Page last updated: 2024-12-07

tebufenozide

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

Description

Tebufenozide is an insecticide that belongs to the class of insect growth regulators. It disrupts the molting process in insects by mimicking the action of the insect hormone ecdysone. Tebufenozide is a synthetic compound, originally developed by the company Rohm and Haas. It acts by interfering with the synthesis of chitin, a key component of the insect exoskeleton. This disruption prevents insects from molting properly, leading to their death. Tebufenozide is effective against a wide range of insect pests, including caterpillars, beetles, and moths. It is commonly used in agriculture and forestry to control pests that damage crops and trees. Tebufenozide has been studied extensively due to its selectivity for insect pests, meaning it has minimal impact on beneficial insects and other wildlife. It is also considered relatively safe for humans and the environment. Research continues to investigate the mechanisms of action, potential environmental impact, and development of resistance in insect populations.'

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

tebufenozide : A carbohydrazide that is hydrazine in which the amino hydrogens have been replaced by tert-butyl, 3,5-dimethylbenzoyl and 4-ethylbenzoyl groups respectively. It is an insecticide used widely against caterpillars. [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 CID91773
CHEMBL ID226968
CHEBI ID38452
SCHEMBL ID64845
MeSH IDM0218669

Synonyms (49)

Synonym
AC-12582
CHEBI:38452 ,
3,5-dimethylbenzoic acid 1-(1,1-dimethylethyl)-2-(4-ethylbenzoyl)hydrazide
112410-23-8
n-tert-butyl-n'-(4-ethylbenzoyl)-3,5-dimethylbenzohydrazide
n'-(t-butyl)-n'-(3,5-dimethylbenzoyl)-n-(4-ethylbenzoyl)hydrazine
tebufenozide
tebufenozide [iso]
benzoic acid, 3,5-dimethyl-, 1-(1,1-dimethylethyl)-2-(4-ethylbenzoyl)hydrazide
hsdb 7050
rh-5992
NCGC00142339-01
NCGC00142339-02
NCGC00142339-03
CHEMBL226968
A802573
n-tert-butyl-n'-(4-ethylbenzoyl)-3,5-dimethyl-benzohydrazide;tebufenozide
NCGC00142339-04
C18526
tox21_300685
NCGC00254593-01
dtxsid4034948 ,
dtxcid2014948
cas-112410-23-8
unii-tnn5mi5ekf
ec 412-850-3
tnn5mi5ekf ,
142583-69-5
mimic
confirm
FT-0603185
AKOS015907787
tebufenozide [hsdb]
3,5-dimethylbenzoic acid 1-(1,1-dimethylethyl)-2-(4-ethylbenzoyl)hydrazine
tebufenozide [mi]
SCHEMBL64845
KS-5034
Q-201782
QYPNKSZPJQQLRK-UHFFFAOYSA-N
tebufenozide, pestanal(r), analytical standard
tebufenozide 10 microg/ml in acetonitrile
tebufenozide 100 microg/ml in acetone
bdbm50178988
F21406
mfcd00467963
Q7692088
CS-0014147
HY-B2054
n-(tert-butyl)-n'-(4-ethylbenzoyl)-3,5-dimethylbenzohydrazide

Research Excerpts

Overview

Tebufenozide is a nonsteroid ecdysone agonist that causes premature and incomplete molting in Lepidoptera. It is considered to be safe for mammals and environmentally friendly.

ExcerptReferenceRelevance
"Tebufenozide is a nonsteroid ecdysone agonist that causes premature and incomplete molting in Lepidoptera. "( An investigation into the formation of tebufenozide's toxic aromatic amine metabolites in human in vitro hepatic microsomes.
Abass, KM, 2016
)
2.15
"Tebufenozide is a non-steroidal insect growth regulator and is extensively used to control pests, although it is considered to be safe for mammals and environmentally friendly. "( Tebufenozide induces G1/S cell cycle arrest and apoptosis in human cells.
Cao, H; Tao, L; Wang, B; Xu, W; Xu, Z; Yang, M; Yang, Y; Zhang, Y, 2017
)
3.34
"Tebufenozide is a synthetic non-steroidal ecdysone agonist insecticide and regarded as potential endocrine-disrupting chemical (EDC)."( Cloning and functional analysis of the ecdysteroid receptor complex in the opossum shrimp Neomysis integer (Leach, 1814).
Christiaens, O; Cooreman, K; De Wilde, R; Janssen, CR; Rougé, P; Smagghe, G; Soin, T; Swevers, L, 2013
)
1.11
"Tebufenozide is a nonsteroid ecdysone agonist that causes premature and incomplete molting in Lepidoptera and is used on crops and in forest spray programs. "( Effects of tebufenozide on some aspects of lake trout (Salvelinus namaycush) immune response.
Hamoutene, D; Payne, JF; Volkoff, H, 2008
)
2.18

Effects

ExcerptReferenceRelevance
"Tebufenozide has been used as a key insecticide for controlling beet armyworm, Spodoptera exigua (Hübner). "( Inheritance, fitness cost and mechanism of resistance to tebufenozide in Spodoptera exigua (Hübner) (Lepidoptera: Noctuidae).
Gao, C; Jia, B; Liu, X; Liu, Y; Shen, J; Zhu, YC, 2009
)
2.04

Treatment

ExcerptReferenceRelevance
"Tebufenozide treatments strongly reduced Lepidoptera up to 6 weeks after spraying."( Trait-mediated responses of caterpillar communities to spongy moth outbreaks and subsequent tebufenozide treatments.
Bae, S; Hahn, WA; Hebert, PDN; Heidrich, L; Hilmers, T; Hochrein, S; Jacobs, M; Kienlein, S; Kriegel, P; Kuzmina, ML; Lemme, H; Leroy, BML; Müller, J; Pretzsch, H; Püls, M; Rabl, D; Roth, N; Seibold, S; Vogel, S; Weisser, WW; Zakharov, EV, 2023
)
1.85

Toxicity

ExcerptReferenceRelevance
" The possible adverse effects of RH-5992 on nontarget aquatic organisms were studied in two test systems."( Toxicity of a new molt-inducing insecticide (RH-5992) to aquatic macroinvertebrates.
Capell, SS; Eichenberg, DC; Kreutzweiser, DP; Wainio-Keizer, KL, 1994
)
0.29
" 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
)
0.57
" 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
"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
"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

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

Methoxyfenozide exhibited greater activity than tebufenozide against codling moth eggs in dose-response bioassays. Dose-response regression lines were parallel across populations, suggesting that the resistance mechanism(s) were quantitatively, but not qualitatively, different.

ExcerptRelevanceReference
" In all these bioassays on Drosophila larvae, the two purely synthetic hydrazines exhibited similar dose-response relationships as did the natural steroid hormone, 20-hydroxyecdysone."( Effect of bisacylhydrazine ecdysteroid mimics (RH-5849 and RH-5992) on chromosomal puffing, imaginal disc proliferation and pupariation in larvae of Drosophila melanogaster.
Farkas, R; Sláma, K, 1999
)
0.3
" 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
)
0.59
" 4-n-nonylphenol contamination caused an inverted dose-response curve."( Environmental chemicals with known endocrine potential affect yolk protein content in the aquatic insect Chironomus riparius.
Hahn, T; Schenk, K; Schulz, R, 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
" Dose-response experiments revealed that RH-5992 was even more potent than 20E."( Comparative effects of a non-steroidal ecdysone agonist RH-5992 and 20-hydroxyecdysone in a lepidopteran cell line (IAL-PID2).
Auzoux-Bordenave, S; Bozzolan, F; Debernard, S; Mottier, V; Porcheron, P; Queguiner, I; Siaussat, D; Solvar, M, 2005
)
0.33
" Evidence is provided that this dose-response difference is related to whether or not an effective dose of tebufenozide is ingested by the first instar prior to the peak of moulting hormone (20-hydroxyecdysone) in first instars."( Diapause disruption with tebufenozide for early-instar control of the spruce budworm, Choristoneura fumiferana.
Arif, B; Bauce, E; Cusson, M; Doucet, D; Frisco, C; Palli, SR; Retnakaran, A; Tomkins, B, 2007
)
0.86
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (3)

RoleDescription
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.
environmental contaminantAny minor or unwanted substance introduced into the environment that can have undesired effects.
ecdysone agonistnull
[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 (1)

ClassDescription
carbohydrazideA hydrazide consisting of hydrazine carrying one or more carboacyl groups.
[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 (66)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
pregnane X receptorRattus norvegicus (Norway rat)Potency8.91250.025127.9203501.1870AID651751
RAR-related orphan receptor gammaMus musculus (house mouse)Potency64.86010.006038.004119,952.5996AID1159521; AID1159523
AR proteinHomo sapiens (human)Potency60.16580.000221.22318,912.5098AID1259243; AID1259247; AID743035; AID743042; AID743054; AID743063
estrogen receptor 2 (ER beta)Homo sapiens (human)Potency48.55770.000657.913322,387.1992AID1259378
nuclear receptor subfamily 1, group I, member 3Homo sapiens (human)Potency38.58090.001022.650876.6163AID1224838; AID1224839; AID1224893
glucocorticoid receptor [Homo sapiens]Homo sapiens (human)Potency21.87240.000214.376460.0339AID720691
retinoid X nuclear receptor alphaHomo sapiens (human)Potency61.64480.000817.505159.3239AID1159527
estrogen-related nuclear receptor alphaHomo sapiens (human)Potency36.62480.001530.607315,848.9004AID1224841; AID1224842; AID1224848; AID1224849; AID1259401; AID1259403
farnesoid X nuclear receptorHomo sapiens (human)Potency39.74110.375827.485161.6524AID743217; AID743220
pregnane X nuclear receptorHomo sapiens (human)Potency5.62340.005428.02631,258.9301AID720659
estrogen nuclear receptor alphaHomo sapiens (human)Potency58.10800.000229.305416,493.5996AID1259244; AID743069; AID743078
peroxisome proliferator-activated receptor deltaHomo sapiens (human)Potency39.81070.001024.504861.6448AID588535
thyroid stimulating hormone receptorHomo sapiens (human)Potency16.97930.001628.015177.1139AID1224843; AID1224895
nuclear factor erythroid 2-related factor 2 isoform 1Homo sapiens (human)Potency63.61690.000627.21521,122.0200AID651741; AID743202; AID743219
cytochrome P450 3A4 isoform 1Homo sapiens (human)Potency3.98110.031610.279239.8107AID884; AID885
Gamma-aminobutyric acid receptor subunit piRattus norvegicus (Norway rat)Potency3.98111.000012.224831.6228AID885
Voltage-dependent calcium channel gamma-2 subunitMus musculus (house mouse)Potency54.48270.001557.789015,848.9004AID1259244
Cellular tumor antigen p53Homo sapiens (human)Potency10.87070.002319.595674.0614AID651631
Gamma-aminobutyric acid receptor subunit beta-1Rattus norvegicus (Norway rat)Potency3.98111.000012.224831.6228AID885
Gamma-aminobutyric acid receptor subunit deltaRattus norvegicus (Norway rat)Potency3.98111.000012.224831.6228AID885
Gamma-aminobutyric acid receptor subunit gamma-2Rattus norvegicus (Norway rat)Potency3.98111.000012.224831.6228AID885
Glutamate receptor 2Rattus norvegicus (Norway rat)Potency54.48270.001551.739315,848.9004AID1259244
Gamma-aminobutyric acid receptor subunit alpha-5Rattus norvegicus (Norway rat)Potency3.98111.000012.224831.6228AID885
Gamma-aminobutyric acid receptor subunit alpha-3Rattus norvegicus (Norway rat)Potency3.98111.000012.224831.6228AID885
Gamma-aminobutyric acid receptor subunit gamma-1Rattus norvegicus (Norway rat)Potency3.98111.000012.224831.6228AID885
Gamma-aminobutyric acid receptor subunit alpha-2Rattus norvegicus (Norway rat)Potency3.98111.000012.224831.6228AID885
Gamma-aminobutyric acid receptor subunit alpha-4Rattus norvegicus (Norway rat)Potency3.98111.000012.224831.6228AID885
Gamma-aminobutyric acid receptor subunit gamma-3Rattus norvegicus (Norway rat)Potency3.98111.000012.224831.6228AID885
Gamma-aminobutyric acid receptor subunit alpha-6Rattus norvegicus (Norway rat)Potency3.98111.000012.224831.6228AID885
Gamma-aminobutyric acid receptor subunit alpha-1Rattus norvegicus (Norway rat)Potency3.98111.000012.224831.6228AID885
Gamma-aminobutyric acid receptor subunit beta-3Rattus norvegicus (Norway rat)Potency3.98111.000012.224831.6228AID885
Gamma-aminobutyric acid receptor subunit beta-2Rattus norvegicus (Norway rat)Potency3.98111.000012.224831.6228AID885
GABA theta subunitRattus norvegicus (Norway rat)Potency3.98111.000012.224831.6228AID885
Gamma-aminobutyric acid receptor subunit epsilonRattus norvegicus (Norway rat)Potency3.98111.000012.224831.6228AID885
[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)
UltraspiracleNezara viridula (southern green stink bug)IC50 (µMol)24.00000.13001.33674.5000AID1111843; AID1111844
UltraspiracleNezara viridula (southern green stink bug)Ki22.17810.10001.01673.0000AID1111829; AID1111830; AID1111831; AID1111843; AID1111844
20-hydroxy-ecdysone receptor Nezara viridula (southern green stink bug)IC50 (µMol)24.00000.13001.33674.5000AID1111843; AID1111844
20-hydroxy-ecdysone receptor Nezara viridula (southern green stink bug)Ki22.17810.10001.01673.0000AID1111829; AID1111830; AID1111831; AID1111843; AID1111844
Ecdysone receptorHeliothis virescens (tobacco budworm)Ki0.00320.00320.00320.0032AID1111841
Ecdysone receptorLucilia cuprina (Australian sheep blowfly)Ki0.15850.15850.15850.1585AID1111836
UltraspiracleChironomus tentansKi0.01000.01000.01000.0100AID1111837
Protein ultraspiracle homologChoristoneura fumiferana (eastern spruce budworm)Ki0.00050.00050.00050.0005AID1111842
20-hydroxy-ecdysone receptor Choristoneura fumiferana (eastern spruce budworm)Ki0.00050.00050.00050.0005AID1111842
ATP-dependent translocase ABCB1Homo sapiens (human)IC50 (µMol)21.50000.00022.318510.0000AID1306283
Protein ultraspiracleDrosophila melanogaster (fruit fly)Ki0.25120.25120.25120.2512AID1111835
Ecdysone receptorDrosophila melanogaster (fruit fly)Ki0.25120.25120.25120.2512AID1111835
Ecdysone receptorAedes aegypti (yellow fever mosquito)Ki0.02510.02510.02510.0251AID1111838
Ecdysone receptorChironomus tentansKi0.01000.01000.01000.0100AID1111837
Ultraspiracle Leptinotarsa decemlineata (Colorado potato beetle)Ki7.55052.51192.51192.5119AID1111832; AID1111834
20-hydroxy-ecdysone receptor Leptinotarsa decemlineata (Colorado potato beetle)Ki2.51192.51192.51192.5119AID1111834
USPPlodia interpunctella (Indianmeal moth)Ki0.00320.00320.00320.0032AID1111839
20-hydroxy-ecdysone receptor Plodia interpunctella (Indianmeal moth)Ki0.00320.00320.00320.0032AID1111839
Gene regulation proteinHeliothis virescens (tobacco budworm)Ki0.00320.00320.00320.0032AID1111841
UltraspiracleChilo suppressalis (striped riceborer)Ki0.00130.00130.00130.0013AID1111840
20-hydroxy-ecdysone receptor Chilo suppressalis (striped riceborer)Ki0.00130.00130.00130.0013AID1111840
Ultraspiracle proteinLucilia cuprina (Australian sheep blowfly)Ki0.15850.15850.15850.1585AID1111836
Ultraspiracle isoform-AAedes aegypti (yellow fever mosquito)Ki0.02510.02510.02510.0251AID1111838
[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)0.00220.00220.35121.2882AID1111388
Protein ultraspiracleDrosophila melanogaster (fruit fly)EC50 (µMol)3.56590.52484.17857.7625AID1111599; AID1111606
Ecdysone receptorDrosophila melanogaster (fruit fly)EC50 (µMol)3.56590.52484.17857.7625AID1111599; AID1111606
Ecdysone receptorBombyx mori (domestic silkworm)EC50 (µMol)0.00120.00100.11410.4365AID1111391; AID1111600
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Other Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Cytochrome P450 3A4Homo sapiens (human)Km6.80001.93005.90608.7000AID1248422
Cytochrome P450 2C19Homo sapiens (human)Km1.70001.70005.38338.7500AID1248424
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Biological Processes (161)

