Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Serdar, Burmaoglu"'
Autor:
Serdar Burmaoglu, Arzu Gobek, Derya Aktas Anil, Mehmet Abdullah Alagoz, Adem Guner, Cem Güler, Ceylan Hepokur, N. Ulku Karabay Yavasoglu, Oztekin Algul
Publikováno v:
Polycyclic Aromatic Compounds. :1-16
Autor:
Serdar Burmaoglu, Oztekin Algul, Arzu Gobek, Derya Aktas Anil, Mahmut Ulger, Busra Gul Erturk, Engin Kaplan, Aylin Dogen, Gönül Aslan
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 32, Iss 1, Pp 490-495 (2017)
Owing to ever-increasing bacterial and fungal drug resistance, we attempted to develop novel antitubercular and antimicrobial agents. For this purpose, we developed some new fluorine-substituted chalcone analogs (3, 4, 9–15, and 20–23) using a st
Externí odkaz:
https://doaj.org/article/77706c4888f74a14bb0edeae9d7d7fb6
Publikováno v:
Future Medicinal Chemistry. 14:1027-1048
Background: Phortress produces reactive electrophilic metabolites that form DNA adducts only in sensitive tumor cells. The authors converted the 2-phenylbenzothiazole nucleus in phortress to 2-aryl and -heteroaryl benzoxazole derivatives (11 new and
Autor:
Ronak Haj Ersan, Burak Kuzu, Derya Yetkin, Mehmet Abdullah Alagoz, Aylin Dogen, Serdar Burmaoglu, Oztekin Algul
Publikováno v:
Medicinal Chemistry Research. 31:1192-1208
The inability to meet the desired outcomes of anticancer treatment and decrease in treatment success of bacterial and fungal infections accelerated research in these areas. Our research group has conducted numerous studies, especially on benzimidazol
Autor:
Bayan Zoatier, Metin Yildirim, Mehmet Abdullah Alagoz, Derya Yetkin, Burcin Turkmenoglu, Serdar Burmaoglu, Oztekin Algul
Publikováno v:
Journal of Molecular Structure. 1285:135513
Publikováno v:
Pharmaceutical Chemistry Journal. 55:149-158
In an attempt to design and synthesize a potent class of antimicrobials, 1,2-phenylenediamine derivatives were reacted with various aliphatic and heteroaliphatic dicarboxylic acids to generate a small library of 26 head-to-head bisbenzimidazole compo
Publikováno v:
Future medicinal chemistry. 14(14)
There is an urgent need to develop potent and selective anticancer agents. In this study, the design and applications of compounds sensitive to specific cancer cells and targeting cancer cells were investigated. The results show that the synthesized
Autor:
Gozde Yalcin-Ozkat, Ronak H. Ersan, Mahmut Ulger, Seda T. Ulger, Serdar Burmaoglu, Ilkay Yildiz, Oztekin Algul
Publikováno v:
Journal of biomolecular structuredynamics.
The increase in the drug-resistant strains of Mycobacterium tuberculosis has led researchers to new drug targets. The development of new compounds that have effective inhibitory properties with the selective vital structure of Mycobacterium tuberculo
Autor:
Derya Aktas Anil, M. Fatih Polat, Ruya Saglamtas, Ayse H. Tarikogullari, M. Abdullah Alagoz, Ilhami Gulcin, Oztekin Algul, Serdar Burmaoglu
Enzyme inhibition is a very active area of research in drug design and development. Chalcone derivatives have a broad enzyme inhibitory activity and function as potential molecules in the development of new drugs. In this study, the synthesized novel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36c5aba484208c0a9195d9e91e6614ab
https://hdl.handle.net/11454/76484
https://hdl.handle.net/11454/76484
In an attempt to develop potent and selective anticancer agents, some 5- or 6- and N-substituted benzoxazol-2-carboxamide derivatives were designed, synthesized, and evaluated for their cyclooxygenase inhibitory, antioxidant, and anti-proliferative a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ef38e755b1dafda95ffea03a350c6a7
https://avesis.yyu.edu.tr/publication/details/af031494-3555-46f2-9673-d4d869000bc9/oai
https://avesis.yyu.edu.tr/publication/details/af031494-3555-46f2-9673-d4d869000bc9/oai