Exploring the Conformational Effects of <i>N</i>- and <i>C</i>-Methylation of <i>N</i>-Acylhydrazones. [PDF]
Franco LS +11 more
europepmc +1 more source
Selective sensing of cyanide ions: impact of molecular design and assembly on the response of π-conjugated acylhydrazone compounds. [PDF]
Barkale HV, Dey N.
europepmc +1 more source
Iron-Based Nanoparticles as Delivery Tools. [PDF]
Parang K +5 more
europepmc +1 more source
Design, Synthesis, and Bioactivity Assessment of Modified Vemurafenib Analog. [PDF]
Guerra FS +5 more
europepmc +1 more source
Injectable, self-healing and degradable dynamic hydrogels with tunable mechanical properties and stability by thermal-induced micellization. [PDF]
Lin C +6 more
europepmc +1 more source
A new <i>N</i>-acylhydrazone oxadiazole derivative with activity against mycobacteria. [PDF]
Souza IV +10 more
europepmc +1 more source
Related searches:
Acylhydrazone derivatives: a patent review
Expert Opinion on Therapeutic Patents, 2014The N-acylhydrazone (NAH) moiety has been characterized as a privileged structure, capable of providing ligands points for more than one type of bioreceptor. Modifications of the subunits bonded to its acyl and imine functions resulted in several derivatives, which modulate a great diversity of molecular targets.
Rodolfo do Couto, Maia +2 more
openaire +4 more sources
Discovery of novel acylhydrazone neuraminidase inhibitors
European Journal of Medicinal Chemistry, 2019Neuraminidase (NA) plays a crucial role in the replication and transmission of influenza virus. NA inhibitors have been developed as effective treatments for influenza A and B infections. In this paper, a new lead neuraminidase inhibitor 6a (IC50 = 7.10 ± 0.2 μM) was discovered by ligand-based virtual screening, receptor-based virtual screening ...
Zhi Xiang Zhao +4 more
openaire +4 more sources
Over the last two decades, N-acylhydrazone (NAH) has been proven to be a very versatile and promising motif in drug design and medicinal chemistry. Herein, we discuss the current and future challenges in the emergence of bioactive NAH-based scaffolds and to developing strategies to overcome the failures in drug discovery. The NAH-related approved drugs
Sreekanth, Thota +5 more
openaire +2 more sources
N-Acylhydrazones as inhibitors of PDE10A
Bioorganic & Medicinal Chemistry Letters, 2011Cyclic nucleotide phosphodiesterases (PDEs) are represented by a large superfamily of enzymes. A series of hydrazone-based inhibitors was synthesized and shown to be novel, potent, and selective against PDE10A. Optimized compounds of this class were efficacious in animal models of schizophrenia and may be useful for the treatment of this disease.
Jennifer L, Gage +13 more
openaire +2 more sources