Processvia Protein(s)Taxonomy
negative regulation of cell population proliferationCellular tumor antigen p53Homo sapiens (human)
regulation of cell cycleCellular tumor antigen p53Homo sapiens (human)
regulation of cell cycle G2/M phase transitionCellular tumor antigen p53Homo sapiens (human)
DNA damage responseCellular tumor antigen p53Homo sapiens (human)
ER overload responseCellular tumor antigen p53Homo sapiens (human)
cellular response to glucose starvationCellular tumor antigen p53Homo sapiens (human)
intrinsic apoptotic signaling pathway in response to DNA damage by p53 class mediatorCellular tumor antigen p53Homo sapiens (human)
regulation of apoptotic processCellular tumor antigen p53Homo sapiens (human)
positive regulation of transcription by RNA polymerase IICellular tumor antigen p53Homo sapiens (human)
positive regulation of miRNA transcriptionCellular tumor antigen p53Homo sapiens (human)
negative regulation of transcription by RNA polymerase IICellular tumor antigen p53Homo sapiens (human)
mitophagyCellular tumor antigen p53Homo sapiens (human)
in utero embryonic developmentCellular tumor antigen p53Homo sapiens (human)
somitogenesisCellular tumor antigen p53Homo sapiens (human)
release of cytochrome c from mitochondriaCellular tumor antigen p53Homo sapiens (human)
hematopoietic progenitor cell differentiationCellular tumor antigen p53Homo sapiens (human)
T cell proliferation involved in immune responseCellular tumor antigen p53Homo sapiens (human)
B cell lineage commitmentCellular tumor antigen p53Homo sapiens (human)
T cell lineage commitmentCellular tumor antigen p53Homo sapiens (human)
response to ischemiaCellular tumor antigen p53Homo sapiens (human)
nucleotide-excision repairCellular tumor antigen p53Homo sapiens (human)
double-strand break repairCellular tumor antigen p53Homo sapiens (human)
regulation of DNA-templated transcriptionCellular tumor antigen p53Homo sapiens (human)
regulation of transcription by RNA polymerase IICellular tumor antigen p53Homo sapiens (human)
protein import into nucleusCellular tumor antigen p53Homo sapiens (human)
autophagyCellular tumor antigen p53Homo sapiens (human)
DNA damage responseCellular tumor antigen p53Homo sapiens (human)
DNA damage response, signal transduction by p53 class mediator resulting in cell cycle arrestCellular tumor antigen p53Homo sapiens (human)
DNA damage response, signal transduction by p53 class mediator resulting in transcription of p21 class mediatorCellular tumor antigen p53Homo sapiens (human)
transforming growth factor beta receptor signaling pathwayCellular tumor antigen p53Homo sapiens (human)
Ras protein signal transductionCellular tumor antigen p53Homo sapiens (human)
gastrulationCellular tumor antigen p53Homo sapiens (human)
neuroblast proliferationCellular tumor antigen p53Homo sapiens (human)
negative regulation of neuroblast proliferationCellular tumor antigen p53Homo sapiens (human)
protein localizationCellular tumor antigen p53Homo sapiens (human)
negative regulation of DNA replicationCellular tumor antigen p53Homo sapiens (human)
negative regulation of cell population proliferationCellular tumor antigen p53Homo sapiens (human)
determination of adult lifespanCellular tumor antigen p53Homo sapiens (human)
mRNA transcriptionCellular tumor antigen p53Homo sapiens (human)
rRNA transcriptionCellular tumor antigen p53Homo sapiens (human)
response to salt stressCellular tumor antigen p53Homo sapiens (human)
response to inorganic substanceCellular tumor antigen p53Homo sapiens (human)
response to X-rayCellular tumor antigen p53Homo sapiens (human)
response to gamma radiationCellular tumor antigen p53Homo sapiens (human)
positive regulation of gene expressionCellular tumor antigen p53Homo sapiens (human)
cardiac muscle cell apoptotic processCellular tumor antigen p53Homo sapiens (human)
positive regulation of cardiac muscle cell apoptotic processCellular tumor antigen p53Homo sapiens (human)
glial cell proliferationCellular tumor antigen p53Homo sapiens (human)
viral processCellular tumor antigen p53Homo sapiens (human)
glucose catabolic process to lactate via pyruvateCellular tumor antigen p53Homo sapiens (human)
cerebellum developmentCellular tumor antigen p53Homo sapiens (human)
negative regulation of cell growthCellular tumor antigen p53Homo sapiens (human)
DNA damage response, signal transduction by p53 class mediatorCellular tumor antigen p53Homo sapiens (human)
negative regulation of transforming growth factor beta receptor signaling pathwayCellular tumor antigen p53Homo sapiens (human)
mitotic G1 DNA damage checkpoint signalingCellular tumor antigen p53Homo sapiens (human)
negative regulation of telomere maintenance via telomeraseCellular tumor antigen p53Homo sapiens (human)
T cell differentiation in thymusCellular tumor antigen p53Homo sapiens (human)
tumor necrosis factor-mediated signaling pathwayCellular tumor antigen p53Homo sapiens (human)
regulation of tissue remodelingCellular tumor antigen p53Homo sapiens (human)
cellular response to UVCellular tumor antigen p53Homo sapiens (human)
multicellular organism growthCellular tumor antigen p53Homo sapiens (human)
positive regulation of mitochondrial membrane permeabilityCellular tumor antigen p53Homo sapiens (human)
cellular response to glucose starvationCellular tumor antigen p53Homo sapiens (human)
intrinsic apoptotic signaling pathway in response to DNA damage by p53 class mediatorCellular tumor antigen p53Homo sapiens (human)
positive regulation of apoptotic processCellular tumor antigen p53Homo sapiens (human)
negative regulation of apoptotic processCellular tumor antigen p53Homo sapiens (human)
entrainment of circadian clock by photoperiodCellular tumor antigen p53Homo sapiens (human)
mitochondrial DNA repairCellular tumor antigen p53Homo sapiens (human)
regulation of DNA damage response, signal transduction by p53 class mediatorCellular tumor antigen p53Homo sapiens (human)
positive regulation of neuron apoptotic processCellular tumor antigen p53Homo sapiens (human)
transcription initiation-coupled chromatin remodelingCellular tumor antigen p53Homo sapiens (human)
negative regulation of proteolysisCellular tumor antigen p53Homo sapiens (human)
negative regulation of DNA-templated transcriptionCellular tumor antigen p53Homo sapiens (human)
positive regulation of DNA-templated transcriptionCellular tumor antigen p53Homo sapiens (human)
positive regulation of RNA polymerase II transcription preinitiation complex assemblyCellular tumor antigen p53Homo sapiens (human)
positive regulation of transcription by RNA polymerase IICellular tumor antigen p53Homo sapiens (human)
response to antibioticCellular tumor antigen p53Homo sapiens (human)
fibroblast proliferationCellular tumor antigen p53Homo sapiens (human)
negative regulation of fibroblast proliferationCellular tumor antigen p53Homo sapiens (human)
circadian behaviorCellular tumor antigen p53Homo sapiens (human)
bone marrow developmentCellular tumor antigen p53Homo sapiens (human)
embryonic organ developmentCellular tumor antigen p53Homo sapiens (human)
positive regulation of peptidyl-tyrosine phosphorylationCellular tumor antigen p53Homo sapiens (human)
protein stabilizationCellular tumor antigen p53Homo sapiens (human)
negative regulation of helicase activityCellular tumor antigen p53Homo sapiens (human)
protein tetramerizationCellular tumor antigen p53Homo sapiens (human)
chromosome organizationCellular tumor antigen p53Homo sapiens (human)
neuron apoptotic processCellular tumor antigen p53Homo sapiens (human)
regulation of cell cycleCellular tumor antigen p53Homo sapiens (human)
hematopoietic stem cell differentiationCellular tumor antigen p53Homo sapiens (human)
negative regulation of glial cell proliferationCellular tumor antigen p53Homo sapiens (human)
type II interferon-mediated signaling pathwayCellular tumor antigen p53Homo sapiens (human)
cardiac septum morphogenesisCellular tumor antigen p53Homo sapiens (human)
positive regulation of programmed necrotic cell deathCellular tumor antigen p53Homo sapiens (human)
protein-containing complex assemblyCellular tumor antigen p53Homo sapiens (human)
intrinsic apoptotic signaling pathway in response to endoplasmic reticulum stressCellular tumor antigen p53Homo sapiens (human)
thymocyte apoptotic processCellular tumor antigen p53Homo sapiens (human)
positive regulation of thymocyte apoptotic processCellular tumor antigen p53Homo sapiens (human)
necroptotic processCellular tumor antigen p53Homo sapiens (human)
cellular response to hypoxiaCellular tumor antigen p53Homo sapiens (human)
cellular response to xenobiotic stimulusCellular tumor antigen p53Homo sapiens (human)
cellular response to ionizing radiationCellular tumor antigen p53Homo sapiens (human)
cellular response to gamma radiationCellular tumor antigen p53Homo sapiens (human)
cellular response to UV-CCellular tumor antigen p53Homo sapiens (human)
stem cell proliferationCellular tumor antigen p53Homo sapiens (human)
signal transduction by p53 class mediatorCellular tumor antigen p53Homo sapiens (human)
intrinsic apoptotic signaling pathway by p53 class mediatorCellular tumor antigen p53Homo sapiens (human)
reactive oxygen species metabolic processCellular tumor antigen p53Homo sapiens (human)
cellular response to actinomycin DCellular tumor antigen p53Homo sapiens (human)
positive regulation of release of cytochrome c from mitochondriaCellular tumor antigen p53Homo sapiens (human)
cellular senescenceCellular tumor antigen p53Homo sapiens (human)
replicative senescenceCellular tumor antigen p53Homo sapiens (human)
oxidative stress-induced premature senescenceCellular tumor antigen p53Homo sapiens (human)
intrinsic apoptotic signaling pathwayCellular tumor antigen p53Homo sapiens (human)
oligodendrocyte apoptotic processCellular tumor antigen p53Homo sapiens (human)
positive regulation of execution phase of apoptosisCellular tumor antigen p53Homo sapiens (human)
negative regulation of mitophagyCellular tumor antigen p53Homo sapiens (human)
regulation of mitochondrial membrane permeability involved in apoptotic processCellular tumor antigen p53Homo sapiens (human)
regulation of intrinsic apoptotic signaling pathway by p53 class mediatorCellular tumor antigen p53Homo sapiens (human)
positive regulation of miRNA transcriptionCellular tumor antigen p53Homo sapiens (human)
negative regulation of G1 to G0 transitionCellular tumor antigen p53Homo sapiens (human)
negative regulation of miRNA processingCellular tumor antigen p53Homo sapiens (human)
negative regulation of glucose catabolic process to lactate via pyruvateCellular tumor antigen p53Homo sapiens (human)
negative regulation of pentose-phosphate shuntCellular tumor antigen p53Homo sapiens (human)
intrinsic apoptotic signaling pathway in response to hypoxiaCellular tumor antigen p53Homo sapiens (human)
regulation of fibroblast apoptotic processCellular tumor antigen p53Homo sapiens (human)
negative regulation of reactive oxygen species metabolic processCellular tumor antigen p53Homo sapiens (human)
positive regulation of reactive oxygen species metabolic processCellular tumor antigen p53Homo sapiens (human)
negative regulation of stem cell proliferationCellular tumor antigen p53Homo sapiens (human)
positive regulation of cellular senescenceCellular tumor antigen p53Homo sapiens (human)
positive regulation of intrinsic apoptotic signaling pathwayCellular tumor antigen p53Homo sapiens (human)
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)
lipid hydroxylationCytochrome P450 3A4Homo sapiens (human)
lipid metabolic processCytochrome P450 3A4Homo sapiens (human)
steroid catabolic processCytochrome P450 3A4Homo sapiens (human)
xenobiotic metabolic processCytochrome P450 3A4Homo sapiens (human)
steroid metabolic processCytochrome P450 3A4Homo sapiens (human)
cholesterol metabolic processCytochrome P450 3A4Homo sapiens (human)
androgen metabolic processCytochrome P450 3A4Homo sapiens (human)
estrogen metabolic processCytochrome P450 3A4Homo sapiens (human)
alkaloid catabolic processCytochrome P450 3A4Homo sapiens (human)
monoterpenoid metabolic processCytochrome P450 3A4Homo sapiens (human)
calcitriol biosynthetic process from calciolCytochrome P450 3A4Homo sapiens (human)
xenobiotic catabolic processCytochrome P450 3A4Homo sapiens (human)
vitamin D metabolic processCytochrome P450 3A4Homo sapiens (human)
vitamin D catabolic processCytochrome P450 3A4Homo sapiens (human)
retinol metabolic processCytochrome P450 3A4Homo sapiens (human)
retinoic acid metabolic processCytochrome P450 3A4Homo sapiens (human)
long-chain fatty acid biosynthetic processCytochrome P450 3A4Homo sapiens (human)
aflatoxin metabolic processCytochrome P450 3A4Homo sapiens (human)
oxidative demethylationCytochrome P450 3A4Homo sapiens (human)
long-chain fatty acid metabolic processCytochrome P450 2C19Homo sapiens (human)
xenobiotic metabolic processCytochrome P450 2C19Homo sapiens (human)
steroid metabolic processCytochrome P450 2C19Homo sapiens (human)
monoterpenoid metabolic processCytochrome P450 2C19Homo sapiens (human)
epoxygenase P450 pathwayCytochrome P450 2C19Homo sapiens (human)
xenobiotic catabolic processCytochrome P450 2C19Homo sapiens (human)
omega-hydroxylase P450 pathwayCytochrome P450 2C19Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Molecular Functions (73)

