Page last updated: 2024-09-04

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

5,11-dimethyl-5h-indolo(2,3-b)quinoline has been researched along with ellipticine in 1 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
(ellipticine)
Trials
(ellipticine)
Recent Studies (post-2010) (ellipticine)
11054540178

Protein Interaction Comparison

ProteinTaxonomy5,11-dimethyl-5h-indolo(2,3-b)quinoline (IC50)ellipticine (IC50)
Cytochrome P450 1A1Homo sapiens (human)0.0193
Mast/stem cell growth factor receptor KitHomo sapiens (human)0.2
DNA topoisomerase 2-alphaHomo sapiens (human)3.3

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (100.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Boratyński, J; Kaczmarek, L; Peczyńska-Czoch, W; Pognan, F1

Other Studies

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

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