Eliezer Jesus de Lacerda Barreiro
Instituição:
Universidade Federal do Rio de Janeiro
Centro:
Centro de Ciências da Saúde
Unidade:
Instituto de Ciências Biomédicas
Departamento:
Docentes/ICB
Formação:
-
Université Joseph Fourier - Grenoble I
| Pós-Doutorado | 1987 - 1987
-
Université Joseph Fourier - Grenoble I
Chimie Médicale | Doutorado | 1974 - 1978
-
Universidade Federal do Rio de Janeiro
Química de Produtos Naturais | Mestrado | 1971 - 1973
-
Universidade Federal do Rio de Janeiro
Faculdade de Farmácia | Graduação | 1967 - 1970
Laboratórios:
Nuvens de Palavras:
Artigos:
(45.52% artigos com DOI)
Titulo | DOI | Ano |
---|---|---|
Design, Synthesis and Phenotypic Profiling of Simplified Gedatolisib Analogues | 10.3390/ph16020209 | 2023 |
Pharmacokinetic Profile Evaluation of Novel Combretastatin Derivative, LASSBio-1920, as a Promising Colorectal Anticancer Agent | 10.3390/pharmaceutics15041282 | 2023 |
Comparative chemical and biological hydrolytic stability of homologous esters and isosteres | 10.1080/14756366.2022.2027933 | 2022 |
Discovery of Putative Dual Inhibitor of Tubulin and EGFR by Phenotypic Approach on LASSBio-1586 Homologs | 10.3390/ph15080913 | 2022 |
Methyl Effect on the Metabolism, Chemical Stability, and Permeability Profile of Bioactive N -Sulfonylhydrazones | 10.1021/acsomega.2c04368 | 2022 |
Pre-clinical evaluation of LASSBio-1491: From in vitro pharmacokinetic study to in vivo leishmanicidal activity | 10.1371/journal.pone.0269447 | 2022 |
Identification of LASSBio-1945 as an inhibitor of SARS-CoV-2 main protease (M PRO ) through in silico screening supported by molecular docking and a fragment-based pharmacophore model | 10.1039/d0md00282h | 2021 |
Design and Synthesis In Silico Drug-like Prediction and Pharmacological Evaluation of Cyclopolymethylenic Homologous of LASSBio-1514 | 10.3390/molecules26164828 | 2021 |
Supplementation with Spirulina platensis Prevents Uterine Diseases Related to Muscle Reactivity and Oxidative Stress in Rats Undergoing Strength Training | 10.3390/nu13113763 | 2021 |
Effect of S-Se Bioisosteric Exchange on Affinity and Intrinsic Efficacy of Novel N-acylhydrazone Derivatives at the Adenosine A2A Receptor | 10.3390/molecules26237364 | 2021 |
LASSBio-596: a New Pre-clinical Candidate for Rheumatoid Arthritis? | 10.1007/s10753-021-01564-2 | 2021 |
Novel VEGFR-2 inhibitors with an N -acylhydrazone scaffold | 10.1002/ardp.202000130 | 2020 |
New Benzofuran N-Acylhydrazone Reduces Cardiovascular Dysfunction in Obese Rats by Blocking TNF-Alpha Synthesis |
10.2147/dddt.s258459 | 2020 |
Carbamoyl- N -aryl-imine-urea: a new framework to obtain a putative leishmanicidal drug-candidate | 10.1039/d0ra00287a | 2020 |
Bioisosteric Replacement of Arylamide-Linked Spine Residues with N -Acylhydrazones and Selenophenes as a Design Strategy to Novel Dibenzosuberone Derivatives as Type I 1/2 p38α MAP Kinase Inhibitors | 10.1021/acs.jmedchem.0c00508 | 2020 |
Novel phosphatidylinositol 4-kinases III beta (PI4KIIIβ) inhibitors discovered by virtual screening using free energy models | 10.1007/s10822-020-00327-9 | 2020 |
β-lactam antibiotics: An overview from a medicinal chemistry perspective | 10.1016/j.ejmech.2020.112829 | 2020 |
In Vitro, In Vivo and In Silico Effectiveness of LASSBio-1386, an N-Acyl Hydrazone Derivative Phosphodiesterase-4 Inhibitor, Against Leishmania amazonensis | 10.3389/fphar.2020.590544 | 2020 |
A novel scaffold for EGFR inhibition: Introducing N-(3-(3-phenylureido)quinoxalin-6-yl) acrylamide derivatives | 10.1038/s41598-018-36846-7 | 2019 |
Chemical Intuition in Drug Design and Discovery | 10.2174/1568026619666190620144142 | 2019 |
Semicarbazone derivatives as promising therapeutic alternatives in leishmaniasis | 10.1016/j.exppara.2019.04.003 | 2019 |
What is hidden in the biodiversity? The role of natural products and medicinal chemistry in the drug discovery process | 10.1590/0001-3765201920190306 | 2019 |
Reduction of cardiac and renal dysfunction by new inhibitor of DPP4 in diabetic rats | 10.1016/j.pharep.2019.07.005 | 2019 |
Evaluation of Functional Selectivity of Haloperidol, Clozapine, and LASSBio-579, an Experimental Compound With Antipsychotic-Like Actions in Rodents, at G Protein and Arrestin Signaling Downstream of the Dopamine D2 Receptor | 10.3389/fphar.2019.00628 | 2019 |
Gastroprotective effects of N-acylarylhydrazone derivatives on ethanol-induced gastric lesions in mice are dependent on the NO/cGMP/KATP pathway | 10.1016/j.bcp.2019.113629 | 2019 |
LASSBio-596 protects gastric mucosa against the development of ethanol-induced gastric lesions in mice | 10.1016/j.ejphar.2019.172662 | 2019 |
Discovery of naphthyl- N -acylhydrazone p38α MAPK inhibitors with in vivo anti-inflammatory and anti-TNF-α activity | 10.1111/cbdd.13085 | 2018 |
Lung and liver responses to 1- and 7-day treatments with LASSBio-596 in mice subchronically intoxicated by microcystin-LR | 10.1016/j.toxicon.2017.10.029 | 2018 |
Ru(II) Compounds: Next-generation anticancer metallotherapeutics? | 10.1021/acs.jmedchem.7b01689 | 2018 |
Oxidative imbalance in mice intoxicated by microcystin-LR can be minimized | 10.1016/j.toxicon.2018.02.008 | 2018 |
Synthesis, X-ray diffraction study and pharmacological evaluation of 3-amino-4-methylthiophene-2-acylcarbohydrazones | 10.1590/0001-3765201820170796 | 2018 |
Synthesis, Aqueous Solubility, Metabolic Stability and Pharmacological Profile of Simplified Urea Derivatives | 10.2174/1570180814666171012155204 | 2018 |
Synthesis, Pharmacological Evaluation and Docking Study of a New | 2018 | |
LASSBio-1586, an N-acylhydrazone derivative, attenuates nociceptive behavior and the inflammatory response in mice | 10.1371/journal.pone.0199009 | 2018 |
N-Acylhydrazones as drugs | 10.1016/j.bmcl.2018.07.015 | 2018 |
Potent immunosuppressive activity of a phosphodiesterase-4 inhibitor N-acylhydrazone in models of lipopolysaccharide-induced shock and delayed-type hypersensitivity reaction | 10.1016/j.intimp.2018.09.047 | 2018 |
The Bench of Science | 10.21577/1984-6835.20180001 | 2018 |
The novel piperazine-containing compound LQFM018: Necroptosis cell death mechanisms, dopamine D 4 receptor binding and toxicological assessment | 10.1016/j.biopha.2018.02.120 | 2018 |
Design, Synthesis, Experimental and Theoretical Characterization of a New Multitarget 2-Thienyl-N-Acylhydrazone Derivative | 10.3390/ph11040119 | 2018 |
