Nuria Cirauqui Díaz
Instituição:
Universidade Federal do Rio de Janeiro
Centro:
Centro de Ciências da Saúde
Unidade:
Faculdade de Farmácia
Departamento:
Departamento de Fármacos e Medicamentos
Formação:
-
Ecole Polytechnique Fédérale de Lausanne
| Pós-Doutorado | 2015 - 2016
-
Universidade Federal do Rio de Janeiro
| Pós-Doutorado | 2009 - Agora
-
Universidad de Navarra
Desenho, síntese e evacuação biológica de fármacos | Doutorado | 2004 - 2009
-
Universidad de Navarra
Química | Graduação | 1999 - 2004
Laboratórios:
Nuvens de Palavras:
Artigos:
(72.73% artigos com DOI)
| Titulo | DOI | Ano |
|---|---|---|
| A step towards development of promising trypanocidal agents: Synthesis, characterization and in vitro biological evaluation of ferrocenyl Mannich base-type derivatives | 10.1016/j.ejmech.2018.12.005 | 2019 |
| Second Generation of Mannich Base-Type Derivatives with Activity against | 10.1021/acs.jmedchem.8b00468 | 2018 |
| Mapping the sensing spots of aerolysin for single oligonucleotides analysis | 10.1038/s41467-018-05108-5 | 2018 |
| BK polyomavirus genotypes Ia and Ib1 exhibit different biological properties in renal transplant recipients | 10.1016/j.virusres.2017.10.018 | 2018 |
| Structural, physicochemical and dynamic features conserved within the aerolysin pore-forming toxin family | 10.1038/s41598-017-13714-4 | 2017 |
| Phylogenetic and structural analysis of merkel cell polyomavirus VP1 in Brazilian samples | 10.1016/j.virusres.2016.05.004 | 2016 |
| Design, Synthesis and Evaluation of New Fluoroamodiaquine Analogues | 10.1248/cpb.c15-01001 | 2016 |
| Cryo-EM structure of aerolysin variants reveals a novel protein fold and the pore-formation process | 10.1038/ncomms12062 | 2016 |
| In Vitro and in Vivo Anti- Activity of New Arylamine Mannich Base-Type Derivatives | 10.1021/acs.jmedchem.6b00784 | 2016 |
| Analysis of worldwide sequence mutations in Zika virus proteins E, NS1, NS3 and NS5 from a structural point of view | 10.1039/c6mb00645k | 2016 |
| Molecular modeling study of a series of amodiaquine analogues with antimalarial activity | 10.1007/s00044-015-1403-z | 2015 |
| Genetic and structural analysis of polyomavirus BK T-antigens reveal a higher density of mutations at inter-domain and hexamerization regions, regardless the status of infection | 10.1002/jmv.24192 | 2015 |
| Genetic and Structural Analysis of Merkel Cell Polyomavirus Large T Antigen from Diverse Biological Samples | 10.1159/000363241 | 2014 |
| Novel sulfonylurea derivatives as H3 receptor antagonists. Preliminary SAR studies | 10.1016/j.ejmech.2012.02.049 | 2012 |
| Building a MCHR1 homology model provides insight into the receptor-antagonist contacts that are important for the development of new anti-obesity agents | 10.1016/j.bmc.2010.09.014 | 2010 |
| New amide derivatives as melanin-concentrating hormone receptor 1 antagonists for the treatment of obesity | 2008 | |
| Melanin-Concentrating Hormone Receptor 1 Antagonists: A New Perspective for the Pharmacologic Treatment of Obesity | 2008 | |
| New biphenylmethyl urea derivatives as MCH-R1 and H3 receptors antagonists for the treatment of obesity | 2008 | |
| Synthesis and biological evaluation of new urea derivatives targeting the MCH-R1 and histamine H3 receptors for the treatment of obesity | 2008 | |
| Novel series of substituted biphenylmethyl urea derivatives as MCH-R1 antagonists for the treatment of obesity | 10.1016/j.bmc.2007.02.049 | 2007 |
| Synthesis and biological evaluation of arylamide derivatives as melanin-concentrating hormone receptor 1 antagonists | 2006 | |
| Arylsulfonamide derivatives as melanin-concentrating hormone receptor 1 antagonists | 2006 |
Eventos:
(0.00% eventos com DOI)