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 |
|