Synergistic interaction between a PDE5 inhibitor (sildenafil) and a new adenosine A2A receptor agonist (LASSBio-1359) improves pulmonary hypertension in rats | 10.1371/journal.pone.0195047 | 2018 |
Recent Advances in Development of Polyphenols as Anticancer Agents | 10.2174/1389557518666180220122113 | 2018 |
Adenosine A2A receptor agonist prevents cardiac remodeling and dysfunction in spontaneously hypertensive male rats after myocardial infarction | 10.2147/dddt.s113289 | 2017 |
LASSBio-1422 | 10.1097/FBP.0000000000000267 | 2017 |
Structural and physicochemical characterization of sulfonylhydrazone derivatives designed as hypoglycemic agents | 10.1039/C7NJ00074J | 2017 |
Structural characterization and cytotoxicity studies of different forms of a combretastatin A4 analogue | 10.1016/j.molstruc.2017.06.093 | 2017 |
A combined experimental and in silico characterization to highlight additional structural features and properties of a potentially new drug | 10.1016/j.molstruc.2017.06.061 | 2017 |
The antithrombotic and haemostatic effects of LASSBio-752: a synthetic, orally active compound in an arterial and venous thrombosis model in rats | 10.1111/jphp.12771 | 2017 |
Multi-gram Preparation of 7-Nitroquinoxalin-2-amine | 10.21577/0103-5053.20170018 | 2017 |
Adenosine Receptors As Drug Targets for Treatment of Pulmonary Arterial Hypertension | 10.3389/fphar.2017.00858 | 2017 |
LASSBio-897 Reduces Lung Injury Induced by Silica Particles in Mice: Potential Interaction with the A2A Receptor | 10.3389/fphar.2017.00778 | 2017 |
Discovery of naphthyl- N -acylhydrazone p38α MAPK inhibitors with in vivo anti-inflammatory and anti-TNF-α activity | 10.1111/cbdd.13085 | 2017 |
LASSBio-1425, an analog of thalidomide, decreases triglyceride and increases HDL cholesterol levels by inhibition of TNF-α production | 10.1016/j.ijcard.2015.09.071 | 2016 |
The total synthesis of calcium atorvastatin | 10.1039/c5ob02546j | 2016 |
Respiratory and Systemic Effects of LASSBio596 Plus Surfactant in Experimental Acute Respiratory Distress Syndrome | 10.1159/000443037 | 2016 |
Synthesis, characterization, DNA binding, DNA cleavage, protein binding and cytotoxic activities of Ru(II) complexes | 10.1016/j.ijbiomac.2015.09.045 | 2016 |
Non-competitive inhibitor of nucleoside hydrolase from Leishmania donovani identified by fragment-based drug discovery | 10.1039/c6ra15143d | 2016 |
Synthesis, Pharmacological Profile and Docking Studies of New Sulfonamides Designed as Phosphodiesterase-4 Inhibitors | 10.1371/journal.pone.0162895 | 2016 |
Design, synthesis, structural characterization and in vitro cytotoxic activity of mononuclear Ru(II)complexes | 10.1007/s00044-016-1625-8 | 2016 |
Treatment with Adenosine Receptor Agonist Ameliorates Pain Induced by Acute and Chronic Inflammation | 10.1124/jpet.115.231241 | 2016 |
LASSBio-579, a prototype antipsychotic drug, and clozapine are effective in novel object recognition task, a recognition memory model | 10.1097/FBP.0000000000000200 | 2016 |
Synthesis, solubility, plasma stability, and pharmacological evaluation of novel sulfonylhydrazones designed as anti-diabetic agents | 10.2147/DDDT.S108327 | 2016 |
Investigating the therapeutic effects of LASSBio-596 in an in vivo model of cylindrospermopsin-induced lung injury | 10.1016/j.toxicon.2014.12.004 | 2015 |
Novel Orally Active Analgesic and Anti-Inflammatory Cyclohexyl-N-Acylhydrazone Derivatives | 10.3390/molecules20023067 | 2015 |
Novel Agonist of Adenosine Receptor Induces Relaxation of Corpus Cavernosum in Guinea Pigs: An In Vitro and In Vivo Study | 10.1016/j.urology.2015.02.006 | 2015 |
Partial agonism and fast dissociation of LASSBio-579 at dopamine D2 receptor | 10.1016/j.pnpbp.2015.04.003 | 2015 |
Design, synthesis and in vitro trypanocidal and leishmanicidal activities of novel semicarbazone derivatives | 10.1016/j.ejmech.2015.05.046 | 2015 |
Structural features evolution - from fluids to solid phase - and crystal morphology study of LASSBio 1601: a cyclohexyl-N-acylhydrazone derivative | 10.1039/c5ra02696b | 2015 |
Design, synthesis, characterization, cytotoxic and structure activity relationships of novel Ru(II) complexes | 10.1016/j.cclet.2015.03.011 | 2015 |
Prevention and Reversal of Morphine-Induced Tolerance by Novel Muscarinic Receptor Agonist in Rats with Neuropathic Pain | 10.4172/2155-9562.1000282 | 2015 |
Synthesis and Biological Evaluation of Pyrazolo[3,4-b]pyridin-4-ones as a New Class of Topoisomerase II Inhibitors | 10.2174/1573406411666141210141317 | 2015 |
In vivo effect of LASSBio-785, a lipid-lowering and anti-inflammatory agent, on cardiac Ca2+-ATPases from hypercholesterolemic rats | 10.1016/j.ijcard.2015.08.091 | 2015 |
Therapeutic effects of LASSBio-596 in an elastase-induced mouse model of emphysema | 10.3389/fphys.2015.00267 | 2015 |
Simple HPLC-UV for the quantification of a new leishmanicidal candidate (E)-1-4 (trifluoromethyl) benzylidene) - 5 - (2-4-dichlorozoyl) carbonylhydrazine (LASSBio-1736) in rat plasma for pharmacokinetics assessment | 10.1002/bmc.3646 | 2015 |
LASSBio-579, a prototype antipsychotic drug, and clozapine are effective in novel object recognition task, a recognition memory model | 10.1097/fbp.0000000000000200 | 2015 |
Structural characterization of LASSBio-1289: a new vasoactive N-methyl-N-acylhydrazone derivative | 10.1039/C4CE02011A | 2015 |
Novel 2-chloro-4-anilino-quinazoline derivatives as EGFR and VEGFR-2 dual inhibitors | 10.1016/j.ejmech.2013.10.058 | 2014 |
N-acylhydrazone improves exercise intolerance in rats submitted to myocardial infarction by the recovery of calcium homeostasis in skeletal muscle | 10.1016/j.lfs.2013.11.012 | 2014 |
LASSBio-1135: A Dual TRPV1 Antagonist and Anti-TNF-Alpha Compound Orally Effective in Models of Inflammatory and Neuropathic Pain | 10.1371/journal.pone.0099510 | 2014 |
In Vitro Microsomal Hepatic Metabolism of Antiasthmatic Prototype LASSBio-448 | 10.2174/1568026614666140506123718 | 2014 |
Pulmonary And Hepatic Injuries Caused By The Subchronic Exposure To Microcystin-lr: Role Of The Duration Of Treatment With LASSBio 596 | 2014 | |
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 Antiproliferative Activity of N-Acylhydrazone Derivatives Designed as Combretastatin A4 Analogues | 10.1371/journal.pone.0085380 | 2014 |
Vasodilator and antihypertensive effects of a novel N -acylhydrazone derivative mediated by the inhibition of L-type Ca 2+ channels | 10.1111/j.1472-8206.2012.01076.x | 2014 |
Synthesis, Antiproliferative and Anti-inflammatory Activities of Novel Simplified Imatinib Analogues | 2014 | |
