mortality measured after 4 days2012Pest management science, Jun, Volume: 68, Issue:6
Development of a rapid resistance monitoring bioassay for codling moth larvae.
AID1111605Agonist activity at ecdysone receptor in Drosophila melanogaster S2 cells at 100 uM after 24 hr by luciferase reporter gene assay relative to 20-hydroxyecdysone2010Pest management science, Nov, Volume: 66, Issue:11
Comparison of the activity of non-steroidal ecdysone agonists between dipteran and lepidopteran insects, using cell-based EcR reporter assays.
AID1111391Agonist activity at ecdysone receptor in Bombyx mori Bm5 cells after 24 hr by luciferase reporter gene assay2010Pest management science, May, Volume: 66, Issue:5
Assessment of species specificity of moulting accelerating compounds in Lepidoptera: comparison of activity between Bombyx mori and Spodoptera littoralis by in vitro reporter and in vivo toxicity assays.
AID1112688Insecticidal activity against Bactrocera oleae assessed as insect mortality at 96 mg Ai/L applied through oral ingestion measured after 7 days (Rvb = 2.5 +/- 2.5%)2013Pest management science, Jan, Volume: 69, Issue:1
Insect growth regulators as potential insecticides to control olive fruit fly (Bactrocera oleae Rossi): insect toxicity bioassays and molecular docking approach.
AID1111004Antifeedant activity against third-instar larval stage of Helicoverpa zea (corn earworm) infested compound-treated leaf assessed as reduction in feeding damage at 467 mg a.i/L after 48 hr by leaf disk assay relative to untreated control2009Pest management science, Sep, Volume: 65, Issue:9
Feeding cessation effects of chlorantraniliprole, a new anthranilic diamide insecticide, in comparison with several insecticides in distinct chemical classes and mode-of-action groups.
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).
AID1112187Insecticidal activity against po dosed 10 day-old larvae of Cydia pomonella (codling moth) Gilbert reared on apple assessed as mortality measured after 4 days2012Pest management science, Jun, Volume: 68, Issue:6
Development of a rapid resistance monitoring bioassay for codling moth larvae.
AID1111596Ratio of EC50 for EcR in Drosophila melanogaster S2 cells to EC50 for EcR in Bombyx mori Bm5 cells2010Pest management science, Nov, Volume: 66, Issue:11
Comparison of the activity of non-steroidal ecdysone agonists between dipteran and lepidopteran insects, using cell-based EcR reporter assays.
AID1081865Stomach toxicity against third-instar Plutella xylostella (diamondback moth) in compound treated fresh cabbage leaves assessed as insecticidal activity at 50 mg/L measured after 3 days by leaf-dip method2011Journal of agricultural and food chemistry, Jan-26, Volume: 59, Issue:2
Synthesis, crystal structures, insecticidal activities, and structure--activity relationships of novel N'-tert-Butyl-N'-substituted-benzoyl-N-[di(octa)hydro]benzofuran{(2,3-dihydro)benzo[1,3]([1,4])dioxine}carbohydrazide derivatives.
AID1110998Antifeedant activity against third-instar larval stage of Helicoverpa zea (corn earworm) infested compound-treated leaf assessed as time required to stop feeding at 467 mg a.i/L after 48 hr by leaf disk assay (Rvb = > 2880 min)2009Pest management science, Sep, Volume: 65, Issue:9
Feeding cessation effects of chlorantraniliprole, a new anthranilic diamide insecticide, in comparison with several insecticides in distinct chemical classes and mode-of-action groups.
AID1112690Insecticidal activity against Bactrocera oleae assessed as insect mortality at 96 mg Ai/L applied through oral ingestion measured after 24 hr (Rvb = 0%)2013Pest management science, Jan, Volume: 69, Issue:1
Insect growth regulators as potential insecticides to control olive fruit fly (Bactrocera oleae Rossi): insect toxicity bioassays and molecular docking approach.
