Results 71 to 80 of about 1,413 (178)

Difluoromethyl-1,3,4-oxadiazoles Are Selective, Mechanism-Based, and Essentially Irreversible Inhibitors of Histone Deacetylase 6. [PDF]

open access: yesJ Med Chem, 2023
König B   +6 more
europepmc   +1 more source

1,3,4-Oxadiazole as an Anticancer Agent

open access: yesInternational Journal For Multidisciplinary Research
The modern era's fastest-growing disease is cancer, it poses a serious threat to people's lives. For the treatment of various cancers, the FDA has approved a number of medications. However, because of the rise in drug toxicity incidents, there is a continual need for the discovery of novel anti-cancer drugs.
Vaishnavi Chopade -, Vinayak Gaware -
openaire   +1 more source

A Graphene Acid - TiO2 Nanohybrid as Multifunctional Heterogeneous Photocatalyst for the Synthesis of 1,3,4-Oxadiazoles. [PDF]

open access: yesACS Appl Mater Interfaces, 2022
Sciarretta M   +5 more
europepmc   +1 more source

Modular and Computational Access to Innocuous Multistep Metal-Free Synthesis of 1,3,4-Oxadiazoles as Enzyme Inhibitors. [PDF]

open access: yesACS Omega, 2023
Umair M   +8 more
europepmc   +1 more source

Difluoromethyl-1,3,4-oxadiazoles are slow-binding substrate analog inhibitors of histone deacetylase 6 with unprecedented isotype selectivity. [PDF]

open access: yesJ Biol Chem, 2023
Cellupica E   +12 more
europepmc   +1 more source

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