Structure via PubChem · Public domain (PubChem)
chlorantraniliprole
Sign in to saveAlso known as DPX-E2Y45, 3-bromo-N-{4-chloro-2-methyl-6-[(methylamino)carbonyl]phenyl}-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxamide
Chlorantraniliprole is an insecticide of the diamide class used for insects found on fruit and vegetable crops as well as ornamental plants.
Chemical data
- Formula
- C18H14BrCl2N5O2
- Molecular weight
- 483.1 g/mol
- IUPAC name
- 3-bromo-N-[4-chloro-2-methyl-6-(methylcarbamoyl)phenyl]-1-(3-chloro-2-pyridinyl)pyrazole-5-carboxamide
- SMILES
- CC1=CC(=CC(=C1NC(=O)C2=CC(=NN2C3=C(C=CC=N3)Cl)Br)C(=O)NC)Cl
- InChIKey
- PSOVNZZNOMJUBI-UHFFFAOYSA-N
- XLogP
- 4.8
- Polar surface area
- 88.9 Ų
- H-bond donors
- 2
- H-bond acceptors
- 4
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Molecule type
- Small molecule
via ChEMBL · EBI
Research
1,003 papers- Chlorantraniliprole in foods: Determination, dissipation and decontamination.Food chemistry · 2023
- Sublethal effects of chlorantraniliprole on growth, biochemical and molecular parameters in two chironomids, Chironomus kiiensis and Chironomus javanus.Ecotoxicology and environmental safety · 2023
- Potential health risk analysis of chlorantraniliprole in vivo.Science bulletin · 2023
- Chlorantraniliprole Resistance in Spodoptera frugiperda: Resistance Monitoring, Resistance Risk, and Resistance Mechanisms.Journal of agricultural and food chemistry · 2024
- Chlorantraniliprole resistance associated with diamondback moth (Lepidoptera: Plutellidae) outbreaks in Arizona Brassica crops.Journal of economic entomology · 2024
via PubMed
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 480.970792
- Has use
- insecticide
Show 3 more facts
- canonical SMILES
- CC1=C(C(=CC(=C1)Cl)C(=O)NC)NC(=O)C2=CC(=NN2C3=C(C=CC=N3)Cl)Br
- chemical formula
- C₁₈H₁₄BrCl₂N₅O₂
- Commons category
- Chlorantraniliprole
Sources (2)
via Wikidata · CC0
~1 min read
Encyclopedic overview
1 sectionsContents
- References
Chlorantraniliprole is an insecticide of the diamide class used for insects found on fruit and vegetable crops as well as ornamental plants.
Chlorantraniliprole opens muscular calcium channels, in particular the ryanodine receptor, rapidly causing paralysis and ultimately death of sensitive species (IRAC class 28). The differential selectivity chlorantraniliprole has towards insect ryanodine receptors explains its low mammalian toxicity receptor. Chlorantraniliprole is active on chewing pest insects primarily by ingestion and secondarily by contact.
Excerpted from Wikipedia’s “chlorantraniliprole” article, available under the CC BY-SA 4.0 licence.