Novel Partial Agonist of PPAR-Gamma for Treatment of Diabetic Neuropathy in Rats | 2014 | |
Toxicological in vitro and subchronic evaluation of LASSBio-596 | 10.1016/j.fct.2014.07.037 | 2014 |
Structural characterization of LASSBio-1289: a new vasoactive N-methyl-N-acylhydrazone derivative | 10.1039/c4ce02011a | 2014 |
N-acylhydrazone derivative ameliorates monocrotaline-induced pulmonary hypertension through the modulation of adenosine AA2R activity | 10.1016/j.ijcard.2014.02.022 | 2014 |
Adenosine A2A Receptor as a Target of Treatment for Pulmonary Arterial Hypertensio | 2014 | |
Synchrotron X-ray powder diffraction data of LASSBio-1515: A new N-acylhydrazone derivative compound | 10.1016/j.radphyschem.2013.02.014 | 2014 |
3-Aminothiophene-2-Acylhydrazones: Non-Toxic, Analgesic and Anti-Inflammatory Lead-Candidates | 10.3390/molecules19068456 | 2014 |
Novel vasodilator prototype drug LASSBio 897 and its action on the cardiovascular system of dogs | 2014 | |
Pharmacological profile of the cardioactive prototype LASSBio-897: a preliminar study of its potencial vasodilatory activity | 2014 | |
Beneficial effects of a novel agonist of the adenosine A 2A receptor on monocrotaline-induced pulmonary hypertension in rats | 10.1111/bph.12193 | 2013 |
A novel Ca²+ channel antagonist reverses cardiac hypertrophy and pulmonary arteriolar remodeling in experimental pulmonary hypertension | 10.1016/j.ejphar.2013.01.050 | 2013 |
Antihyperalgesic effects of a novel muscarinic agonist (LASSBio-873) in spinal nerve ligation in rats | 10.1111/1440-1681.12090 | 2013 |
Hybrid furoxanyl N-acylhydrazone derivatives as hits for the development of neglected diseases drug candidates | 10.1016/j.ejmech.2012.10.047 | 2013 |
Synchrotron X-ray powder diffraction data of LASSBio-1515: A new N-acylhydrazone derivative compound | 10.1016/j.radphyschem.2013.02.014 | 2013 |
XII National Meeting of Pharmaceutical Chemistry Professors: could we have now a subarea of Pharmaceutical and Medicinal Chemistry in the CNPq Pharmacy Comittee? | 10.1590/S1984-82502013000100001 | 2013 |
Impairment of locomotor activity induced by the novel N-acylhydrazone derivatives LASSBio-785 and LASSBio-786 in mice | 10.1590/1414-431X20122085 | 2013 |
Biotransformation of LASSBio-579 and pharmacological evaluation of p-hydroxylated metabolite a N-phenylpiperazine antipsychotic lead compound | 10.1016/j.ejmech.2012.08.011 | 2013 |
Synthesis and pharmacological evaluation of new N-phenylpiperazine derivatives designed as homologues of the antipsychotic lead compound LASSBio-579 | 10.1016/j.ejmech.2013.05.027 | 2013 |
Anti-atherogenic Effects of a New Thienylacylhydrazone Derivative, LASSBio-788, in Rats Fed a Hypercholesterolemic Diet | 10.1254/jphs.13016FP | 2013 |
Oral Antithrombotic Effects of Acylhydrazone Derivatives | 10.5551/jat.14886 | 2013 |
Desafios da indústria farmacêutica brasileira | 10.1590/s0100-40422013001000012 | 2013 |
Characterization of Amide Bond Conformers for a Novel Heterocyclic Template of N-acylhydrazone Derivatives | 10.3390/molecules181011683 | 2013 |
Structure Re-determination of LASSBio-294 - a cardioactive compound of the N-acylhydrazone class - using X-ray powder diffraction data | 10.1017/S0885715613000808 | 2013 |
As Longas Pernas do Laboratório de Avaliação e Síntese de Substâncias Bioativas (LASSBio®;http://www.farmacia.ufrj.br/lassbio): Histórico e Perspectivas | 2013 | |
Opportunities and Challenges for Innovation in Pharmaceuticals: Now or Never. | 2013 | |
THIONYL CHLORIDE (CAS No 7719-09-7) - MÉTODO DE PREPARAÇÃO INDUSTRIAL DE SOLVENTES E REAGENTES QUÍMICOS | 2013 | |
A Novel Adenosine A2a Receptor Agonist Attenuates the Progression of Monocrotaline-induced Pulmonary Hypertension in Rats | 2013 | |
Novel vasodilator prototype drug LASSBio 897 and its action on the cardiovascular system of dogs | 2013 | |
Pharmacological profile of the ptototypes LASSBio-294 and LASSBio-897: a comparative preliminar study of their metabolites' effects on myocardial contraction. | 2013 | |
New oxidovanadium(IV) N-acylhydrazone complexes: Promising antileishmanial and antitrypanosomal agents | 10.1016/j.ejmech.2012.12.036 | 2013 |
Novel furfurylidene N-acylhydrazones derived from natural safrole: discovery of LASSBio-1215, a new potent antiplatelet prototype | 10.3109/14756366.2011.578575 | 2012 |
Discovery of new orally effective analgesic and anti-inflammatory hybrid furoxanyl N-acylhydrazone derivatives | 10.1016/j.bmc.2012.01.034 | 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 |
Design, Synthesis, and Pharmacological Evaluation of N -Acylhydrazones and Novel Conformationally Constrained Compounds as Selective and Potent Orally Active Phosphodiesterase-4 Inhibitors | 10.1021/jm300514y | 2012 |
Benzenesulfonamide attenuates monocrotaline-induced pulmonary arterial hypertension in a rat model | 10.1016/j.ejphar.2012.05.043 | 2012 |
Antihypertensive profile of 2-thienyl-3,4-methylenedioxybenzoylhydrazone is mediated by activation of the A2A adenosine receptor | 10.1016/j.ejmech.2012.06.056 | 2012 |
Synthesis and characterization of the atropisomeric relationships of a substituted N-phenyl-bipyrazole derivative with anti-inflammatory properties | 10.1002/chir.22016 | 2012 |
Synthesis, Biological Evaluation, and Structure-activity Relationship of Clonazepam, Meclonazepam, and 1,4-Benzodiazepine Compounds with Schistosomicidal Activity | 10.1111/j.1747-0285.2012.01354.x | 2012 |
Molecular docking and molecular dynamic studies of semi-synthetic piperidine alkaloids as acetylcholinesterase inhibitors | 10.1590/s0103-50532012000100023 | 2012 |
New insights into pharmacological profile of LASSBio-579, a multi-target N-phenylpiperazine derivative active on animal models of schizophrenia | 10.1016/j.bbr.2012.09.016 | 2012 |
Design, Synthesis, Antinociceptive and Anti-Inflammatory Activities of Novel Piroxicam Analogues | 10.3390/molecules171214126 | 2012 |
Synthesis and Pharmacological Evaluation of Novel Phenyl Sulfonamide Derivatives Designed as Modulators of Pulmonary Inflammatory Response | 10.3390/molecules171214651 | 2012 |
Antinociceptive effects of an extract, fraction and an isolated compound of the stem bark of Maytenus rigida | 10.1590/s0102-695x2012005000007 | 2012 |
Docking, synthesis and pharmacological activity of novel urea-derivatives designed as p38 MAPK inhibitors | 10.1016/j.ejmech.2012.05.006 | 2012 |
