Synthesis of paeonol ester derivatives and their insecticidal, nematicidal, and anti-oomycete activities.
Paeonia suffruticosa
botanical pesticide
paeonol
pesticidal activity
structural modification
Journal
Pest management science
ISSN: 1526-4998
Titre abrégé: Pest Manag Sci
Pays: England
ID NLM: 100898744
Informations de publication
Date de publication:
Aug 2022
Aug 2022
Historique:
revised:
06
04
2022
received:
25
01
2022
accepted:
14
05
2022
pubmed:
15
5
2022
medline:
16
7
2022
entrez:
14
5
2022
Statut:
ppublish
Résumé
Paeonol is extracted and isolated as a rich and sustainable natural bioresource from the root bark of Paeonia suffruticosa, the derivatives of which exhibit numerous biological activities. It is well known that ester compounds play a very important role in pest control, such as organophosphorus, carbamate and pyrethroid pesticides. To discover biorational natural product-based pesticides, three series of (60) paeonol ester derivatives (7a-t, 8g,p, 9g,p, 10g-j,n-u, 11g,u, 12g,u, 13a-p, 14b,c, and 15b,c) were prepared by structural modification of paeonol, and their structures were well characterized by proton nuclear magnetic resonance ( This study suggested that the introduction of a nitro at the C5 or C3 position of paeonol could improve its bioactivity against M. separata, H. glycines, and Phytophthora capsici. © 2022 Society of Chemical Industry.
Sections du résumé
BACKGROUND
BACKGROUND
Paeonol is extracted and isolated as a rich and sustainable natural bioresource from the root bark of Paeonia suffruticosa, the derivatives of which exhibit numerous biological activities. It is well known that ester compounds play a very important role in pest control, such as organophosphorus, carbamate and pyrethroid pesticides.
RESULTS
RESULTS
To discover biorational natural product-based pesticides, three series of (60) paeonol ester derivatives (7a-t, 8g,p, 9g,p, 10g-j,n-u, 11g,u, 12g,u, 13a-p, 14b,c, and 15b,c) were prepared by structural modification of paeonol, and their structures were well characterized by proton nuclear magnetic resonance (
CONCLUSION
CONCLUSIONS
This study suggested that the introduction of a nitro at the C5 or C3 position of paeonol could improve its bioactivity against M. separata, H. glycines, and Phytophthora capsici. © 2022 Society of Chemical Industry.
Substances chimiques
Acetophenones
0
Antinematodal Agents
0
Esters
0
Insecticides
0
Pesticides
0
paeonol
3R834EPI82
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
3442-3455Subventions
Organisme : Young Teacher Funding Program of the Henan Higher School
Organisme : National Natural Science Foundation of China
Informations de copyright
© 2022 Society of Chemical Industry.
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