Synthesis of thiazole derivatives as cholinesterase inhibitors with antioxidant activity
Year 2023,
Volume: 2 Issue: 3, 118 - 124, 29.12.2023
Abdüllatif Karakaya
,
Zahra Maryam
,
Tugba Ercetin
,
Ulviye Acar Çevik
Abstract
In the present research, we synthesized two unique series of thiazole compounds having 5-bromothiophene and 3-methylthiophene (2a-2f) in their structure. After that, spectroscopic methods were used to analyze the chemical compositions of the newly synthesized molecules. Then in vitro evaluation was done to determine acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE) activity of the synthesized compounds using galantamine as reference standard. The compounds’ antioxidant properties were assessed using DPPH radical scavenging and ferrous ion-chelating techniques. The results of the study showed weak anticholinesterase activity against AChE and BuChE enzymes for all the final compounds. The synthesized analogs also showed significant DPPH radical scavenging activities with IC50 values in the range of 29.16 ± 0.009 to 33.09 ± 0.004 µM (for DDPH) incomparison to standard gallic acid with IC50 = 31.13 ± 0.008 µM (for DDPH). Especially, compound 2c showed the best antioxidant activity with IC50 value of 29.16 ± 0.009 µM.
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Year 2023,
Volume: 2 Issue: 3, 118 - 124, 29.12.2023
Abdüllatif Karakaya
,
Zahra Maryam
,
Tugba Ercetin
,
Ulviye Acar Çevik
References
- Gupta SM, Behera A, Jain NK, Tripathi A, Rishipathak D, Singh S, Ahemad N, Erol M, & Kumar D. Development of substituted benzylidene derivatives as novel dual cholinesterase inhibitors for Alzheimer’s treatment. RSC Adv. (2023); 13(38): 26344-26356. https://doi.org/10.1039/D3RA03224H.
- Siddiqui SZ, Arfan M, Abbasi MA, Shah SAA, Parveen R, Ashraf M, Solangi M, Hussain S, & Khan KM. Design, synthesis of triazole-based scaffolds, N-(substitutedphenyl)-2-(5-(4-methoxyphenyl)-4-phenyl-4H-1,2,4-triazol-3-ylthiol) acetamides: As potential anti-cholinesterase agents for neurodegenerative diseases. J Mol Struct. (2023); 135885. https://doi.org/10.1016/j.molstruc.2023.135885.
- Gutti G, Leifeld J, Kakarla R, Bajad NG, Ganeshpurkar A, Kumar A, Krishnamurthy S, Klein-Schmidt C, Tapken D, Hollmann M, & Singh SK. Discovery of triazole-bridged aryl adamantane analogs as an intriguing class of multifunctional agents for treatment of Alzheimer’s disease. Eur J Med Chem. (2023); 259: 115670. https://doi.org/10.1016/j.ejmech.2023.115670.
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- Tuğrak M, Gül Hİ, & Gülçin İ. Acetylcholinesterase inhibitory potencies of new pyrazoline derivatives. J Res Pharm. (2020); 24(4): 464-471. https://doi.org/10.35333/jrp.2020.194.
- Temel HE, Altintop MD, & Özdemir A. Synthesis and evaluation of a new series of thiazolyl-pyrazoline derivatives as cholinesterase inhibitors. Turk J Pharm Sci. (2018); 15(3): 333-338. https://doi.org/10.4274/tjps.20982.
- Budak Y, Kocyigit UM, Gürdere MB, Özcan K, Taslimi P, Gülçin İ, & Ceylan M. Synthesis and investigation of antibacterial activities and carbonic anhydrase and acetyl cholinesterase inhibition profiles of novel 4, 5-dihydropyrazol and pyrazolyl-thiazole derivatives containing methanoisoindol-1, 3-dion unit. Synth Commun. (2017); 47(24): 2313-2323. https://doi.org/10.1080/00397911.2017.1373406.
- Ellman GL, Courtney KD, Andres Jr V, & Featherstone RM. A new and rapid colorimetric determination of acetylcholinesterase activity. Biochem Pharmacol. (1961); 7(2): 88-95. https://doi.org/10.1016/0006-2952(61)90145-9.
- Dinis TCP, Madeira VMC., & Almeida LM. Action of phenolic derivatives (acetaminophen, salicylate, and 5-aminosalicylate) as inhibitors of membrane lipid peroxidation and peroxyl radical scavengers. Arch Biochem Biophys. (1994); 315: 161–169. https://doi.org/10.1006/abbi.1994.1485.
- Ercetin T, Senol FS, Orhan IE, and Toker G. Comparative assessment of antioxidant and cholinesterase inhibitory properties of the marigold extracts from Calendula arvensis L. and Calendula officinalis L. Ind Crops Prod. (2012); 36(1): 203-208. https://doi.org/10.1016/j.indcrop.2011.09.007.
- Blois MS. Antioxidant determinations by the use of a stable free radical. Nature. (1958); 181(4617): 1199-1200. https://doi.org/10.1038/1811199a0.