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Название: Synthesis, Fungicidal Activity and Plant Protective Properties of 1,2,3-Thiadiazole and Isothiazole-Based N-acyl-N-arylalaninates
Авторы: Kalinina, T. A.
Balandina, V. I.
Obydennov, K. L.
Slepukhin, P. A.
Fan, Z.
Bakulev, V. A.
Glukhareva, T. V.
Дата публикации: 2023
Издатель: MDPI
Библиографическое описание: Kalinina, TA, Balandina, VI, Obydennov, KL, Slepukhin, PA, Fan, Z, Bakulev, VA & Glukhareva, TV 2023, 'Synthesis, Fungicidal Activity and Plant Protective Properties of 1,2,3-Thiadiazole and Isothiazole-Based N-acyl-N-arylalaninates', Molecules, Том. 28, № 1, 419. https://doi.org/10.3390/molecules28010419
Kalinina, T. A., Balandina, V. I., Obydennov, K. L., Slepukhin, P. A., Fan, Z., Bakulev, V. A., & Glukhareva, T. V. (2023). Synthesis, Fungicidal Activity and Plant Protective Properties of 1,2,3-Thiadiazole and Isothiazole-Based N-acyl-N-arylalaninates. Molecules, 28(1), [419]. https://doi.org/10.3390/molecules28010419
Аннотация: The addition of active groups of known fungicides, or systemic acquired resistance inducers, into novel compound molecules to search for potential antifungal compounds is a popular and effective strategy. In this work, a new series of N-acyl-N-arylalanines was developed and synthesized, in which 1,2,3-thiadiazol-5-ylcarbonyl or 3,4-dichloroisothiazol-5-ylcarbonyl (fragments from synthetic plant resistance activators tiadinil and isotianil, respectively) and a fragment of N-arylalanine, the toxophoric group of acylalanine fungicides. Several new synthesized compounds have shown moderate antifungal activity against fungi in vitro, such as B. cinerea, R. solani and S. sclerotiorum. In vivo tests against A. brassicicola showed that compound 1d was 92% effective at a concentration of 200 µg/mL, similar to level of tiadinil, a known inducer of systemic resistance. Thus, 1d could be considered a new candidate fungicide for further detailed study. The present results will advance research and influence the search for more promising fungicides for disease control in agriculture. © 2023 by the authors.
Ключевые слова: 1,2,3-THIADIAZOLES
ACYLALANINE FUNGICIDES
ANTIFUNGAL ACTIVITY
ISOTHIAZOLES
ISOTIANIL
N-ACYL-N-ARYLALANINES
PLANT PROTECTION
TIADINIL
ANTIFUNGAL AGENT
FUNGICIDE
N-(3-CHLORO-4-METHYLPHENYL)-4-METHYL-1,2,3-THIADIAZOLE-5-CARBOXAMIDE
THIADIAZOLE DERIVATIVE
CHEMICAL STRUCTURE
PLANT
STRUCTURE ACTIVITY RELATION
ANTIFUNGAL AGENTS
FUNGICIDES, INDUSTRIAL
MOLECULAR STRUCTURE
PLANTS
STRUCTURE-ACTIVITY RELATIONSHIP
THIADIAZOLES
URI: http://elar.urfu.ru/handle/10995/130492
Условия доступа: info:eu-repo/semantics/openAccess
cc-by
Текст лицензии: https://creativecommons.org/licenses/by/4.0/
Идентификатор SCOPUS: 85145692224
Идентификатор WOS: 000909975500001
Идентификатор PURE: 33314854
ISSN: 1420-3049
DOI: 10.3390/molecules28010419
Сведения о поддержке: Russian Science Foundation, RSF: 22-26-20124
This research was supported by the Russian Science Foundation and Government of Sverdlovsk region, Joint Grant No 22-26-20124, https://rscf.ru/en/project/22-26-20124/ (accessed on 1 January 2023).
Карточка проекта РНФ: 22-29-01514
Располагается в коллекциях:Научные публикации ученых УрФУ, проиндексированные в SCOPUS и WoS CC

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