Journals / International Journal of Chemistry and Technology / 2022 / Cilt: 6 - Sayı: 1

Synthesis and biological activities of new hybrid chalcones with benzoic acid ring

Benzoik asit halkali yeni hibrit kalkonlarin sentezi ve biyolojik aktiviteleri

Pages
7–14
Publication Date
2022-07-06
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

It was found that the most active compound against AChE enzyme in anticholinesterase inhibition activity was compound 1.

📌 3 Key Takeaways

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Objective & Hypothesis:A series of E-4-(3-oxo-3-(substituted)prop-1-en-1-yl)benzoic acid derivatives (1-5) were synthesized by the Claisen-Schmidt condensation of various ketones with 4-formylbenzoic acid.
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Key Findings & Data:The anticholinesterase (AChE and BChE), tyrosinase, and urease inhibition activities of the synthesized compounds (1-5) were examined.
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Conclusion & Impact:It was found that the most active compound against AChE enzyme in anticholinesterase inhibition activity was compound 1.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Chalcone · Anticholinesterase activity · Tyrosinase inhibitory activity

Abstract

A series of E-4-(3-oxo-3-(substituted)prop-1-en-1-yl)benzoic acid derivatives (1-5) were synthesized by the Claisen-Schmidt condensation of various ketones with 4-formylbenzoic acid. The anticholinesterase (AChE and BChE), tyrosinase, and urease inhibition activities of the synthesized compounds (1-5) were examined. It was found that the most active compound against AChE enzyme in anticholinesterase inhibition activity was compound 1. Compound 4 was the most active compound in tyrosinase inhibition activity, while compound 3 was the most active compound in urease psychological activity.

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Cite This Article

AKTAR, B. S. K., SICAK, Y., ORUÇ-EMRE, E. E. (2022). Synthesis and biological activities of new hybrid chalcones with benzoic acid ring. International Journal of Chemistry and Technology, Cilt: 6 - Sayı: 1, 7–14. https://ajindex.com/articles/764927

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