Yazar "Abdelgawad, M.A." için Araştırma Çıktıları | Scopus İndeksli Yayınlar Koleksiyonu listeleme

Toplam kayıt 3, listelenen: 1-3

Design, synthesis, and biological evaluation of pyridazinones containing the (2-fluorophenyl) piperazine moiety as selective MAO-B inhibitors

Çeçen, M.; Oh, J.M.; Özdemir, Z.; Büyüktuncel, S.E.; Uysal, M.; Abdelgawad, M.A.; Musa, A.; Gambacorta, N.; Nicolotti, O.; Mathew, B.; Kim, H. (2020)

Twelve pyridazinones (T1–T12) containing the (2-fluorophenyl) piperazine moiety were designed, synthesized, and evaluated for monoamine oxidase (MAO) -A and -B inhibitory activities. T6 was found to be the most potent MAO-B ...
Synthesis of new 1-aryl-2-(3,5-dimethylpyrazol-1-yl)ethanone oxime ether derivatives and investigation of their cytotoxic effects

Alagöz, M.A.; Karakurt, A.; Hepokur, C.; Şalva, E.; Önkol, T.; Ghoneim, M.M.; Abdelgawad, M.A.; Khames, A.; Kim, H.; Mathew, B. (2021)

In this study, 12 new 1-aryl-2-(3,5-dimethylpyrazol-1-yl)ethanone oxime ether derivatives were designed and synthesized to investigate their cytotoxic effects. The in vitro cytotoxic activities of the compounds were evaluated ...
Development of a Novel Class of Pyridazinone Derivatives as Selective MAO-B Inhibitors

Alagöz, M.A.; Oh, J.M.; Zenni, Y.N.; Özdemir, Z.; Abdelgawad, M.A.; Naguib, I.A.; Ghoneim, M.M.; Gambacorta, N.; Nicolotti, O.; Kim, H.; Mathew, B. (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 ...

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