Processvia Protein(s)Taxonomy
transcription cis-regulatory region bindingCellular tumor antigen p53Homo sapiens (human)
RNA polymerase II cis-regulatory region sequence-specific DNA bindingCellular tumor antigen p53Homo sapiens (human)
DNA-binding transcription factor activity, RNA polymerase II-specificCellular tumor antigen p53Homo sapiens (human)
cis-regulatory region sequence-specific DNA bindingCellular tumor antigen p53Homo sapiens (human)
core promoter sequence-specific DNA bindingCellular tumor antigen p53Homo sapiens (human)
TFIID-class transcription factor complex bindingCellular tumor antigen p53Homo sapiens (human)
DNA-binding transcription repressor activity, RNA polymerase II-specificCellular tumor antigen p53Homo sapiens (human)
DNA-binding transcription activator activity, RNA polymerase II-specificCellular tumor antigen p53Homo sapiens (human)
protease bindingCellular tumor antigen p53Homo sapiens (human)
p53 bindingCellular tumor antigen p53Homo sapiens (human)
DNA bindingCellular tumor antigen p53Homo sapiens (human)
chromatin bindingCellular tumor antigen p53Homo sapiens (human)
DNA-binding transcription factor activityCellular tumor antigen p53Homo sapiens (human)
mRNA 3'-UTR bindingCellular tumor antigen p53Homo sapiens (human)
copper ion bindingCellular tumor antigen p53Homo sapiens (human)
protein bindingCellular tumor antigen p53Homo sapiens (human)
zinc ion bindingCellular tumor antigen p53Homo sapiens (human)
enzyme bindingCellular tumor antigen p53Homo sapiens (human)
receptor tyrosine kinase bindingCellular tumor antigen p53Homo sapiens (human)
ubiquitin protein ligase bindingCellular tumor antigen p53Homo sapiens (human)
histone deacetylase regulator activityCellular tumor antigen p53Homo sapiens (human)
ATP-dependent DNA/DNA annealing activityCellular tumor antigen p53Homo sapiens (human)
identical protein bindingCellular tumor antigen p53Homo sapiens (human)
histone deacetylase bindingCellular tumor antigen p53Homo sapiens (human)
protein heterodimerization activityCellular tumor antigen p53Homo sapiens (human)
protein-folding chaperone bindingCellular tumor antigen p53Homo sapiens (human)
protein phosphatase 2A bindingCellular tumor antigen p53Homo sapiens (human)
RNA polymerase II-specific DNA-binding transcription factor bindingCellular tumor antigen p53Homo sapiens (human)
14-3-3 protein bindingCellular tumor antigen p53Homo sapiens (human)
MDM2/MDM4 family protein bindingCellular tumor antigen p53Homo sapiens (human)
disordered domain specific bindingCellular tumor antigen p53Homo sapiens (human)
general transcription initiation factor bindingCellular tumor antigen p53Homo sapiens (human)
molecular function activator activityCellular tumor antigen p53Homo sapiens (human)
promoter-specific chromatin bindingCellular tumor antigen p53Homo sapiens (human)
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)
monooxygenase activityCytochrome P450 3A4Homo sapiens (human)
steroid bindingCytochrome P450 3A4Homo sapiens (human)
iron ion bindingCytochrome P450 3A4Homo sapiens (human)
protein bindingCytochrome P450 3A4Homo sapiens (human)
steroid hydroxylase activityCytochrome P450 3A4Homo sapiens (human)
retinoic acid 4-hydroxylase activityCytochrome P450 3A4Homo sapiens (human)
oxidoreductase activityCytochrome P450 3A4Homo sapiens (human)
oxygen bindingCytochrome P450 3A4Homo sapiens (human)
enzyme bindingCytochrome P450 3A4Homo sapiens (human)
heme bindingCytochrome P450 3A4Homo sapiens (human)
vitamin D3 25-hydroxylase activityCytochrome P450 3A4Homo sapiens (human)
caffeine oxidase activityCytochrome P450 3A4Homo sapiens (human)
quinine 3-monooxygenase activityCytochrome P450 3A4Homo sapiens (human)
testosterone 6-beta-hydroxylase activityCytochrome P450 3A4Homo sapiens (human)
1-alpha,25-dihydroxyvitamin D3 23-hydroxylase activityCytochrome P450 3A4Homo sapiens (human)
anandamide 8,9 epoxidase activityCytochrome P450 3A4Homo sapiens (human)
anandamide 11,12 epoxidase activityCytochrome P450 3A4Homo sapiens (human)
anandamide 14,15 epoxidase activityCytochrome P450 3A4Homo sapiens (human)
aromatase activityCytochrome P450 3A4Homo sapiens (human)
vitamin D 24-hydroxylase activityCytochrome P450 3A4Homo sapiens (human)
estrogen 16-alpha-hydroxylase activityCytochrome P450 3A4Homo sapiens (human)
estrogen 2-hydroxylase activityCytochrome P450 3A4Homo sapiens (human)
1,8-cineole 2-exo-monooxygenase activityCytochrome P450 3A4Homo sapiens (human)
monooxygenase activityCytochrome P450 2C19Homo sapiens (human)
iron ion bindingCytochrome P450 2C19Homo sapiens (human)
steroid hydroxylase activityCytochrome P450 2C19Homo sapiens (human)
oxidoreductase activityCytochrome P450 2C19Homo sapiens (human)
(S)-limonene 6-monooxygenase activityCytochrome P450 2C19Homo sapiens (human)
(S)-limonene 7-monooxygenase activityCytochrome P450 2C19Homo sapiens (human)
oxygen bindingCytochrome P450 2C19Homo sapiens (human)
enzyme bindingCytochrome P450 2C19Homo sapiens (human)
heme bindingCytochrome P450 2C19Homo sapiens (human)
(R)-limonene 6-monooxygenase activityCytochrome P450 2C19Homo sapiens (human)
aromatase activityCytochrome P450 2C19Homo sapiens (human)
long-chain fatty acid omega-1 hydroxylase activityCytochrome P450 2C19Homo sapiens (human)
arachidonic acid epoxygenase activityCytochrome P450 2C19Homo sapiens (human)
oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygenCytochrome P450 2C19Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Ceullar Components (27)

Processvia Protein(s)Taxonomy
nuclear bodyCellular tumor antigen p53Homo sapiens (human)
nucleusCellular tumor antigen p53Homo sapiens (human)
nucleoplasmCellular tumor antigen p53Homo sapiens (human)
replication forkCellular tumor antigen p53Homo sapiens (human)
nucleolusCellular tumor antigen p53Homo sapiens (human)
cytoplasmCellular tumor antigen p53Homo sapiens (human)
mitochondrionCellular tumor antigen p53Homo sapiens (human)
mitochondrial matrixCellular tumor antigen p53Homo sapiens (human)
endoplasmic reticulumCellular tumor antigen p53Homo sapiens (human)
centrosomeCellular tumor antigen p53Homo sapiens (human)
cytosolCellular tumor antigen p53Homo sapiens (human)
nuclear matrixCellular tumor antigen p53Homo sapiens (human)
PML bodyCellular tumor antigen p53Homo sapiens (human)
transcription repressor complexCellular tumor antigen p53Homo sapiens (human)
site of double-strand breakCellular tumor antigen p53Homo sapiens (human)
germ cell nucleusCellular tumor antigen p53Homo sapiens (human)
chromatinCellular tumor antigen p53Homo sapiens (human)
transcription regulator complexCellular tumor antigen p53Homo sapiens (human)
protein-containing complexCellular tumor antigen p53Homo sapiens (human)
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)
cytoplasmCytochrome P450 3A4Homo sapiens (human)
endoplasmic reticulum membraneCytochrome P450 3A4Homo sapiens (human)
intracellular membrane-bounded organelleCytochrome P450 3A4Homo sapiens (human)
plasma membraneGamma-aminobutyric acid receptor subunit gamma-2Rattus norvegicus (Norway rat)
plasma membraneGlutamate receptor 2Rattus norvegicus (Norway rat)
endoplasmic reticulum membraneCytochrome P450 2C19Homo sapiens (human)
plasma membraneCytochrome P450 2C19Homo sapiens (human)
intracellular membrane-bounded organelleCytochrome P450 2C19Homo sapiens (human)
intracellular membrane-bounded organelleCytochrome P450 2C19Homo sapiens (human)
cytoplasmCytochrome P450 2C19Homo sapiens (human)
plasma membraneGamma-aminobutyric acid receptor subunit alpha-1Rattus norvegicus (Norway rat)
plasma membraneGamma-aminobutyric acid receptor subunit beta-2Rattus norvegicus (Norway rat)
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (137)

