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dc.contributor.authorKalinina, T. A.en
dc.contributor.authorBalandina, V. I.en
dc.contributor.authorObydennov, K. L.en
dc.contributor.authorSlepukhin, P. A.en
dc.contributor.authorFan, Z.en
dc.contributor.authorBakulev, V. A.en
dc.contributor.authorGlukhareva, T. V.en
dc.date.accessioned2024-04-05T16:22:26Z-
dc.date.available2024-04-05T16:22:26Z-
dc.date.issued2023-
dc.identifier.citationKalinina, 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/molecules28010419harvard_pure
dc.identifier.citationKalinina, 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/molecules28010419apa_pure
dc.identifier.issn1420-3049-
dc.identifier.otherFinal2
dc.identifier.otherAll Open Access, Gold, Green3
dc.identifier.otherhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85145692224&doi=10.3390%2fmolecules28010419&partnerID=40&md5=006269e854f70e1c2016dceb39c7d35c1
dc.identifier.otherhttps://www.mdpi.com/1420-3049/28/1/419/pdf?version=1672735384pdf
dc.identifier.urihttp://elar.urfu.ru/handle/10995/130492-
dc.description.abstractThe 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.sponsorshipRussian Science Foundation, RSF: 22-26-20124en
dc.description.sponsorshipThis 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.mimetypeapplication/pdfen
dc.language.isoenen
dc.publisherMDPIen
dc.relationinfo:eu-repo/grantAgreement/RSF//22-29-01514en
dc.rightsinfo:eu-repo/semantics/openAccessen
dc.rightscc-byother
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/unpaywall
dc.sourceMolecules2
dc.sourceMoleculesen
dc.subject1,2,3-THIADIAZOLESen
dc.subjectACYLALANINE FUNGICIDESen
dc.subjectANTIFUNGAL ACTIVITYen
dc.subjectISOTHIAZOLESen
dc.subjectISOTIANILen
dc.subjectN-ACYL-N-ARYLALANINESen
dc.subjectPLANT PROTECTIONen
dc.subjectTIADINILen
dc.subjectANTIFUNGAL AGENTen
dc.subjectFUNGICIDEen
dc.subjectN-(3-CHLORO-4-METHYLPHENYL)-4-METHYL-1,2,3-THIADIAZOLE-5-CARBOXAMIDEen
dc.subjectTHIADIAZOLE DERIVATIVEen
dc.subjectCHEMICAL STRUCTUREen
dc.subjectPLANTen
dc.subjectSTRUCTURE ACTIVITY RELATIONen
dc.subjectANTIFUNGAL AGENTSen
dc.subjectFUNGICIDES, INDUSTRIALen
dc.subjectMOLECULAR STRUCTUREen
dc.subjectPLANTSen
dc.subjectSTRUCTURE-ACTIVITY RELATIONSHIPen
dc.subjectTHIADIAZOLESen
dc.titleSynthesis, Fungicidal Activity and Plant Protective Properties of 1,2,3-Thiadiazole and Isothiazole-Based N-acyl-N-arylalaninatesen
dc.typeArticleen
dc.typeinfo:eu-repo/semantics/articleen
dc.type|info:eu-repo/semantics/publishedVersionen
dc.identifier.doi10.3390/molecules28010419-
dc.identifier.scopus85145692224-
local.contributor.employeeKalinina, 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 Federationen
local.contributor.employeeBalandina, 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 Federationen
local.contributor.employeeObydennov, 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 Federationen
local.contributor.employeeSlepukhin, P.A., Postovsky Institute of Organic Synthesis, Ural Branch of Russian Academy of Sciences, 22/20 S. Kovalevskaya Street, Ekaterinburg, 620108, Russian Federationen
local.contributor.employeeFan, Z., State Key Laboratory of Elemento-Organic Chemistry, College of Chemistry, Nankai University, No. 94, Weijin Road, Tianjin, 300071, Chinaen
local.contributor.employeeBakulev, 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 Federationen
local.contributor.employeeGlukhareva, 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 Federationen
local.issue1-
local.volume28-
dc.identifier.wos000909975500001-
local.contributor.departmentInstitute of Chemical Engineering, Ural Federal University Named after the First President of Russia B.N. Yeltsin, 19 Mira Street, Ekaterinburg, 620002, Russian Federationen
local.contributor.departmentPostovsky Institute of Organic Synthesis, Ural Branch of Russian Academy of Sciences, 22/20 S. Kovalevskaya Street, Ekaterinburg, 620108, Russian Federationen
local.contributor.departmentState Key Laboratory of Elemento-Organic Chemistry, College of Chemistry, Nankai University, No. 94, Weijin Road, Tianjin, 300071, Chinaen
local.identifier.pure33314854-
local.description.order419-
local.identifier.eid2-s2.0-85145692224-
local.fund.rsf22-29-01514-
local.identifier.wosWOS:000909975500001-
local.identifier.pmid36615609-
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