Studies on imidazopyridine derivatives as acetylcholinesterase inhibitors

Yıl 2012, Cilt: 2 Sayı: 3, 119 - 123, 30.01.2014

Usama Abu Mohsen

Öz

Objective: In this study we aimed to synthesize some hydrazide derivatives of imidazo[1,2-a]pyridine and to evaluate their anti-cholinesterase activities. 

Method: The reaction of imidazo[1,2-a]pyridine-2-carboxylic acid hydrazides with various benzaldehydes gave N-(benzylidene)imidazo[1,2-a]pyridine-2-carboxylic acid hydrazide derivatives. The chemical structures of the compounds were elucidated by IR, 1H-NMR, FAB+-MS spectral data and elemental analysis. In the pharmacological study, anti-cholinesterase activities of these compounds have been evaluated by using modified Ellman’s spectrophotometric method.

Results: Three of the synthesized compounds (2, 3 and 4) can be identified as promising anticholinesterase agents due to their inhibitory effect on AChE with IC50 value of 74.42±4.29, 43.26±7.28 and 18.29±2.31 μM, respectively when compared with Donepezil (IC50=0.058±0.002 μM).

Conclusion: The halogen substitutions on phenyl ring have a crucial influence on anticholinesterase activity.

Key words: Imidazo[1,2-a]pyridine, hydrazone, cholinesterase inhibitors

Anahtar Kelimeler

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Asetilkolinesteraz inhibitörleri olarak imidazopiridin türevleri üzerine çalışmalar

Öz

Amaç: Bu çalışmada, imidazo[1,2-a]piridinin bazı hidrazid türevlerinin sentezlenmesi ve antikolinesteraz aktivitelerinin araştırılması amaçlandı. 

Yöntem: İmidazo[1,2-a]piridin-2-karboksilik asid hidrazidi ile çeşitli benzaldehit türevlerinin reaksiyonu ile hedef bileşikler olan N-(benziliden)imidazo[1,2-a]piridin-2-karboksilik asid hidrazid türevlerine ulaşıldı. Bileşiklerin kimyasal yapıları, IR, 1H-NMR ve FAB+-MS spektral verileri ve elementel analiz verileri ile aydınlatıldı. Modifiye edilmiş Ellman spektrofotometrik metodu kullanılarak, elde edilen tüm bileşiklerin asetilkolinesteraz (AChE) inhibisyonları incelendi.

Bulgular: Donepezil (IC50=0.058±0.002 μM) ile kıyaslandığında, sentezlenen bileşiklerin üç tanesinin (2, 3 ve 4), IC50 değerleri sırasıyla 74.42±4.29, 43.26±7.28 ve 18.29±2.31 μM olarak ölçülmüş ve AChE üzerinde ümit verici inhibisyonları gözlenmiştir.

Sonuçlar: Fenil halkası üzerindeki halojen sübstitisyonunun, antikolinesteraz etki üzerinde önemli katkısı vardır.

Anahtar Kelimeler : İmidazo[1,2-a]piridin, hidrazon, kolinesteraz inhibitörleri

Anahtar Kelimeler

İmidazo[1, 2-a]piridin, hidrazon, kolinesteraz inhibitörleri

Kaynakça

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