Page last updated: 2024-12-07

rh-0345

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

Description

N-4-chlorobenzoyl-N'-benzoyl-N'-tert-butylhydrazine: structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID114994
CHEMBL ID226969
CHEBI ID38451
SCHEMBL ID55120
MeSH IDM0465088

Synonyms (43)

Synonym
4-chlorobenzoic acid 2-benzoyl-2-(1,1-dimethylethyl)hydrazide
112226-61-6
n'-benzoyl-n'-tert-butyl-4-chlorobenzohydrazide
CHEBI:38451 ,
halofenozide
benzoic acid, 4-chloro-, 2-benzoyl-2-(1,1-dimethylethyl)hydrazide
rh 0345
halofenozide [iso]
NCGC00163832-01
CHEMBL226969
n-(1,6-dihydro-6-oxopurin-2-yl)-benzamide
C18791
dtxcid2012619
NCGC00256749-01
cas-112226-61-6
tox21_302655
dtxsid4032619 ,
n-4-chlorobenzoyl-n'-benzoyl-n'-tert-butylhydrazine
unii-c81k20pelv
rh0345
rh-0345
hsdb 7949
benzoic acid, n-tert-butyl-n'-(4-chlorobenzoyl)hydrazide
ec 431-600-4
n'-benzoyl-4-chloro-n'-(2-methyl-2-propanyl)benzohydrazide
c81k20pelv ,
FT-0631061
mach 2
rg 100864
mach 2 (dow agrosci.)
n-tert-butyl-n'-(4-chlorobenzoyl)benzohydrazide
halofenozide [mi]
SCHEMBL55120
CNKHSLKYRMDDNQ-UHFFFAOYSA-N
n'-tert-butyl-n-(4-chlorobenzoyl)-n'-benzoylhydrazine
halofenozide, analytical standard
mfcd03158909
bdbm50488461
Q27117858
n'-benzoyl-n'-(tert-butyl)-4-chlorobenzohydrazide
AKOS037515578
HY-113890
CS-0063255

Research Excerpts

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
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (2)

ClassDescription
bisacylhydrazine insecticide
monochlorobenzenesAny member of the class of chlorobenzenes containing a mono- or poly-substituted benzene ring in which only one substituent is chlorine.
[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 (13)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
pregnane X receptorRattus norvegicus (Norway rat)Potency44.66840.025127.9203501.1870AID651751
GLI family zinc finger 3Homo sapiens (human)Potency38.33560.000714.592883.7951AID1259392
AR proteinHomo sapiens (human)Potency43.38500.000221.22318,912.5098AID743063
estrogen-related nuclear receptor alphaHomo sapiens (human)Potency35.48800.001530.607315,848.9004AID1224848; AID1224849; AID1259403
pregnane X nuclear receptorHomo sapiens (human)Potency35.13080.005428.02631,258.9301AID1346982; AID720659
vitamin D (1,25- dihydroxyvitamin D3) receptorHomo sapiens (human)Potency0.00200.023723.228263.5986AID588543
thyroid stimulating hormone receptorHomo sapiens (human)Potency22.41750.001628.015177.1139AID1224843; AID1224895
thyroid hormone receptor beta isoform aHomo sapiens (human)Potency0.39810.010039.53711,122.0200AID588547
thyroid hormone receptor beta isoform 2Rattus norvegicus (Norway rat)Potency35.44260.000323.4451159.6830AID743065; AID743067
[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)0.45710.00220.35121.2882AID1111388
Protein ultraspiracleDrosophila melanogaster (fruit fly)EC50 (µMol)7.76250.52484.17857.7625AID1111606
Ecdysone receptorDrosophila melanogaster (fruit fly)EC50 (µMol)7.76250.52484.17857.7625AID1111606
Ecdysone receptorBombyx mori (domestic silkworm)EC50 (µMol)0.08240.00100.11410.4365AID1111391; AID1111600
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (32)

Assay IDTitleYearJournalArticle
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.
AID1111605Agonist activity at ecdysone receptor in Drosophila melanogaster S2 cells at 100 uM after 24 hr by luciferase reporter gene assay relative to 20-hydroxyecdysone2010Pest management science, Nov, Volume: 66, Issue:11
Comparison of the activity of non-steroidal ecdysone agonists between dipteran and lepidopteran insects, using cell-based EcR reporter assays.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
AID1091176Stomach toxicity against Mythimna separata (Oriental armyworm) fourth-instar larvae reared on compound pre-treated corn leaves assessed as insect mortality at 50 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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (28)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's17 (60.71)29.6817
2010's8 (28.57)24.3611
2020's3 (10.71)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 19.39

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be moderate demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index19.39 (24.57)
Research Supply Index3.40 (2.92)
Research Growth Index5.85 (4.65)
Search Engine Demand Index13.88 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (19.39)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews1 (3.45%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other28 (96.55%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]