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新型吲哚席夫碱化合物的合成及其抗真菌活性。

Synthesis of Novel Indole Schiff Base Compounds and Their Antifungal Activities.

机构信息

College of Sciences, Henan Agricultural University, Zhengzhou 450002, China.

出版信息

Molecules. 2022 Oct 13;27(20):6858. doi: 10.3390/molecules27206858.

Abstract

A series of novel indole Schiff base derivatives (-) containing a 1,3,4-thiadiazole scaffold modified with a thioether group were synthesized, and their structures were confirmed using FT-IR, H NMR, C NMR, and HR-MS. In addition, the antifungal activity of synthesized indole derivatives was investigated against (), (, (), ), and var. ( var. ) using the mycelium growth rate method. Among the synthesized indole derivatives, compound showed the highest inhibition rates of 100%, 95.7%, 89%, and 76.5% at a concentration of 500 μg/mL against , , , and var. , respectively. Similarly, compounds and exhibited higher inhibition rates of 81.9% and 83.7% at a concentration of 500 μg/mL against . In addition, compound has been recognized as a potential compound for further investigation in the field of fungicides.

摘要

一系列新型吲哚席夫碱衍生物(-)被合成,其中含有一个噻二唑支架,并用硫醚基团进行了修饰。它们的结构通过傅里叶变换红外光谱(FT-IR)、核磁共振氢谱(H NMR)、核磁共振碳谱(C NMR)和高分辨质谱(HR-MS)得到了确认。此外,采用菌丝生长速率法,研究了合成的吲哚衍生物对()、(、(、)和(var. (var. )的抗真菌活性。在所合成的吲哚衍生物中,化合物在 500μg/mL 浓度下对、、、和 var. 的抑制率最高,分别为 100%、95.7%、89%和 76.5%。类似地,化合物和在 500μg/mL 浓度下对的抑制率也较高,分别为 81.9%和 83.7%。此外,化合物被认为是杀菌剂领域进一步研究的潜在化合物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b16c/9609699/fa27e2227181/molecules-27-06858-g001.jpg

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