Please use this identifier to cite or link to this item:
https://hdl.handle.net/20.500.11851/10518
Title: | Design and Synthesis of Some Arylhydrazone Derivatives as Potential Faah Inhibitors | Other Titles: | Potansiyel Faah İnhibitörü Olarak Bazı Arilhidrazon Türevi Bileşiklerin Tasarımı ve Sentezi | Authors: | Gür, Maz, T. Turanlı, S. Çalışkan, H.B. |
Keywords: | Arylhydrazones FAAH heterocycles inflammation arylhydrazone derivative fatty acid amidase inhibitor n (3 pyridazinyl) 4 [3 (5 trifluoromethyl 2 pyridinyloxy)benzylidene] 1 piperidinecarboxamide n' [(4 phenoxyphenyl)methylidene]pyridine 3 carbohydrazide n' [[ 4 (pyridin 2 yloxy)phenyl]methylidene]pyridine 3 carbohydrazide n' [[4 (benzyloxy)phenyl]methylidene]pyridine 3 carbohydrazide n' [[4 [(4 cyanophenyl)methoxy]phenyl]methylidene]pyridine 3 carbohydrazide n' [[4 [(4 fluorophenyl)methoxy]phenyl]methylidene]benzohydrazide n' [[4 [(4 fluorophenyl)methoxy]phenyl]methylidene]pyridine 3 carbohydrazide n' [[4 [(4 methoxyphenyl)methoxy]phenyl]methylidene]pyridine 3 carbohydrazide unclassified drug Article carbon nuclear magnetic resonance chemical structure chemotype controlled study drug design drug synthesis enzyme active site enzyme inhibition human hydrogen bond liquid chromatography-mass spectrometry melting point molecular docking molecular model proton nuclear magnetic resonance X ray crystallography |
Publisher: | University of Ankara | Abstract: | Objective: The aim was to design, synthesis and investigation of possible interactions in the enzyme active site of a series of arylhydrazone derivatives for the inhibition of the FAAH enzyme.” Material and Method: Arylhydrazone derivatives were obtained through the reaction of nicotinic hydrazide or benzohydrazide with appropriate aldehyde derivatives, and the obtained crude product was recrystallized from ethanol. After elucidating chemical structures of the compounds via spectroscopic methods, the inhibitory activities against hFAAH were screened. The results were further supported with molecular modeling studies. Result and Discussion: In this study, a new series of seven arylhydrazone derivatives were screened against hFAAH. 4-phenoxyphenyl bearing derivative 5 was found to inhibit hFAAH 40 % at 10 µM which indicates that newly developed inhibitor could serve as a starting point for improving inhibitory effect of the new series. © 2023 University of Ankara. All rights reserved. | URI: | https://doi.org/10.33483/jfpau.1181948 https://hdl.handle.net/20.500.11851/10518 |
ISSN: | 2564-6524 |
Appears in Collections: | Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection |
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