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首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Design, synthesis and antifungal activities of novel pyrrole alkaloid analogs.
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Design, synthesis and antifungal activities of novel pyrrole alkaloid analogs.

机译:新型吡咯生物碱类似物的设计,合成和抗真菌活性。

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摘要

A series of novel analogs of pyrrole alkaloid were designed and synthesized by a facile method and their structures were characterized by 1H NMR, 13C NMR and high-resolution mass spectrometry (HRMS). The structure of compound 2a was identified by 2D NMR including heteronuclear multiple-quantum coherence (HMQC), heteronuclear multiple-bond correlation (HMBC) and H-H correlation spectrometry (H-H COSY) spectra. Their antifungal activities against five fungi were evaluated, and the results indicated that some of the title compounds showed moderate fungicidal activities in vitro against Alternaria solani, Cercospora arachidicola, Fusarium omysporum, Gibberella zeae and Physalospora piricola at the dosage of 50 mug mL(-1). Compound 2a and 3a exhibited good activities against P. piricola at low dosage.
机译:设计并合成了一系列新颖的吡咯生物碱类似物,并通过1H NMR,13C NMR和高分辨质谱(HRMS)对其结构进行了表征。化合物2a的结构通过2D NMR鉴定,包括异核多量子相干(HMQC),异核多键相关(HMBC)和H-H相关光谱(H-H COSY)光谱。评估了它们对五种真菌的抗真菌活性,结果表明,某些标题化合物在50杯毫升(-1)的剂量下对solternaria solani,Cercospora arachidicola,Fusarium omysporum,Gibberella zeae和Physalospora piricola表现出中等的杀真菌活性。 )。化合物2a和3a在低剂量下显示出对P. piricola的良好活性。

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