Assay IDTitleYearJournalArticle
AID1248416Drug metabolism in yeast cells expressing human CYP3A4 assessed as human CYP3A4-mediated metabolite-M4 formation by measuring compound production ratio at 200 uM pre-incubated for 2 mins at 37 degC before NADPH addition by LC/MS method2015Bioorganic & medicinal chemistry, Oct-15, Volume: 23, Issue:20
Identification and in silico prediction of metabolites of the model compound, tebufenozide by human CYP3A4 and CYP2C19.
AID1091174Stomach toxicity against Mythimna separata (Oriental armyworm) fourth-instar larvae reared on compound pre-treated corn leaves assessed as insect mortality at 10 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.
AID506706Activation of Bombyx mori Ecdysone receptor (amino acids 272-606) expressed in HEK293 cells transfected with cytomegalovirus promoter-driven expression construct encoding chimeric transactivator composed of DBD and homodimerization domains of yeast Gal4 (2007Nature chemical biology, Mar, Volume: 3, Issue:3
Small-molecule regulation of zebrafish gene expression.
AID1248426Selectivity index, ratio of Km for human CYP2C19-mediated metabolite-M1 formation to Km for human CYP3A4-mediated metabolite-M1 formation2015Bioorganic & medicinal chemistry, Oct-15, Volume: 23, Issue:20
Identification and in silico prediction of metabolites of the model compound, tebufenozide by human CYP3A4 and CYP2C19.
AID1111837Binding affinity to Chironomus tentans EcR2011Pest management science, Nov, Volume: 67, Issue:11
Isoforms of the heteropteran Nezara viridula ecdysone receptor: protein characterisation, RH5992 insecticide binding and homology modelling.
AID1081285Larvicidal activity against fourth-instar larval stage of Mythimna separata (Oriental armyworm) in compound-pretreated corn leaves assessed as mortality at 10 mg/l after 4 days2010Journal of agricultural and food chemistry, Feb-10, Volume: 58, Issue:3
Synthesis and insecticidal evaluation of N-tert-butyl-N'-thio[1-(6-chloro-3-pyridylmethyl)-2-nitroiminoimidazolidine]-N,N'-diacylhydrazines.
AID1248422Drug metabolism in yeast cells expressing human CYP3A4 assessed as human CYP3A4-mediated metabolite-M1 formation at 200 uM pre-incubated for 2 mins at 37 degC before NADPH addition by LC/MS method2015Bioorganic & medicinal chemistry, Oct-15, Volume: 23, Issue:20
Identification and in silico prediction of metabolites of the model compound, tebufenozide by human CYP3A4 and CYP2C19.
AID506695Activation of Bombyx mori Ecdysone receptor (amino acids 272-606) expressed in AB zebrafish embryos transfected with cytomegalovirus promoter-driven expression construct encoding chimeric transactivator composed of DBD and homodimerization domains of yeas2007Nature chemical biology, Mar, Volume: 3, Issue:3
Small-molecule regulation of zebrafish gene expression.
AID1081851Insecticidal activity against Culex pipiens pallens (mosquito) fourth-instar larvae assessed as insect mortality at 2 ug/mL measured 96 hr post compound exposure2011Journal of agricultural and food chemistry, Jan-26, Volume: 59, Issue:2
Synthesis and insecticidal activity of N-tert-butyl-N,N'-diacylhydrazines containing 1,2,3-thiadiazoles.
AID1111827Binding affinity to Myzus persicae EcR (green peach aphid)2011Pest management science, Nov, Volume: 67, Issue:11
Isoforms of the heteropteran Nezara viridula ecdysone receptor: protein characterisation, RH5992 insecticide binding and homology modelling.
AID1081284Larvicidal activity against fourth-instar larval stage of Mythimna separata (Oriental armyworm) in compound-pretreated corn leaves assessed as mortality at 5 mg/l after 4 days2010Journal of agricultural and food chemistry, Feb-10, Volume: 58, Issue:3
Synthesis and insecticidal evaluation of N-tert-butyl-N'-thio[1-(6-chloro-3-pyridylmethyl)-2-nitroiminoimidazolidine]-N,N'-diacylhydrazines.
AID1112677Insecticidal activity against Bactrocera oleae assessed as insect mortality at 180 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.
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.
AID1081853Insecticidal activity against Plutella xylostella (diamondback moth) second-instar larvae grown on compound treated fresh cabbage leaves assessed as insect mortality at 200 ug/mL measured 96 hr post compound exposure by leaf film feeding method2011Journal of agricultural and food chemistry, Jan-26, Volume: 59, Issue:2
Synthesis and insecticidal activity of N-tert-butyl-N,N'-diacylhydrazines containing 1,2,3-thiadiazoles.
AID1248424Drug metabolism in yeast cells expressing human CYP2C19 assessed as human CYP2C19-mediated metabolite-M1 formation at 200 uM pre-incubated for 2 mins at 37 degC before NADPH addition by LC/MS method2015Bioorganic & medicinal chemistry, Oct-15, Volume: 23, Issue:20
Identification and in silico prediction of metabolites of the model compound, tebufenozide by human CYP3A4 and CYP2C19.
AID1081850Insecticidal activity against Plutella xylostella (diamondback moth) second-instar larvae grown on compound treated fresh cabbage leaves assessed as insect mortality measured 96 hr post compound exposure by leaf film feeding method2011Journal of agricultural and food chemistry, Jan-26, Volume: 59, Issue:2
Synthesis and insecticidal activity of N-tert-butyl-N,N'-diacylhydrazines containing 1,2,3-thiadiazoles.
AID1111833Binding affinity to Locusta migratoria ecdysone receptor (EcR)2011Pest management science, Nov, Volume: 67, Issue:11
Isoforms of the heteropteran Nezara viridula ecdysone receptor: protein characterisation, RH5992 insecticide binding and homology modelling.
AID506705Activation of Bombyx mori Ecdysone receptor (amino acids 272-606) expressed in HEK293 cells transfected with cytomegalovirus promoter-driven expression construct encoding chimeric transactivator composed of DBD and homodimerization domains of yeast Gal4 (2007Nature chemical biology, Mar, Volume: 3, Issue:3
Small-molecule regulation of zebrafish gene expression.
AID1111844Displacement of [3H]PonA from recombinant Nezara viridula EcR112011Pest management science, Nov, Volume: 67, Issue:11
Isoforms of the heteropteran Nezara viridula ecdysone receptor: protein characterisation, RH5992 insecticide binding and homology modelling.
AID1719918Drug metabolism in microsomes containing baculovirus expressing human CYP3A4 assessed as CYP3A4-mediated hydroxylation at t-butyl group at 200 uM preincubated for 2 mins followed by NADPH addition and measured after 1 hr by LC/MS/MS analysis relative to c2020Bioorganic & medicinal chemistry, 05-01, Volume: 28, Issue:9
Identification and in silico prediction of metabolites of tebufenozide derivatives by major human cytochrome P450 isoforms.
AID506699Activation of Bombyx mori Ecdysone receptor (amino acids 272-606) expressed in AB zebrafish embryos transfected with cytomegalovirus promoter-driven expression construct encoding chimeric transactivator composed of DBD and homodimerization domains of yeas2007Nature chemical biology, Mar, Volume: 3, Issue:3
Small-molecule regulation of zebrafish gene expression.
AID1248425Drug metabolism in yeast cells expressing human CYP2C19 assessed as human CYP2C19-mediated metabolite-M1 formation per mol of protein at 200 uM pre-incubated for 2 mins at 37 degC before NADPH addition by LC/MS method2015Bioorganic & medicinal chemistry, Oct-15, Volume: 23, Issue:20
Identification and in silico prediction of metabolites of the model compound, tebufenozide by human CYP3A4 and CYP2C19.
AID506709Activation of Bombyx mori Ecdysone receptor V454I and Y474E mutant (amino acids 272-606)-mediated mylz2 gene expression expressed in AB zebrafish embryos transfected with cytomegalovirus promoter-driven expression construct encoding chimeric transactivato2007Nature chemical biology, Mar, Volume: 3, Issue:3
Small-molecule regulation of zebrafish gene expression.
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.
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.
AID506694Activation of Bombyx mori Ecdysone receptor V454I and Y474E mutant (amino acids 272-606)-mediated myl7 gene expression expressed in AB zebrafish embryos transfected with cytomegalovirus promoter-driven expression construct encoding chimeric transactivator2007Nature chemical biology, Mar, Volume: 3, Issue:3
Small-molecule regulation of zebrafish gene expression.
AID1090840Stomach toxicity against fourth-instar larval stage of Mythimna separata (Oriental armyworm) in compound-pretreated corn leaves assessed as mortality at 5 mg/kg at 25+/-1 degC measured after 4 days2007Journal of agricultural and food chemistry, Nov-14, Volume: 55, Issue:23
Synthesis and insecticidal activities of novel N-sulfenyl-N'-tert-butyl-N,N'-diacylhydrazines. 1. N-alkoxysulfenate derivatives.
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.
AID1080454Larvicidal activity against fourth-instar larval stage of Mythimna separata (Oriental armyworm) in compound-pretreated corn leaves assessed as mortality at 10 mg/kg at 25 +/-1 degC measured after 4 days2008Journal of agricultural and food chemistry, Nov-26, Volume: 56, Issue:22
Synthesis and insecticidal activities of novel N-sulfenyl-N'-tert-butyl-N,N'-diacylhydrazines. 3. N-(alkyldithio), n-(aminothio), and N,N-dithio 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.
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.
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.
AID1248415Drug metabolism in yeast cells expressing human CYP3A4 assessed as human CYP3A4-mediated metabolite-M3 formation by measuring compound production ratio at 200 uM pre-incubated for 2 mins at 37 degC before NADPH addition by LC/MS method2015Bioorganic & medicinal chemistry, Oct-15, Volume: 23, Issue:20
Identification and in silico prediction of metabolites of the model compound, tebufenozide by human CYP3A4 and CYP2C19.
