New 2-aryl-6-methyl-3,4-dihydro-β-carbolin-2-iums as potential antifungal agents: Synthesis, bioactivity and structure-activity relationship
Autor: | Le Zhou, Xing-Qiang Li, Wei Zhao, Xin-Juan Yang, Shanshan Yang, Bingyu Zhang |
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Jazyk: | angličtina |
Rok vydání: | 2019 |
Předmět: |
0301 basic medicine
Antifungal Agents Stereochemistry lcsh:Medicine Microbial Sensitivity Tests Article 03 medical and health sciences chemistry.chemical_compound Structure-Activity Relationship 0302 clinical medicine Structure–activity relationship lcsh:Science IC50 Mycelium Plant Diseases Degree of unsaturation Multidisciplinary Molecular Structure Carbendazim Aryl lcsh:R Fungi Plants Fungicides Industrial High-Throughput Screening Assays Fungicide 030104 developmental biology chemistry Azoxystrobin lcsh:Q 030217 neurology & neurosurgery |
Zdroj: | Scientific Reports, Vol 9, Iss 1, Pp 1-12 (2019) Scientific Reports |
ISSN: | 2045-2322 |
DOI: | 10.1038/s41598-018-38222-x |
Popis: | Thirty new title compounds along with five known analogues were prepared from commercially available 2-arylhydrazin-1-ium chlorides and α-ketoglutaric acid. The mycelium growth rate method was used to evaluate inhibition activity against six strains of plant pathogenic fungi. Most of the compounds displayed the activity for each the fungi at 150 μΜ, higher than azoxystrobin, a positive drug. Compound 6-2 showed the lowest average IC50 value of 4.58 μg/mL for all the fungi where F. solani exhibited the highest susceptibility to most of the compounds. For F. solani, some compounds were more active with IC50 values of 2.67–8.48 μM than thiabendazole (IC50 = 9.30 μM) and/or carbendazim (IC50 = 3.36 μM). The SAR showed that the activity is significantly affected by substituents on the A-ring and/or D-ring along with the degree of unsaturation of the C-ring. Thus, a series of new β-carboline compounds with potent antifungal potential were found. |
Databáze: | OpenAIRE |
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