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2-methoxy-1,4-naphthoquinone and alpha-lapachone

2-methoxy-1,4-naphthoquinone has been researched along with alpha-lapachone in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (33.33)29.6817
2010's2 (66.67)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Carroll, PJ; DuHadaway, JB; Jaller, D; Kumar, S; LaLonde, JM; Malachowski, WP; Metz, R; Muller, AJ; Prendergast, GC1
Bourguignon, SC; Carneiro, PF; do Nascimento, SB; dos Santos JĂșnior, HM; Ferreira, VF; Lechuga, GC; Pinto, AV; Pinto, Mdo C; Resende, JA; Santos, DO1
Alves, HG; Barbosa, GS; Carneiro, PF; da Silva, FC; de Vasconcellos, MC; Ferreira, VF; Lima, ES; Marra, RKF; Pinto, MCRF; Pohlit, AM; Resende, JALC; Rocha E Silva, LF1

Other Studies

3 other study(ies) available for 2-methoxy-1,4-naphthoquinone and alpha-lapachone

ArticleYear
Indoleamine 2,3-dioxygenase is the anticancer target for a novel series of potent naphthoquinone-based inhibitors.
    Journal of medicinal chemistry, 2008, Mar-27, Volume: 51, Issue:6

    Topics: Animals; Antineoplastic Agents; Binding Sites; Cell Proliferation; Cell Survival; Computer Simulation; Crystallography, X-Ray; Disease Models, Animal; Dose-Response Relationship, Drug; Drug Screening Assays, Antitumor; Enzyme Inhibitors; Indoleamine-Pyrrole 2,3,-Dioxygenase; Mice; Mice, Knockout; Mice, Nude; Models, Molecular; Molecular Structure; Naphthoquinones; Pyrones; Stereoisomerism; Structure-Activity Relationship; Vitamin K 3

2008
New oxirane derivatives of 1,4-naphthoquinones and their evaluation against T. cruzi epimastigote forms.
    Bioorganic & medicinal chemistry, 2012, Aug-15, Volume: 20, Issue:16

    Topics: Animals; Cell Death; Cell Survival; Chlorocebus aethiops; Dose-Response Relationship, Drug; Drug Evaluation, Preclinical; Ethylene Oxide; Models, Molecular; Molecular Structure; Naphthoquinones; Parasitic Sensitivity Tests; Structure-Activity Relationship; Trypanocidal Agents; Trypanosoma cruzi; Vero Cells

2012
Synthesis and antimalarial activity of quinones and structurally-related oxirane derivatives.
    European journal of medicinal chemistry, 2016, Jan-27, Volume: 108

    Topics: Antimalarials; Cell Line; Cell Survival; Dose-Response Relationship, Drug; Ethylene Oxide; Fibroblasts; Humans; Molecular Structure; Parasitic Sensitivity Tests; Plasmodium falciparum; Quinones; Structure-Activity Relationship

2016