Sonochemical Synthesis of 2'-Hydroxy-Chalcone Derivatives with Potential Anti-Oomycete Activity.
Identifieur interne : 000052 ( Main/Exploration ); précédent : 000051; suivant : 000053Sonochemical Synthesis of 2'-Hydroxy-Chalcone Derivatives with Potential Anti-Oomycete Activity.
Auteurs : Génesis L Pez [Chili] ; Marco Mellado [Chili] ; Enrique Werner [Chili] ; Bastián Said [Chili] ; Patricio Godoy [Chili] ; Nelson Caro [Chili] ; Ximena Besoain [Chili] ; Iván Montenegro [Chili] ; Alejandro Madrid [Chili]Source :
- Antibiotics (Basel, Switzerland) [ 2079-6382 ] ; 2020.
Abstract
This work reports on the synthesis of eight new 2'-hydroxy-chalcones with potential anti-phytopathogenic applications in agroindustry, among others, via Claisen-Schmidt condensation and ultrasound assisted reaction. Assays showed three chalcones with allyl moieties strongly inhibited growth of phytopathogenic oomycete Phytophthora infestans; moreover, compound 8a had a half maximal effective concentration (EC50) value (32.5 µg/mL) similar to that of metalaxyl (28.6 µg/mL). A software-aided quantitative structure-activity relationship (QSAR) analysis of the whole series suggests that the structural features of these new chalcones-namely, the fluoride, hydroxyl, and amine groups over the carbon 3' of the chalcone skeleton-increase anti-oomycete activity.
DOI: 10.3390/antibiotics9090576
PubMed: 32899705
PubMed Central: PMC7560025
Affiliations:
Links toward previous steps (curation, corpus...)
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<front><div type="abstract" xml:lang="en">This work reports on the synthesis of eight new 2'-hydroxy-chalcones with potential anti-phytopathogenic applications in agroindustry, among others, via Claisen-Schmidt condensation and ultrasound assisted reaction. Assays showed three chalcones with allyl moieties strongly inhibited growth of phytopathogenic oomycete <i>Phytophthora infestans</i>
; moreover, compound <b>8a</b>
had a half maximal effective concentration (EC<sub>50</sub>
) value (32.5 µg/mL) similar to that of metalaxyl (28.6 µg/mL). A software-aided quantitative structure-activity relationship (QSAR) analysis of the whole series suggests that the structural features of these new chalcones-namely, the fluoride, hydroxyl, and amine groups over the carbon 3' of the chalcone skeleton-increase anti-oomycete activity.</div>
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; moreover, compound <b>8a</b>
had a half maximal effective concentration (EC<sub>50</sub>
) value (32.5 µg/mL) similar to that of metalaxyl (28.6 µg/mL). A software-aided quantitative structure-activity relationship (QSAR) analysis of the whole series suggests that the structural features of these new chalcones-namely, the fluoride, hydroxyl, and amine groups over the carbon 3' of the chalcone skeleton-increase anti-oomycete activity.</AbstractText>
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<affiliations><list><country><li>Chili</li>
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