AID506690Toxicity in zebrafish AB embryos assessed as induction of patterning deffects at 10 uM single dose measured 72 hrs post fertilization2007Nature chemical biology, Mar, Volume: 3, Issue:3
Small-molecule regulation of zebrafish gene expression.
AID1112683Insecticidal activity against Bactrocera oleae assessed as insect survival lifespan at 180 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.
AID1081848Insecticidal activity against Culex pipiens pallens (mosquito) fourth-instar larvae assessed as insect mortality at 0.5 ug/mL measured 96 hr post compound exposure2011Journal of agricultural and food chemistry, Jan-26, Volume: 59, Issue:2
Synthesis and insecticidal activity of N-tert-butyl-N,N'-diacylhydrazines containing 1,2,3-thiadiazoles.
AID1080450Larvicidal activity against fourth-instar larval stage of Mythimna separata (Oriental armyworm) in compound-pretreated corn leaves assessed as mortality at 30 mg/kg at 25 +/-1 degC measured after 4 days2008Journal of agricultural and food chemistry, Nov-26, Volume: 56, Issue:22
Synthesis and insecticidal activities of novel N-sulfenyl-N'-tert-butyl-N,N'-diacylhydrazines. 3. N-(alkyldithio), n-(aminothio), and N,N-dithio derivatives.
AID1111832Binding affinity to Anthonomus grandis ecdysone receptor (EcR)2011Pest management science, Nov, Volume: 67, Issue:11
Isoforms of the heteropteran Nezara viridula ecdysone receptor: protein characterisation, RH5992 insecticide binding and homology modelling.
AID1090835Contact toxicity against fourth-instar larval stage of Mythimna separata (Oriental armyworm) assessed as mortality at 25 +/-1 degC applied topically on the thoracic tergite measured per larva after 96 hr2007Journal of agricultural and food chemistry, Nov-14, Volume: 55, Issue:23
Synthesis and insecticidal activities of novel N-sulfenyl-N'-tert-butyl-N,N'-diacylhydrazines. 1. N-alkoxysulfenate derivatives.
AID1719950Drug metabolism in microsomes containing baculovirus expressing human CYP1A2 assessed as CYP1A2-mediated hydroxylation at 200 uM preincubated for 2 mins followed by NADPH addition and measured after 1 hr by LC/MS/MS analysis2020Bioorganic & medicinal chemistry, 05-01, Volume: 28, Issue:9
Identification and in silico prediction of metabolites of tebufenozide derivatives by major human cytochrome P450 isoforms.
AID1112685Insecticidal activity against Bactrocera oleae assessed as insect mortality at 180 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.
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.
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.
AID1111840Binding affinity to Chilo suppressalis (rice stem borer) EcR2011Pest management science, Nov, Volume: 67, Issue:11
Isoforms of the heteropteran Nezara viridula ecdysone receptor: protein characterisation, RH5992 insecticide binding and homology modelling.
AID1719917Drug metabolism in microsomes containing baculovirus expressing human CYP3A4 assessed as CYP3A4-mediated hydroxylation at ethyl-CH2 group of B-ring at 200 uM preincubated for 2 mins followed by NADPH addition and measured after 1 hr by LC/MS/MS analysis r2020Bioorganic & medicinal chemistry, 05-01, Volume: 28, Issue:9
Identification and in silico prediction of metabolites of tebufenozide derivatives by major human cytochrome P450 isoforms.
AID1111830Binding affinity to Nezara viridula EcR112011Pest management science, Nov, Volume: 67, Issue:11
Isoforms of the heteropteran Nezara viridula ecdysone receptor: protein characterisation, RH5992 insecticide binding and homology modelling.
AID1090832Toxic ratio of RH-5992 LD90 to compound LD90 for fourth-instar larval stage of Mythimna separata (Oriental armyworm) measured after 96 hr2007Journal of agricultural and food chemistry, Nov-14, Volume: 55, Issue:23
Synthesis and insecticidal activities of novel N-sulfenyl-N'-tert-butyl-N,N'-diacylhydrazines. 1. N-alkoxysulfenate derivatives.
AID1081849Insecticidal activity against Culex pipiens pallens (mosquito) fourth-instar larvae assessed as insect mortality at 1 ug/mL measured 96 hr post compound exposure2011Journal of agricultural and food chemistry, Jan-26, Volume: 59, Issue:2
Synthesis and insecticidal activity of N-tert-butyl-N,N'-diacylhydrazines containing 1,2,3-thiadiazoles.
AID1111603Agonist activity at ecdysone receptor in Drosophila melanogaster S2 cells at 10 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.
AID1248419Drug metabolism in yeast cells expressing human CYP2C19 assessed as human CYP2C19-mediated metabolite-M5 formation by measuring compound production ratio at 200 uM pre-incubated for 2 mins at 37 degC before NADPH addition by LC/MS method2015Bioorganic & medicinal chemistry, Oct-15, Volume: 23, Issue:20
Identification and in silico prediction of metabolites of the model compound, tebufenozide by human CYP3A4 and CYP2C19.
AID1080458Larvicidal activity against fourth-instar larval stage of Mythimna separata (Oriental armyworm) in compound-pretreated corn leaves assessed as mortality at 200 mg/kg at 25 +/-1 degC measured after 4 days2008Journal of agricultural and food chemistry, Nov-26, Volume: 56, Issue:22
Synthesis and insecticidal activities of novel N-sulfenyl-N'-tert-butyl-N,N'-diacylhydrazines. 3. N-(alkyldithio), n-(aminothio), and N,N-dithio derivatives.
AID1111836Binding affinity to Lucilia cuprina EcR2011Pest management science, Nov, Volume: 67, Issue:11
Isoforms of the heteropteran Nezara viridula ecdysone receptor: protein characterisation, RH5992 insecticide binding and homology modelling.
AID1112689Insecticidal activity against Bactrocera oleae assessed as insect mortality at 180 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.
AID1091168Contact toxicity against Ostrinia furnacalis (Asian corn borer) fourth-instar larvae exposed to compound on thoracic tergite region assessed as insect mortality measured 48 hr 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.
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.
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.
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.
AID1080457Larvicidal activity against fourth-instar larval stage of Mythimna separata (Oriental armyworm) in compound-pretreated corn leaves assessed as mortality at 100 mg/kg at 25 +/-1 degC measured after 4 days2008Journal of agricultural and food chemistry, Nov-26, Volume: 56, Issue:22
Synthesis and insecticidal activities of novel N-sulfenyl-N'-tert-butyl-N,N'-diacylhydrazines. 3. N-(alkyldithio), n-(aminothio), and N,N-dithio derivatives.
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.
AID1080453Larvicidal activity against fourth-instar larval stage of Mythimna separata (Oriental armyworm) in compound-pretreated corn leaves assessed as mortality at 5 mg/kg at 25 +/-1 degC measured after 4 days2008Journal of agricultural and food chemistry, Nov-26, Volume: 56, Issue:22
Synthesis and insecticidal activities of novel N-sulfenyl-N'-tert-butyl-N,N'-diacylhydrazines. 3. N-(alkyldithio), n-(aminothio), and N,N-dithio derivatives.
AID1091170Contact toxicity against Spodoptera litura fourth-instar larvae exposed to compound on thoracic tergite region assessed as insect mortality measured 48 hr 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.
AID1719916Drug metabolism in microsomes containing baculovirus expressing human CYP3A4 assessed as CYP3A4-mediated hydroxylation at methyl group of A-ring at 200 uM preincubated for 2 mins followed by NADPH addition and measured after 1 hr by LC/MS/MS analysis rela2020Bioorganic & medicinal chemistry, 05-01, Volume: 28, Issue:9
Identification and in silico prediction of metabolites of tebufenozide derivatives by major human cytochrome P450 isoforms.
AID1111834Binding affinity to Leptinotarsa decemlineata EcR2011Pest management science, Nov, Volume: 67, Issue:11
Isoforms of the heteropteran Nezara viridula ecdysone receptor: protein characterisation, RH5992 insecticide binding and homology modelling.
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.
AID1248417Drug metabolism in yeast cells expressing human CYP2C19 assessed as human CYP2C19-mediated metabolite-M1 formation by measuring compound production ratio at 200 uM pre-incubated for 2 mins at 37 degC before NADPH addition by LC/MS method2015Bioorganic & medicinal chemistry, Oct-15, Volume: 23, Issue:20
Identification and in silico prediction of metabolites of the model compound, tebufenozide by human CYP3A4 and CYP2C19.
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.
AID1091171Stomach toxicity against Spodoptera litura third-instar larvae reared on compound pre-treated cabbage leaves assessed as insect mortality measured 3 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.
AID1090831Toxic ratio of RH-5992 LD50 to compound LD50 for fourth-instar larval stage of Spodoptera litura measured after 48 hr2007Journal of agricultural and food chemistry, Nov-14, Volume: 55, Issue:23
Synthesis and insecticidal activities of novel N-sulfenyl-N'-tert-butyl-N,N'-diacylhydrazines. 1. N-alkoxysulfenate derivatives.
AID506697Activation of Bombyx mori Ecdysone receptor (amino acids 272-606) expressed in AB zebrafish embryos transfected with cytomegalovirus promoter-driven expression construct encoding chimeric transactivator composed of DBD and homodimerization domains of yeas2007Nature chemical biology, Mar, Volume: 3, Issue:3
Small-molecule regulation of zebrafish gene expression.
AID1248427Selectivity index, ratio of Vmax for human CYP3A4-mediated metabolite-M1 formation to Vmax for human CYP2C19-mediated metabolite-M1 formation2015Bioorganic & medicinal chemistry, Oct-15, Volume: 23, Issue:20
Identification and in silico prediction of metabolites of the model compound, tebufenozide by human CYP3A4 and CYP2C19.
AID1081281Insecticidal activity against apterous adult stage of Aphis fabae (black bean aphids) in soybean tender shoots assessed as induction of premature, abnormal and lethal larva moult at 10 mg/l treated for 5 secs measured after 3 days by modified FAO dip test2010Journal of agricultural and food chemistry, Feb-10, Volume: 58, Issue:3
