Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/21533
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dc.contributor.authorAksenov, N. A.-
dc.contributor.authorАксенов, Н. А.-
dc.date.accessioned2022-10-28T07:06:43Z-
dc.date.available2022-10-28T07:06:43Z-
dc.date.issued2022-
dc.identifier.citationVasilin, V.K., Kanishcheva, E.A., Stroganova, T.A., Dmitrieva, I.G., Taranenko, V.V., Tumskiy, R.S., Tumskaia, A.V., Aksenov, N.A., Krapivin, G.D. Design, Synthesis, and Screening of Pyridothieno[3,2- b ]indole and Pyridothieno[3,2- c ]cinnoline Derivatives as Potential Biologically Active Molecules // Synthesis (Germany). - 2022. - Том 54. - Выпуск 14. - Стр.: 3249 - 326. - Номер статьи ss-2021-c0801-op. - DOI10.1055/a-1785-7191ru
dc.identifier.urihttp://hdl.handle.net/20.500.12258/21533-
dc.description.abstractNew pyridothieno[3,2-b]indole and pyridothieno[3,2-c]cinnoline derivatives are designed and prepared from the corresponding 3- amino-2-arylthieno[2,3-b]pyridines. By a molecular docking method novel potential inhibitors of DNA gyrase B are identified among the thieno[2,3-b]pyridine derivatives. In addition, some of the prepared pyridothienoindoles exhibit in vivo antidote activity against the herbicide 2,4-D.ru
dc.language.isoenru
dc.publisherGeorg Thieme Verlagru
dc.relation.ispartofseriesSynthesis (Germany)-
dc.subjectADMETru
dc.subjectPyridothienoindolesru
dc.subjectAntidote activityru
dc.subjectAzideru
dc.subjectDNA gyrase inhibitorsru
dc.subjectMolecular dockingru
dc.subjectThermolysisru
dc.titleDesign, Synthesis, and Screening of Pyridothieno[3,2- b ]indole and Pyridothieno[3,2- c ]cinnoline Derivatives as Potential Biologically Active Moleculesru
dc.typeСтатьяru
vkr.instХимико-фармацевтический факультетru
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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