Preparation and cytotoxicity evaluation of some amino acid methyl ester schiff bases
Yazarlar (3)
Dr. Öğr. Üyesi Nilay Akkuş Taş Tokat Gaziosmanpaşa Üniversitesi, Türkiye
Doç. Dr. Ayşegül ŞENOCAK Tokat Gaziosmanpaşa Üniversitesi, Türkiye
Prof. Dr. Ali Aydın Tokat Gaziosmanpaşa Üniversitesi, Türkiye
Makale Türü Açık Erişim Özgün Makale (SCOPUS dergilerinde yayınlanan tam makale)
Dergi Adı Journal of the Turkish Chemical Society Section A Chemistry
Dergi ISSN 2149-0120 Scopus Dergi
Makale Dili İngilizce Basım Tarihi 01-2018
Cilt / Sayı / Sayfa 5 / 2 / 585–606 DOI 10.18596/jotcsa.373904
Makale Linki https://dergipark.org.tr/en/download/article-file/453905
UAK Araştırma Alanları
Fen Bilimleri ve Matematik
Özet
In this study, we prepared nine Schiff bases by condensation of amino acid methyl esters (isoleucine, phenylalanine, and methionine) with salicylaldehyde derivatives (2,4-dihydroxybenzaldehyde, 2-hydroxy-3-methoxybenzaldehyde, and 5-bromo-2-hydroxybenzaldehyde) and characterized by various spectroscopic methods (FT-IR, UV-Vis, and NMR techniques). FT-IR and UV-Vis spectra exhibited characteristic peaks for all imine compounds. NMR spectra pointed out the imine bond which is the indicator of the formation of Schiff bases. Besides, antiproliferative and cytotoxic features of the Schiff bases were examined by using MTT cell proliferation and LDH cytotoxicity assays, respectively. Amongst the synthesized Schiff bases, compound 3d exhibited a very strong antiproliferative effect against all cells except A549. The experimental studies revealed that the Schiff bases synthesized in this study, especially 3d, have an important potential to enter drug developmental studies.
Anahtar Kelimeler
Amino acid Schiff bases | Antiproliferative activity | Cytotoxicity | NMR spectra | Salicylaldehyde
BM Sürdürülebilir Kalkınma Amaçları
Atıf Sayıları
Scopus 9
Google Scholar 10
Preparation and cytotoxicity evaluation of some amino acid methyl ester schiff bases

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