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http://elar.urfu.ru/handle/10995/130492
Полная запись метаданных
Поле DC | Значение | Язык |
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dc.contributor.author | Kalinina, T. A. | en |
dc.contributor.author | Balandina, V. I. | en |
dc.contributor.author | Obydennov, K. L. | en |
dc.contributor.author | Slepukhin, P. A. | en |
dc.contributor.author | Fan, Z. | en |
dc.contributor.author | Bakulev, V. A. | en |
dc.contributor.author | Glukhareva, T. V. | en |
dc.date.accessioned | 2024-04-05T16:22:26Z | - |
dc.date.available | 2024-04-05T16:22:26Z | - |
dc.date.issued | 2023 | - |
dc.identifier.citation | 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 | harvard_pure |
dc.identifier.citation | 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 | apa_pure |
dc.identifier.issn | 1420-3049 | - |
dc.identifier.other | Final | 2 |
dc.identifier.other | All Open Access, Gold, Green | 3 |
dc.identifier.other | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85145692224&doi=10.3390%2fmolecules28010419&partnerID=40&md5=006269e854f70e1c2016dceb39c7d35c | 1 |
dc.identifier.other | https://www.mdpi.com/1420-3049/28/1/419/pdf?version=1672735384 | |
dc.identifier.uri | http://elar.urfu.ru/handle/10995/130492 | - |
dc.description.abstract | 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. | en |
dc.description.sponsorship | Russian Science Foundation, RSF: 22-26-20124 | en |
dc.description.sponsorship | 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). | en |
dc.format.mimetype | application/pdf | en |
dc.language.iso | en | en |
dc.publisher | MDPI | en |
dc.relation | info:eu-repo/grantAgreement/RSF//22-29-01514 | en |
dc.rights | info:eu-repo/semantics/openAccess | en |
dc.rights | cc-by | other |
dc.rights.uri | https://creativecommons.org/licenses/by/4.0/ | unpaywall |
dc.source | Molecules | 2 |
dc.source | Molecules | en |
dc.subject | 1,2,3-THIADIAZOLES | en |
dc.subject | ACYLALANINE FUNGICIDES | en |
dc.subject | ANTIFUNGAL ACTIVITY | en |
dc.subject | ISOTHIAZOLES | en |
dc.subject | ISOTIANIL | en |
dc.subject | N-ACYL-N-ARYLALANINES | en |
dc.subject | PLANT PROTECTION | en |
dc.subject | TIADINIL | en |
dc.subject | ANTIFUNGAL AGENT | en |
dc.subject | FUNGICIDE | en |
dc.subject | N-(3-CHLORO-4-METHYLPHENYL)-4-METHYL-1,2,3-THIADIAZOLE-5-CARBOXAMIDE | en |
dc.subject | THIADIAZOLE DERIVATIVE | en |
dc.subject | CHEMICAL STRUCTURE | en |
dc.subject | PLANT | en |
dc.subject | STRUCTURE ACTIVITY RELATION | en |
dc.subject | ANTIFUNGAL AGENTS | en |
dc.subject | FUNGICIDES, INDUSTRIAL | en |
dc.subject | MOLECULAR STRUCTURE | en |
dc.subject | PLANTS | en |
dc.subject | STRUCTURE-ACTIVITY RELATIONSHIP | en |
dc.subject | THIADIAZOLES | en |
dc.title | Synthesis, Fungicidal Activity and Plant Protective Properties of 1,2,3-Thiadiazole and Isothiazole-Based N-acyl-N-arylalaninates | en |
dc.type | Article | en |
dc.type | info:eu-repo/semantics/article | en |
dc.type | |info:eu-repo/semantics/publishedVersion | en |
dc.identifier.doi | 10.3390/molecules28010419 | - |
dc.identifier.scopus | 85145692224 | - |
local.contributor.employee | Kalinina, T.A., Institute of Chemical Engineering, Ural Federal University Named after the First President of Russia B.N. Yeltsin, 19 Mira Street, Ekaterinburg, 620002, Russian Federation | en |
local.contributor.employee | Balandina, V.I., Institute of Chemical Engineering, Ural Federal University Named after the First President of Russia B.N. Yeltsin, 19 Mira Street, Ekaterinburg, 620002, Russian Federation | en |
local.contributor.employee | Obydennov, K.L., Institute of Chemical Engineering, Ural Federal University Named after the First President of Russia B.N. Yeltsin, 19 Mira Street, Ekaterinburg, 620002, Russian Federation | en |
local.contributor.employee | Slepukhin, P.A., Postovsky Institute of Organic Synthesis, Ural Branch of Russian Academy of Sciences, 22/20 S. Kovalevskaya Street, Ekaterinburg, 620108, Russian Federation | en |
local.contributor.employee | Fan, Z., State Key Laboratory of Elemento-Organic Chemistry, College of Chemistry, Nankai University, No. 94, Weijin Road, Tianjin, 300071, China | en |
local.contributor.employee | Bakulev, V.A., Institute of Chemical Engineering, Ural Federal University Named after the First President of Russia B.N. Yeltsin, 19 Mira Street, Ekaterinburg, 620002, Russian Federation | en |
local.contributor.employee | Glukhareva, T.V., Institute of Chemical Engineering, Ural Federal University Named after the First President of Russia B.N. Yeltsin, 19 Mira Street, Ekaterinburg, 620002, Russian Federation | en |
local.issue | 1 | - |
local.volume | 28 | - |
dc.identifier.wos | 000909975500001 | - |
local.contributor.department | Institute of Chemical Engineering, Ural Federal University Named after the First President of Russia B.N. Yeltsin, 19 Mira Street, Ekaterinburg, 620002, Russian Federation | en |
local.contributor.department | Postovsky Institute of Organic Synthesis, Ural Branch of Russian Academy of Sciences, 22/20 S. Kovalevskaya Street, Ekaterinburg, 620108, Russian Federation | en |
local.contributor.department | State Key Laboratory of Elemento-Organic Chemistry, College of Chemistry, Nankai University, No. 94, Weijin Road, Tianjin, 300071, China | en |
local.identifier.pure | 33314854 | - |
local.description.order | 419 | - |
local.identifier.eid | 2-s2.0-85145692224 | - |
local.fund.rsf | 22-29-01514 | - |
local.identifier.wos | WOS:000909975500001 | - |
local.identifier.pmid | 36615609 | - |
Располагается в коллекциях: | Научные публикации ученых УрФУ, проиндексированные в SCOPUS и WoS CC |
Файлы этого ресурса:
Файл | Описание | Размер | Формат | |
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2-s2.0-85145692224.pdf | 3,15 MB | Adobe PDF | Просмотреть/Открыть |
Лицензия на ресурс: Лицензия Creative Commons