Synthesis and insecticidal evaluation of N-tert-butyl-N'-thio[1-(6-chloro-3-pyridylmethyl)-2-nitroiminoimidazolidine]-N,N'-diacylhydrazines.
AID506707Activation of Bombyx mori Ecdysone receptor (amino acids 272-606) expressed in HEK293 cells transfected with cytomegalovirus promoter-driven expression construct encoding chimeric transactivator composed of DBD and homodimerization domains of yeast Gal4 (2007Nature chemical biology, Mar, Volume: 3, Issue:3
Small-molecule regulation of zebrafish gene expression.
AID1111835Binding affinity to Drosophila melanogaster EcR2011Pest management science, Nov, Volume: 67, Issue:11
Isoforms of the heteropteran Nezara viridula ecdysone receptor: protein characterisation, RH5992 insecticide binding and homology modelling.
AID1248414Drug metabolism in yeast cells expressing human CYP3A4 assessed as human CYP3A4-mediated metabolite-M1 formation by measuring compound production ratio at 200 uM pre-incubated for 2 mins at 37 degC before NADPH addition by LC/MS method2015Bioorganic & medicinal chemistry, Oct-15, Volume: 23, Issue:20
Identification and in silico prediction of metabolites of the model compound, tebufenozide by human CYP3A4 and CYP2C19.
AID1112687Insecticidal activity against Bactrocera oleae assessed as insect mortality at 180 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.
AID506692Activation of Bombyx mori Ecdysone receptor V454I and Y474E mutant (amino acids 272-606) expressed in AB zebrafish embryos transfected with cytomegalovirus promoter-driven expression construct encoding chimeric transactivator composed of DBD and homodimer2007Nature chemical biology, Mar, Volume: 3, Issue:3
Small-molecule regulation of zebrafish gene expression.
AID1090839Stomach toxicity against fourth-instar larval stage of Mythimna separata (Oriental armyworm) in compound-pretreated corn leaves assessed as mortality at 2.5 mg/kg at 25+/-1 degC measured after 4 days2007Journal of agricultural and food chemistry, Nov-14, Volume: 55, Issue:23
Synthesis and insecticidal activities of novel N-sulfenyl-N'-tert-butyl-N,N'-diacylhydrazines. 1. N-alkoxysulfenate derivatives.
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.
AID1090830Contact toxicity against fourth-instar larval stage of Ostrinia furnacalis (Asian corn borer) assessed as mortality at 25 +/-1 degC applied topically on the thoracic tergite measured per gm of larva after 48 hr2007Journal of agricultural and food chemistry, Nov-14, Volume: 55, Issue:23
Synthesis and insecticidal activities of novel N-sulfenyl-N'-tert-butyl-N,N'-diacylhydrazines. 1. N-alkoxysulfenate derivatives.
AID506708Activation of Bombyx mori Ecdysone receptor (amino acids 272-606) expressed in HEK293 cells transfected with cytomegalovirus promoter-driven expression construct encoding chimeric transactivator composed of DBD and homodimerization domains of yeast Gal4 (2007Nature chemical biology, Mar, Volume: 3, Issue:3
Small-molecule regulation of zebrafish gene expression.
AID1090838Stomach toxicity against third-instar larval stage of Spodoptera exigua in cabbage leaves assessed as mortality at 25 +/-1 degC treated for 3 secs before larval infestation measured after 3 days by leaf-dip method2007Journal of agricultural and food chemistry, Nov-14, Volume: 55, Issue:23
Synthesis and insecticidal activities of novel N-sulfenyl-N'-tert-butyl-N,N'-diacylhydrazines. 1. N-alkoxysulfenate derivatives.
AID1719922Drug metabolism in microsomes containing baculovirus expressing human CYP2D6 assessed as CYP2D6-mediated hydroxylation at ethyl-CH2 group of B-ring at 200 uM preincubated for 2 mins followed by NADPH addition and measured after 1 hr by LC/MS/MS analysis r2020Bioorganic & medicinal chemistry, 05-01, Volume: 28, Issue:9
Identification and in silico prediction of metabolites of tebufenozide derivatives by major human cytochrome P450 isoforms.
AID1248423Drug metabolism in yeast cells expressing human CYP3A4 assessed as human CYP3A4-mediated metabolite-M1 formation per mol of protein at 200 uM pre-incubated for 2 mins at 37 degC before NADPH addition by LC/MS method2015Bioorganic & medicinal chemistry, Oct-15, Volume: 23, Issue:20
Identification and in silico prediction of metabolites of the model compound, tebufenozide by human CYP3A4 and CYP2C19.
AID1090841Stomach toxicity against fourth-instar larval stage of Mythimna separata (Oriental armyworm) in compound-pretreated corn leaves assessed as mortality at 10 mg/kg at 25+/-1 degC measured after 4 days2007Journal of agricultural and food chemistry, Nov-14, Volume: 55, Issue:23
Synthesis and insecticidal activities of novel N-sulfenyl-N'-tert-butyl-N,N'-diacylhydrazines. 1. N-alkoxysulfenate derivatives.
AID1111828Binding affinity to Bemisia tabaci (sweet potato whitefly) ecdysone receptor (EcR)2011Pest management science, Nov, Volume: 67, Issue:11
Isoforms of the heteropteran Nezara viridula ecdysone receptor: protein characterisation, RH5992 insecticide binding and homology modelling.
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.
AID1080449Larvicidal activity against fourth-instar larval stage of Mythimna separata (Oriental armyworm) in compound-pretreated corn leaves assessed as mortality at 20 mg/kg at 25 +/-1 degC measured after 4 days2008Journal of agricultural and food chemistry, Nov-26, Volume: 56, Issue:22
Synthesis and insecticidal activities of novel N-sulfenyl-N'-tert-butyl-N,N'-diacylhydrazines. 3. N-(alkyldithio), n-(aminothio), and N,N-dithio derivatives.
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.
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.
AID1112679Insecticidal activity against Bactrocera oleae assessed as insect mortality at 180 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.
AID1111843Displacement of [3H]PonA from recombinant Nezara viridula EcR102011Pest management science, Nov, Volume: 67, Issue:11
Isoforms of the heteropteran Nezara viridula ecdysone receptor: protein characterisation, RH5992 insecticide binding and homology modelling.
AID506696Activation of Bombyx mori Ecdysone receptor (amino acids 272-606) expressed in AB zebrafish embryos transfected with cytomegalovirus promoter-driven expression construct encoding chimeric transactivator composed of DBD and homodimerization domains of yeas2007Nature chemical biology, Mar, Volume: 3, Issue:3
Small-molecule regulation of zebrafish gene expression.
AID1080447Toxic ratio of RH-5992 LC50 to compound LC50 for second-instar larval stage of Plutella xylostella (diamondback moth) measured after 6 days by leaf-dip method2008Journal of agricultural and food chemistry, Nov-26, Volume: 56, Issue:22
Synthesis and insecticidal activities of novel N-sulfenyl-N'-tert-butyl-N,N'-diacylhydrazines. 3. N-(alkyldithio), n-(aminothio), and N,N-dithio derivatives.
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.
AID1090828Toxic ratio of RH-5992 LD50 to compound LD50 for fourth-instar larval stage of Ostrinia furnacalis (Asian corn borer) measured after 48 hr2007Journal of agricultural and food chemistry, Nov-14, Volume: 55, Issue:23
Synthesis and insecticidal activities of novel N-sulfenyl-N'-tert-butyl-N,N'-diacylhydrazines. 1. N-alkoxysulfenate derivatives.
AID506701Activation of Bombyx mori Ecdysone receptor V454I and Y474E mutant (amino acids 272-606) expressed in AB zebrafish embryos transfected with cytomegalovirus promoter-driven expression construct encoding chimeric transactivator composed of DBD and homodimer2007Nature chemical biology, Mar, Volume: 3, Issue:3
Small-molecule regulation of zebrafish gene expression.
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.
AID1248418Drug metabolism in yeast cells expressing human CYP2C19 assessed as human CYP2C19-mediated metabolite-M2 formation by measuring compound production ratio at 200 uM pre-incubated for 2 mins at 37 degC before NADPH addition by LC/MS method2015Bioorganic & medicinal chemistry, Oct-15, Volume: 23, Issue:20
Identification and in silico prediction of metabolites of the model compound, tebufenozide by human CYP3A4 and CYP2C19.
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).
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.
AID1090827Toxic ratio of RH-5992 LD50 to compound LD50 for fourth-instar larval stage of Helicoverpa armigerameasured after 48 hr2007Journal of agricultural and food chemistry, Nov-14, Volume: 55, Issue:23
Synthesis and insecticidal activities of novel N-sulfenyl-N'-tert-butyl-N,N'-diacylhydrazines. 1. N-alkoxysulfenate derivatives.
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.
AID506704Activation of Bombyx mori Ecdysone receptor (amino acids 272-606) expressed in HEK293 cells transfected with cytomegalovirus promoter-driven expression construct encoding chimeric transactivator composed of DBD and homodimerization domains of yeast Gal4 (2007Nature chemical biology, Mar, Volume: 3, Issue:3
Small-molecule regulation of zebrafish gene expression.
AID506702Activation of Bombyx mori Ecdysone receptor V454I and Y474E mutant (amino acids 272-606) expressed in AB zebrafish embryos transfected with cytomegalovirus promoter-driven expression construct encoding chimeric transactivator composed of DBD and homodimer2007Nature chemical biology, Mar, Volume: 3, Issue:3
Small-molecule regulation of zebrafish gene expression.
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.
AID1080456Larvicidal activity against fourth-instar larval stage of Mythimna separata (Oriental armyworm) in compound-pretreated corn leaves assessed as mortality at 50 mg/kg at 25 +/-1 degC measured after 4 days2008Journal of agricultural and food chemistry, Nov-26, Volume: 56, Issue:22
Synthesis and insecticidal activities of novel N-sulfenyl-N'-tert-butyl-N,N'-diacylhydrazines. 3. N-(alkyldithio), n-(aminothio), and N,N-dithio derivatives.
