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Design of cinnamaldehyde amino acid Schiff base compounds based on the quantitative structure–activity relationship
Cinnamaldehyde amino acid Schiff base (CAAS) is a new class of safe, bioactive compounds which could be developed as potential antifungal agents for fungal infections. To design new cinnamaldehyde amino acid Schiff base compounds with high bioactivity, the quantitative structure–activity relationshi...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society Publishing
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5627098/ https://www.ncbi.nlm.nih.gov/pubmed/28989758 http://dx.doi.org/10.1098/rsos.170516 |
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author | Wang, Hui Jiang, Mingyue Li, Shujun Hse, Chung-Yun Jin, Chunde Sun, Fangli Li, Zhuo |
author_facet | Wang, Hui Jiang, Mingyue Li, Shujun Hse, Chung-Yun Jin, Chunde Sun, Fangli Li, Zhuo |
author_sort | Wang, Hui |
collection | PubMed |
description | Cinnamaldehyde amino acid Schiff base (CAAS) is a new class of safe, bioactive compounds which could be developed as potential antifungal agents for fungal infections. To design new cinnamaldehyde amino acid Schiff base compounds with high bioactivity, the quantitative structure–activity relationships (QSARs) for CAAS compounds against Aspergillus niger (A. niger) and Penicillium citrinum (P. citrinum) were analysed. The QSAR models (R(2) = 0.9346 for A. niger, R(2) = 0.9590 for P. citrinum,) were constructed and validated. The models indicated that the molecular polarity and the Max atomic orbital electronic population had a significant effect on antifungal activity. Based on the best QSAR models, two new compounds were designed and synthesized. Antifungal activity tests proved that both of them have great bioactivity against the selected fungi. |
format | Online Article Text |
id | pubmed-5627098 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | The Royal Society Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-56270982017-10-08 Design of cinnamaldehyde amino acid Schiff base compounds based on the quantitative structure–activity relationship Wang, Hui Jiang, Mingyue Li, Shujun Hse, Chung-Yun Jin, Chunde Sun, Fangli Li, Zhuo R Soc Open Sci Chemistry Cinnamaldehyde amino acid Schiff base (CAAS) is a new class of safe, bioactive compounds which could be developed as potential antifungal agents for fungal infections. To design new cinnamaldehyde amino acid Schiff base compounds with high bioactivity, the quantitative structure–activity relationships (QSARs) for CAAS compounds against Aspergillus niger (A. niger) and Penicillium citrinum (P. citrinum) were analysed. The QSAR models (R(2) = 0.9346 for A. niger, R(2) = 0.9590 for P. citrinum,) were constructed and validated. The models indicated that the molecular polarity and the Max atomic orbital electronic population had a significant effect on antifungal activity. Based on the best QSAR models, two new compounds were designed and synthesized. Antifungal activity tests proved that both of them have great bioactivity against the selected fungi. The Royal Society Publishing 2017-09-06 /pmc/articles/PMC5627098/ /pubmed/28989758 http://dx.doi.org/10.1098/rsos.170516 Text en © 2017 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Chemistry Wang, Hui Jiang, Mingyue Li, Shujun Hse, Chung-Yun Jin, Chunde Sun, Fangli Li, Zhuo Design of cinnamaldehyde amino acid Schiff base compounds based on the quantitative structure–activity relationship |
title | Design of cinnamaldehyde amino acid Schiff base compounds based on the quantitative structure–activity relationship |
title_full | Design of cinnamaldehyde amino acid Schiff base compounds based on the quantitative structure–activity relationship |
title_fullStr | Design of cinnamaldehyde amino acid Schiff base compounds based on the quantitative structure–activity relationship |
title_full_unstemmed | Design of cinnamaldehyde amino acid Schiff base compounds based on the quantitative structure–activity relationship |
title_short | Design of cinnamaldehyde amino acid Schiff base compounds based on the quantitative structure–activity relationship |
title_sort | design of cinnamaldehyde amino acid schiff base compounds based on the quantitative structure–activity relationship |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5627098/ https://www.ncbi.nlm.nih.gov/pubmed/28989758 http://dx.doi.org/10.1098/rsos.170516 |
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