Génesis LópezMarco MelladoEnrique WernerBastián SaidPatricio GodoyNelson CaroXimena BesoainAlejandro MadridMontenegro, IvánIvánMontenegro2025-04-132025-04-132020-09-0410.3390/antibiotics90905762-s2.0-85090625159https://cris-uv-2.scimago.es/handle/123456789/2154WOS:000581509500001This 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.enacceso abiertoBiochemistryInfectious DiseasesMicrobiologyPharmacology And PharmacyPharmacologyPharmacology, Toxicology And Pharmaceuticsarticle