Page last updated: 2024-08-22

2-methoxy-1,4-naphthoquinone and lawsone

2-methoxy-1,4-naphthoquinone has been researched along with lawsone in 8 studies

Research

Studies (8)

TimeframeStudies, this research(%)All Research%
pre-19901 (12.50)18.7374
1990's0 (0.00)18.2507
2000's2 (25.00)29.6817
2010's1 (12.50)24.3611
2020's4 (50.00)2.80

Authors

AuthorsStudies
Dunn, WJ; Hodnett, EM; Marrs, P; Wongwiechintana, C1
Cordingley, MG; Graham, PL; Reamer, RA; Singh, SB1
Carroll, PJ; DuHadaway, JB; Jaller, D; Kumar, S; LaLonde, JM; Malachowski, WP; Metz, R; Muller, AJ; Prendergast, GC1
Abdeen, S; Chapman, E; Chitre, S; Hoang, QQ; Johnson, SM; Park, Y; Ray, AM; Salim, N; Sivinski, J; Stevens, M; Washburn, A1
Cao, L; Ding, H; Han, J; Hou, Z; Li, Y; Luo, C; Min, W; Niu, A; Yang, P; Zhang, R1
Afraj, SN; Barve, BD; Ho, HO; Hung, CC; Kuo, LY; Kuo, YH; Lin, ZH; Shen, CC1
Chai, JY; Foong, LC; Ho, ASH; Lim, YM; Tam, SM; Yeo, BPH1
Barnaś, K; Dziuba, J; Kapsiak, M; Nowicka, B; Suchoń, A; Walczak, J1

Other Studies

8 other study(ies) available for 2-methoxy-1,4-naphthoquinone and lawsone

ArticleYear
Substituted 1,4-naphthoquinones vs. the ascitic sarcoma 180 of mice.
    Journal of medicinal chemistry, 1983, Volume: 26, Issue:4

    Topics: Animals; Lethal Dose 50; Magnetic Resonance Spectroscopy; Mathematics; Mice; Naphthoquinones; Sarcoma 180; Structure-Activity Relationship

1983
Discovery, total synthesis, HRV 3C-protease inhibitory activity, and structure-activity relationships of 2-methoxystypandrone and its analogues.
    Bioorganic & medicinal chemistry letters, 2001, Dec-17, Volume: 11, Issue:24

    Topics: 3C Viral Proteases; Cysteine Endopeptidases; Naphthoquinones; Protease Inhibitors; Structure-Activity Relationship; Viral Proteins

2001
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
HSP60/10 chaperonin systems are inhibited by a variety of approved drugs, natural products, and known bioactive molecules.
    Bioorganic & medicinal chemistry letters, 2019, 05-01, Volume: 29, Issue:9

    Topics: Biological Products; Chaperonin 10; Chaperonin 60; Escherichia coli; Humans; Inhibitory Concentration 50; Protein Folding; Rafoxanide; Salicylanilides; Suramin

2019
Lead discovery, chemical optimization, and biological evaluation studies of novel histone methyltransferase SET7 small-molecule inhibitors.
    Bioorganic & medicinal chemistry letters, 2020, 05-01, Volume: 30, Issue:9

    Topics: Antineoplastic Agents; Cell Proliferation; Computer Simulation; Drug Discovery; Histone-Lysine N-Methyltransferase; Humans; Inhibitory Concentration 50; MCF-7 Cells; Models, Molecular; Molecular Structure; Structure-Activity Relationship

2020
Synthesis, biological evaluation, and correlation of cytotoxicity versus redox potential of 1,4-naphthoquinone derivatives.
    Bioorganic & medicinal chemistry letters, 2021, 06-01, Volume: 41

    Topics: Antineoplastic Agents; Cell Proliferation; DNA Topoisomerases, Type I; Dose-Response Relationship, Drug; Drug Screening Assays, Antitumor; HeLa Cells; Humans; KB Cells; Molecular Structure; Naphthoquinones; Oxidation-Reduction; Structure-Activity Relationship; Topoisomerase I Inhibitors

2021
Comparative transcriptome analysis to identify candidate genes involved in 2-methoxy-1,4-naphthoquinone (MNQ) biosynthesis in Impatiens balsamina L.
    Scientific reports, 2020, 09-30, Volume: 10, Issue:1

    Topics: Flowers; Gene Expression Profiling; Gene Expression Regulation, Plant; Gene Ontology; Impatiens; Molecular Sequence Annotation; Naphthoquinones; Plant Leaves; Plants, Medicinal; Transcriptome

2020
Impact of cytotoxic plant naphthoquinones, juglone, plumbagin, lawsone and 2-methoxy-1,4-naphthoquinone, on Chlamydomonas reinhardtii reveals the biochemical mechanism of juglone toxicity by rapid depletion of plastoquinol.
    Plant physiology and biochemistry : PPB, 2023, Volume: 197

    Topics: Antioxidants; Chlamydomonas reinhardtii; Naphthoquinones; Plants; Reactive Oxygen Species

2023