Journals / Ankara Üniversitesi Eczacılık Fakültesi Dergisi / 1983 / Cilt: 13 - Sayı: 1

The synthesis and biological activity of some antiviral 3,5-disubstitue1,2,4-triazolederivatives

(s)-Triazol-N-Glikozitleri. VII - Antivira l etkili baz ı 3,5-disübs - titüe- l .2.4-triazol türevlerini n sentezleri v e biyoloji k etkileri

Pages
78–88
Publication Date
1983-06-01
DOI
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AI Summary & Key Takeaways

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⚡ TL;DR(Too Long; Didn't Read)

The water soluble derivatives, A3G d , B 3 G d and C 3 G d obtained by deacylation of corresponding N-glucosides, were compared with A2 , B 2 , C 2 - All compounds were tested for their antiviral activity and it was found that they were highly active against poliomyelitis type-3 virus.

📌 3 Key Takeaways

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Objective & Hypothesis:In this study, 5-thioeter derivatives; 1, 2, 4-triazole-5-thioacetic acid = A2 , 3-methyl-l, 2, 4-triazole-5-thioacetic acid = B 2 , 3-ethyl-l, 2, 4-triazole-5-thioacetic acid = C2 and their ethyl esters 1, 2, 4-triazole-5-thioacetic acid ethyl ester = A3 , 3-methyl-l, 2, 4-triazole-5- thioacetic acid ethyl ester = B 3 , 3-ethyl-l,2,4-triazole-5-thioacetic acid ethyl ester = C3 were prepared using 3-substitued-5-mercapto-l, 2, 4-triazoles synthesised previously.
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Key Findings & Data:In order to investigate the effect of the ose molecule on activity, the compounds were converted to their nucleosides.
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Conclusion & Impact:The water soluble derivatives, A3G d , B 3 G d and C 3 G d obtained by deacylation of corresponding N-glucosides, were compared with A2 , B 2 , C 2 - All compounds were tested for their antiviral activity and it was found that they were highly active against poliomyelitis type-3 virus.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:antiviral · 5-disubstitue · 4-triazolederivatives

Abstract

In this study, 5-thioeter derivatives; 1, 2, 4-triazole-5-thioacetic acid = A2 , 3-methyl-l, 2, 4-triazole-5-thioacetic acid = B 2 , 3-ethyl-l, 2, 4-triazole-5-thioacetic acid = C2 and their ethyl esters 1, 2, 4-triazole-5-thioacetic acid ethyl ester = A3 , 3-methyl-l, 2, 4-triazole-5- thioacetic acid ethyl ester = B 3 , 3-ethyl-l,2,4-triazole-5-thioacetic acid ethyl ester = C3 were prepared using 3-substitued-5-mercapto-l, 2, 4-triazoles synthesised previously. In order to investigate the effect of the ose molecule on activity, the compounds were converted to their nucleosides. The water soluble derivatives, A3G d , B 3 G d and C 3 G d obtained by deacylation of corresponding N-glucosides, were compared with A2 , B 2 , C 2 - All compounds were tested for their antiviral activity and it was found that they were highly active against poliomyelitis type-3 virus.

Özet

Bu çalışmada daha önce sentezleri gerçekleştirilen (1), 3-sübstitüe-5-merkapto-l, 2, 4-triazol'lerden hareketle 5-tiyoeter türevleri olan; 1, 2, 4-triazol-5-tiyoasetik asit = A2 , 3-metil-l, 2, 4-triazol-5- tiyoasetik asit = B 2 , 3-etil-l, 2, 4-triazol-5-tiyoasetik asit = C 2 , 1, 2, 4-triazol-5-tiyoasetikasit etil esteri= A3 , 3-metil-l, 2, 4-triazol-5-tiyoasetik asit etil esteri = B3 , 3-etil-l, 2, 4-triazol-5-tiyoasetik asit etil esteri = C 2 türevleri sentez edildi. Bu bileşiklerden A3 , B3 ve C2 türevlerinin antiviral etkileri karşılaştırılarak A2 , B 2 , C2 türevlerine ozun getireceği etkiyi incelemek ve suda çözünür hale dönüştürmek üzere glikozaminle nükleozitleri hazırlandı. Elde edilen nükleozitlerin deasetilasyonlarıyla A3G d , B 3 G d ve C 3 G d elde edildi. Daha sonra antiviral etkileri araştırıldı. RN A grubu viruslardan poliomielitis Tip-3 virusuna etkili oldukları görüldü.

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Cite This Article

ERTAN, M., ERSAN, S. (1983). The synthesis and biological activity of some antiviral 3,5-disubstitue1,2,4-triazolederivatives. Ankara Üniversitesi Eczacılık Fakültesi Dergisi, Cilt: 13 - Sayı: 1, 78–88. https://ajindex.com/articles/118781

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