Synthesis, Fungicidal, and Insecticidal Activities of β-Methoxyacrylate-Containing N-Acetyl Pyrazoline Derivatives
| Autor: | Guang-Fu Yang, Ming-Zhi Zhang, Fu Wang, Zu-Ming Liu, Wei Huang, Pei-Liang Zhao |
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| Rok vydání: | 2008 |
| Předmět: |
Insecticides
biology Stereochemistry Pyrazoline General Chemistry Pyrazoline derivatives biology.organism_classification Fungicides Industrial Fungicide Rhizoctonia solani Structure-Activity Relationship chemistry.chemical_compound Acrylates chemistry Pyrazoles Tetranychus Benzodioxoles Pharmacophore General Agricultural and Biological Sciences Sphaerotheca Botrytis cinerea |
| Zdroj: | Journal of Agricultural and Food Chemistry. 56:10767-10773 |
| ISSN: | 1520-5118 0021-8561 |
| DOI: | 10.1021/jf802343p |
| Popis: | 1-Acetyl-3,-5-diarylpyrazolines have received considerable interests from the fields of medicinal and agricultural chemistry due to their broad spectrum of biological activities. To discover new lead compounds exhibiting both fungicidal and insecticidal activities, a series of pyrazoline derivatives were designed and synthesized by introducing the beta-methoxyacrylate pharmacophore into the scaffold of 1-acetyl-3,5-diarylpyrazoline. The fungicidal activities against Pseudoperoniospora cubensis, Sphaerotheca fuliginea, Botrytis cinerea, and Rhizoctonia solani and the insecticidal activities against Aphis medicagini, Nilaparvata legen, Mythima separata, and Tetranychus cinnabarnus were screened. The most potent compound 13, 1-aceto-3-[m-[o-(E-1-methoxycarboxyl-2-methoxy)-1-yl]benzyloxy]phenyl-5-(benzo-[1,3]-dioxolyl)-4,5-dihydro- pyrazoline, was identified. Its fungicidal IC(50) values against P. cubensis and S. fuliginea are 26.6 and 57.6 microg mL(-1), respectively, while its insecticidal LC(50) value against M. separata is 26.6 microg mL(-1). These results indicated that compound 13 could be used as a lead for further developing new pyrazoline type products exhibiting both fungicidal and insecticidal activities. |
| Databáze: | OpenAIRE |
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