Structure via PubChem · Public domain (PubChem)
Resmethrin
Sign in to saveAlso known as (5-(Phenylmethyl)-3-furanyl)methyl 2,2-dimethyl-3-(2-methyl-1-propenyl)cyclopropanecarboxylate, 5-Benzyl-3-furylmethyl (1RS,3RS;1RS,3SR)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropanecarboxylate, 5-Benzyl-3-furylmethyl (+-)-cis,trans-chrysanthemate
Gruppe von Stereoisomeren
Chemical data
- Formula
- C22H26O3
- Molecular weight
- 338.4 g/mol
- IUPAC name
- (5-benzylfuran-3-yl)methyl 2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate
- SMILES
- CC(=CC1C(C1(C)C)C(=O)OCC2=COC(=C2)CC3=CC=CC=C3)C
- InChIKey
- VEMKTZHHVJILDY-UHFFFAOYSA-N
- XLogP
- 6.1
- Polar surface area
- 39.4 Ų
- H-bond donors
- 0
- H-bond acceptors
- 3
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Molecule type
- Small molecule
via ChEMBL · EBI
Research
163 papers- Resmethrin, the first modern pyrethroid insecticide.Pest management science · 2015
- Resmethrin disrupts mitochondria-associated membranes and activates endoplasmic reticulum stress, leading to proliferation inhibition in cultured mouse Leydig and Sertoli cells.Pesticide biochemistry and physiology · 2024
- Evaluation of Resmethrin Toxicity to Neonatal Testes in Organ Culture.Toxicological sciences : an official journal of the Society of Toxicology · 2020
- Resmethrin induces implantation failure by disrupting calcium homeostasis and forcing mitochondrial defects in porcine trophectoderm and uterine luminal epithelial cells.The Science of the total environment · 2024
- Case Report: Fatal Neurotoxicity Following Resmethrin Poisoning in a Child.Frontiers in pediatrics · 2021
via PubMed
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 338.188
- Has use
- insecticide
Show 4 more facts
- chemical formula
- C₂₂H₂₆O₃
- canonical SMILES
- CC(=CC1C(C1(C)C)C(=O)OCC2=COC(=C2)CC3=CC=CC=C3)C
- subject has role
- carcinogen
- Commons category
- Resmethrin
via Wikidata · CC0
Article · Deutsch
Resmethrin ist ein Pflanzenschutzmittel aus der Gruppe der Pyrethroide. Es ist ein Gemisch aus vier Stereoisomeren; eines davon ist das (R,R)-Isomer, als Bioresmethrin bekannt. Es wurde in den 1960er Jahren von der Gruppe von Michael Elliott (Rothamsted Research) entwickelt.
Abstract from DBpedia / Wikipedia · CC BY-SA
Available in 9 languages
via Wikidata sitelinks · CC0