Page last updated: 2024-09-04

5,11-dimethyl-5h-indolo(2,3-b)quinoline and neocryptolepine

5,11-dimethyl-5h-indolo(2,3-b)quinoline has been researched along with neocryptolepine in 2 studies

Compound Research Comparison

Studies
(5,11-dimethyl-5h-indolo(2,3-b)quinoline)
Trials
(5,11-dimethyl-5h-indolo(2,3-b)quinoline)
Recent Studies (post-2010)
(5,11-dimethyl-5h-indolo(2,3-b)quinoline)
Studies
(neocryptolepine)
Trials
(neocryptolepine)
Recent Studies (post-2010) (neocryptolepine)
110539024

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (50.00)18.2507
2000's0 (0.00)29.6817
2010's1 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Boratyński, J; Kaczmarek, L; Peczyńska-Czoch, W; Pognan, F1
Cmoch, P; Jaromin, A; Kaczmarek, L; Peczyńska-Czoch, W; Piętka-Ottlik, M; Sidoryk, K; Switalska, M; Szczepek, W; Wietrzyk, J; Zagrodzka, J1

Other Studies

2 other study(ies) available for 5,11-dimethyl-5h-indolo(2,3-b)quinoline and neocryptolepine

ArticleYear
Synthesis and structure-activity relationship of methyl-substituted indolo[2,3-b]quinolines: novel cytotoxic, DNA topoisomerase II inhibitors.
    Journal of medicinal chemistry, 1994, Oct-14, Volume: 37, Issue:21

    Topics: Animals; Antineoplastic Agents; Candida albicans; Carbolines; Cattle; Cell Division; DNA; DNA Topoisomerases, Type II; Gram-Positive Bacteria; Hot Temperature; Humans; Indoles; KB Cells; Methylation; Molecular Structure; Nucleic Acid Denaturation; Quinolines; Structure-Activity Relationship; Topoisomerase II Inhibitors; Trichophyton

1994
Synthesis and biological evaluation of new amino acid and dipeptide derivatives of neocryptolepine as anticancer agents.
    Journal of medicinal chemistry, 2012, Jun-14, Volume: 55, Issue:11

    Topics: Alkaloids; Amino Acids; Animals; Antineoplastic Agents; Carbolines; Cell Line, Tumor; Dipeptides; Drug Screening Assays, Antitumor; Hemolysis; Humans; Hydrophobic and Hydrophilic Interactions; Mice; Quinolines; Structure-Activity Relationship

2012