Use este identificador para citar ou linkar para este item: http://repositorio.ufla.br/jspui/handle/1/42616
Título: Trends in the recent patent literature on cholinesterase reactivators (2016-2019)
Palavras-chave: Organophosphorus compounds
Acetylcholinesterase
Therapeutic potential
Reactivation process
New trends in reactivators
Data do documento: 2020
Editor: Multidisciplinary Digital Publishing Institute
Citação: CASTRO, A. A. de et al. Trends in the recent patent literature on cholinesterase reactivators (2016-2019). Biomolecules, [S.l.], v. 10, n. 3, 2020.
Resumo: Acetylcholinesterase (AChE) is the key enzyme responsible for deactivating the ACh neurotransmitter. Irreversible or prolonged inhibition of AChE, therefore, elevates synaptic ACh leading to serious central and peripheral adverse effects which fall under the cholinergic syndrome spectra. To combat the toxic effects of some AChEI, such as organophosphorus (OP) nerve agents, many compounds with reactivator effects have been developed. Within the most outstanding reactivators, the substances denominated oximes stand out, showing good performance for reactivating AChE and restoring the normal synaptic acetylcholine (ACh) levels. This review was developed with the purpose of covering the new advances in AChE reactivation. Over the past years, researchers worldwide have made efforts to identify and develop novel active molecules. These researches have been moving farther into the search for novel agents that possess better effectiveness of reactivation and broad-spectrum reactivation against diverse OP agents. In addition, the discovery of ways to restore AChE in the aged form is also of great importance. This review will allow us to evaluate the major advances made in the discovery of new acetylcholinesterase reactivators by reviewing all patents published between 2016 and 2019. This is an important step in continuing this remarkable research so that new studies can begin.
URI: https://www.mdpi.com/2218-273X/10/3/436
http://repositorio.ufla.br/jspui/handle/1/42616
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