Synthesis and in vitro anticancer evaluation of 1,4-phenylene-bis-pyrimidine-2-amine derivatives      
Yazarlar (5)
Prof. Dr. Meliha Burcu GÜRDERE Tokat Gaziosmanpaşa Üniversitesi, Türkiye
Erdoğan Kamo
Tokat Gaziosmanpaşa Üniversitesi, Türkiye
Ayşe Şahin Yağlıoğlu
Çankırı Karatekin Üniversitesi, Türkiye
Prof. Dr. Yakup BUDAK Tokat Gaziosmanpaşa Üniversitesi, Türkiye
Prof. Dr. Mustafa CEYLAN Tokat Gaziosmanpaşa Üniversitesi, Türkiye
Makale Türü Özgün Makale
Makale Alt Türü SSCI, AHCI, SCI, SCI-Exp dergilerinde yayınlanan tam makale
Dergi Adı Turkish Journal of Chemistry
Dergi ISSN 1300-0527 Wos Dergi Scopus Dergi
Dergi Tarandığı Indeksler SCI-Expanded
Dergi Grubu Q4
Makale Dili İngilizce
Basım Tarihi 01-2017
Cilt No 41
Sayı 2
Sayfalar 263 / 271
DOI Numarası 10.3906/kim-1603-112
Makale Linki http://online.journals.tubitak.gov.tr/openDoiPdf.htm?mKodu=kim-1603-112
Özet
A series of 1,4-phenylene-bis-chalcones 3a 3h were synthesized by the reaction of terephthalaldehyde with substituted arylketones in this study. The novel 1,4-phenylene-bis-pyrimidine-2-amine derivatives 5a 5h were obtained by the addition of guanidine hydrochloride to 1,4-phenylene-bis-chalcone 3a 3h in ethanolic KOH under reflux conditions. The structure of the compounds was explained by means of IR, 1 H NMR, 13 C NMR, and elemental analyses. The anticancer activities of 3a 3h and 5a 5h were investigated against rat brain tumor cells and human uterus carcinoma in vitro. Activity tests were performed as dose-dependent assays at eight concentrations. The positive control was 5- fluorouracil (5-FU). Compounds 3c and 3d were examined and they showed high activities as compared to 5-FU against C6 (rat brain tumor) and HeLa (human uterus carcinoma) cells. The anticancer activity of 5h was better than that of 5-FU at high concentrations cell-selectively against C6 cells.
Anahtar Kelimeler
1,4-Phenylene-bis-chalcone | 1,4-phenylene-bis-pyrimidine | HeLa | C6 | anticanceractivity | 5-fluorouracil