Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Dilan Ozmen Ozgun"'
Autor:
Gonca Alak, Cem Yamali, Arzu Uçar, Telat Yanik, Dilan Ozmen Ozgun, Rana Almuhur, Muhammed Atamanalp, Veysel Parlak, Halise Inci Gul, Mahmut Kocaman, Ahmed O. Maslat
Publikováno v:
In Vitro Cellular & Developmental Biology - Animal. 57:17-20
[Abstract Not Available]
Autor:
Feyza Sena Engin, Mehtap Tugrak, Yusuf Özkay, Cem Yamali, Halise Inci Gul, Serkan Levent, Sinan Bilginer, Begüm Nurpelin Sağlık, Dilan Ozmen Ozgun, Gulsen Ozli
Publikováno v:
Journal of Heterocyclic Chemistry. 58:161-171
Chalcones targeting neurodegenerative diseases have been known as attractive structures in drug design and discovery. In this study, phenothiazine-based chalcones as ChEs and MAOs inhibitors were designed and synthesizedviabase-catalyzed Claisen-Schm
Autor:
Cem Yamali, Veysel Parlak, Gonca Alak, Dilan Ozmen Ozgun, Mahmut Kocaman, Arzu Uçar, Ahmad Maslat, Telat Yanik, Halise Inci Gul, Muhammed Atamanalp, Sinan Bilginer
Publikováno v:
Pakistan Journal of Zoology. 53
Autor:
Cem Yamali, Kaspars Tars, Claudiu T. Supuran, Halise Inci Gul, Dilan Ozmen Ozgun, Janis Leitans, Andris Kazaks, Andrea Angeli, Hiroshi Sakagami
Publikováno v:
Bioorganic Chemistry. 77:411-419
In this study, new 4-13-(aryl)-5-substitutedphenyl-4,5-dihydro-1H-pyrazole-1-yllbenzensulfonamides (19-36) were synthesized and evaluated their cytotoxic/anticancer and CA inhibitory effects. According to results obtained, the compounds 34 (4-[5-(2,3
Autor:
Halise Inci Gul, Noriyuki Okudaira, Hiroshi Sakagami, Dilan Ozmen Ozgun, Cem Yamali, Cavit Kazaz
Publikováno v:
Medicinal Chemistry Research. 26:2015-2023
The compounds titled 1-(2,5/3,5-difluorophenyl)-3-(2,3/2,4/2,5/3,4-dimethoxyphenyl)-2-propen-1-ones (1-8) were synthesized via Claisen-Schmidt condensation under basic condition. The chemical structure of the compounds were identified using several s
Autor:
Dilan Ozmen Ozgun, Telat Yanik, İlhami Gülçin, Claudiu T. Supuran, Cem Yamali, Halise Inci Gul, Parham Taslimi
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry. 31:1498-1501
The effects of isatin Mannich bases incorporating (1-[piperidin-1-yl (P1)/morpholin-4-yl (P2)/N-methylpiperazin-1-yl (P3)]methyl)-1H-indole-2,3-dione) moieties against human (h) carbonic anhydrase (CA, EC 4.2.1.1) isoenzymes hCA I and hCA II, acetylc
Pyrazolines are reported with a broad range of bioactivities, excellent fluorescence properties and easy synthesis. But unfortunately, there is no or very limited information available about their pH sensor application. Additionally, there is a littl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::489b812ac89d406bacb194f7cc6956c9
https://hdl.handle.net/20.500.12501/763
https://hdl.handle.net/20.500.12501/763
Autor:
Naoki Umemura, Cavit Kazaz, Halise Inci Gul, Hiroshi Sakagam, Cem Yamali, Mustafa Gul, Dilan Ozmen Ozgun
Publikováno v:
Anti-Cancer Agents in Medicinal Chemistry. 17
Background: Although anticancer chemotherapeutics are available in markets, side effects related to the drugs in clinical use lead to researchers to investigate new drug candidates which are more safe, potent and selective than others. Chalcones are