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Synthesis of Novel Indole Schiff Base Compounds and Their Antifungal Activities

A series of novel indole Schiff base derivatives (2a–2t) containing a 1,3,4-thiadiazole scaffold modified with a thioether group were synthesized, and their structures were confirmed using FT-IR, (1)H NMR, (13)C NMR, and HR-MS. In addition, the antifungal activity of synthesized indole derivatives w...

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Detalles Bibliográficos
Autores principales: Wang, Caixia, Fan, Liangxin, Pan, Zhenliang, Fan, Sufang, Shi, Lijun, Li, Xu, Zhao, Jinfang, Wu, Lulu, Yang, Guoyu, Xu, Cuilian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9609699/
https://www.ncbi.nlm.nih.gov/pubmed/36296452
http://dx.doi.org/10.3390/molecules27206858
Descripción
Sumario:A series of novel indole Schiff base derivatives (2a–2t) containing a 1,3,4-thiadiazole scaffold modified with a thioether group were synthesized, and their structures were confirmed using FT-IR, (1)H NMR, (13)C NMR, and HR-MS. In addition, the antifungal activity of synthesized indole derivatives was investigated against Fusarium graminearum (F. graminearum), Fusarium oxysporum (F. oxysporum), Fusarium moniliforme (F. moniliforme), Curvularia lunata (C. lunata), and Phytophthora parasitica var. nicotiana (P. p. var. nicotianae) using the mycelium growth rate method. Among the synthesized indole derivatives, compound 2j showed the highest inhibition rates of 100%, 95.7%, 89%, and 76.5% at a concentration of 500 μg/mL against F. graminearum, F. oxysporum, F. moniliforme, and P. p. var. nicotianae, respectively. Similarly, compounds 2j and 2q exhibited higher inhibition rates of 81.9% and 83.7% at a concentration of 500 μg/mL against C. lunata. In addition, compound 2j has been recognized as a potential compound for further investigation in the field of fungicides.