Potential Inhibitory Effect of LASSBio-596, a New Thalidomide Hybrid, on Inflammatory Corneal Angiogenesis in Rabbits | 10.1159/000337137 | 2012 |
LASSBio-542: Novel Thalidomide Analog Distinctly Modulates IL-10 and Inhibits Angiogenesis | 10.2174/157340712801784778 | 2012 |
Docking, Synthesis and Anti-Diabetic Activity of Novel Sulfonylhydrazone Derivatives Designed as PPAR-Gamma Agonists | 10.2174/156802612804910205 | 2012 |
Combination of docking, molecular dynamics and quantum mechanical calculations for metabolism prediction of 3,4-methylenedioxybenzoyl-2-thienylhydrazone | 10.1007/s00894-011-1219-9 | 2012 |
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 |
The Role of Natural Products in the Discovery of New Drug Candidates for the Treatment of Neurodegenerative Disorders I: Parkinson?s Disease | 2011 | |
Structure-based design and biological profile of (E)-N-(4-Nitrobenzylidene)-2-naphthohydrazide, a novel small molecule inhibitor of I?B kinase-? | 10.1016/j.ejmech.2011.01.045 | 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 |
The Methylation Effect in Medicinal Chemistry | 10.1021/cr200060g | 2011 |
Binuclear zinc(II) complexes with the anti-inflammatory compounds salicylaldehyde semicarbazone and salicylaldehyde-4-chlorobenzoyl hydrazone (H2LASSBio-1064) | 10.1016/j.poly.2011.04.024 | 2011 |
Analgesic and Anti-Inflammatory Activities of Salicylaldehyde 2-Chlorobenzoyl Hydrazone (H2LASSBio-466), Salicylaldehyde 4-Chlorobenzoyl Hydrazone (H2LASSBio-1064) and Their Zinc(II) Complexes | 10.3390/molecules16086902 | 2011 |
LASSBio 596 per os avoids pulmonary and hepatic inflammation induced by microcystin-LR | 10.1016/j.toxicon.2011.05.018 | 2011 |
MAOS and Medicinal Chemistry: Some Important Examples from the Last Years | 10.3390/molecules16119274 | 2011 |
Anti-inflammatory effects of LASSBio-998, a new drug candidate designed to be a p38 MAPK inhibitor, in an experimental model of lubg inflammation | 2011 | |
Combination of docking, molecular dynamics and quantum mechanical calculations for metabolism prediction of 3,4-methylenedioxybenzoyl-2-thienylhydrazone | 10.1007/s00894-011-1219-9 | 2011 |
Determination of the cardioactive prototype LASSBio-294 and its metabolites in dog plasma by LCâ¿¿MS/MS: Application for a pharmacokinetic study | 10.1016/j.jpba.2011.02.031 | 2011 |
Therapeutic approaches for tumor necrosis factor inhibition | 2011 | |
Vasodilatory activity and antihypertensive profile mediated by inhibition of phosphodiesterase type 1 induced by a novel sulfonamide compound | 10.1111/j.1472-8206.2011.00999.x | 2011 |
Microwave-assisted synthesis and structure¿activity relationships of neuroactive pyrazolo[3,4-b]pyrrolo[3,4-d]pyridine derivatives | 10.1016/j.bmcl.2009.11.038 | 2010 |
Characterization of the conformational ensemble from bioactive N-acylhydrazone derivatives | 10.1016/j.jmgm.2009.10.004 | 2010 |
Searching for multi-target antipsychotics: Discovery of orally active heterocyclic N-phenylpiperazine ligands of D2-like and 5-HT1A receptors | 10.1016/j.bmc.2010.01.040 | 2010 |
Design of new dopamine D2 receptor ligands: Biosynthesis and pharmacological evaluation of the hydroxylated metabolite of LASSBio-581 | 10.1016/j.bmcl.2010.03.034 | 2010 |
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 |
Structure-based prediction and biosynthesis of the major mammalian metabolite of the cardioactive prototype LASSBio-294 | 10.1016/j.bmcl.2010.04.073 | 2010 |
Novel thienylacylhydrazone derivatives inhibit platelet aggregation through cyclic nucleotides modulation and thromboxane A2 synthesis inhibition | 10.1016/j.ejphar.2010.04.003 | 2010 |
A Theoretical Investigation on the Pleiotropic Effects of Statins as p38 | 2010 | |
Can LASSBio 596 and dexamethasone treat acute lung and liver inflammation induced by microcystin-LR? | 10.1016/j.toxicon.2010.06.005 | 2010 |
Synthesis and pharmacological evaluation of pyrazine N-acylhydrazone derivatives designed as novel analgesic and anti-inflammatory drug candidates | 10.1016/j.bmc.2010.06.002 | 2010 |
Cardiovascular effects induced by N-(4'-dihydro)-piperoylthiomorpholine in normotensive rats | 10.1111/j.2042-7158 | 2010 |
LASSBio-294, A Compound With Inotropic and Lusitropic Activity, Decreases CardiacRemodeling and Improves Ca2+ InfluxSarcoplasmic Reticulum After Myocardial Infarction Into | 2010 | |
Antimicrobial activity of Pterogyne nitens Tul., Fabaceae, against opportunistic fungi | 10.1590/S0102-695X2010005000017 | 2010 |
2-Acetylpyridine thiosemicarbazones: Cytotoxic activity in nanomolar doses against malignant gliomas | 10.1016/j.ejmech.2010.09.021 | 2010 |
Descoberta de novos protótipos N-fenilpiperazínicos heteroarilazólicos candidatos a fármacos antipsicóticos atípicos | 2010 | |
Espectalina, cassina e análogos semissintéticos como potenciais candidatos a fármacos para o tratamento da doença de Alzheimer | 2010 | |
LASSBio - 596: da descoberta aos ensaios pré - clínicos | 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 |
Synthesis, trypanocidal activity and docking studies of novel quinoxaline-N-acylhydrazones, designed as cruzain inhibitors candidates | 10.1016/j.bmc.2008.11.065 | 2009 |
Biodiversidade: fonte potencial para a descoberta de fármacos | 2009 | |
Synthesis, pharmacological evaluation and docking studies of new sulindac analogues | 10.1016/j.ejmech.2008.11.012 | 2009 |
Synthesis and pharmacological evaluation of N-phenyl-acetamide sulfonamides designed as novel non-hepatotoxic analgesic candidates | 10.1016/j.ejmech.2009.02.026 | 2009 |
Studies towards the identification of putative bioactive conformation of potent vasodilator arylidene N-acylhydrazone derivatives | 10.1016/j.ejmech.2009.04.044 | 2009 |
Design, synthesis and analgesic properties of novel conformationally-restricted N-acylhydrazones (NAH) | 10.1016/j.bmcl.2009.07.075 | 2009 |
Novel 6-methanesulfonamide-3,4-methylenedioxyphenyl-N-acylhydrazones: Orally effective anti-inflammatory drug candidates | 10.1016/j.bmc.2008.12.045 | 2009 |
From nature to drug discovery:the indole scaffold as a 'privileged structure' | 2009 | |
Sedation and antinociception induced by a new pyrazolo[3,4-b]pyrrolo[3,4-d]pyridine derivative (LASSBio-873) is modulated by activation of muscarinic receptors | 10.1016/j.pbb.2009.07.008 | 2009 |
Structural insights into IKK? inhibition by natural products staurosporine and quercetin | 10.1016/j.bmcl.2009.10.076 | 2009 |
