Design, Synthesis, and Insecticidal Activity of Novel Doramectin Derivatives Containing Acylurea and Acylthiourea Based on Hydrogen Bonding.
acylthiourea
acylurea
corn borer
diamondback moth
insecticidal activities
molecular docking
oriental armyworm
Journal
Journal of agricultural and food chemistry
ISSN: 1520-5118
Titre abrégé: J Agric Food Chem
Pays: United States
ID NLM: 0374755
Informations de publication
Date de publication:
27 May 2020
27 May 2020
Historique:
pubmed:
2
5
2020
medline:
8
1
2021
entrez:
2
5
2020
Statut:
ppublish
Résumé
Our recent investigation on the insecticidal activities of several doramectin derivatives preliminarily revealed that the presence of hydrogen bonds at the C4″ position of the molecule with target protein γ-aminobutyric acid (GABA) receptor was crucial for retaining high insecticidal activity. As a continuation of our research work on the development of new insecticides, two series of novel acylurea and acylthiourea doramectin derivatives were designed and synthesized. The bioassay results indicated that the newly synthesized compounds (
Identifiants
pubmed: 32356977
doi: 10.1021/acs.jafc.0c00230
doi:
Substances chimiques
Insecticides
0
Ivermectin
70288-86-7
Thiourea
GYV9AM2QAG
doramectin
KGD7A54H5P
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM