Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/11286
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dc.contributor.authorPetronijević, Jelena-
dc.contributor.authorJanković, Nenad-
dc.contributor.authorBugarčić Z.-
dc.date.accessioned2021-04-20T17:58:16Z-
dc.date.available2021-04-20T17:58:16Z-
dc.date.issued2018-
dc.identifier.issn1570-193X-
dc.identifier.urihttps://scidar.kg.ac.rs/handle/123456789/11286-
dc.description.abstract© 2018 Bentham Science Publishers. Background: Quinoxaline-based derivatives present a group of very important heterocyclic pharmacophores which occupied the attention of a large number of scientists in the last few decades. Compounds with quinoxaline fragment have significant antitumor and antiviral potential, proved by an in vitro or/and in vivo study, and possess therapeutic potential. Conclusion: In this review article, we present an overview of the developments in the area of synthesis of compounds that contain quinoxaline scaffold with antitumor or antiviral activities.-
dc.rightsrestrictedAccess-
dc.sourceMini-Reviews in Organic Chemistry-
dc.titleSynthesis of Quinoxaline-Based Compounds and Their Antitumor and Antiviral Potentials-
dc.typereview-
dc.identifier.doi10.2174/1570193X14666171201143357-
dc.identifier.scopus2-s2.0-85047610369-
Appears in Collections:Faculty of Science, Kragujevac
Institute for Information Technologies, Kragujevac

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