Synthesis, characterization, crystal structures, theoretical calculations and biological evaluations of novel substituted tacrine derivatives as cholinesterase and carbonic … S Ökten, M Ekiz, ÜM Koçyiğit, A Tutar, İ Çelik, M Akkurt, F Gökalp, ... Journal of Molecular Structure 1175, 906-915, 2019 | 78 | 2019 |
Efficient and selective synthesis of quinoline derivatives A Sahin, O Cakmak, I Demirtas, S Okten, A Tutar Tetrahedron 64 (43), 10068-10074, 2008 | 69 | 2008 |
Simple and convenient preparation of novel 6, 8-disubstituted quinoline derivatives and their promising anticancer activities S ÖKTEN, O Cakmak, R Erenler, ÖY ŞAHİN, Ş TEKİN Turkish Journal of Chemistry 37 (6), 896-908, 2013 | 66 | 2013 |
Quinoline‐based promising anticancer and antibacterial agents, and some metabolic enzyme inhibitors S Ökten, A Aydın, ÜM Koçyiğit, O Çakmak, S Erkan, CA Andac, P Taslimi, ... Archiv der Pharmazie 353 (9), 2000086, 2020 | 41 | 2020 |
Biological evaluation of some quinoline derivatives with different functional groups as anticancer agents TK Köprülü, S Ökten, Ş Tekin, O Çakmak Journal of Biochemical and Molecular Toxicology 33 (3), e22260, 2019 | 41 | 2019 |
Synthesis, characterization, and SAR of arylated indenoquinoline‐based cholinesterase and carbonic anhydrase inhibitors M Ekiz, A Tutar, S Ökten, B Bütün, ÜM Koçyiğit, P Taslimi, G Topçu Archiv der Pharmazie 351 (9), 1800167, 2018 | 38 | 2018 |
A SAR Study: Evaluation of bromo derivatives of 8-substituted quinolines as novel anticancer agents S Okten, O Cakmak, S Tekin, TK Koprulu Letters in Drug Design & Discovery 14 (12), 1415-1424, 2017 | 30 | 2017 |
Synthesis of novel cyano quinoline derivatives S Ökten, O Çakmak Tetrahedron letters 56 (39), 5337-5340, 2015 | 30 | 2015 |
Novel Piperazine and Morpholine Substituted Quinolines: Selective Synthesis through Activation of 3,6,8-Tribromoquinoline, Characterization and Their Some Metabolic Enzymes … O Çakmak, S Ökten, D Alımlı, CC Ersanlı, ÜM Koçyiğit, P Taslimi Journal of Molecular Structure, 2020 | 27 | 2020 |
Synthesis of brominated quinolines S ÖKTEN, D EYİGÜN, O Cakmak Sigma Journal of Engineering and Natural Sciences 33 (1), 8-15, 2015 | 24 | 2015 |
Convenient synthesis of disubstituted tacrine derivatives via electrophilic and copper induced reactions M Ekiz, A Tutar, S Ökten Tetrahedron 72 (35), 5323-5330, 2016 | 23 | 2016 |
The SAR study of 6,8-disubstituted quinoline derivatives as anti cancer agents S ÖKTEN, O ÇAKMAK, Ş TEKİN Turkish Journal of Clinics and Laboratory 8 (4), 152-159, 2017 | 19* | 2017 |
SAR evaluation of disubstituted tacrine analogues as promising cholinesterase and carbonic anhydrase inhibitors B BÜTÜN, G TOPÇU, S ÖKTEN, M EKIZ, A TUTAR, ÜM Koçyiğit, İ Gülçin Indian Journal of Pharmaceutical Education 53 (2), 23-29, 2019 | 16 | 2019 |
In vitro antiproliferative/cytotoxic activity of 2, 3'-biindole against various cancer cell lines S ÖKTEN, R Erenler, TKUL KÖPRÜLÜ, Ş TEKİN Turkish Journal of Biology 39 (1), 15-22, 2015 | 16 | 2015 |
Decision making for promising quinoline‐based anticancer agents through combined methodology E Özcan, S Ökten, T Eren Journal of Biochemical and Molecular Toxicology 34 (9), e22522, 2020 | 15 | 2020 |
Regioselective bromination: Synthesis of brominated methoxyquinolines O Çakmak, S Ökten Tetrahedron 73 (36), 5389-5396, 2017 | 15 | 2017 |
Biological activity and molecular docking studies of some new quinolines as potent anticancer agents T Kul Köprülü, S Ökten, V Enisoğlu Atalay, Ş Tekin, O Çakmak Medical Oncology 38 (7), 84, 2021 | 14 | 2021 |
Reinvestigation of bromination of 8-substituted quinolines and synthesis of novel phthalonitriles S Ökten, O Çakmak, A Saddiqa, B Keskin, S Özdemir, M İnal Org. Commun 9 (4), 82-93, 2016 | 14 | 2016 |
Activation of 6-bromoquinoline by nitration: synthesis of morpholinyl and piperazinyl quinolines O Çakmak, S Ökten, D Alımlı, A Saddiqa, CC Ersanlı Arkivoc 2018 (iii), 362-374, 2018 | 11* | 2018 |
In vitro antiproliferative/cytotoxic activity of novel quinoline compound SO-18 against various cancer cell lines S Ökten, ÖY Şahin, Ş Tekin, O Çakmak J. Biotechn 185, S106, 2014 | 11 | 2014 |