Leandro Louback da Silva
Instituição:
Universidade Federal do Rio de Janeiro
Centro:
Campus de Macaé
Unidade:
Direção Geral/Macaé
Departamento:
Docentes do Campus UFRJ/Macaé
Formação:
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Universidade Federal do Rio de Janeiro
Farmacologia e Química Medicinal | Doutorado | 2009 - 2014
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Universidade Federal do Rio de Janeiro
Ciências Biológicas (Farmacologia e Química Medicinal) | Mestrado | 2007 - 2009
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Universidade Federal do Rio de Janeiro
Farmácia | Graduação | 2003 - 2007
Laboratórios:
Nenhum laboratório cadastrado
Nuvens de Palavras:
Artigos:
(100.00% artigos com DOI)
Titulo | DOI | Ano |
---|---|---|
Evaluation of Camphor Hydrazone Derivatives as Inhibitors of Myeloperoxidase and Acetylcholinesterase Enzymes: Targets for the Development of Agents against Alzheimer?s Disease | 10.21127/yaoyimr20230002 | 2023 |
Effects of bisphenol A and S on blood coagulation: in vivo , in vitro and in silico approaches in toxicodynamic | 10.1080/15376516.2020.1836102 | 2021 |
Ethyl Acetate Fraction and Isolated Phenolics Derivatives from Mandevilla moricandiana Identified by UHPLC-DAD-ESI-MSn with Pharmacological Potential for the Improvement of Obesity-Induced Endothelial Dysfunction | 10.3390/pharmaceutics13081173 | 2021 |
A combined injectable contraceptive improves plasma redox status and does not induce vascular changes in female rats | 10.1590/0001-3765202120201924 | 2021 |
Acylhydrazones as isoniazid derivatives with multi-target profiles for the treatment of Alzheimer?s disease: radical scavenging, Myeloperoxidase/Acetylcholinesterase inhibition and Biometal chelation | 10.1016/j.bmc.2020.115470 | 2020 |
Isolation and characterization of flavonoids from Tapirira guianensis leaves with vasodilatory and myeloperoxidase-inhibitory activities | 10.1080/14786419.2020.1784170 | 2020 |
Acetylcholinesterase as a target of halogenated marine natural products from Laurencia dendroidea | 10.1016/j.algal.2020.102130 | 2020 |
Taurine supplementation prevents endothelial dysfunction and attenuates structural changes in aortas from hypothalamic obese rats | 10.1007/s00394-018-1616-2 | 2018 |
Antinociceptive and anti-inflammatory effects of a Geissospermum vellosii stem bark fraction | 10.1590/0001-3765201520140374 | 2016 |
Novel Potent Imidazo[1,2-a]pyridine-N-Glycinyl-Hydrazone Inhibitors of TNF-α Production: In Vitro and In Vivo Studies | 10.1371/journal.pone.0091660 | 2014 |
Docking, synthesis and pharmacological activity of novel urea-derivatives designed as p38 MAPK inhibitors | 10.1016/j.ejmech.2012.05.006 | 2012 |
Discovery of Novel Orally Active Anti-Inflammatory N-Phenylpyrazolyl-N-Glycinyl-Hydrazone Derivatives That Inhibit TNF-α Production | 10.1371/journal.pone.0046925 | 2012 |
Structure-based design and biological profile of (E)-N-(4-Nitrobenzylidene)-2-naphthohydrazide, a novel small molecule inhibitor of I¿B kinase-ß | 10.1016/j.ejmech.2011.01.045 | 2011 |
CYP1A2-mediated biotransformation of cardioactive 2-thienylidene-3,4-methylenedioxybenzoylhydrazine (LASSBio-294) by rat liver microsomes and human recombinant CYP enzymes | 10.1016/j.ejmech.2010.11.024 | 2011 |
Discovery of LASSBio-772, a 1,3-benzodioxole N-phenylpiperazine derivative with potent alpha 1A/D-Adrenergic receptor blocking properties | 10.1016/j.ejmech.2011.04.032 | 2011 |
LASSBio-881: an N-acylhydrazone transient receptor potential vanilloid subfamily type 1 antagonist orally effective against the hypernociception induced by capsaicin or partial sciatic ligation | 10.1111/j.1476-5381.2010.00672.x | 2010 |
Discovery of novel analgesic and anti-inflammatory 3-arylamine-imidazo[1,2-a]pyridine symbiotic prototypes | 10.1016/j.bmc.2008.11.018 | 2009 |
Development of CoMFA and CoMSIA models of affinity and selectivity for indole ligands of cannabinoid CB1 and CB2 receptors | 10.1016/j.ejmech.2009.01.026 | 2009 |
Synthesis and analgesic profile of conformationally constrained N-acylhydrazone analogues: Discovery of novel N-arylideneamino quinazolin-4(3H)-one compounds derived from natural safrole | 10.1016/j.bmc.2009.08.009 | 2009 |
Eventos:
(0.00% eventos com DOI)