AID1111599Agonist activity at ecdysone receptor in Drosophila melanogaster B2 cells assessed as reduction in cell density2010Pest 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.
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).
AID1081283Insecticidal activity against apterous adult stage of Aphis fabae ( black bean aphids) in soybean tender shoots assessed as death rate at 200 mg/l treated for 5 secs measured after 48 hr by modified FAO dip test2010Journal of agricultural and food chemistry, Feb-10, Volume: 58, Issue:3
Synthesis and insecticidal evaluation of N-tert-butyl-N'-thio[1-(6-chloro-3-pyridylmethyl)-2-nitroiminoimidazolidine]-N,N'-diacylhydrazines.
AID1112681Insecticidal activity against Bactrocera oleae assessed as insect mortality at 180 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.
AID506700Activation of Bombyx mori Ecdysone receptor (amino acids 272-606) expressed in AB zebrafish embryos transfected with cytomegalovirus promoter-driven expression construct encoding chimeric transactivator composed of DBD and homodimerization domains of yeas2007Nature chemical biology, Mar, Volume: 3, Issue:3
Small-molecule regulation of zebrafish gene expression.
AID506693Induction of nuclear translocation of Bombyx mori Ecdysone receptor V454I and Y474E mutant (amino acids 272-606) expressed in AB zebrafish embryos transfected with cytomegalovirus promoter-driven expression construct encoding chimeric transactivator compo2007Nature chemical biology, Mar, Volume: 3, Issue:3
Small-molecule regulation of zebrafish gene expression.
AID1080448Larvicidal activity against second-instar larval stage of Plutella xylostella (diamondback moth) in cabbage leaves assessed as mortality at 25 +/-1 degC treated for 15 secs before larval infestation measured after 6 days by leaf-dip method2008Journal of agricultural and food chemistry, Nov-26, Volume: 56, Issue:22
Synthesis and insecticidal activities of novel N-sulfenyl-N'-tert-butyl-N,N'-diacylhydrazines. 3. N-(alkyldithio), n-(aminothio), and N,N-dithio derivatives.
AID1111838Binding affinity to Aedes aegypti EcR2011Pest management science, Nov, Volume: 67, Issue:11
Isoforms of the heteropteran Nezara viridula ecdysone receptor: protein characterisation, RH5992 insecticide binding and homology modelling.
AID1111839Binding affinity to Plodia interpunctella (Indian meal moth ) EcR2011Pest management science, Nov, Volume: 67, Issue:11
Isoforms of the heteropteran Nezara viridula ecdysone receptor: protein characterisation, RH5992 insecticide binding and homology modelling.
AID1090837Toxic ratio of RH-5992 LC90 to compound LC90 for third-instar larval stage of Spodoptera exigua measured after 3 days by leaf-dip method2007Journal of agricultural and food chemistry, Nov-14, Volume: 55, Issue:23
Synthesis and insecticidal activities of novel N-sulfenyl-N'-tert-butyl-N,N'-diacylhydrazines. 1. N-alkoxysulfenate derivatives.
AID313184Larvicidal activity against Oriental armyworm2008Bioorganic & medicinal chemistry, Jan-01, Volume: 16, Issue:1
Synthesis and insecticidal evaluation of novel N'-tert-butyl-N'-substitutedbenzoyl-N-5-chloro-6-chromanecarbohydrazide derivatives.
AID1111842Binding affinity to Choristoneura fumiferana EcR2011Pest management science, Nov, Volume: 67, Issue:11
Isoforms of the heteropteran Nezara viridula ecdysone receptor: protein characterisation, RH5992 insecticide binding and homology modelling.
AID1080452Larvicidal activity against fourth-instar larval stage of Mythimna separata (Oriental armyworm) in compound-pretreated corn leaves assessed as mortality at 2.5 mg/kg at 25 +/-1 degC measured after 4 days2008Journal of agricultural and food chemistry, Nov-26, Volume: 56, Issue:22
Synthesis and insecticidal activities of novel N-sulfenyl-N'-tert-butyl-N,N'-diacylhydrazines. 3. N-(alkyldithio), n-(aminothio), and N,N-dithio derivatives.
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.
AID1090833Contact toxicity against fourth-instar larval stage of Spodoptera litura assessed as mortality at 25 +/-1 degC applied topically on the thoracic tergite measured per gm of larva after 48 hr2007Journal of agricultural and food chemistry, Nov-14, Volume: 55, Issue:23
Synthesis and insecticidal activities of novel N-sulfenyl-N'-tert-butyl-N,N'-diacylhydrazines. 1. N-alkoxysulfenate derivatives.
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.
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).
AID1090834Toxic ratio of RH-5992 LD50 to compound LD50 for fourth-instar larval stage of Mythimna separata (Oriental armyworm) measured after 96 hr2007Journal of agricultural and food chemistry, Nov-14, Volume: 55, Issue:23
Synthesis and insecticidal activities of novel N-sulfenyl-N'-tert-butyl-N,N'-diacylhydrazines. 1. N-alkoxysulfenate derivatives.
AID1719920Drug metabolism in microsomes containing baculovirus expressing human CYP2C9 assessed as CYP2C9-mediated hydroxylation at ethyl-CH2 group of B-ring at 200 uM preincubated for 2 mins followed by NADPH addition and measured after 1 hr by LC/MS/MS analysis r2020Bioorganic & medicinal chemistry, 05-01, Volume: 28, Issue:9
Identification and in silico prediction of metabolites of tebufenozide derivatives by major human cytochrome P450 isoforms.
AID1111829Binding affinity to Nezara viridula EcR2011Pest management science, Nov, Volume: 67, Issue:11
Isoforms of the heteropteran Nezara viridula ecdysone receptor: protein characterisation, RH5992 insecticide binding and homology modelling.
AID1090829Contact toxicity against fourth-instar larval stage of Helicoverpa armigeraassessed as mortality at 25 +/-1 degC applied topically on the thoracic tergite measured per gm of larva after 48 hr2007Journal of agricultural and food chemistry, Nov-14, Volume: 55, Issue:23
Synthesis and insecticidal activities of novel N-sulfenyl-N'-tert-butyl-N,N'-diacylhydrazines. 1. N-alkoxysulfenate derivatives.
AID506698Activation of Bombyx mori Ecdysone receptor (amino acids 272-606) expressed in AB zebrafish embryos transfected with cytomegalovirus promoter-driven expression construct encoding chimeric transactivator composed of DBD and homodimerization domains of yeas2007Nature chemical biology, Mar, Volume: 3, Issue:3
Small-molecule regulation of zebrafish gene expression.
AID1111831Binding affinity to Nezara viridula EcR102011Pest management science, Nov, Volume: 67, Issue:11
Isoforms of the heteropteran Nezara viridula ecdysone receptor: protein characterisation, RH5992 insecticide binding and homology modelling.
AID1719919Drug metabolism in microsomes containing baculovirus expressing human CYP2C9 assessed as CYP2C9-mediated hydroxylation at methyl group of A-ring at 200 uM preincubated for 2 mins followed by NADPH addition and measured after 1 hr by LC/MS/MS analysis rela2020Bioorganic & medicinal chemistry, 05-01, Volume: 28, Issue:9
Identification and in silico prediction of metabolites of tebufenozide derivatives by major human cytochrome P450 isoforms.
AID1719921Drug metabolism in microsomes containing baculovirus expressing human CYP2C19 assessed as CYP2C19-mediated hydroxylation at ethyl-CH2 group of B-ring at 200 uM preincubated for 2 mins followed by NADPH addition and measured after 1 hr by LC/MS/MS analysis2020Bioorganic & medicinal chemistry, 05-01, Volume: 28, Issue:9
Identification and in silico prediction of metabolites of tebufenozide derivatives by major human cytochrome P450 isoforms.
AID1091169Contact toxicity against Helicoverpa armigerafourth-instar larvae exposed to compound on thoracic tergite region assessed as insect mortality measured 48 hr 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.
AID506703Activation of Bombyx mori Ecdysone receptor (amino acids 272-606) expressed in HEK293 cells transfected with cytomegalovirus promoter-driven expression construct encoding chimeric transactivator composed of DBD and homodimerization domains of yeast Gal4 (2007Nature chemical biology, Mar, Volume: 3, Issue:3
Small-molecule regulation of zebrafish gene expression.
AID1090836Toxic ratio of RH-5992 LC50 to compound LC50 for third-instar larval stage of Spodoptera exigua measured after 3 days by leaf-dip method2007Journal of agricultural and food chemistry, Nov-14, Volume: 55, Issue:23
Synthesis and insecticidal activities of novel N-sulfenyl-N'-tert-butyl-N,N'-diacylhydrazines. 1. N-alkoxysulfenate derivatives.
AID1080451Larvicidal activity against fourth-instar larval stage of Mythimna separata (Oriental armyworm) in compound-pretreated corn leaves assessed as mortality at 40 mg/kg at 25 +/-1 degC measured after 4 days2008Journal of agricultural and food chemistry, Nov-26, Volume: 56, Issue:22
Synthesis and insecticidal activities of novel N-sulfenyl-N'-tert-butyl-N,N'-diacylhydrazines. 3. N-(alkyldithio), n-(aminothio), and N,N-dithio derivatives.
AID1111841Binding affinity to Heliothis virescens (tobacco budworm) EcR2011Pest management science, Nov, Volume: 67, Issue:11
Isoforms of the heteropteran Nezara viridula ecdysone receptor: protein characterisation, RH5992 insecticide binding and homology modelling.
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.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (151)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's16 (10.60)18.2507
2000's83 (54.97)29.6817
2010's43 (28.48)24.3611
2020's9 (5.96)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 39.05

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 Index39.05 (24.57)
Research Supply Index5.05 (2.92)
Research Growth Index4.79 (4.65)
Search Engine Demand Index61.15 (26.88)
Search Engine Supply Index2.18 (0.95)

This Compound (39.05)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews1 (0.65%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other154 (99.35%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]