Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Mehmet Abdullah Alagoz"'
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:
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
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
Publikováno v:
Foods and Raw Materials, Vol 11, Iss 1, Pp 84-93 (2023)
The olive (Olea europaea L.) is one of the most important plants grown in many Mediterranean countries that has a high economic value. Olives, which are specific to each region, have different bioactive components. In this study, we investigated the
Externí odkaz:
https://doaj.org/article/5e36b6f6819c4f61808b46002cc6c0ca
Autor:
Zeynep Özdemir, Semra Utku, Bijo Mathew, Simone Carradori, Giustino Orlando, Simonetta Di Simone, Mehmet Abdullah Alagöz, Azime Berna Özçelik, Mehtap Uysal, Claudio Ferrante
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 35, Iss 1, Pp 1100-1109 (2020)
Novel 3(2H)-pyridazinone derivatives were designed, synthesised in satisfactory yields and evaluated in different experimental assays to assess their preliminary toxicity in vivo and anti-proliferative effects against HCT116 cell lines in vitro. Arte
Externí odkaz:
https://doaj.org/article/77aec80aff0d46378d800e0973455166
Autor:
Mehmet Abdullah Alagöz, Jong Min Oh, Yaren Nur Zenni, Zeynep Özdemir, Mohamed A. Abdelgawad, Ibrahim A. Naguib, Mohammed M. Ghoneim, Nicola Gambacorta, Orazio Nicolotti, Hoon Kim, Bijo Mathew
Publikováno v:
Molecules, Vol 27, Iss 12, p 3801 (2022)
Sixteen compounds (TR1–TR16) were synthesized and evaluated for their inhibitory activities against monoamine oxidase A and B (MAOs). Most of the derivatives showed potent and highly selective MAO-B inhibition. Compound TR16 was the most potent inh
Externí odkaz:
https://doaj.org/article/e1a4adf7fd08419ea40b9eb3e9ca8419
Autor:
Mehmet Abdullah Alagöz, Zeynep Özdemir, Mehtap Uysal, Simone Carradori, Marialucia Gallorini, Alessia Ricci, Susi Zara, Bijo Mathew
Publikováno v:
Pharmaceuticals, Vol 14, Iss 3, p 183 (2021)
Novel twenty-three 3(2H)-pyridazinone derivatives were designed and synthesized based on the chemical requirements related to the anti-proliferative effects previously demonstrated within this scaffold. The introduction of a piperazinyl linker betwee
Externí odkaz:
https://doaj.org/article/47501730cd0f45b3b1533e2d93a2d506