Design, Synthesis, and Structure-Activity Relationship Studies of (4-Alkoxyphenyl)glycinamides and Bioisosteric 1,3,4-Oxadiazoles as GPR88 Agonists. [PDF]
Rahman MT +9 more
europepmc +1 more source
Synthesis of 2-(β-D-glucopyranosyl)-5-(substituted-amino)-1,3,4-oxa-and -thiadiazoles for the inhibition of glycogen phosphorylase [PDF]
Docsa, Tibor +4 more
core +1 more source
Synthesis and antimicrobial evaluation of hybrids methoxynaphthalene-<i>N</i>-acylhydrazones/1,3,4-oxadiazoles. [PDF]
Frederico Rozada AM +9 more
europepmc +1 more source
SYNTHESIS OF 1,3,4-OXADIAZOLES AS SELECTIVE T-TYPE CALCIUM CHANNEL INHIBITORS. [PDF]
Zhang M +10 more
europepmc +1 more source
2:1 Adducts Arising from Reactions between Benzynes and 1,3,4-Oxadiazoles. [PDF]
Guzman AL, Kevorkian PV, Hoye TR.
europepmc +1 more source
In Vitro and In Silico Evaluation of Anticancer Activity of New Indole-Based 1,3,4-Oxadiazoles as EGFR and COX-2 Inhibitors. [PDF]
Sever B +12 more
europepmc +1 more source
1,3,4-oxadiazoles as inhibitors of the atypical member of the BET family bromodomain factor 3 from Trypanosoma cruzi (TcBDF3). [PDF]
Alonso VL +7 more
europepmc +1 more source
Synthesis of 1,3,4-oxadiazoles derivatives with antidepressant activity and their binding to the 5-HT1A receptor. [PDF]
Wang S +5 more
europepmc +1 more source
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
2-(Difluoromethyl)-1,3,4-oxadiazoles: The Future of Selective Histone Deacetylase 6 Modulation? [PDF]
König B, Hansen FK.
europepmc +1 more source

