New synthesis and biological evaluation of benzothiazole derivates as antifungal agents
- PMID: 25797910
- DOI: 10.1021/acs.jafc.5b00150
New synthesis and biological evaluation of benzothiazole derivates as antifungal agents
Abstract
In search of new antifungal agrochemicals that could replace commercially available, aryl-2-mercaptobenzothiazoles were synthesized. They were prepared by two methodologies, using both photostimulated reaction and microwave assisted reaction. These reactions took place without the use of metallic catalyst by a one-pot procedure with excellent yields (70-98%). Synthesized compounds were evaluated for fungal growth inhibition against Botrytis cinerea. Most of the compounds have an excellent antifungal activity, and three of these showed a superior inhibitory effect to commercial fungicide Triadimefon. IC50 values observed for 2-(phenylthio)benzothiazole, 2-(2-chlorophenylthio)benzothiazole, and 2-(3-chlorophenyl thio)benzothiazole were 0.75, 0.69, and 0.65 μg mL(-1), respectively.
Keywords: Botrytis cinerea; antifungal activities; microwave irradiation; synthesis.
Similar articles
-
Green Synthesis of Potential Antifungal Agents: 2-Benzyl Substituted Thiobenzoazoles.J Agric Food Chem. 2017 Nov 29;65(47):10325-10331. doi: 10.1021/acs.jafc.7b04130. Epub 2017 Nov 9. J Agric Food Chem. 2017. PMID: 29099589
-
Microwave-assisted, one-pot syntheses and fungicidal activity of polyfluorinated 2-benzylthiobenzothiazoles.Bioorg Med Chem. 2006 Dec 15;14(24):8280-5. doi: 10.1016/j.bmc.2006.09.016. Epub 2006 Sep 27. Bioorg Med Chem. 2006. PMID: 17008103
-
Synthesis and fungicidal activity of novel 2,5-disubstituted-1,3,4-oxadiazole derivatives.J Agric Food Chem. 2012 Nov 28;60(47):11649-56. doi: 10.1021/jf303807a. Epub 2012 Nov 15. J Agric Food Chem. 2012. PMID: 23134289
-
Mechanisms of resistance to fungicides in field strains of Botrytis cinerea.Pest Manag Sci. 2002 Sep;58(9):876-88. doi: 10.1002/ps.566. Pest Manag Sci. 2002. PMID: 12233177 Review.
-
Synthesis and Biological Importance of 2-(thio)ureabenzothiazoles.Molecules. 2022 Sep 19;27(18):6104. doi: 10.3390/molecules27186104. Molecules. 2022. PMID: 36144837 Free PMC article. Review.
Cited by
-
Selective and eco-friendly procedures for the synthesis of benzimidazole derivatives. The role of the Er(OTf)3 catalyst in the reaction selectivity.Beilstein J Org Chem. 2016 Nov 16;12:2410-2419. doi: 10.3762/bjoc.12.235. eCollection 2016. Beilstein J Org Chem. 2016. PMID: 28144309 Free PMC article.
-
Design, Synthesis, and Spectral Properties of Novel 2-Mercaptobenzothiazole Derivatives.Materials (Basel). 2024 Jan 2;17(1):246. doi: 10.3390/ma17010246. Materials (Basel). 2024. PMID: 38204100 Free PMC article.
-
Control Effect and Mechanism of Trichoderma asperellum TM11 against Blueberry Root Rot.Pol J Microbiol. 2023 Sep 20;72(3):325-337. doi: 10.33073/pjm-2023-034. eCollection 2023 Sep 1. Pol J Microbiol. 2023. PMID: 37725898 Free PMC article.
-
A Green Approach to 2-Substituted Benzo- and Naphthothiazoles via N-bromosuccinimide/Bromide-Mediated C(aryl)-S Bond Formation.Molecules. 2022 Nov 15;27(22):7876. doi: 10.3390/molecules27227876. Molecules. 2022. PMID: 36431980 Free PMC article.
-
Modern Approaches to the Synthesis and Transformations of Practically Valuable Benzothiazole Derivatives.Molecules. 2021 Apr 10;26(8):2190. doi: 10.3390/molecules26082190. Molecules. 2021. PMID: 33920281 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources