Recent Advances in Design, Synthesis, and Biological Activity Studies of 1,3-Selenazoles

The review examines recent advances in the design and synthesis of 1,3-selenazole derivatives since 2000. Various synthetic approaches to 1,3-selenazoles and reaction conditions are discussed. The beneficial properties of 1,3-selenazoles, especially their biological activity, are emphasized. Compoun...

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Main Authors: Nataliya A. Makhaeva, Svetlana V. Amosova, Andrey S. Filippov, Vladimir A. Potapov, Maxim V. Musalov
Format: Article
Language:English
Published: MDPI AG 2024-12-01
Series:Biomolecules
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Online Access:https://www.mdpi.com/2218-273X/14/12/1546
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author Nataliya A. Makhaeva
Svetlana V. Amosova
Andrey S. Filippov
Vladimir A. Potapov
Maxim V. Musalov
author_facet Nataliya A. Makhaeva
Svetlana V. Amosova
Andrey S. Filippov
Vladimir A. Potapov
Maxim V. Musalov
author_sort Nataliya A. Makhaeva
collection DOAJ
description The review examines recent advances in the design and synthesis of 1,3-selenazole derivatives since 2000. Various synthetic approaches to 1,3-selenazoles and reaction conditions are discussed. The beneficial properties of 1,3-selenazoles, especially their biological activity, are emphasized. Compounds with antitumor, antiviral (HIV-1 and HIV-2), antibacterial, antifungal, antiproliferative, anticonvulsant, and antioxidant activity are highlighted.
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publishDate 2024-12-01
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series Biomolecules
spelling doaj-art-e88b4977b55b4231a4b6824c3d8b4f052024-12-27T14:13:45ZengMDPI AGBiomolecules2218-273X2024-12-011412154610.3390/biom14121546Recent Advances in Design, Synthesis, and Biological Activity Studies of 1,3-SelenazolesNataliya A. Makhaeva0Svetlana V. Amosova1Andrey S. Filippov2Vladimir A. Potapov3Maxim V. Musalov4A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, 1 Favorsky Str., Irkutsk 664033, RussiaA. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, 1 Favorsky Str., Irkutsk 664033, RussiaA. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, 1 Favorsky Str., Irkutsk 664033, RussiaA. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, 1 Favorsky Str., Irkutsk 664033, RussiaA. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, 1 Favorsky Str., Irkutsk 664033, RussiaThe review examines recent advances in the design and synthesis of 1,3-selenazole derivatives since 2000. Various synthetic approaches to 1,3-selenazoles and reaction conditions are discussed. The beneficial properties of 1,3-selenazoles, especially their biological activity, are emphasized. Compounds with antitumor, antiviral (HIV-1 and HIV-2), antibacterial, antifungal, antiproliferative, anticonvulsant, and antioxidant activity are highlighted.https://www.mdpi.com/2218-273X/14/12/1546heterocycles1,3-selenazolessynthesisbiological activity1,3-selenazole derivatives
spellingShingle Nataliya A. Makhaeva
Svetlana V. Amosova
Andrey S. Filippov
Vladimir A. Potapov
Maxim V. Musalov
Recent Advances in Design, Synthesis, and Biological Activity Studies of 1,3-Selenazoles
Biomolecules
heterocycles
1,3-selenazoles
synthesis
biological activity
1,3-selenazole derivatives
title Recent Advances in Design, Synthesis, and Biological Activity Studies of 1,3-Selenazoles
title_full Recent Advances in Design, Synthesis, and Biological Activity Studies of 1,3-Selenazoles
title_fullStr Recent Advances in Design, Synthesis, and Biological Activity Studies of 1,3-Selenazoles
title_full_unstemmed Recent Advances in Design, Synthesis, and Biological Activity Studies of 1,3-Selenazoles
title_short Recent Advances in Design, Synthesis, and Biological Activity Studies of 1,3-Selenazoles
title_sort recent advances in design synthesis and biological activity studies of 1 3 selenazoles
topic heterocycles
1,3-selenazoles
synthesis
biological activity
1,3-selenazole derivatives
url https://www.mdpi.com/2218-273X/14/12/1546
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AT svetlanavamosova recentadvancesindesignsynthesisandbiologicalactivitystudiesof13selenazoles
AT andreysfilippov recentadvancesindesignsynthesisandbiologicalactivitystudiesof13selenazoles
AT vladimirapotapov recentadvancesindesignsynthesisandbiologicalactivitystudiesof13selenazoles
AT maximvmusalov recentadvancesindesignsynthesisandbiologicalactivitystudiesof13selenazoles