Chaquip Daher Netto
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
| Pós-Doutorado | 2007 - 2008
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Universidade Federal do Rio de Janeiro
Química de Produtos Naturais | Doutorado | 2003 - 2007
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Universidade Federal do Rio de Janeiro
Química de Produtos Naturais | Mestrado | 2001 - 2003
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Universidade Federal do Rio de Janeiro
Farmácia | Graduação | 1996 - 2000
Laboratórios:
Nenhum laboratório cadastrado
Nuvens de Palavras:
Artigos:
(91.89% artigos com DOI)
| Titulo | DOI | Ano |
|---|---|---|
| Flavonoids as Inspiration for the Design and Synthesis of New Antiproliferative, Antiparasitic and Antiviral Compounds: An Account | 10.21577/0103-5053.20240056 | 2024 |
| LQB-118 Suppresses Migration and Invasion of Prostate Cancer Cells by Modulating the Akt/GSK3β Pathway and MMP-9/Reck Gene Expression | 10.21873/anticanres.16171 | 2023 |
| Copper(I)/Triphenylphosphine Complexes Containing Naphthoquinone Ligands as Potential Anticancer Agents | 10.3390/inorganics11090367 | 2023 |
| Partial characterization and anticoagulant activity of sulfated galactan from the green seaweed Halimeda opuntia | 10.1590/0001-3765202320211002 | 2023 |
| Effects of |
10.1002/ps.6900 | 2022 |
| Novel Ru(II)-bipyridine/phenanthroline-lapachol complexes as potential anti-cancer agents | 10.1016/j.jinorgbio.2022.112005 | 2022 |
| Lapachol in the Design of a New Ruthenium(II)-Diphosphine Complex as a Promising Anticancer Metallodrug | 10.1016/j.jinorgbio.2020.111289 | 2021 |
| The pterocarpanquinone LQB¿118 compound induces apoptosis of cytarabine¿resistant acute myeloid leukemia cells | 10.3892/ijo.2021.5204 | 2021 |
| Cross-Coupling Reactions with 2-Amino-/Acetylamino-Substituted 3-Iodo-1,4-naphthoquinones: Convenient Synthesis of Novel Alkenyl- and Alkynylnaphthoquinones and Derivatives | 10.1055/s-0037-1610781 | 2021 |
| The pterocarpanquinone LQB 118 inhibits inflammation triggered by zymosan in vivo and in vitro | 10.1016/j.intimp.2020.106399 | 2020 |
| Medicinal Electrochemistry of Halogenated and Nitrated Pterocarpanquinones | 10.21577/0103-5053.20190161 | 2019 |
| LQB-118 compound inhibits migration and induces cell death in glioblastoma cells | 10.3892/or.2019.7402 | 2019 |
| New strategies for the synthesis of naphthoquinones employing Cu(II) complexes: Crystal structures and cytotoxicity | 10.1016/j.molstruc.2017.08.066 | 2018 |
| Second-generation pterocarpanquinones: synthesis and antileishmanial activity | 10.1186/s40409-018-0174-7 | 2018 |
| Preparative Chiral Separation and Absolute Configuration of the Synthetic Pterocarpanquinone LQB-118 | 10.1002/chir.22696 | 2017 |
| Synthesis of Stilbene-Quinone Hybrids through Heck Reactions in PEG-400 | 10.1055/s-0036-1589095 | 2017 |
| In vitro and in vivo antineoplastic and immunological effects of pterocarpanquinone LQB-118 | 10.1007/s10637-016-0359-2 | 2016 |
| Preclinical studies of LQB-118: subacute toxicity and therapeutic evaluation in experimental visceral leishmaniasis. | 10.1128/aac.01787-15 | 2016 |
| Anti-Inflammatory Properties of Pterocarpanquinone LQB-118 in Mice | 10.1016/j.bmc.2016.07.046 | 2016 |
| ROS release, alkylating ability and DNA interaction of a pterocarpanquinone: a test case for electrochemistry | 10.1002/celc.201600504 | 2016 |
| Palladium-Catalyzed Oxyarylation, Azaarylation and | 10.2174/157017941206150828112502 | 2015 |
| Further evidence that naphthoquinone inhibits Toxoplasma gondii growth in vitro | 10.1016/j.parint.2015.08.010 | 2015 |
| Ligand-Free Palladium-Catalyzed Oxyarylation of Dihydronaphthalenes and Chromenequinone with o-Iodophenols and 3-Iodolawsone in PEG-400: An Efficient Synthesis of 5-Carbapterocarpans and Pterocarpanquinones | 10.1055/s-0034-1378745 | 2015 |
| The pterocarpanquinone LQB-118 inhibits tumor cell proliferation by downregulation of c-Myc and cyclins D1 and B1 mRNA and upregulation of p21 cell cycle inhibitor expression | 10.1016/j.bmc.2014.04.025 | 2014 |
| LQB-118, an orally active pterocarpanquinone, induces selective oxidative stress and apoptosis in Leishmania amazonensis | 10.1093/jac/dks498 | 2013 |
| Purification of a synthetic naphthoquinone pterocarpanquinone by counter-current chromatography | 2012 | |
| A new type of pterocarpanquinone that affects Toxoplasma gondii tachyzoites in vitro | 10.1016/j.vetpar.2011.11.008 | 2012 |
| LQB-118, a pterocarpanquinone structurally related to lapachol [2-hydroxy-3-(3-methyl-2-butenyl)-1,4-naphthoquinone]: a novel class of agent with high apoptotic effect in chronic myeloid leukemia cells | 10.1007/s10637-010-9453-z | 2011 |
| Pterocarpanquinones, aza-pterocarpanquinone and derivatives: Synthesis, antineoplasic activity on human malignant cell lines and antileishmanial activity on Leishmania amazonensis | 10.1016/j.bmc.2011.09.025 | 2011 |
| Effectiveness of the local or oral delivery of the novel naphthopterocarpanquinone LQB-118 against cutaneous leishmaniasis | 10.1093/jac/dkr158 | 2011 |
| New pterocarpanquinones: Synthesis, antineoplasic activity on cultured human malignant cell lines and TNF-a modulation in human PBMC cells | 10.1016/j.bmc.2009.12.073 | 2010 |
| Comparison of the cytotoxic effect of lapachol, ?-lapachone and pentacyclic 1,4-naphthoquinones on human leukemic cells | 10.1007/s10637-009-9231-y | 2010 |
| Antitumoral, Antileishmanial and Antimalarial Activity of Pentacyclic 1,4-Naphthoquinone Derivatives | 2009 | |
| (±)-3,4-Dihydroxy-8,9-methylenedioxypterocarpan and derivatives: Cytotoxic effect on human leukemia cell lines | 10.1016/j.ejmech.2008.01.027 | 2009 |
| Insights into the mechanism of Na+/K+-ATPase inhibition by 2-methoxy-3,8,9-trihydroxy coumestan | 10.1016/j.bmc.2008.09.007 | 2008 |
| Structure?activity relationship of wedelolactone analogues: Structural requirements for inhibition of Na+,K+-ATPase and binding to the central benzodiazepine receptor | 10.1016/j.bmc.2006.07.053 | 2006 |
| The First Synthesis of (±)-3,4-Dihydroxy-8,9-methylenedioxypterocarpan, an AntitumoralAgent and its Coumestan Derivative | 2004 |
Eventos:
(0.00% eventos com DOI)