Pharmacological Characterization of (3-Thienylidene)-3,4-Methylenedioxybenzoylhydrazide: A Novel Muscarinic Agonist With Antihypertensive Profile | 10.1038/ajh.2009.238 | 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 |
Cytotoxic Guanidine Alkaloids from Pterogyne nitens - | 10.1021/np800612x | 2009 |
New Insights for Multifactorial Disease Therapy: The Challenge of the Symbiotic Drugs | 2008 | |
Serotonergic neurotransmission mediates hypothermia induced by the N-phenylpiperazine antipsychotic prototypes LASSBio-579 and LASSBio-581 | 10.1016/j.pbb.2007.10.018 | 2008 |
Synthesis and anti-platelet activity of novel arylsulfonate-acylhydrazone derivatives, designed as antithrombotic candidates | 10.1016/j.ejmech.2007.03.032 | 2008 |
Improved solvent-free Dakin oxidation protocol | 10.1080/00397910701820673 | 2008 |
CNS-selective noncompetitive cholinesterase inhibitors derived from the natural piperidine alkaloid (-)-spectaline | 10.1016/j.ejphar.2007.11.035 | 2008 |
Antinociceptive Profile of 2,3,6-Trisubstituted Piperidine Alkaloids:3-O-Acetyl-spectaline and Semi-synthetic Derivatives of (-)-Spectaline | 2008 | |
Flavonols from Pterogyne nitens and their evaluation as myeloperoxidase inhibitors | 10.1016/j.phytochem.2008.01.006 | 2008 |
NSAIDs revisited: Putative molecular basis of their interactions with peroxisome proliferator-activated gamma receptor (PPAR?) | 10.1016/j.ejmech.2007.11.031 | 2008 |
Pharmacokinetic evaluation of LASSBio-579: an N-phenylpiperazine antipsychotic prototype | 2008 | |
Constituintes Químicos das Flores de Pterogyne nitens | 2008 | |
Studies of trypanocidal (inhibitory) power of naphthoquinones:Evaluation of quantum chemical molecular descriptors for structureeactivity relationships | 10.1016/j.ejmech.2007.12.023 | 2008 |
1-Methyl-7-(4-nitrophenyl)-3-phenylpyrazolo[3,4- b ]pyrrolo[3,4- d ]pyridine-6,8(3 H ,7 H )-dione | 10.1107/s1600536808037240 | 2008 |
Pharmacokinetic evaluation of LASSBio-579: an N -phenylpiperazine antipsychotic prototype | 10.1211/jpp.60.6.0004 | 2008 |
Development and validation of a LC-MS/MS method with electrospray ionization for determination of LASSBio-579 in rat plasma | 10.1016/j.jpba.2006.07.052 | 2007 |
Synthesis, Pharmacological Evaluation and Electrochemical Studies of Novel6-Nitro-3,4-Methylenedioxyphenyl-N-Acylhydrazone Derivatives: Discovery ofLASSBio-881, a New Ligand of Cannabinoid Receptors | 10.1016/j.bmc.2007.01.013 | 2007 |
Molecular Hybridization: A usful tool in the design of new drug prototypes | 2007 | |
A Descoberta Racional de Fármacos | 2007 | |
The molecular basis of COX-2 versus COX-1 selectivity of lumiracoxib bymolecular docking studies | 2007 | |
Privileged Structures: A Useful Concept for the Rational Design of New Lead Drugs Candidates | 2007 | |
High performance liquid chromatography method for quantification of the N-phenylpiperazine derivative LASSBio-579 in the rat plasma | 2007 | |
Uma visão da Química Bioinorgânica Medicinal | 2007 | |
Medicinal chemistry of N-acylhydrazones: New lead-compounds of analgesic, antiinflammatory ad antithrombotic drugs | 2006 | |
Thalidomide and analogs as antiinflammatory and immunomodulator drug candidates | 2006 | |
Protective Effects of Phosphodiesterase Inhibiors on Lung Function and Remodeling in a Murine Model of Chronic Asthma | 2006 | |
Os Produtos Naturais e a Química Medicinal Moderna | 2006 | |
New potent 5-nitrofuryl derivatives as inhibitors of Trypanosoma cruzi growth. 3D-QSAR (CoMFA) studies | 10.1016/j.bmc.2005.07.072 | 2006 |
Molecular docking study and development of na empirical binding free energy model for phosphodiesterase 4 inhibitors | 10.1016/j.bmc.2006.05.017 | 2006 |
Development of new CoMFA and CoMSIA 3D-QSAR models for anti-inflammatory phhalimide-containing TNFalpha modulators | 10.1016/j.bmc.2006.06.042 | 2006 |
Design and synthesis of 3,4-methylenedioxy-6-nitrophenoxyacetylhydrazone derivatives obtained from natural safrole: New lead-agents with analgesic and antipyretic properties | 10.1016/j.bmc.2006.07.046 | 2006 |
ASPECTOS QUÍMICOS, BIOLÓGICOS E ETNOFARMACOLÓGICOS DO GÊNERO Cassia | 2006 | |
Design, Synthesis and Pharmacological Evaluation of Neuroactive Pyrazolo[3,4-d]pyridine derivatives | 10.1016/j.bmc.2005.08.042 | 2006 |
Protective effects of phosphodiesterase inhibitors on lung function and remodeling in a murine model of chronic asthma | 10.1590/s0100-879x2006000200016 | 2006 |
LASSBio-468, a new achiral thalidomide analogue which modulates TNF-alpha and NO production and inhibits endotoxic ahock and arthitis in an animal model | 10.1016/j.intimp.2004.10.017 | 2005 |
Bioisosterism: A Useful Strategy for Molecular Modification and Drug Desing | 2005 | |
Um Paradigma Da Quimica Medicinal: A Flexibilidade Dos Ligantes E Receptores | 2005 | |
Desing, synthesis and antiinflammatory activity of novel phthalimide derivatives, structurally related to thalidomide | 10.1016/j.bmcl.2004.12.012 | 2005 |
Evaluating the prophylactic potential of the phtalimide derivative LASSBio 552 on allergen-evoked inflammation in rats | 10.1016/j.ejphar.2005.02.011 | 2005 |
Synthesis and vasodilatory activity of new N-acylhydrazone derivatives, designed as LASSBio-294 analogues | 10.1016/j.bmc.2005.03.003 | 2005 |
Design, synthesis and pharmacological evaluation of new nonsteroidal antiinflammatory 1,3,4-thiadiazole derivatives | 2005 | |
New selective acetylcholinesterase inhibitors designed from natural piperidine alkaloids | 10.1016/j.bmc.2005.04.030 | 2005 |
New anti-Alzheimer drugs from biodiversity: the role of the natural acetylcholinestarse inhibitors | 2005 | |
Pharmacokinetis and tissue distribuition of a new heterocyclic N-phenylpiperazine derivative (LASSBio-581) in rats | 10.1016/j.ejps.2005.06.002 | 2005 |
Aplicação de análise de componentes principais para verificação de atribuições de sinais nos espectros de RMN 1H. O caso dos 3-aril(1,2,4)-oxadiazolil-5-carboidrazida | 2005 | |
Hydrolisis of new phthalimide-derived esters catalyzed by immobilized lipase | 2005 | |
Chemo-selective hydrolisis of the iminic moiety in salicylaldehyde semicarbazone promoted by ruthenium | 10.1016/j.ica.2005.04.021 | 2005 |
Electronspray ionization mass and tandem mass spectra of a series of N-pyrazolylmethyl and N-triazolylmethyl N-phenylpiperazines: new dopaminergic ligands with potential antipsychotic properties | 2005 | |
The molecular basis for coxib inhibition of p38alpha MAP kinase | 10.1016/j.bmcl.2005.05.107 | 2005 |
