Cargando…

Design, synthesis and antimicrobial activities of novel 1,3,5-thiadiazine-2-thione derivatives containing a 1,3,4-thiadiazole group

A series of novel 1,3,5-thiadiazine-2-thione derivatives containing a 1,3,4-thiadiazole group was designed and synthesized. The structures of all the compounds were well characterized using (1)H NMR, (13)C NMR and high-resolution mass spectrometer, and further confirmed by the X-ray diffraction anal...

Descripción completa

Detalles Bibliográficos
Autores principales: Yan, Jinghua, Si, Weijie, Hu, Haoran, Zhao, Xu, Chen, Min, Wang, Xiaobin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6733239/
https://www.ncbi.nlm.nih.gov/pubmed/31534848
http://dx.doi.org/10.7717/peerj.7581
_version_ 1783449947428880384
author Yan, Jinghua
Si, Weijie
Hu, Haoran
Zhao, Xu
Chen, Min
Wang, Xiaobin
author_facet Yan, Jinghua
Si, Weijie
Hu, Haoran
Zhao, Xu
Chen, Min
Wang, Xiaobin
author_sort Yan, Jinghua
collection PubMed
description A series of novel 1,3,5-thiadiazine-2-thione derivatives containing a 1,3,4-thiadiazole group was designed and synthesized. The structures of all the compounds were well characterized using (1)H NMR, (13)C NMR and high-resolution mass spectrometer, and further confirmed by the X-ray diffraction analysis of 8d. The antimicrobial activities of all the target compounds against Xanthomonas oryzae pv. oryzicola, X. oryzae pv. oryzae, Rhizoctonia solani and Fusarium graminearum were evaluated. The in vitro antimicrobial bioassays indicated that some title compounds exhibited noteworthy antimicrobial effects against the above strains. Notably, the compound N-(5-(ethylthio)-1,3,4-thiadiazol-2-yl)-2-(5-methyl-6-thioxo-1,3,5-thiadiazinan-3-yl)acetamide (8a) displayed obvious antibacterial effects against X. oryzae pv. oryzicola and X. oryzae pv. oryzae at 100 μg/mL with the inhibition rates of 30% and 56%, respectively, which was better than the commercial bactericide thiodiazole-copper. In addition, the anti-R. solani EC(50) value of 8a was 33.70 μg/mL, which was more effective than that of the commercial fungicide hymexazol (67.10 μg/mL). It was found that the substitutes in the 1,3,5-thiadiazine-2-thione and the 1,3,4-thiadiazole rings played a vital role in the antimicrobial activities of the title compounds. More active title compounds against phytopathogenic microorganisms might be obtained via further structural modification.
format Online
Article
Text
id pubmed-6733239
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher PeerJ Inc.
record_format MEDLINE/PubMed
spelling pubmed-67332392019-09-18 Design, synthesis and antimicrobial activities of novel 1,3,5-thiadiazine-2-thione derivatives containing a 1,3,4-thiadiazole group Yan, Jinghua Si, Weijie Hu, Haoran Zhao, Xu Chen, Min Wang, Xiaobin PeerJ Agricultural Science A series of novel 1,3,5-thiadiazine-2-thione derivatives containing a 1,3,4-thiadiazole group was designed and synthesized. The structures of all the compounds were well characterized using (1)H NMR, (13)C NMR and high-resolution mass spectrometer, and further confirmed by the X-ray diffraction analysis of 8d. The antimicrobial activities of all the target compounds against Xanthomonas oryzae pv. oryzicola, X. oryzae pv. oryzae, Rhizoctonia solani and Fusarium graminearum were evaluated. The in vitro antimicrobial bioassays indicated that some title compounds exhibited noteworthy antimicrobial effects against the above strains. Notably, the compound N-(5-(ethylthio)-1,3,4-thiadiazol-2-yl)-2-(5-methyl-6-thioxo-1,3,5-thiadiazinan-3-yl)acetamide (8a) displayed obvious antibacterial effects against X. oryzae pv. oryzicola and X. oryzae pv. oryzae at 100 μg/mL with the inhibition rates of 30% and 56%, respectively, which was better than the commercial bactericide thiodiazole-copper. In addition, the anti-R. solani EC(50) value of 8a was 33.70 μg/mL, which was more effective than that of the commercial fungicide hymexazol (67.10 μg/mL). It was found that the substitutes in the 1,3,5-thiadiazine-2-thione and the 1,3,4-thiadiazole rings played a vital role in the antimicrobial activities of the title compounds. More active title compounds against phytopathogenic microorganisms might be obtained via further structural modification. PeerJ Inc. 2019-09-06 /pmc/articles/PMC6733239/ /pubmed/31534848 http://dx.doi.org/10.7717/peerj.7581 Text en © 2019 Yan et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Agricultural Science
Yan, Jinghua
Si, Weijie
Hu, Haoran
Zhao, Xu
Chen, Min
Wang, Xiaobin
Design, synthesis and antimicrobial activities of novel 1,3,5-thiadiazine-2-thione derivatives containing a 1,3,4-thiadiazole group
title Design, synthesis and antimicrobial activities of novel 1,3,5-thiadiazine-2-thione derivatives containing a 1,3,4-thiadiazole group
title_full Design, synthesis and antimicrobial activities of novel 1,3,5-thiadiazine-2-thione derivatives containing a 1,3,4-thiadiazole group
title_fullStr Design, synthesis and antimicrobial activities of novel 1,3,5-thiadiazine-2-thione derivatives containing a 1,3,4-thiadiazole group
title_full_unstemmed Design, synthesis and antimicrobial activities of novel 1,3,5-thiadiazine-2-thione derivatives containing a 1,3,4-thiadiazole group
title_short Design, synthesis and antimicrobial activities of novel 1,3,5-thiadiazine-2-thione derivatives containing a 1,3,4-thiadiazole group
title_sort design, synthesis and antimicrobial activities of novel 1,3,5-thiadiazine-2-thione derivatives containing a 1,3,4-thiadiazole group
topic Agricultural Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6733239/
https://www.ncbi.nlm.nih.gov/pubmed/31534848
http://dx.doi.org/10.7717/peerj.7581
work_keys_str_mv AT yanjinghua designsynthesisandantimicrobialactivitiesofnovel135thiadiazine2thionederivativescontaininga134thiadiazolegroup
AT siweijie designsynthesisandantimicrobialactivitiesofnovel135thiadiazine2thionederivativescontaininga134thiadiazolegroup
AT huhaoran designsynthesisandantimicrobialactivitiesofnovel135thiadiazine2thionederivativescontaininga134thiadiazolegroup
AT zhaoxu designsynthesisandantimicrobialactivitiesofnovel135thiadiazine2thionederivativescontaininga134thiadiazolegroup
AT chenmin designsynthesisandantimicrobialactivitiesofnovel135thiadiazine2thionederivativescontaininga134thiadiazolegroup
AT wangxiaobin designsynthesisandantimicrobialactivitiesofnovel135thiadiazine2thionederivativescontaininga134thiadiazolegroup