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Journals / Marmara Pharmaceutical Journal / 2017 / Cilt: 21 - Sayı: 1

The synthesis and evaluation of anti-acetylcholinesterase activity of some 4(3H)-quinazolinone derivatives bearing substituted 1,3,4- thiadiazole

1,3,4-tiyadiazol içeren bazı 4(3H)-kinazolinon türevlerinin sentezi ve anti-asetilkolinesteraz aktiviteleri

Zafer Asım KAPLANCIKLI
Sevgi KARAKUŞ
Sevim ROLLAS
Usama ABU MOHSEN
Mine URAZ
Pages
96–101
Publication Date
2022-10-18
DOI
—
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AI Summary & Key Takeaways

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⚡ TL;DR(Too Long; Didn't Read)

The structures of the synthesized compounds were confirmed by elemental analysis, ıR, 1h-nMR and mass spectroscopic (5b and 5f) methods. each derivative was evaluated for its ability to inhibit acetylcholinesterase (Ache) using a modification of ellman’s spectrophotometric method. compounds 2-methyl-3-{4-[5-(ethylamino)-1,3,4-thiadiazol2-yl]phenyl}quinazolin-4(3H)-one (5b) and 2-methyl-3-{4-[5(cyclohexylamino)-1,3,4-thiadiazol-2-yl]phenyl}quinazolin4(3H)-one (5d) can be identified as promising anticholinesterase agents due to their inhibitory effect when compared with donepezil as a reference drug.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:ın the present study, a series of 4(3H)-quinazolinone derivatives (5a-f) were synthesized through the cylization reaction of substituted 1,3,4-thiadiazoles containing an aromatic primary amin and anthranilic acid in the presence of acetic anhydride and acetic acid.
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Key Findings & Data:ın the present study, a series of 4(3H)-quinazolinone derivatives (5a-f) were synthesized through the cylization reaction of substituted 1,3,4-thiadiazoles containing an aromatic primary amin and anthranilic acid in the presence of acetic anhydride and acetic acid.
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Conclusion & Impact:The structures of the synthesized compounds were confirmed by elemental analysis, ıR, 1h-nMR and mass spectroscopic (5b and 5f) methods. each derivative was evaluated for its ability to inhibit acetylcholinesterase (Ache) using a modification of ellman’s spectrophotometric method. compounds 2-methyl-3-{4-[5-(ethylamino)-1,3,4-thiadiazol2-yl]phenyl}quinazolin-4(3H)-one (5b) and 2-methyl-3-{4-[5(cyclohexylamino)-1,3,4-thiadiazol-2-yl]phenyl}quinazolin4(3H)-one (5d) can be identified as promising anticholinesterase agents due to their inhibitory effect when compared with donepezil as a reference drug.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

ın the present study, a series of 4(3H)-quinazolinone derivatives (5a-f) were synthesized through the cylization reaction of substituted 1,3,4-thiadiazoles containing an aromatic primary amin and anthranilic acid in the presence of acetic anhydride and acetic acid. The structures of the synthesized compounds were confirmed by elemental analysis, ıR, 1h-nMR and mass spectroscopic (5b and 5f) methods. each derivative was evaluated for its ability to inhibit acetylcholinesterase (Ache) using a modification of ellman’s spectrophotometric method. compounds 2-methyl-3-{4-[5-(ethylamino)-1,3,4-thiadiazol2-yl]phenyl}quinazolin-4(3H)-one (5b) and 2-methyl-3-{4-[5(cyclohexylamino)-1,3,4-thiadiazol-2-yl]phenyl}quinazolin4(3H)-one (5d) can be identified as promising anticholinesterase agents due to their inhibitory effect when compared with donepezil as a reference drug.

Özet

Bu çalışmada, aromatik pirimer amin içeren sübstitüe 1,3,4-tiyadiazoller ile antranilik asitin asetik asit ve asetik anhidritli ortamdaki siklizasyonundan bir seri 4(3H)kinazolinon türevi (5a-f) sentez edildi. Bileşiklerin yapıları ıR, 1h-nMR, kütle spektroskopisi (5b ve 5f) ve elementel analiz yöntemleri kullanılarak aydınlatıldı. Bileşiklerin aktivite tayini ellman’ın modifiye edilmiş spektrofotometrik yöntemi kullanılarak yapıldı. Donepezil standardı ile karşılaştırıldığında bileşik 5b (2-metil-3-{4-[5-(etilamino)-1,3,4-tiyadiazol-2-il] fenil}kinazolin-4(3H)-on) ve bileşik 5d (2-metil-3-{4-[5(siklohegzilamino)-1,3,4-tiyadiazol-2-il]fenil}kinazolin-4(3H)on) inhibitör etkilerine göre antikolinesteraz ajanları olarak tanımlanabilirler.

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Cite This Article

KAPLANCIKLI, Z. A., KARAKUŞ, S., ROLLAS, S., MOHSEN, U. A., URAZ, M. (2022). The synthesis and evaluation of anti-acetylcholinesterase activity of some 4(3H)-quinazolinone derivatives bearing substituted 1,3,4- thiadiazole. Marmara Pharmaceutical Journal, Cilt: 21 - Sayı: 1, 96–101. https://ajindex.com/articles/578549

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