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Synthesis and antifungal activity of new hydrazide derivatives

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Al-Azhar University – Gaza
Turan-Zitouni G.; Altintop M.D.; Özdemir A.; Demirci F.; Mohsen U.A.; Kaplancikli Z.A.
Turan-Zitouni, Gülhan (7003906101); Altintop, Mehlika Dilek (38662171400); Özdemir, Ahmet (7006505091); Demirci, Fatih (35071145000); Mohsen, Usama Abu (6505829502); Kaplancikli, Zafer Asim (6602311259)
7003906101; 38662171400; 7006505091; 35071145000; 6505829502; 6602311259
2013
Journal of Enzyme Inhibition and Medicinal Chemistry
Synthesis and antifungal activity of new hydrazide derivatives
28
6
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1216
Faculty of Pharmacy, Department of Pharmaceutical Chemistry, Anadolu University, Eskisehir, Turkey; Graduate School of Health Sciences, Faculty of Pharmacy, Anadolu University, 26470 Eskisehir, Turkey; Faculty of Pharmacy, Department of Pharmacognosy, Anadolu University, Eskisehir, Turkey; Faculty of Pharmacy, Department of Pharmaceutical Chemistry, Al-Azhar University, Gaza, Palestine
Turan-Zitouni G., Faculty of Pharmacy, Department of Pharmaceutical Chemistry, Anadolu University, Eskisehir, Turkey; Altintop M.D., Faculty of Pharmacy, Department of Pharmaceutical Chemistry, Anadolu University, Eskisehir, Turkey; Özdemir A., Faculty of Pharmacy, Department of Pharmaceutical Chemistry, Anadolu University, Eskisehir, Turkey; Demirci F., Graduate School of Health Sciences, Faculty of Pharmacy, Anadolu University, 26470 Eskisehir, Turkey, Faculty of Pharmacy, Department of Pharmacognosy, Anadolu University, Eskisehir, Turkey; Mohsen U.A., Faculty of Pharmacy, Department of Pharmaceutical Chemistry, Al-Azhar University, Gaza, Palestine; Kaplancikli Z.A., Faculty of Pharmacy, Department of Pharmaceutical Chemistry, Anadolu University, Eskisehir, Turkey, Graduate School of Health Sciences, Faculty of Pharmacy, Anadolu University, 26470 Eskisehir, Turkey
Z.A. Kaplancikli; Graduate School of Health Sciences, Faculty of Pharmacy, Anadolu University, 26470 Eskisehir, Turkey; email: zakaplan@anadolu.edu.tr
26
10.3109/14756366.2012.723208
Anticandidal activity; Antifungal activity; Hydrazide-hydrazone; Tetrahydronaphthalene
Antifungal Agents; Candida; Dose-Response Relationship, Drug; Hydrazines; Microbial Sensitivity Tests; Molecular Structure; Naphthalenes; Structure-Activity Relationship; 2 [(5,6,7,8 tetrahydronaphthalen 2 yl)oxy]acetohydrazide derivative; acetophenone derivative; benzaldehyde derivative; hydrazide derivative; ketoconazole; n' (1 phenylethylidene) 2 [(5,6,7,8 tetrahydronaphthalen 2 yl)oxy]acetohydrazide; n' (2 chlorobenzylidene) 2 [(5,6,7,8 tetrahydronaphthalen 2 yl)oxy]acetohydrazide; n' (3 Nitrobenzylidene) 2 [(5,6,7,8 tetrahydronaphthalen 2 yl)oxy]acetohydrazide; n' (4 chlorobenzylidene) 2 [(5,6,7,8 tetrahydronaphthalen 2 yl)oxy]acetohydrazide; n' (4 methoxybenzylidene) 2 [(5,6,7,8 tetrahydronaphthalen 2 yl)oxy]acetohydrazide; n' (4 methylbenzylidene) 2 [(5,6,7,8 tetrahydronaphthalen 2 yl)oxy]acetohydrazide; n' (4 nitrobenzylidene) 2 [(5,6,7,8 tetrahydronaphthalen 2 yl)oxy]acetohydrazide; n' [1 (4 hydroxyphenyl)ethylidene] 2 [(5,6,7,8 tetrahydronaphthalen 2 yl)oxy]acetohydrazide; n' [4 (dimethylamino)benzylidene] 2 [(5,6,7,8 tetrahydro naphthalen 2 yl)oxy]acetohydrazide; unclassified drug; agar diffusion; antifungal activity; article; broth dilution; Candida albicans; Candida glabrata; Candida krusei; Candida parapsilosis; Candida tropicalis; Candida zeylanoides; drug purification; drug screening; drug structure; drug synthesis; fungal strain; Pichia jadinii; priority journal; proton nuclear magnetic resonance