Compounds > naphtho(2,3-b)furan-4,9-dione
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naphtho(2,3-b)furan-4,9-dione and naphthoquinones

naphtho(2,3-b)furan-4,9-dione has been researched along with naphthoquinones in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (20.00)18.2507
2000's2 (40.00)29.6817
2010's2 (40.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Ferreira, VF; Pinto, AV; Pinto, Mdo C1
Koyanagi, J; Nakayama, K; Ogawa, M; Ohguchi, H; Sugaya, A; Tanaka, A; Tsuda, T; Yamamoto, K1
Hashimoto, K; Kikuchi, H; Koyanagi, J; Kurihara, T; Motohashi, N; Nakamura, Y; Ogawa, M; Sakagami, H; Takano, A; Tanaka, A; Wakabayashi, H; Yamamoto, K1
Bannwitz, S; Kalin, T; Krane, D; Lindenschmidt, C; Müller, K; Prinz, H; Tentrop, J; Vortherms, S; Zahedi Golpayegani, N1
Chamni, S; Chanvorachote, P; Chaotham, C; De-Eknamkul, W; Karnsomwan, W; Prateep, A; Sumkhemthong, S1

Other Studies

5 other study(ies) available for naphtho(2,3-b)furan-4,9-dione and naphthoquinones

ArticleYear
NBS bromination reactions of dihydronaphthofuran quinones: a new fragmentation type reaction in the chemistry of quinones.
    Anais da Academia Brasileira de Ciencias, 1990, Volume: 62, Issue:4

    Topics: Furans; Naphthoquinones; Oxidation-Reduction

1990
Cytotoxic activity toward KB cells of 2-substituted naphtho[2,3-b]furan-4,9-diones and their related compounds.
    Bioscience, biotechnology, and biochemistry, 2006, Volume: 70, Issue:4

    Topics: Cell Proliferation; Humans; KB Cells; Molecular Structure; Naphthoquinones; Structure-Activity Relationship

2006
Tumor-specific cytotoxicity and type of cell death induced by naphtho[2,3-b]furan-4,9-diones and related compounds in human tumor cell lines: relationship to electronic structure.
    Anticancer research, 2009, Volume: 29, Issue:1

    Topics: Cell Death; Cell Line, Tumor; Drug Screening Assays, Antitumor; HL-60 Cells; Humans; Naphthoquinones; Structure-Activity Relationship

2009
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
Avicequinone B sensitizes anoikis in human lung cancer cells.
    Journal of biomedical science, 2018, Apr-09, Volume: 25, Issue:1

    Topics: Anoikis; Antineoplastic Agents; Cell Line, Tumor; Down-Regulation; Humans; Naphthoquinones; Proto-Oncogene Mas; Signal Transduction

2018