A proposed molecular basis for the selective resveratrol inhibition of the PGHS-1 peroxidase activity | 10.1016/j.bmc.2005.07.028 | 2005 |
New potent 5-substituted benzofuroxans as inhibitors of Trypanosoma cruzi growth: Quantitative structure-activity relationship studies. | 2005 | |
A questão da inovação em fármacos no Brasil: proposta de criação do programa nacional de fármacos (Pronfar). | 2005 | |
Cysteinyl Leukotriene Receptor Antagonists and Thromboxane Synthase Inhibitors: New targets to treat Asthma | 2004 | |
Studies on diastereoselective reduction of cyclic beta-ketoesters with boron hydrides. Part 4: The reductive profile of functionalized cyclohexanone derivatives | 2004 | |
A novel 3D-QSAR comparative molecular field analysis (CoMFA) model of imidazole and quinazolinone functinalized p38 MAP kinase inhibitor | 2004 | |
Further bioactive piperidine alkaloids from the flowers and green fruits of Cassia spectabilis | 2004 | |
Esquizofrenia, Quarenta Anos da hipotese Dopaminergica Sob A Otica da Quimica Medicinal | 2004 | |
Selective PGHS-2 Inhibitors, A Rational Approach for Treatment of the Inflammation | 2004 | |
New optimized piperamide analogues with potent in vivo hypotensive properties | 2004 | |
Produtos Naturais Como Candidatos a Farmacos Uteis No Tratamento Do Mal De Alzheimer | 2004 | |
New class of potent antinociceptive and antiplatelet 10H-phenothiazine-1-acylhydrazone derivatives | 2004 | |
Enzymatic hydrolysis by immobilized lipase applied to a new prototype anti-asthma drug | 2004 | |
Agentes Dopaminergicos e o Tratamento da Disfuncão Eretil | 2004 | |
Studies of Chiral GC Separation of gamma-Butyrolactone Derivatives on 2,3-di-O-Methyl-6-O-t-Butyldimethylsilyl-beta-cyclodextrin | 2003 | |
Design, synthesis, and pharmacological profile of novel fused pyrazolo[4,3-d]pyridine and pyrazolo[3,4-b][1,8]naphthyridine isosteres: a new class of potent and selective acetylcholinesterase inhibitors | 2003 | |
Antiplatelet properties of novel N-substituted-phenyl-1,2,3-triazole-4-acylhydrazone derivatives | 2003 | |
Highly Stereocontrolle Synthesis of Natural Barbacenic Acid. Novel Bisnorditerpene from Barbacenia flava | 2003 | |
Therapeutic potential of a new phosphodiesterase inhibitor in acute lung injury | 2003 | |
Dopaminergic Profile of New Heterocyclic of N-phenylpiperazine Derivatives | 2003 | |
Novas Estratégias Terapêuticas para o Tratamento da Depressão: Uma Visão da Química Medicinal | 2003 | |
Thienylhydrazone derivative increases sarcoplasmatic reticulum Ca+2 release in mammalian skeletal muscle. | 2003 | |
The Medicinal Chemistry and Drug Discovery: A new cardioactive lead-compound, LASSBio-294. | 2003 | |
Antinociceptive Profile of (-) ¿ Spectaline: A Piperidine Alkaloid From Cassia Leptophylla | 2003 | |
Validated HPLC method for determination of LASSBio-581, a new heterocyclic N-phenylhydrazine derivative, in rat plasma | 2003 | |
Desing, Synthesis and Pharmacological Profile of New Tacrine Isosteres: A New Class of Potent and Selective Acetycholonesterase Inhibitors | 2003 | |
Desing, Synthesis and Pharmacological Profile of Novel Doámine D2 Receptor Ligands | 2003 | |
Design,Synthesis and Pharmacological Evaluation of Novel Pyrazolo [3,4-b ]thieno [2,3-d ]pyridine Acid Derivatives:A New Class of Anti-in flammatory and Anti-platelet Agents | 2002 | |
Vasodilatory Properties of LASSBio 294 and its Dependence on cGMP Increase | 2002 | |
A Química Medicinal de N-acilidrazonas: Novos compostos-protótipos de fármacos analgésicos, antiinflamatórios e antitrombóticos | 2002 | |
Highly Diastereoselective mercury mediated synthesis of funstionalyzed 2-azabicyclo[3.3.0]octane derivatives | 2002 | |
Molecular Modeling of New Derivatives 1H-Pyrazolo[3,4-b]pyridine Designed as Isosters of Antimalarial Mefloquine | 2002 | |
New isoxazole derivatives designed as nicotinic acetylcholine receptor ligand candidates | 2002 | |
Local intersection volume: a new 3D descriptor applied to develop a 3D-QSAR pharmacophore model for benzodiazepine receptor | 2002 | |
Studies on the diastereoselective reduction of 2-acetyl-2-alkyl-gama-butyrolactones with boron hydrides | 2002 | |
Novel Phthalimide Derivatives, Designed as Leukotriene D4 Receptor Antagonists | 2002 | |
Structure-Activity Relationship of the Antimalarial Agent Artemisinin. 6 . The Development of Predictive in Vitro Potency Models Using CoMFA and HQSAR Methodologies | 2002 | |
Molecular Modeling of novel 1H-pyrazolo[3,4-b»pyridine Derivatives Designed as Isosters of the Antimalarial Mefloquine | 2002 | |
Selective PGHS-2 inhibitors: A rational approach for treatment of the inflammation | 2002 | |
Synthesis and Anti-inflammatory Activity of phthalimide derivatives, esigned as new thalidomide analogues | 2002 | |
Agentes Antiasmaticos Modernos: Antagonistas de receptores de leucotrienos cisteínicos | 2002 | |
Synthesis and biological evaluation of new imidazo[1-2a]pyridine derivatives designed as mefloquine analogues | 2002 | |
Estratégica de Simplificação Molecular no Planejamento Racional de Fármacos: A Descoberta de Novo Agente Cardioativo | 2002 | |
Synthesis and pharmacological evaluation of novel antinociceptive N-substituted-phenylimidazolyl-4-acylhydrazone derivatives | 2002 | |
Synthesis of Natural Amide Alkaloid Piperdardine and a New Bioactive Analogue | 2001 | |
Synthesis and Pharmacological Evaluation of new 2-azabicyclo[3.3.0]octane derivative | 2001 | |
Sobre a Química dos Remédios, dos Fármacos e dos Medicamentos | 2001 | |
A Importância da Síntese de Fármacos | 2001 | |
O Renascimento de um Fármaco: Talidomida | 2001 | |
LASSBio 294, a Novel Cardionotropic Agent, Increases the Calcium Content in the Sarcoplasmatic Reticulum of Saponin-Skinned Cardiac Fibres | 2001 | |
A novel thienylhydrazone, (2-thienylidene)3,4-methylenedioxybenzoylhydrazine, increases inotropism and decreases fatigue of skeletal muscle | 2001 | |
Estratégias em Química Medicinal para o planejamento de fármacos | 2001 | |
Asymmetric synthesis of 3beta-angeloyloxy-4beta-hydroxyeudesman-8-one, purported sesquiterpene from Puchea quitoc | 2000 | |
Synthesis and non-addictive analgesic activity of novel N-acylarylhydrazones and isosters, derived from natural safrole | 2000 | |
Electron impact mass spectrometry of some 3-[3-(4-aryl)-1,2,4-oxadiazole-5-yl]acyl arylaldehyde hydrazone derivatives | 2000 | |
A possible molecular mechanism for the inhibition of cysteine proteases by salicilaldehyde N-acylhydrazones and related compounds | 2000 | |
