New thiopyrano[2,3-d][1,3]thiazole derivatives as potential antiviral agents
A series of novel thiopyrano[2,3-d][1,3]thiazole derivatives were synthesized and evaluated for their antiviral activity in vitro within AACF NIAID programme. Compounds were studied towards Dengue Virus Type 2, Venezuelan Equine Encephalitis Virus, Respiratory Syncytial Virus, SARS Coronavirus, Rift...
| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
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National Academy of Sciences of Ukraine, Palladin Institute of Biochemistry
2016-04-01
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| Series: | The Ukrainian Biochemical Journal |
| Online Access: | http://ukrbiochemjournal.org/wp-content/uploads/2016/07/Zelisko_88_Sp_is.pdf |
| _version_ | 1797422242470035456 |
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| author | N. I. Zelisko I. L. Demchuk R. B. Lesyk |
| author_facet | N. I. Zelisko I. L. Demchuk R. B. Lesyk |
| author_sort | N. I. Zelisko |
| collection | DOAJ |
| description | A series of novel thiopyrano[2,3-d][1,3]thiazole derivatives were synthesized and evaluated for their antiviral activity in vitro within AACF NIAID programme. Compounds were studied towards Dengue Virus Type 2, Venezuelan Equine Encephalitis Virus, Respiratory Syncytial Virus, SARS Coronavirus, Rift Valley Fever Virus, Tacaribe Virus, Influenza Virus Types A and B. Among the tested thiopyrano[2,3-d][1,3]thiazoles, alkyl rel-(5R,5aR,11bS)-2,6-dioxo-3,5a,6,11b-tetrahydro-2Н,5H-chromeno[4’,3’:4,5]thiopyrano[2,3-d][1,3]thiazole-5-carboxylates 8 and 11 were found to be the most active and showed significant antiviral activity against Influenza Virus Types A H3N2 and H5N1. |
| first_indexed | 2024-03-09T07:30:24Z |
| format | Article |
| id | doaj.art-8e5a128c0a6e44dc9378e9627ed9b338 |
| institution | Directory Open Access Journal |
| issn | 2409-4943 2413-5003 |
| language | English |
| last_indexed | 2024-03-09T07:30:24Z |
| publishDate | 2016-04-01 |
| publisher | National Academy of Sciences of Ukraine, Palladin Institute of Biochemistry |
| record_format | Article |
| series | The Ukrainian Biochemical Journal |
| spelling | doaj.art-8e5a128c0a6e44dc9378e9627ed9b3382023-12-03T06:27:17ZengNational Academy of Sciences of Ukraine, Palladin Institute of BiochemistryThe Ukrainian Biochemical Journal2409-49432413-50032016-04-0188SI0110511210.15407/ubj88.si01.105New thiopyrano[2,3-d][1,3]thiazole derivatives as potential antiviral agentsN. I. Zelisko0I. L. Demchuk1R. B. Lesyk 2Danylo Halytsky Lviv National Medical University, UkraineDanylo Halytsky Lviv National Medical University, UkraineDanylo Halytsky Lviv National Medical University, UkraineA series of novel thiopyrano[2,3-d][1,3]thiazole derivatives were synthesized and evaluated for their antiviral activity in vitro within AACF NIAID programme. Compounds were studied towards Dengue Virus Type 2, Venezuelan Equine Encephalitis Virus, Respiratory Syncytial Virus, SARS Coronavirus, Rift Valley Fever Virus, Tacaribe Virus, Influenza Virus Types A and B. Among the tested thiopyrano[2,3-d][1,3]thiazoles, alkyl rel-(5R,5aR,11bS)-2,6-dioxo-3,5a,6,11b-tetrahydro-2Н,5H-chromeno[4’,3’:4,5]thiopyrano[2,3-d][1,3]thiazole-5-carboxylates 8 and 11 were found to be the most active and showed significant antiviral activity against Influenza Virus Types A H3N2 and H5N1.http://ukrbiochemjournal.org/wp-content/uploads/2016/07/Zelisko_88_Sp_is.pdf |
| spellingShingle | N. I. Zelisko I. L. Demchuk R. B. Lesyk New thiopyrano[2,3-d][1,3]thiazole derivatives as potential antiviral agents The Ukrainian Biochemical Journal |
| title | New thiopyrano[2,3-d][1,3]thiazole derivatives as potential antiviral agents |
| title_full | New thiopyrano[2,3-d][1,3]thiazole derivatives as potential antiviral agents |
| title_fullStr | New thiopyrano[2,3-d][1,3]thiazole derivatives as potential antiviral agents |
| title_full_unstemmed | New thiopyrano[2,3-d][1,3]thiazole derivatives as potential antiviral agents |
| title_short | New thiopyrano[2,3-d][1,3]thiazole derivatives as potential antiviral agents |
| title_sort | new thiopyrano 2 3 d 1 3 thiazole derivatives as potential antiviral agents |
| url | http://ukrbiochemjournal.org/wp-content/uploads/2016/07/Zelisko_88_Sp_is.pdf |
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