Discovery of hybrid Glypromate conjugates with neuroprotective activity against paraquat-induced toxicity

Author:

Silva-Reis Sara C.12ORCID,Costa Vera M.23,da Silva Daniela Correia4,Pereira David M.4ORCID,Correia Xavier Cruz1ORCID,García-Mera Xerardo5ORCID,Rodríguez-Borges José E.1ORCID,Sampaio-Dias Ivo E.1ORCID

Affiliation:

1. LAQV/REQUIMTE, Department of Chemistry and Biochemistry, Faculty of Sciences, University of Porto, 4169-007 Porto, Portugal

2. UCIBIO/REQUIMTE, Laboratory of Toxicology, Faculty of Pharmacy, University of Porto, 4050-313 Porto, Portugal

3. Associate Laboratory i4HB – Institute for Health and Bioeconomy, Faculty of Pharmacy, University of Porto, 4050-313 Porto, Portugal

4. LAQV/REQUIMTE, Laboratory of Pharmacognosy, Department of Chemical Sciences, Faculty of Pharmacy, University of Porto, 4050-313 Porto, Portugal

5. Department of Organic Chemistry, Faculty of Pharmacy, University of Santiago de Compostela, E-15782 Santiago de Compostela, Spain

Abstract

A series of bicyclic-based Glypromate conjugates with reduction of protein aggregation elicited by Aβ25–35 and neuroprotective activity against paraquat-induced toxicity is reported, paving the way for the discovery of novel neurotherapeutics.

Funder

Xunta de Galicia

Fundação para a Ciência e a Tecnologia

Publisher

Royal Society of Chemistry (RSC)

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