Chiral gas chromatographic separation of 2-oxabicyclo[3.3.0]octane derivatives and their synthetic precursors | 2000 | |
O-Alkylation of bioactive phthalimide derivatives under microwave irradiation in dry media | 2000 | |
Synthesis of Functinalized g-Spirolactone and 2-oxabicyclo[3.3.0]octane Derivatives from Nuclephilic Oxirane Ring Opening | 2000 | |
Synthesis and Biological Activity of New Potential Antimalarial: 1H-pyrazolo[3,4-b]pyridine derivatives | 2000 | |
Design and Synthesis of Novel Potent Antinociceptive Agents: Methyl-imidazolyl N-Acylarylhydrazones Derivatives | 2000 | |
Synthesis and Evaluation of Novel Heterotricyclic Acylhydrazones Derivatives, Designed as PAF Antagonist Candidates | 2000 | |
A New Nicotinic Pseudoreceptor Model: A Theoretical Thermodynamic Analysis of Simultaneous Cation-p and Hydrogen Bond Interactions | 2000 | |
Synthesis and analgesic activity of novel N-acylarylhydrazones and isosters, derived from natural safrole##This paper represents contribution # 36 of the LASSBio, UFRJ (Br.) (LASSBio, http://acd.ufrj.br/≈pharma/lassbio); For contribution # 35, see [24]. | 10.1016/s0223-5234(00)00120-3 | 2000 |
Studies on Antiplatelet Agents from Natural Safrole. II. Synthesis and Pharmacological Properties of Novel; Functionalized Oxime O-benzylether Derivatives | 1999 | |
A Utilização do Safrol, Principal Componente Químico do Óleo de Sassafrás, na Síntese de Substancias Bioativas na Cascata do Ácido Araquidônico: Anti-inflamatórios, Analgésicos e Anti-trombóticos | 1999 | |
Synthesis and Analgesic Pofile of Novel N-Containing Heterocycle Derivatives: Arylidedne 3-Phenyl-1,2,4-oxadiazole-5-carbohydrazine | 1999 | |
New Antithrombotic Aryl-semicarbazide Derivative Synthesized from Natural Safrole | 1999 | |
Toward a Platelet-activating Factor Pseudo-receptor 2. A Three Dimensional Semiempirical Model for Agonist and Antagonist Binding | 1999 | |
"Synthesis of New Isosteric Heterocyclic Derivatives: Pyrazolo[3,4-b]thieno[2,3-e]pyridine, Pyrazolo[3,4-b]pyrrolo[2,3-b]pyridine and Pyrazolo[3,4-b]furo[2,3-e]pyridine | 1999 | |
Síntese de Novos Análogos de Piperamidas Hipotensoras | 1999 | |
Proposal of a New PAF Pharmacophoric Map by the AM1 Method | 1999 | |
Synthesis and Anti-platelet Evaluation of Novel Aryl-sulfonamides Derivatives, from Natural Safrole | 1999 | |
Anti-inflammatory Profile of N-Phenylpyrazole Arylhydrazones Derivatives | 1999 | |
Synthesis of Piperamides from Natural Safrole | 1999 | |
Synthesis and Antinociceptive Profile of Novel Acidic Sulfonylhydrazone Derivatives, from Natural Safrole | 1999 | |
Planning and Synthesis of novel 2-oxabicyclo[3.3.0]octane derivatives as potencial lead-compounds with anti-platelet properties | 1999 | |
Synthesis And Pharmacological Evaluation Of New Flosulide Analogues, Synthesized From Natural Safrole | 1998 | |
Diastereomeric Analysis Of Bioactive N-Phenylpyrazole-4-Acylhydrazone Derivatives By High Resolution Gas Chromatography | 1998 | |
Synthesis Of New Benzylic Ethers Of Oximes Derived From 1-Phenyl Pyrazole Compounds | 1998 | |
Toward A Platelet-Activating Factor Pseudoreceptor: Semiempirical Modeling Of Cation-Pi And Hydrogen Bond Interactions In Agonist Binding | 1998 | |
Synthesis And Analgesic Properties Of New 5-Thioaryl Pyrazole Derivatives | 1998 | |
Synthesis Of New 2-Pyridinylarylhydrazones And Evaluation Of Their Analgesic, Antiinflammatory And Antiplatelet Profile | 1998 | |
Synthesis And Analgesic Profile Of New Planned Imidazo[1,2-A]Pyridine Acylaryl Hydrazones Derivatives | 1998 | |
Synthesis Of New 1,2-Benzothiazin-3-One Derivatives, Designed As Dual Cyclooxigenase And 5-Lipoxigenase Inhibitors Candidates | 1998 | |
Synthesis And Pharmacological Profile Of A New Class Of Bicyclic Phospholipids Analogues, Designed As Platelet Activating Factor Antagonist Candidates | 1998 | |
Inibidores Seletivos de Prostaglandina Endoperoxido Sintase-2 (Pghs-2): Nova Estratégia Para O Tratamento da Inflamação | 1998 | |
1H And 13C Of New Bioactive Isochromanylacylhydrazone Derivatives | 1998 | |
Four-Dimensional Quantitative Structure-Activity Relationship Analysis Of A Series Of Interphenylene 7-Oxabicycloheptane Oxazole Thromboxane A2 Receptor Antagonists | 1998 | |
Studies on Diastereoselective Synthesis of 3-Vinyl-5-Carbomethoxy-2-Oxabicyclo{3.3.0]Octane Derivatives Employing Palladium II Oxidative Cyclization | 1998 | |
1H and13C NMR of bioactive isochromanylacetylarylhydrazone derivatives | 10.1002/(SICI)1097-458X(199807)36:7<533::AID-OMR328>3.0.CO;2-V | 1998 |
Reduction Of 2-Allyl-2-Carbomethoxycyclopentanone Derivatives With Sodium Borohydride. Part 2. The Elucidation Of Diastereoselective Control. | 1997 | |
Improvement Of Enantioselective Synthesis And Chiral High Resolution Gas Chromatography Analysis Of (+)-2-Allyl-2-Carbethoxycyclopentanol | 1997 | |
The Synthesis Of New Isochromanylacetylhydrazones Designed As Probable Non-Addictive Analgesic Agents | 1997 | |
On The Modeling Of Some Active Antiinflammatory And Antithrombotic Drugs By Am1 | 1997 | |
Modelagem Molecular, Ferramenta Para O Planejamento Racional de Fármacos | 1997 | |
Síintese de Beta-Ceto-Ésteres Ciclícos: Novo Procedimento Para Ciclizações de Dieckman Empregando Alcl3 e Trietilamina | 1997 | |
Substâncias Enantiomericamente Puras (Sep): A Questão dos Fármacos | 1997 | |
2-Pyridylhydrazone Derivatives, A New Class Of Platelet Aggregation Inhibitors | 1996 | |
Synthesis And Anti-Platelet Evaluation Of New Tricyclic Paf Antagonists, Designed As Structurally Related To Hetrazepines Class - Web 2086 | 1996 | |
Synthesis Of Condensed Tricyclic Pyrazolo[2,3-B]Thieno[2,3-D]Pyridine And Related Isostere Derivatives | 1996 | |
Synthesis And Analgesic Properties Of New 4-Arylhydrazone 1h-Pyrazolo[3,4-B]Pyridine Derivatives | 1996 | |
A Semiempirical Study Of Pyrazole Acylhydrazones As Potential Antimalarial Agents | 1996 | |
Enantiofacial Selective Reduction Of 2-Allyl-2-Carbethoxycyclopentanone Madiated By Baker'S Yeast | 1996 | |
Design And Synthesis Of A New 4-Oxa-8w-11-Deoxy-5,6-Dihydroprostacyclin Analogue | 1996 | |
Asymmetric Friedel-Crafts Reaction: An Application To The Synthesis Of An Etodolac Analogue | 1996 | |
Cardiotônicos: Histórico & Perspectivas de Uma Antiga e Importante Classe de Agentes Terapêuticos | 1996 | |
Noções Sobre Metabolismo de Fármacos | 1996 | |
Molecular Modeliing On Paf And New Proposed Paf Antagonists | 1996 | |
