Zobrazeno 1 - 10
of 110
pro vyhledávání: '"Oztekin Algul"'
Publikováno v:
Future Medicinal Chemistry. 15:365-377
Aim: Investigating molecules having toxicity and chemical similarity to find hit molecules. Methods: The machine learning (ML) model was developed to predict the arylhydrocarbon receptor activity of anti-Parkinson's and US FDA-approved drugs. The ML
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
The main aim of the study was to reveal the effects of endoplasmic reticulum (ER) stress on human bronchial epithelial cells BEAS-2B at gene and protein levels under oxidative stress conditions. The second aim of the study was to investigate whether
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f954318b5f1c7f27537952894a81c947
https://doi.org/10.21203/rs.3.rs-2332298/v1
https://doi.org/10.21203/rs.3.rs-2332298/v1
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:
ChemistrySelect. 6:2529-2538
thtgerIn this study, Mitsunobu reagent, DEAD (diethyl azodicarbox-ylate) and PPh3, and ethyl-oxalamide derivatives of 2-amino-phenol were reacted under mild reaction conditions. As a resultof the cyclization reaction, benzoxazole derivatives bearing
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