AID1091172Stomach toxicity against Mythimna separata (Oriental armyworm) fourth-instar larvae reared on compound pre-treated corn leaves assessed as insect mortality at 2.5 mg/kg measured 4 days post compound treatment2008Journal of agricultural and food chemistry, Jul-09, Volume: 56, Issue:13
Synthesis and insecticidal activities of novel N-sulfenyl-N'-tert-butyl-N,N'-diacylhydrazines. 2. N-substituted phenoxysulfenate derivatives.
AID1112192Insecticidal activity against po dosed 10 day-old larvae of Cydia pomonella (codling moth) lab-s measured after 4 days2012Pest management science, Jun, Volume: 68, Issue:6
Development of a rapid resistance monitoring bioassay for codling moth larvae.
AID1112680Insecticidal activity against Bactrocera oleae assessed as insect mortality at 96 mg Ai/L applied through residual contact on glass surfaces measured after 7 days (Rvb = 4.0 +/- 4.0%)2013Pest management science, Jan, Volume: 69, Issue:1
Insect growth regulators as potential insecticides to control olive fruit fly (Bactrocera oleae Rossi): insect toxicity bioassays and molecular docking approach.
AID1081860Stomach toxicity against third-instar Spodoptera exigua in compound treated fresh cabbage leaves assessed as insecticidal activity at 100 mg/L measured after 3 days by leaf-dip method2011Journal of agricultural and food chemistry, Jan-26, Volume: 59, Issue:2
Synthesis, crystal structures, insecticidal activities, and structure--activity relationships of novel N'-tert-Butyl-N'-substituted-benzoyl-N-[di(octa)hydro]benzofuran{(2,3-dihydro)benzo[1,3]([1,4])dioxine}carbohydrazide derivatives.
AID1081861Stomach toxicity against third-instar Spodoptera exigua in compound treated fresh cabbage leaves assessed as insecticidal activity at 50 mg/L measured after 3 days by leaf-dip method2011Journal of agricultural and food chemistry, Jan-26, Volume: 59, Issue:2
Synthesis, crystal structures, insecticidal activities, and structure--activity relationships of novel N'-tert-Butyl-N'-substituted-benzoyl-N-[di(octa)hydro]benzofuran{(2,3-dihydro)benzo[1,3]([1,4])dioxine}carbohydrazide derivatives.
AID1081863Stomach toxicity against third-instar Plutella xylostella (diamondback moth) in compound treated fresh cabbage leaves assessed as insecticidal activity at 200 mg/L measured after 3 days by leaf-dip method2011Journal of agricultural and food chemistry, Jan-26, Volume: 59, Issue:2
Synthesis, crystal structures, insecticidal activities, and structure--activity relationships of novel N'-tert-Butyl-N'-substituted-benzoyl-N-[di(octa)hydro]benzofuran{(2,3-dihydro)benzo[1,3]([1,4])dioxine}carbohydrazide derivatives.
AID1110979Antifeedant activity against third-instar larval stage of Spodoptera exigua infested compound-treated leaf assessed as time required to stop feeding at 467 mg a.i/L after 48 hr by leaf disk assay (Rvb = > 2880 min)2009Pest management science, Sep, Volume: 65, Issue:9
Feeding cessation effects of chlorantraniliprole, a new anthranilic diamide insecticide, in comparison with several insecticides in distinct chemical classes and mode-of-action groups.
AID1103874Toxicity against Metaseiulus occidentalis adults in bean leaf disk infested with two-spotted spider mites assessed as average number of eggs laid (fecundity) at 0.3767 g AI/L treated using worst-case laboratory exposure procedure measured after 72 hr (Rvb2009Pest management science, Jun, Volume: 65, Issue:6
Effect of seven new orchard pesticides on Galendromus occidentalis in laboratory studies.
AID1111385Selectivity ratio of EC50 for ecdysone receptor in Bombyx mori Bm5 cells to EC50 for ecdysone receptor in Spodoptera littoralis Sl2 cells2010Pest management science, May, Volume: 66, Issue:5
Assessment of species specificity of moulting accelerating compounds in Lepidoptera: comparison of activity between Bombyx mori and Spodoptera littoralis by in vitro reporter and in vivo toxicity assays.
