CHEBI:38452 - tebufenozide

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ChEBI Name tebufenozide
ChEBI ID CHEBI:38452
Definition A carbohydrazide that is hydrazine in which the amino hydrogens have been replaced by tert-butyl, 3,5-dimethylbenzoyl and 4-ethylbenzoyl groups respectively.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.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C22H28N2O2
Net Charge 0
Average Mass 352.47000
Monoisotopic Mass 352.21508
InChI InChI=1S/C22H28N2O2/c1-7-17-8-10-18(11-9-17)20(25)23-24(22(4,5)6)21(26)19-13-15(2)12-16(3)14-19/h8-14H,7H2,1-6H3,(H,23,25)
InChIKey QYPNKSZPJQQLRK-UHFFFAOYSA-N
SMILES CCc1ccc(cc1)C(=O)NN(C(=O)c1cc(C)cc(C)c1)C(C)(C)C
Roles Classification
Chemical Role(s): environmental contaminant
Any minor or unwanted substance introduced into the environment that can have undesired effects.
Biological Role(s): ecdysone agonist

xenobiotic
A 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.
Application(s): ecdysone agonist

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ChEBI Ontology
Outgoing tebufenozide (CHEBI:38452) has functional parent N'-benzoyl-N-(tert-butyl)benzohydrazide (CHEBI:38457)
tebufenozide (CHEBI:38452) has role ecdysone agonist (CHEBI:38456)
tebufenozide (CHEBI:38452) has role environmental contaminant (CHEBI:78298)
tebufenozide (CHEBI:38452) has role xenobiotic (CHEBI:35703)
tebufenozide (CHEBI:38452) is a carbohydrazide (CHEBI:35363)
IUPAC Name
N-tert-butyl-N'-(4-ethylbenzoyl)-3,5-dimethylbenzohydrazide
Synonyms Sources
3,5-dimethylbenzoic acid 1-(1,1-dimethylethyl)-2-(4-ethylbenzoyl)hydrazide ChemIDplus
N'-(t-butyl)-N'-(3,5-dimethylbenzoyl)-N-(4-ethylbenzoyl)hydrazine ChemIDplus
tebufenozide ChemIDplus
Manual Xrefs Databases
611 PPDB
C18526 KEGG COMPOUND
CN103553255 Patent
CN103766364 Patent
tebufenozide Alan Wood's Pesticides
Tebufenozide Wikipedia
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Registry Numbers Types Sources
112410-23-8 CAS Registry Number KEGG COMPOUND
112410-23-8 CAS Registry Number ChemIDplus
7822297 Reaxys Registry Number Reaxys
7822297 Beilstein Registry Number Beilstein
Citations Waiting for Citations Types Sources
14745824 PubMed citation Europe PMC
15759403 PubMed citation Europe PMC
22730139 PubMed citation Europe PMC
24121094 PubMed citation Europe PMC
Last Modified
14 November 2014