Molecular Docking and In Vitro Studies of Synthesized Oxadiazole Derivatives as Urease Inhibitors
A novel sequence of 1,3,4-oxadiazoles (7a–h) was synthesized. The compounds were characterized by IR, ¹H NMR, and MS analyses. They were also examined to determine whether they could prevent urease from functioning.
Kamran Mehdi +7 more
doaj
Design, synthesis, antimicrobial activity, DFT, and molecular docking studies of pyridine‐pyrazole‐based dihydro‐1,3,4‐oxadiazoles against various bacterial and fungal targets [PDF]
Nisheeth C. Desai +5 more
openalex +1 more source
Synthesis, Urease Inhibition, Antioxidant, Antibacterial, and Molecular Docking Studies of 1,3,4-Oxadiazole Derivatives [PDF]
Muhammad Asif Hanif +5 more
openalex +1 more source
Design, Synthesis and Bioactivity Evaluation of Novel β-carboline 1,3,4-oxadiazole Derivatives [PDF]
Zhijun Zhang +3 more
openalex +1 more source
Chemo- and Regioselective Synthesis of 3,4-Dihydropyrimidin-4-ones from 4,5-Dihydro-1,2,4-oxadiazoles and Chromium Alkoxy Alkynyl Fischer Carbene Complexes. [PDF]
Sánchez-Alonso S +3 more
europepmc +1 more source
A novel and sustainable synthesis-functionalization strategy for the oxidative cyclization towards 2,5-disubstituted-1,3,4-oxadiazoles using bentonite-supported copper(i) iodide as a green catalyst. [PDF]
Tran VQ +4 more
europepmc +1 more source
C-Glucopyranosyl-1,2,4-triazoles As New Potent Inhibitors of Glycogen Phosphorylase [PDF]
Bokor, Éva +3 more
core +1 more source