AID1091955Dissociation constant, pKa of the compound at pH 7.32011Journal of agricultural and food chemistry, Apr-13, Volume: 59, Issue:7
Importance of physicochemical properties for the design of new pesticides.
AID1111600Agonist activity at ecdysone receptor in Bombyx mori Bm5 cells after 24 hr by luciferase reporter gene assay2010Pest management science, Nov, Volume: 66, Issue:11
Comparison of the activity of non-steroidal ecdysone agonists between dipteran and lepidopteran insects, using cell-based EcR reporter assays.
AID1110971Antifeedant activity against third-instar larval stage of Trichoplusia ni (cabbage looper) infested compound-treated leaf assessed as time required to stop feeding at 467 mg a.i/L after 48 hr by leaf disk assay (Rvb = > 2880 min)2009Pest management science, Sep, Volume: 65, Issue:9
Feeding cessation effects of chlorantraniliprole, a new anthranilic diamide insecticide, in comparison with several insecticides in distinct chemical classes and mode-of-action groups.
AID1103880Toxicity against Metaseiulus occidentalis adults in bean leaf disk infested with two-spotted spider mites assessed as average number of eggs laid (fecundity) at 0.3767 g AI/L treated using worst-case laboratory exposure procedure measured after 48 hr (Rvb2009Pest management science, Jun, Volume: 65, Issue:6
Effect of seven new orchard pesticides on Galendromus occidentalis in laboratory studies.
AID229583Ratio of maximum level of gene expression (ecdysone receptor and beta-galactosidase receptor) of compound to maximum level of gene expression with GSTM-E expressed as RMFI2003Bioorganic & medicinal chemistry letters, Jun-02, Volume: 13, Issue:11
Optimization of alpha-acylaminoketone ecdysone agonists for control of gene expression.
AID288189Permeability from basolateral to apical side of the Caco-2 cell membrane2007Bioorganic & medicinal chemistry, Jun-01, Volume: 15, Issue:11
QSAR study on permeability of hydrophobic compounds with artificial membranes.
AID1110964Antifeedant activity against third-instar larval stage of Trichoplusia ni (cabbage looper) infested compound-treated leaf assessed as reduction in feeding damage at 467 mg a.i/L after 48 hr by leaf disk assay relative to untreated control2009Pest management science, Sep, Volume: 65, Issue:9
Feeding cessation effects of chlorantraniliprole, a new anthranilic diamide insecticide, in comparison with several insecticides in distinct chemical classes and mode-of-action groups.
AID1081856Stomach toxicity against third-instar Mythimna separata (Oriental armyworm) in compound treated fresh corn leaves assessed as insecticidal activity at 50 mg/L measured after 4 days by leaf-dip method2011Journal of agricultural and food chemistry, Jan-26, Volume: 59, Issue:2
Synthesis, crystal structures, insecticidal activities, and structure--activity relationships of novel N'-tert-Butyl-N'-substituted-benzoyl-N-[di(octa)hydro]benzofuran{(2,3-dihydro)benzo[1,3]([1,4])dioxine}carbohydrazide derivatives.
AID1091957Apparent permeability of the compound by PAMPA2011Journal of agricultural and food chemistry, Apr-13, Volume: 59, Issue:7
Importance of physicochemical properties for the design of new pesticides.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (186)

TimeframeStudies, This Drug (%)All Drugs %
pre-19904 (2.15)18.7374
1990's10 (5.38)18.2507
2000's103 (55.38)29.6817
2010's48 (25.81)24.3611
2020's21 (11.29)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 36.45

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

MetricThis Compound (vs All)
Research Demand Index36.45 (24.57)
Research Supply Index5.42 (2.92)
Research Growth Index5.36 (4.65)
Search Engine Demand Index79.51 (26.88)
Search Engine Supply Index3.00 (0.95)

This Compound (36.45)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials18 (8.74%)5.53%
Reviews2 (0.97%)6.00%
Case Studies5 (2.43%)4.05%
Observational0 (0.00%)0.25%
Other181 (87.86%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]