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Sonochemical Synthesis of 2'-Hydroxy-Chalcone Derivatives with Potential Anti-Oomycete Activity.

Identifieur interne : 000052 ( Main/Exploration ); précédent : 000051; suivant : 000053

Sonochemical 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 :

RBID : pubmed:32899705

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...)


Le document en format XML

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<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
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<b>8a</b>
had a half maximal effective concentration (EC
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