Antiproliferative Effects against A549, Hep3B and FL Cell Lines of Cyclotriphosphazene‐Based Novel Protic Molten Salts: Spectroscopic, Crystallographic and Thermal Results.    
Yazarlar (6)
Aytuğ Okumuş
Ankara Üniversitesi, Türkiye
Doç. Dr. Hüseyin AKBAŞ Tokat Gaziosmanpaşa Üniversitesi, Türkiye
Ahmet Karadağ
Tokat Gaziosmanpaşa Üniversitesi, Türkiye
Ali Aydın
Tokat Gaziosmanpaşa Üniversitesi, Türkiye
Zeynel Kılıç
Ankara Üniversitesi, Türkiye
Tuncer Hökelek
Hacettepe Üniversitesi, Türkiye
Makale Türü Özgün Makale
Makale Alt Türü SSCI, AHCI, SCI, SCI-Exp dergilerinde yayınlanan tam makale
Dergi Adı Chemistryselect
Dergi ISSN 2365-6549 Wos Dergi Scopus Dergi
Dergi Tarandığı Indeksler SCI-Expanded
Dergi Grubu Q3
Makale Dili İngilizce
Basım Tarihi 06-2017
Cilt No 2
Sayı 18
Sayfalar 4988 / 4999
DOI Numarası 10.1002/slct.201700497
Makale Linki https://doi.org/10.1002/slct.201700497
Özet
The protic molten salts (PMOS) of (1 a- 6 b) have been prepared from the reactions of tetrapyrrolidino (1-3) and tetrapiperidino (4-6) fully substituted phosphazenes with the gentisic and γ-resorcylic acids. The structures of PMOS (1 a-6 b) were characterized by elemental analyses, FTIR and 1H, 13C{1H}, 31P{1H} NMR techniques. The crystal structures of 1 b and 2 b were established by X-ray diffraction method. The thermal properties of PMOS were verified using thermogravimetric instruments. In addition, this study also focused on the pharmacological abilities of the PMOS to affect the cell growth and cell cytotoxicity on A549, Hep3B and normal human amnion (FL) cell lines and to interact with calf thymus DNA (CT-DNA). Studies on the cells displayed that these PMOS demonstrated significant antiproliferative effect in conjunction with caused apoptotic-like changes in morphology. The PMOS are able to strongly bind to CT-DNA through minor groove binding modes with hyperchromic effect. The IC50 and binding constant ranges of the PMOS were found to be as 25–160 μM and 0.5 x 103 −12.0 x 103 M−1, respectively. These findings indicate that the PMOS 1 b-6 b are more antiproliferative than those of the PMOS 1 a-6 a. Moreover, it is observed that the CT-DNA most significantly bound the PMOS 1 b-6 b. Consequently, a good correlation between the antiproliferative effects and their binding activities of these PMOS was observed.
Anahtar Kelimeler
Antiproliferation,Cytotoxicity,DNA cleavage,Phosphazenes,Protic molten