Page last updated: 2024-12-07

n(2),n(6)-dimethyl-9-hydroxyellipticinium

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

N(2),N(6)-dimethyl-9-hydroxyellipticinium: RN given refers to parent cpd; structure given in second source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID125770
CHEMBL ID32580
MeSH IDM0150995

Synonyms (9)

Synonym
CHEMBL32580
69467-90-9
6h-pyrido(4,3-b)carbazolium, 9-hydroxy-2,5,6,11-tetramethyl-
n(2),n(6)-dimethyl-9-hydroxyellipticinium
2,6-dimethyl-9-hydroxyellipticine acetate
2,6-dimethyl-9-hydroxyellipticinium
9-hydroxy-2,6-dimethylellipticinium
2,6-dmhe
9-hydroxy-2,5,6,11-tetramethylpyrido(4,3-b)carbazolium chloride
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (6)

Assay IDTitleYearJournalArticle
AID117502The effect on oxygen consumed in the presence of MPO-H2O2.1981Journal of medicinal chemistry, Mar, Volume: 24, Issue:3
Bioactivation of the antitumor drugs 9-hydroxyellipticine and derivatives by a peroxidase-hydrogen peroxide system.
AID96644Compound was tested for its antitumor activity against murine leukemia L1210 cells in vitro, expressed as ID501981Journal of medicinal chemistry, Mar, Volume: 24, Issue:3
Bioactivation of the antitumor drugs 9-hydroxyellipticine and derivatives by a peroxidase-hydrogen peroxide system.
AID116286Increase in life span over control (10e5 cells) in mice after intraperitoneal treatment of the compound.1981Journal of medicinal chemistry, Mar, Volume: 24, Issue:3
Bioactivation of the antitumor drugs 9-hydroxyellipticine and derivatives by a peroxidase-hydrogen peroxide system.
AID117798The effect on NADH oxidation in the presence of MPO-H2O2.1981Journal of medicinal chemistry, Mar, Volume: 24, Issue:3
Bioactivation of the antitumor drugs 9-hydroxyellipticine and derivatives by a peroxidase-hydrogen peroxide system.
AID96665Growth inhibitory activity against L1210 lymphocytic leukemia cells.1983Journal of medicinal chemistry, Oct, Volume: 26, Issue:10
Autoxidation of the antitumor drug 9-hydroxyellipticine and its derivatives.
AID97904Compound was tested for its cytotoxic activity against murine leukemia L1210 cells in mice after intraperitoneal treatment, expressed as LD0 (highest nonlethal dose).1981Journal of medicinal chemistry, Mar, Volume: 24, Issue:3
Bioactivation of the antitumor drugs 9-hydroxyellipticine and derivatives by a peroxidase-hydrogen peroxide system.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (6)

TimeframeStudies, This Drug (%)All Drugs %
pre-19904 (66.67)18.7374
1990's2 (33.33)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 12.28

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be weak demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index12.28 (24.57)
Research Supply Index2.08 (2.92)
Research Growth Index4.36 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (12.28)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials1 (16.67%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other5 (83.33%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]