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dc.contributor.authorBabu, K. N.en
dc.contributor.authorSravya, G.en
dc.contributor.authorBasha, N. H.en
dc.contributor.authorZyryanov, G. V.en
dc.contributor.authorPadmavathi, V.en
dc.contributor.authorЗырянов, Г. В.ru
dc.date.accessioned2021-08-31T15:08:53Z-
dc.date.available2021-08-31T15:08:53Z-
dc.date.issued2020-
dc.identifier.citationSynthesis of heteroaryl urea derivatives as antimicrobial agents / K. N. Babu, G. Sravya, N. H. Basha, et al. — DOI 10.1063/5.0018631 // AIP Conference Proceedings. — 2020. — Vol. 2280. — 0018631.en
dc.identifier.isbn9780735440104-
dc.identifier.issn0094243X-
dc.identifier.otherFinal2
dc.identifier.otherAll Open Access, Green3
dc.identifier.otherhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85096447787&doi=10.1063%2f5.0018631&partnerID=40&md5=a0441b90239df08fbb1b28a1f009ec2f
dc.identifier.otherhttps://elar.urfu.ru/bitstream/10995/81137/1/978-5-6044427-0-8_2019_097.pdfm
dc.identifier.urihttp://elar.urfu.ru/handle/10995/103297-
dc.description.abstractAzoles are prominent scaffolds in the pharmaceutical arena. In fact, medicinal properties of azole and benzazole containing compounds include anticancer, antimicrobial and antioxidant. Some of the drugs Inthomycin C, Oxaprozin, Tiazofurin, Dacarbazine, Tipifarnib, Albendazole, Febendazole, Omeprazole possess azole/benzazole moiety. Realizing the importance of azoles and benzazoles, it is planned to conjugate these two ligands as heteroaryl substituted urea derivatives and to study their antimicrobial activity. The results pertaining to these aspects will be discussed. © 2020 Author(s).en
dc.description.sponsorshipThe authors K. Narendra Babu and V. Padmavathi are grateful to CSIR (Council of Scientific and Industrial Research), New Delhi for financial assistance under major research project.en
dc.format.mimetypeapplication/pdfen
dc.language.isoenen
dc.publisherAmerican Institute of Physics Inc.en
dc.rightsinfo:eu-repo/semantics/openAccessen
dc.sourceAIP Conf. Proc.2
dc.sourceAIP Conference Proceedingsen
dc.titleSynthesis of heteroaryl urea derivatives as antimicrobial agentsen
dc.typeConference Paperen
dc.typeinfo:eu-repo/semantics/conferenceObjecten
dc.typeinfo:eu-repo/semantics/publishedVersionen
dc.identifier.doi10.1063/5.0018631-
dc.identifier.scopus85096447787-
local.contributor.employeeBabu, K.N., Department of Chemistry, Sri Venkateswara University, Tirupati, Andhra Pradesh, India
local.contributor.employeeSravya, G., Ural Federal University, Chemical Engineering Institute, Yekaterinburg, 620002, Russian Federation
local.contributor.employeeBasha, N.H., Department of Chemistry, Sri Venkateswara University, Tirupati, Andhra Pradesh, India
local.contributor.employeeZyryanov, G.V., Ural Federal University, Chemical Engineering Institute, Yekaterinburg, 620002, Russian Federation, I. Ya. Postovsky Institute of Organic Synthesis, Ural Division of Russian Academy of Sciences, 22 S. Kovalevskoy Street, Yekaterinburg, 620219, Russian Federation
local.contributor.employeePadmavathi, V., Department of Chemistry, Sri Venkateswara University, Tirupati, Andhra Pradesh, India
local.volume2280-
dc.identifier.wos000598468000099-
local.contributor.departmentDepartment of Chemistry, Sri Venkateswara University, Tirupati, Andhra Pradesh, India
local.contributor.departmentUral Federal University, Chemical Engineering Institute, Yekaterinburg, 620002, Russian Federation
local.contributor.departmentI. Ya. Postovsky Institute of Organic Synthesis, Ural Division of Russian Academy of Sciences, 22 S. Kovalevskoy Street, Yekaterinburg, 620219, Russian Federation
local.identifier.pure022aee96-73d9-4222-8183-ecc78639904euuid
local.identifier.pure20135217-
local.description.order0018631-
local.identifier.eid2-s2.0-85096447787-
local.identifier.wosWOS:000598468000099-
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