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Potenciais aplicações medicinais de compostos 1,2,3-triazólicos: uma revisão

H.U. revista, 2022-08, Vol.48, p.1-15

2022

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Inhibitory effects of resveratrol analogs on mushroom tyrosinase activity

Molecules (Basel, Switzerland), 2012-10, Vol.17 (10), p.11816-11825

2012

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Synthesis and In Vivo Antimalarial Activity of Novel Derivatives of 6- Mercaptopurine

Letters in drug design & discovery, 2013-10, Vol.10 (8), p.741-747

2013

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FAST GC-FID METHOD FOR MONITORING ACIDIC AND BASIC CATALYTIC TRANSESTERIFICATION REACTIONS IN VEGETABLE OILS TO METHYL ESTER BIODIESEL PREPARATION

Química Nova, 2016-04, Vol.39 (3), p.352-355

2016

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In vitro and in vivo antiplasmodial activity of novel quinoline derivative compounds by molecular hybridization

European journal of medicinal chemistry, 2021-04, Vol.215, p.113271-113271, Article 113271

2021

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1,2,3-Triazole derivatives: synthesis, docking, cytotoxicity analysis and in vivo antimalarial activity

Chemico-biological interactions, 2021-12, Vol.350, p.109688-109688, Article 109688

2021

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Synthesis and biological activity of novel 4-aminoquinoline/1,2,3-triazole hybrids against Leishmania amazonensis

Biomedicine & pharmacotherapy, 2021-09, Vol.141, p.111857-111857, Article 111857

2021

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Azastilbene Analogs as Tyrosinase Inhibitors: New Molecules with Depigmenting Potential

TheScientificWorld, 2013-01, Vol.2013 (2013), p.1-7

2013

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Quinoline Derivatives as Novel Depigmenting and Antioxidant Agents

Letters in drug design & discovery, 2017-04, Vol.14 (4), p.374-379

2017

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Kinetics and thermodynamics of β-cyclodextrin-NH2/β-carotene complexation: how much energy is required to include a hydrophobic group in the macrocycle cavity?

Journal of inclusion phenomena and macrocyclic chemistry, 2024, Vol.104 (7-8), p.395-405

2024

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A simple quinoline salt derivative is active in vitro against Plasmodiumf alciparum asexual blood stages and inhibits the development of cerebral malaria in murine model

Chemico-biological interactions, 2022-03, Vol.355, p.109848, Article 109848

2022

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RA33, an analogue of resveratrol, improves the development of in vitro -fertilized bovine embryos

Zygote (Cambridge), 2022-12, Vol.30 (6), p.891-894

2022

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Antioxidant Activity of Synthetic Resveratrol Analogs: A Structure- Activity Insight

Letters in drug design & discovery, 2012-09, Vol.9 (7), p.676-679

2012

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Antioxidant Activity of Thio-Schiff Bases

Letters in drug design & discovery, 2013-08, Vol.10 (7), p.557-560

2013

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Biological Properties of Heterocyclic Pyridinylimines and Pyridinylhydrazones

Letters in drug design & discovery, 2016-01, Vol.13 (1), p.107-114

2016

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High efficient Light-Emitting Electrochemical Cells based on ionic liquids 1,2,3-triazolium

Organic electronics, 2019-10, Vol.73, p.172-181

2019

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Photoprotective activity of resveratrol analogues

Bioorganic & medicinal chemistry, 2013-02, Vol.21 (4), p.964-968

2013

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Antioxidant Activity of Resveratrol Analogs

Letters in drug design & discovery, 2012-01, Vol.9 (1), p.8-11

2012

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New group of azastilbene analogs of resveratrol: Synthesis, anticandidal activity and toxicity evaluation

Journal of King Saud University. Science, 2019-04, Vol.31 (2), p.158-163

2019

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Quinolines derivatives as novel sunscreening agents

Bioorganic & medicinal chemistry letters, 2013-08, Vol.23 (16), p.4506-4510

2013

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A cascata dos fosfoinositídeos

Química Nova, 2003-01, Vol.26 (1), p.105-111

2003

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Síntese e avaliação da atividade antileishmanial in vitro de bioisósteros do resveratrol

Principia: Caminhos da Iniciação Científica, 2020-03, Vol.18 (1), p.10

2020

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Human serum albumin-resveratrol complex formation: Effect of the phenolic chemical structure on the kinetic and thermodynamic parameters of the interactions

Food chemistry, 2020-03, Vol.307, p.125514-125514, Article 125514

2020

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Resveratrol analogues present effective antileishmanial activity against promastigotes and amastigotes from distinct Leishmania species by multitarget action in the parasites

Journal of pharmacy and pharmacology, 2019-12, Vol.71 (12), p.1854-1863

2019

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The kinetics of formation of resveratrol-β-cyclodextrin-NH2 and resveratrol analog-β-cyclodextrin-NH2 supramolecular complexes

Food chemistry, 2022-01, Vol.366, p.130612-130612, Article 130612

2022

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Potenciais aplicações medicinais de compostos 1,2,3-triazólicos: uma revisão

Inhibitory effects of resveratrol analogs on mushroom tyrosinase activity

Synthesis and In Vivo Antimalarial Activity of Novel Derivatives of 6- Mercaptopurine

FAST GC-FID METHOD FOR MONITORING ACIDIC AND BASIC CATALYTIC TRANSESTERIFICATION REACTIONS IN VEGETABLE OILS TO METHYL ESTER BIODIESEL PREPARATION

In vitro and in vivo antiplasmodial activity of novel quinoline derivative compounds by molecular hybridization

1,2,3-Triazole derivatives: synthesis, docking, cytotoxicity analysis and in vivo antimalarial activity

Synthesis and biological activity of novel 4-aminoquinoline/1,2,3-triazole hybrids against Leishmania amazonensis

Azastilbene Analogs as Tyrosinase Inhibitors: New Molecules with Depigmenting Potential

Quinoline Derivatives as Novel Depigmenting and Antioxidant Agents

Kinetics and thermodynamics of β-cyclodextrin-NH2/β-carotene complexation: how much energy is required to include a hydrophobic group in the macrocycle cavity?

A simple quinoline salt derivative is active in vitro against Plasmodiumf alciparum asexual blood stages and inhibits the development of cerebral malaria in murine model

RA33, an analogue of resveratrol, improves the development of in vitro -fertilized bovine embryos

Antioxidant Activity of Synthetic Resveratrol Analogs: A Structure- Activity Insight

Antioxidant Activity of Thio-Schiff Bases

Biological Properties of Heterocyclic Pyridinylimines and Pyridinylhydrazones

High efficient Light-Emitting Electrochemical Cells based on ionic liquids 1,2,3-triazolium

Photoprotective activity of resveratrol analogues

Antioxidant Activity of Resveratrol Analogs

New group of azastilbene analogs of resveratrol: Synthesis, anticandidal activity and toxicity evaluation

Quinolines derivatives as novel sunscreening agents

A cascata dos fosfoinositídeos

Síntese e avaliação da atividade antileishmanial in vitro de bioisósteros do resveratrol

Human serum albumin-resveratrol complex formation: Effect of the phenolic chemical structure on the kinetic and thermodynamic parameters of the interactions

Resveratrol analogues present effective antileishmanial activity against promastigotes and amastigotes from distinct Leishmania species by multitarget action in the parasites

The kinetics of formation of resveratrol-β-cyclodextrin-NH2 and resveratrol analog-β-cyclodextrin-NH2 supramolecular complexes

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