Preparation and Anticancer Activities of Some Amino Acid Methyl Ester Schiff Bases      
Yazarlar (3)
Nilay Akkuş Taş
Tokat Gaziosmanpaşa Üniversitesi, Türkiye
Doç. Dr. Ayşegül ŞENOCAK Tokat Gaziosmanpaşa Üniversitesi, Türkiye
Ali Aydın
Tokat Gaziosmanpaşa Üniversitesi, Türkiye
Makale Türü Açık Erişim Özgün Makale
Makale Alt Türü Ulusal alan endekslerinde (TR Dizin, ULAKBİM) yayınlanan tam makale
Dergi Adı Journal of the Turkish Chemical Society, Section A: Chemistry
Dergi ISSN 2149-0120 Scopus Dergi
Dergi Tarandığı Indeksler TR DİZİN
Makale Dili İngilizce
Basım Tarihi 06-2018
Cilt No 11
Sayı 1
Sayfalar 999 / 999
Makale Linki http://dergipark.gov.tr/jotcsa/issue/33408/373904
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 development studies.
Anahtar Kelimeler
Amino acid Schiff base | salicylaldehyde | antiproliferative activity | cytotoxicity | anticancer activity
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