Synthesis of novel oxadiazole derivatives and their cytotoxic activity against various cancer cell lines
| dc.authorid | 0000-0003-0957-6965 | |
| dc.authorid | 0000-0001-6975-6808 | |
| dc.contributor.author | Sucu, Bilgesu Onur | |
| dc.contributor.author | Koç, Elif Beyza | |
| dc.date.accessioned | 2022-09-27T09:44:40Z | |
| dc.date.available | 2022-09-27T09:44:40Z | |
| dc.date.issued | 2022 | |
| dc.department | İstanbul Medipol Üniversitesi, Rektörlük, Sağlık Bilim ve Teknolojileri Araştırma Enstitüsü | |
| dc.department | İstanbul Medipol Üniversitesi, Sağlık Hizmetleri Meslek Yüksekokulu, Tıbbi Laboratuvar Teknikleri Ana Bilim Dalı | |
| dc.description.abstract | Caffeic acid (CA), ferulic acid (FA) and caffeic acid phenethyl ester (CAPE) have a broad anticancer effect on various cell lines. In this study, nine ferulic and caffeic acid-based 1,2,4 and 1,3,4 oxadiazole molecular hybrids were synthesized and their cytotoxic activity was evaluated mainly against Glioblastoma (GBM) cell lines. Compounds 1 and 5 exhibited the highest inhibitory activity against three different GBM cell lines (LN229, T98G, and U87), without toxicity to healthy human mesenchymal stem cells (hMSC). In addition, their cytotoxicity was also evaluated against three additional cancer cell lines and more inhibitory results were found than GBM cell lines. The IC50 values of compound 5 in U87, T98G, LN229, SKOV3, MCF7, and A549 cells were determined as 35.1, 34.4, 37.9, 14.2, 30.9, and 18.3 µM. In the light of biological activity studies, the developed compounds have a high potential to lead studies for the development of new drug candidates for the treatment of cancer. | |
| dc.identifier.citation | Sucu, B. O. ve Koç, E. B. (2022). Synthesis of novel oxadiazole derivatives and their cytotoxic activity against various cancer cell lines. Turkish Journal of Chemistry, 46(4), 1089-1096. https://dx.doi.org/10.55730/1300-0527.3417 | |
| dc.identifier.doi | 10.55730/1300-0527.3417 | |
| dc.identifier.endpage | 1096 | |
| dc.identifier.issn | 1300-0527 | |
| dc.identifier.issue | 4 | |
| dc.identifier.scopus | 2-s2.0-85137398685 | |
| dc.identifier.scopusquality | Q3 | |
| dc.identifier.startpage | 1089 | |
| dc.identifier.trdizinid | 1141983 | |
| dc.identifier.uri | https://dx.doi.org/10.55730/1300-0527.3417 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12511/9756 | |
| dc.identifier.volume | 46 | |
| dc.identifier.wos | 000895319000012 | en_US |
| dc.identifier.wosquality | Q4 | |
| dc.indekslendigikaynak | Web of Science | |
| dc.indekslendigikaynak | Scopus | |
| dc.indekslendigikaynak | TR-Dizin | |
| dc.indekslendigikaynak | PubMed | |
| dc.institutionauthor | Sucu, Bilgesu Onur | |
| dc.institutionauthor | Koç, Elif Beyza | |
| dc.language.iso | en | |
| dc.publisher | TUBITAK | |
| dc.relation.ispartof | Turkish Journal of Chemistry | en_US |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | |
| dc.relation.tubitak | info:eu-repo/grantAgreement/TUBITAK/SOBAG/119Z116 | |
| dc.rights | Attribution 4.0 International | * |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.rights.uri | https://creativecommons.org/licenses/by/4.0/ | * |
| dc.subject | 1,2,4-Oxadiazoles | |
| dc.subject | 1,3,4-Oxadiazoles | |
| dc.subject | Anticancer Activity | |
| dc.subject | Glioblastoma Cancer Cells | |
| dc.title | Synthesis of novel oxadiazole derivatives and their cytotoxic activity against various cancer cell lines | |
| dc.type | Article |
