Abstract
Schiff bases of the tetrahydropyran series have been synthesized by the condensation of 2-(tetrahydropyran-4-yl)ethanamines and tetrahydropyran-4-amine with 4-chloro, 4-fluoro-, and 4-(dimethylamino)benzaldehydes and thiophene-2-carbaldehyde. The synthesized compounds showed lower anti-inflammatory, analgesic, and antipyretic activities than those of diclofenac and indomethacin used as reference drugs.
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Biological experiments were carried out in full compliance with the European Convention and Directives of the European Parliament for the protection of vertebrate animals used for experimental and other scientific purposes [5].
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Isakhanyan, A.U., Hakobyan, N.Z., Muradyan, R.E. et al. Synthesis and Anti-inflammatory, Analgesic, and Antipyretic Activities of Azomethine Derivatives of the Tetrahydropyran Series. Russ J Org Chem 60, 539–542 (2024). https://doi.org/10.1134/S1070428024030230
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DOI: https://doi.org/10.1134/S1070428024030230