Affiliation:
1. Laboratório de Síntese de Moléculas Medicinais (LaSMMed), Departamento de Química, Centro de Ciências Exatas,
Universidade Estadual de Londrina, Londrina, Brazil
Abstract
Abstract:
Some diseases caused by trypanosomatid parasites, like Leishmaniasis, Chagas Disease,
and Human African Trypanosomiasis (HTA), are challenging to manage, mainly concerning pharmacological
therapy because they are associated with vulnerable populations. Unfortunately, there
is a lack of significant investments in the search for new drugs. Therefore, one of the strategies to
aid the discovery of new drugs is to identify and inhibit molecular targets essential to the parasite's
survival, such as the proteasome, which degrades most proteins in the parasite cells. Our study has
presented several proteasome inhibitors with various pharmacophoric cores, and two of them, 5,
and 13, have stood out in the clinical phase of treatment for leishmaniasis.
Publisher
Bentham Science Publishers Ltd.
Subject
Clinical Biochemistry,Drug Discovery,Pharmacology,Molecular Medicine
Cited by
3 articles.
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