Crystal Structure Of Pyrazole Derivatives. Iv. 5-Chloro-4-Chlorosulfonyl-3-Methyl-1-Phenylpyraazole | 1996 | |
Studies Toward The Diastereoseleective Reduction Of 2-Alkoxycarbonyl-2-Allylcyclopentanone Derivatives With Sodium Borohydrides | 1995 | |
The Synthesis And Analgesic Properties Of New Spiro-Isochromanyl Acid Derivatives Synthesized From Natural Safrole | 1995 | |
Semiempirical Calculations On The Mechanism Of Stereoselective Nabh4 Reduction Of 2-Methoxycarbonyl-2-Allyl-Cyclopentanone | 1995 | |
Design Of New Potential 5-Lipoxigenase Inhibitors, Dual Thromboxane Synthase Inhibitors And Thromboxane A2 Receptor Antagonists By Am1 | 1995 | |
Síntese, Avaliação das Propriedades Antiedematogênicas e Relação Estrutura Atividade de Derivados 5-Arilidrazonil-N-Fenil Pirazolas | 1995 | |
Synthesis And Analgesic Properties Of 5-Acylarylhydrazone 1-H Pyrazole (3,4-B}Pyridine Derivatives | 1994 | |
Analgesic and Antiinflammatory Effects of 3-[3-(Phenyl)-1,2,4-Oxadiazol-5-yl]Propionic Acid | 1994 | |
Structures of Pyrazole Derivatives.III. 5-amino-4-ciano-1-phenylpyrazole | 1994 | |
Perspectivas Terapêuticas de Fármacos que Atuem na Cascata do Ácido Araquidônico | 1994 | |
New Pyrazolylhydrazono Derivatives Inhibitors Of Platelet Aggregation | 1993 | |
The Synthesis And Antiinflammatory Activity Of 1-Alkyl-Isochroman- 1-Yl Acetic Acids Derivatives | 1993 | |
Structures Of Pyrazole Derivatives.1 A Potential Bioisoster Of Thromboxane Synthetase Inhibitor | 1993 | |
Structures Of Pyrazole Derivatives.II.A Potential Bioisoster Of Acetazolamide. | 1993 | |
Sintese e Atividade Antiinflamatória de Novos Derivados Pirazolicos Funcionalizados. Parte 1. 5-Amino Pirazolas | 1993 | |
Agentes Antiinflamatórios Não Esteróides. Parte 1. | 1993 | |
Agentes Antiinflamatórios Não Esteróides. Parte 2. | 1993 | |
Agentes Antiinflamatórios Não Esteróides. Parte 3. | 1993 | |
Structures of pyrazole derivatives. I. A potential bioisoster of thromboxane synthetase inhibitors | 10.1107/s0108270192008527 | 1993 |
The Synthesis And Antiinflammatory Properties Of A New Sulindac Analogue Synthesized From Natural Safrole. | 1992 | |
Pyrazole, An Alcohol Dehydrogenase Inhibitor Has Dual Effects On N-Methyl-D-Aspartate Receptors Of Hippocampal Pyramidal Cells: Agonist And Nomcompetitive Antagonist | 1992 | |
Synthesis Of Pyrazole Derivatives As Potential Bioisosteres Of Thromboxane-Synthetase Inhibitors | 1992 | |
Synthesis of a New Benzothiazine Derivative, Related to Oxicams, Synthesized from Natural Safrole | 1992 | |
A Importancia da Sintese de Farmacos Na Producao de Medicamentos | 1991 | |
Bioisosterismo:Importante Estrategia de Modificacao Molecular Para O Plenejamento Racional de Farmacos. Parte 1. | 1991 | |
Substituted Pyrazolylhydrazones: A New Class Of Platelet Aggregation Inhibitors | 1991 | |
Investigation Of The Lipophilicity Of Antiphlogistic Pyrazole Derivatives: Relationships Between Log Kw And Log P Values Of 5-Arylamino And Arylhydrazone-3-Methyl-4-Nitro-1-Phenylpyrazoles | 1991 | |
Antinoceptive Property Of New 4-Acyl-Arylhydrazone Pyrazolic Compounds | 1991 | |
Bioisosterismo:Importante Estrategia de Modificacao Molecular Para O Plenejamento Racional de Farmacos. Parte 2. | 1991 | |
Produtos Naturais Bioativos de Origem Vegetal e O Desenvolvimento de Farmacos | 1990 | |
Anti-Inflammatory Properties Of New Bioisosteres Of Indomethacin Synthesized From Natural Safrole Which Are Sulindac Analogues | 1989 | |
The Synthesis Of A New 8-Azaprostanoid | 1989 | |
Síntese Total de um Sesquiterpeno Natural Isolado de Aplysia brasiliana. Síntese Enantioespecífica do (+)-Brasilenol | 1989 | |
Eicosanóides. Parte 2 | 1988 | |
The Synthesis Of New Hybrid Prostanoid From Natural Safrole | 1987 | |
Expeditious, Stereocontrolled Synthesis Of Racemic And Natural Brasilenol Through Intramolecular Asynetry Transfer. Absolute Stereochemistry Of Brasilenol | 1987 | |
The Synthesis of a New Prostanoid from Natural Safrole | 1987 | |
Eicosanóides.Parte1 | 1987 | |
A Selective Synthesis Of Brasilenol, A Novel Sesquiterpene From The Sea Hare Aplysia Brasiliana And The Red Alga Laurencia Obtusa | 1986 | |
Sintese Estereosseletiva de 2-Oxa Biciclo[3.3.0]Octanos Funcionalizado | 1985 | |
Prostaglandin Analogues. Part 2. Synthesis Of New Derivatives From Safrole Isolated From Sassafraz Oil. | 1985 | |
Prostaglandin Analogues. The Synthesis of New Aromatic Prostanoides from Natural safrole | 1984 | |
Prostaglandin Analogues. The Synthesis of New Thromboxanes Derivatives from Natural Safrole | 1984 | |
Síntese de Análogos de Prostaglandinas a Partir do Ácido Hidnocárpico | 1984 | |
Prostaglandin Analogues. Synthesis Of Tetrahomoprostaglandin Derivatives From Natural Hydnocarpic Acid Isolated From Sapucainha Oil. | 1983 | |
The Synthesis of 6,7-dehydro-1-methyl-5H-pyrrolizidine-7-one (Danaidone) from pyrrolizidine alkaloid | 1983 | |
Nova Síntese da Sarcomicina-Via da Alfa Tropolona | 1983 | |
Utilização de Produtos Naturais Abundantes na Síntese de Substâncias Biologicamente Ativas: Resultados | 1983 | |
A New Synthesis Of Sarkomycin | 1982 | |
The Total Synthesis Of Prostaglandins By Tropolone Route | 1982 | |
An Improved Synthesis From Natural Safrole Of Indole Derivatives Related To Indomethacin | 1982 | |
Síntese de Derivados do Ácido 2,3-Indolilacético a Partir do Safrol | 1982 | |
Síntese de Prostaglandinas a Partir de Produtos Naturais Abundantes | 1982 | |
A Química Orgânica Sintética | 1982 | |
Síntese de Compostos Biologicamente Ativos a Partir de Produtos Naturais Abundantes | 1981 | |
Síntese de Potenciais Agentes Antiinflamtórios Não-Esteróides do Grupo dos Ácidos Heteroaril Carboxílicos | 1981 | |
Constituintes Químicos de Barbacenia Bicolor Mart | 1980 | |
Carbon-13 Nuclear Magnetic Resonance of Pyrrolizidines Alkaloids | 1980 | |
Synthesis of New Allenic Prostanoid | 1979 | |
Prostaglandinas | 1979 | |
Voies Nouvelles en Synthese de Prostaglandines | 1977 | |
The Use of Cyclo (3.2.0)Heptanones in The Synthesis of Natural Products and Modified Natural Products | 1977 | |
Tetracyclic Triterpenes of Barbecenia Biocolor Mart | 1976 | |
Controlled Formation of Allenes | 1976 | |
New Synthesis of Prostaglandins | 1976 | |
Reactions of Aldehydes with Lithium Dimethylcopper | 1975 | |
Asymmetric Induction in Addition of Organocuprates | 1975 | |
Formation of Allenes by Reaction of Lithium Diorganacuprates | 1975 | |
Pequena Contribuição para a Síntese Estereoespecífica de Olefinas | 1973 |
Eventos:
(0.00% eventos com DOI)