Cátia Teixeira

Post-doc Fellowship

Short CV

Researcher ID

ORCID

Cátia Teixeira was graduated in Chemistry in 2003, Department of Chemistry, Faculty of Sciences, University of Porto. Two years later she received M.Sc. degree (Organic Chemistry) in the same faculty. She then moved to France, where she obtained her Ph.D. in Computational Medicinal Chemistry in 2009, ITODYS research centre, University Paris 7 - Paris Diderot. In 2008, Cátia was awarded the L'Oréal France - Unesco 2008 prize for her doctoral research work.

Cátia is now at the Associated Laboratory CICECO of the University of Aveiro and the Centre for Chemical Research of the University of Porto as a Post-Doctoral research fellow. Her post-doctoral project is aimed at novel heteroaromatic-peptidomimetic hybrid constructs able to act as multi-target antimalarials with potent activity against intraerythrocytic Plasmodium falciparum parasites and reduced propensity to elicit resistance.

 

 

Projects

Publications

Cinnamic Derivatives as Antitubercular Agents: Characterization by Quantitative Structure-Activity Relationship Studies

Teixeira, C; Ventura, C; Gomes, JRB; Gomes, P; Martins, F
2020, MOLECULES, 25, 3.
ISBN: 1420-3049

Striking HIV-1 Entry by Targeting HIV-1 gp41. But, Where Should We Target?

Teixeira, C; Barbault, F; Couesnon, T; Gomes, JRB; Gomes, P; Maurel, F
2016, PLOS ONE, 11, 1.

N-Cinnamoylation of Antimalarial Classics: Effects of Using Acyl Groups Other than Cinnamoyl toward Dual-Stage Antimalarials

Gomes, A; Machado, M; Lobo, L; Nogueira, F; Prudencio, M; Teixeira, C; Gomes, P
2015, CHEMMEDCHEM, 10, 8, 1344-1349.

N-Cinnamoylation of Antimalarial Classics: Quinacrine Analogues with Decreased Toxicity and Dual-Stage Activity

Gomes, A; Perez, B; Albuquerque, I; Machado, M; Prudencio, M; Nogueira, F; Teixeira, C; Gomes, P
2014, CHEMMEDCHEM, 9, 2, 305-310.

"Recycling" Classical Drugs for Malaria

Teixeira, C; Vale, N; Perez, B; Gomes, A; Gomes, JRB; Gomes, P
2014, CHEMICAL REVIEWS, 114, 22, 11164-11220.

Is the conformational flexibility of piperazine derivatives important to inhibit HIV-1 replication?

Teixeira, C; Serradji, N; Amroune, S; Storck, K; Rogez-Kreuz, C; Clayette, P; Barbault, F; Maurel, F
2013, JOURNAL OF MOLECULAR GRAPHICS & MODELLING, 44, 91-103.

N-Cinnamoylated Chloroquine Analogues as Dual-Stage Antimalarial Leads

Perez, BC; Teixeira, C; Albuquerque, IS; Gut, J; Rosenthal, PJ; Gomes, JRB; Prudencio, M; Gomes, P
2013, JOURNAL OF MEDICINAL CHEMISTRY, 56, 2, 556-567.

Development of Plasmodium falciparum Protease Inhibitors in the Past Decade (2002-2012)

Perez, B; Teixeira, C; Gomes, JRB; Gomes, P
2013, CURRENT MEDICINAL CHEMISTRY, 20, 25, 3049-3068.

In vitro efficiency of 9-(N-cinnamoylbutyl)aminoacridines against blood- and liver-stage malaria parasites

Perez, B; Teixeira, C; Gomes, AS; Albuquerque, IS; Gut, J; Rosenthal, PJ; Prudencio, M; Gomes, P
2013, BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 23, 3, 610-613.

N-Cinnamoylated Aminoquinolines as Promising Antileishmanial Agents

Vale-Costa, S; Costa-Gouveia, J; Perez, B; Silva, T; Teixeira, C; Gomes, P; Gomes, MS
2013, ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 57, 10, 5112-5115.

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