Synthesis and anticancer and cytotoxic effects of novel 1,4-phenylene-bis-N-thiocarbamoylpyrazole and 1,4-phenylene-bis-pyrazolylthiazole derivatives
Yazarlar (5)
Prof. Dr. Meliha Burcu GÜRDERE Tokat Gaziosmanpaşa Üniversitesi, Türkiye
Erdoğan Kamo Tokat Gaziosmanpaşa Üniversitesi, Türkiye
Prof. Dr. Yakup BUDAK Tokat Gaziosmanpaşa Üniversitesi, Türkiye
Ayşe Şahin Yağlıoğlu Çankırı Karatekin Üniversitesi, Türkiye
Prof. Dr. Mustafa CEYLAN Tokat Gaziosmanpaşa Üniversitesi, Türkiye
| Makale Türü | Özgün Makale (SSCI, AHCI, SCI, SCI-Exp dergilerinde yayınlanan tam makale) | ||
| Dergi Adı | TURKISH JOURNAL OF CHEMISTRY (Q4) | ||
| Dergi ISSN | 1300-0527 Wos Dergi Scopus Dergi | ||
| Dergi Tarandığı Indeksler | SCI-Expanded | ||
| Makale Dili | İngilizce | Basım Tarihi | 01-2017 |
| Cilt / Sayı / Sayfa | 41 / 2 / 179–189 | DOI | 10.3906/kim-1604-84 |
| Makale Linki | http://online.journals.tubitak.gov.tr/openDoiPdf.htm?mKodu=kim-1604-84 | ||
| Özet |
| Thiazolylpyrazoline derivatives were recently reported as potent anticancer agents. In this study, novel 1, 4-phenylene-bis-N-thiocarbamoylpyrazoles (3a–h) and 1, 4-phenylene-bis-pyrazolylthiazoles (5a–h) were prepared and screened for their anticancer activities against C6 (rat brain tumor cells) and HeLa (human uterus carcinoma). Anticancer activity studies were performed as a dose-dependent assay starting with eight concentrations. 5-Fluorouracil (5-FU) was used as a positive control. Compounds 3c, 3d, and 3h were examined and they revealed almost the same activities compared with 5-FU in terms of cell selectivity against C6 cells. Moreover, compounds 3a–h had lower cytotoxicity than 5-FU. The low cytotoxicity values of 3a–h as well as their high antiproliferative activity were encouraging, but further studies are required on the use of these molecules as anticancer drugs. |
| Anahtar Kelimeler |
| Bis-chalcone | bis-N-thiocarbamoylpyrazole | bis-pyrazolylthiazole | HeLa | C6 | anticancer activity | cytotoxicity |
BM Sürdürülebilir Kalkınma Amaçları
| Atıf Sayıları | |
| Google Scholar | 3 |
| Google Scholar | 20 |
| Web of Science | 18 |