Structure via PubChem · Public domain (PubChem)
Lufenuron
Sign in to saveAlso known as N-((2,5-dichloro-4-(1,1,2,3,3,3-hexafluoropropoxy)phenyl)carbamoyl)-2,6-difluorobenzamide, N-({[2,5-dichloro-4-(1,1,2,3,3,3-hexafluoropropoxy)phenyl]amino}carbonyl)-2,6-difluorobenzamide, 1-(2,5-dichloro-4-(1,1,2,3,3,3-hexafluoropropoxy)phenyl)-3-(2,6-difluorobenzoyl)urea, Fluphenacur
médicament
Chemical data
- Formula
- C17H8Cl2F8N2O3
- Molecular weight
- 511.1 g/mol
- IUPAC name
- N-[[2,5-dichloro-4-(1,1,2,3,3,3-hexafluoropropoxy)phenyl]carbamoyl]-2,6-difluorobenzamide
- SMILES
- C1=CC(=C(C(=C1)F)C(=O)NC(=O)NC2=CC(=C(C=C2Cl)OC(C(C(F)(F)F)F)(F)F)Cl)F
- InChIKey
- PWPJGUXAGUPAHP-UHFFFAOYSA-N
- XLogP
- 6.4
- Polar surface area
- 67.4 Ų
- H-bond donors
- 2
- H-bond acceptors
- 11
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Max clinical phase
- Phase 2
- Molecule type
- Small molecule
via ChEMBL · EBI
Research
284 papers- Dissecting the manipulation of lufenuron on chitin synthesis in Helicoverpa armigera.Pesticide biochemistry and physiology · 2024
- Amlodipine and lufenuron as repurposing drugs against Sporothrix brasiliensis.PeerJ · 2023
- EVALUATING BAITS WITH LUFENURON AND NITENPYRAM FOR FLEA CONTROL ON PRAIRIE DOGS (CYNOMYS SPP.) TO MITIGATE PLAGUE.Journal of wildlife diseases · 2023
- Detection of Chitin Synthase Mutations in Lufenuron-Resistant Spodoptera frugiperda in China.Insects · 2022
- Effects of lufenuron treatments on the growth and development of Spodoptera frugiperda (Lepidoptera: Noctuidae).Comparative biochemistry and physiology. Toxicology & pharmacology : CBP · 2023
via PubMed
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 509.978
- Has use
- insecticide
Show 3 more facts
- chemical formula
- C₁₇H₈Cl₂F₈N₂O₃
- canonical SMILES
- C1=CC(=C(C(=C1)F)C(=O)NC(=O)NC2=CC(=C(C=C2Cl)OC(C(C(F)(F)F)F)(F)F)Cl)F
- Commons category
- Lufenuron
via Wikidata · CC0
Article · Français
La lufénurone (DCI) est un composé qui appartient à la famille des benzoylurées. La substance active lufénurone du médicament vétérinaire appartient au groupe des inhibiteurs du développement des insectes (IDI). Elle inhibe la synthèse de la chitine et est utilisée pour détruire les larves d'insectes et certains champignons.
Abstract from DBpedia / Wikipedia · CC BY-SA