Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Abdullah Burak Karaduman"'
Autor:
Asaf Evrim Evren, Abdullah Burak Karaduman, Begüm Nurpelin Sağlik, Yusuf Özkay, Leyla Yurttaş
Publikováno v:
ACS Omega, Vol 8, Iss 1, Pp 1410-1429 (2022)
Externí odkaz:
https://doaj.org/article/195f883847704cf1b9b94e98b219ecf1
Autor:
Ulviye Acar Çevik, Begüm Nurpelin Sağlık, Derya Osmaniye, Serkan Levent, Betül Kaya Çavuşoğlu, Abdullah Burak Karaduman, Özlem Atlı Eklioğlu, Yusuf Özkay, Zafer Asım Kaplancıklı
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 35, Iss 1, Pp 1657-1673 (2020)
In this study, some benzimidazole-oxadiazole derivatives were synthesised and tested for their in vitro anticancer activities on five cancer cell lines, including HeLa, MCF7, A549, HepG2 and C6. Their structures were elucidated by IR, 1H-NMR, 13C-NMR
Externí odkaz:
https://doaj.org/article/8d3d80b3ed0b41ec929c75178d5bc4f6
Autor:
Gülhan Turan-Zitouni, Aouatef Tabbi, Weiam Hussein, Abdullah Burak Karaduman, Begüm Nurpelin Sağlık, Yusuf Özkay
Publikováno v:
Journal of Chemistry, Vol 2018 (2018)
A series of N-[1-(((3,4-diphenylthiazol-2(3H)-ylidene)amino)methyl)cyclopentyl]acetamide derivatives (4a-4i) were synthesized in good yield and assayed for their inhibitory potency against monoamine oxidase (MAO) isoforms. Structures of newly synthes
Externí odkaz:
https://doaj.org/article/16e4833e6a4048ffbd6ae6897708cd5e
Autor:
Derya Osmaniye, Serkan Levent, Abdullah Burak Karaduman, Sinem Ilgın, Yusuf Özkay, Zafer Asım Kaplancıklı
Publikováno v:
Molecules, Vol 23, Iss 5, p 1054 (2018)
During the last five decades, a large number of BT (Benzothiazole) derivatives formed one of the eligible structures in medicinal chemistry as anticancer agents. Most of the studies reveal that various substitutions at specific positions on BT scaffo
Externí odkaz:
https://doaj.org/article/b0ea3a44111d40999efa641702670410
Autor:
Betül Kaya Çavuşoğlu, Begüm Nurpelin Sağlık, Derya Osmaniye, Serkan Levent, Ulviye Acar Çevik, Abdullah Burak Karaduman, Yusuf Özkay, Zafer Asım Kaplancıklı
Publikováno v:
Molecules, Vol 23, Iss 1, p 60 (2017)
Twenty-six novel thiosemicarbazone derivative B1–B26 were synthesized via condensation reactions between the corresponding thiosemicarbazides and aldehydes. The chemical characterization of the compounds was carried out by infrared (IR), mass (MS),
Externí odkaz:
https://doaj.org/article/d82ffb48e6d740eea26bd7f0586b0bfb
Publikováno v:
Proceedings, Vol 1, Iss 6, p 639 (2017)
Benzimidazole derivatives have a great deal of interest in terms of antimicrobial therapy. [...]
Externí odkaz:
https://doaj.org/article/b9a71c809c394e58bd2032ad74f8f8f1
Autor:
Begüm Nurpelin Sağlık, Serkan Levent, Derya Osmaniye, Asaf Evrim Evren, Abdullah Burak Karaduman, Yusuf Özkay, Zafer Asım Kaplancıklı
Publikováno v:
ACS Omega. 7:47378-47404
Autor:
Derya Osmaniye, Serkan Levent, Begum Nurpelin Sağlık, Abdullah Burak Karaduman, Yusuf Özkay, Zafer Asım Kaplancıklı
Publikováno v:
New Journal of Chemistry. 46:7442-7451
The activity of the synthesized compounds against breast cancer was investigated. Molecular docking studies were performed against aromatase, MAO-B, and Caspase-3 enzymes.
Autor:
Begüm Nurpelin, Sağlık, Serkan, Levent, Derya, Osmaniye, Asaf Evrim, Evren, Abdullah Burak, Karaduman, Yusuf, Özkay, Zafer Asım, Kaplancıklı
Publikováno v:
ACS omega. 7(50)
Alzheimer's disease (AD) is a neurological, progressive illness that typically affects the elderly and is clinically distinguished by memory and cognitive decline. Due to a number of factors, including the absence of a radical treatment, an increase
Autor:
Begüm Nurpelin Sağlık, Zafer Asım Kaplancıklı, Betül Kaya Çavuşoğlu, Derya Osmaniye, Serkan Levent, Ahmet Mücahit Şen, Ulviye Acar Çevik, Abdullah Burak Karaduman, Yusuf Özkay, Asaf Evrim Evren
Publikováno v:
Zeitschrift für Naturforschung C. 75:353-362
Inhibition of aromatase enzymes is very important in the prevention of estrogen-related diseases and the regulation of estrogen levels. Aromatase enzyme is involved in the final stage of the biosynthesis of estrogen, in the conversion of androgens to