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dc.date.accessioned | 2019-01-22T20:34:17Z | |
dc.date.available | 2019-01-22T20:34:17Z | |
dc.date.issued | 2018 | |
dc.identifier.issn | 0036-021X | |
dc.identifier.uri | https://dspace.kpfu.ru/xmlui/handle/net/147755 | |
dc.description.abstract | © 2018 Uspekhi Khimii, Russian Academy of Sciences and Turpion Ltd. The present review is concerned with the synthesis and structure-activity relationship studies of Arbidol and its structural analogues. The latter are roughly divided into several unequal parts: indole- and benzofuran-based compounds, benzimidazole and imidazopyridine bioisosteres and ring-expanded quinoline derivatives. Much attention is focused on various types of antiviral activity of the above-mentioned Arbidol congeners, as well as of the parent compound itself. Features of Arbidol synthesis and metabolic changes are also discussed. | |
dc.relation.ispartofseries | Russian Chemical Reviews | |
dc.title | Arbidol: A quarter-century after. Past, present and future of the original Russian antiviral | |
dc.type | Review | |
dc.relation.ispartofseries-issue | 6 | |
dc.relation.ispartofseries-volume | 87 | |
dc.collection | Публикации сотрудников КФУ | |
dc.relation.startpage | 509 | |
dc.source.id | SCOPUS0036021X-2018-87-6-SID85048057986 |