Compounds > beta-lapachone

beta-lapachone and anthralin

beta-lapachone has been researched along with anthralin in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (20.00)18.2507
2000's0 (0.00)29.6817
2010's4 (80.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Müller, K; Sellmer, A; Wiegrebe, W1
Barnes, JC; Bradley, P; Day, NC; Fourches, D; Reed, JZ; Tropsha, A1
Bannwitz, S; Müller, K; Prinz, H; Reichstein, A; Tentrop, J; Vortherms, S1
Bannwitz, S; Kalin, T; Krane, D; Lindenschmidt, C; Müller, K; Prinz, H; Tentrop, J; Vortherms, S; Zahedi Golpayegani, N1
Basoglu, A; Dirkmann, S; Fröhlich, R; Müller, K; Nowottnik, D; Prinz, H; Tentrop, J; Vortherms, S; Zahedi Golpayegani, N1

Other Studies

5 other study(ies) available for beta-lapachone and anthralin

ArticleYear
Potential antipsoriatic agents: lapacho compounds as potent inhibitors of HaCaT cell growth.
    Journal of natural products, 1999, Volume: 62, Issue:8

    Topics: Administration, Topical; Anthralin; Anti-Inflammatory Agents; Cell Division; Cell Line; Humans; Keratinocytes; Keratolytic Agents; L-Lactate Dehydrogenase; Naphthoquinones; Psoriasis; Spectrophotometry, Infrared; Spectrophotometry, Ultraviolet

1999
Cheminformatics analysis of assertions mined from literature that describe drug-induced liver injury in different species.
    Chemical research in toxicology, 2010, Volume: 23, Issue:1

    Topics: Animals; Chemical and Drug Induced Liver Injury; Cluster Analysis; Databases, Factual; Humans; MEDLINE; Mice; Models, Chemical; Molecular Conformation; Quantitative Structure-Activity Relationship

2010
Synthesis and structure-activity relationships of lapacho analogues. 1. Suppression of human keratinocyte hyperproliferation by 2-substituted naphtho[2,3-b]furan-4,9-diones, activation by enzymatic one- and two-electron reduction, and intracellular genera
    Journal of medicinal chemistry, 2012, Aug-23, Volume: 55, Issue:16

    Topics: Cell Line; Cell Membrane; Cell Proliferation; Dermatologic Agents; Dicumarol; Furans; Humans; Keratinocytes; L-Lactate Dehydrogenase; NAD(P)H Dehydrogenase (Quinone); NADPH-Ferrihemoprotein Reductase; Naphthoquinones; Oxadiazoles; Psoriasis; Structure-Activity Relationship; Superoxides

2012
Synthesis and structure-activity relationships of lapacho analogues. 2. Modification of the basic naphtho[2,3-b]furan-4,9-dione, redox activation, and suppression of human keratinocyte hyperproliferation by 8-hydroxynaphtho[2,3-b]thiophene-4,9-diones.
    Journal of medicinal chemistry, 2014, Jul-24, Volume: 57, Issue:14

    Topics: Cell Proliferation; Cells, Cultured; Dose-Response Relationship, Drug; Humans; Keratinocytes; Molecular Structure; Naphthoquinones; Oxidation-Reduction; Structure-Activity Relationship; Tabebuia

2014
Oxadiazole-substituted naphtho[2,3-b]thiophene-4,9-diones as potent inhibitors of keratinocyte hyperproliferation. Structure-activity relationships of the tricyclic quinone skeleton and the oxadiazole substituent.
    European journal of medicinal chemistry, 2017, Jul-07, Volume: 134

    Topics: Cell Line; Cell Proliferation; Humans; Keratinocytes; Oxadiazoles; Quinones; Structure-Activity Relationship; Superoxides; Thiophenes

2017