LAUSR.org creates dashboard-style pages of related content for over 1.5 million academic articles. Sign Up to like articles & get recommendations!

Structure-activity relationships of cinnamaldehyde and eugenol derivatives against plant pathogenic fungi

Photo from wikipedia

Abstract Rhizoctonia solani and Fusarium oxysporum are very well known phytopathogens with worldwide spread that cause one of the most destructive diseases, resulting significant yield losses in crop production. In… Click to show full abstract

Abstract Rhizoctonia solani and Fusarium oxysporum are very well known phytopathogens with worldwide spread that cause one of the most destructive diseases, resulting significant yield losses in crop production. In order to find effective fungicides for controlling phytopathogen, the structure-activity relationships of cinnamaldehyde and eugenol derivatives against R. solani and F. oxysporum were evaluated. Additionally, the composition and fungicidal activity of Cinnamomum cassia and Syzygium aromatica essential oils was assessed. Cinnamaldehyde (49.75%) is the major compound in cinnamon bark oil, and eugenol (89.17%) is most abundant in clove bud oil. The clove bud oil exhibited good antifungal activities against R. solani and F. oxysporum (IC50 = 106.5 and 149.9 μg/mL, respectively). Cinnamon bark oil showed a lower activity than clove bud oil. The fungicidal activity of cinnamaldehyde (IC50 = 75.4 and 156.9 μg/mL, respectively) and eugenol (IC50 = 58.9 and 52.9 μg/mL, respectively) against R. solani and F. oxysporum was also evalutated. Comparisons of the antifungal activities of cinnamaldehyde and eugenol derivatives revealed that α-methylcinnamaldehyde, α-methylcinnamic acid, methyleugenol, acetyleugenol, isoeugenol, methylisoeugenol, and acetylisoeugenol showed good antifungal activities against R. solani and F. oxysporum. In structure-activity relationships, the fungicidal activity of cinnamaldehyde derivatives could be related to conjugated double bond and the length of CH chain outside the ring. In addition, the presence of the lipophilicity may have a considerable influence on the toxicity of phenylpropenes. The present approach may help future work in the search for fungicidal compounds.

Keywords: activity relationships; cinnamaldehyde eugenol; eugenol derivatives; structure activity; activity

Journal Title: Industrial Crops and Products
Year Published: 2017

Link to full text (if available)


Share on Social Media:                               Sign Up to like & get
recommendations!

Related content

More Information              News              Social Media              Video              Recommended



                Click one of the above tabs to view related content.