Page last updated: 2024-12-07

1-hydroxy-5,8-bis(2-((2-hydroxyethyl)amino)ethylamino)-9,10-anthracenedione

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

Description

1-hydroxy-5,8-bis(2-((2-hydroxyethyl)amino)ethylamino)-9,10-anthracenedione is a complex organic compound with a rather long and complicated name. It's more commonly known as **Mitoxantrone**.

**Mitoxantrone** is a synthetic, water-soluble anthracenedione derivative. It is a type of **antineoplastic** drug, meaning it's used to treat cancer.

**Why is it important for research?**

Mitoxantrone is a clinically important drug with several unique features that make it a target for research:

* **Mechanism of action:** Mitoxantrone works by interfering with the DNA replication process of cancer cells, effectively stopping their growth. This makes it an interesting compound for understanding how to target DNA replication for cancer therapy.
* **Applications in various cancers:** Mitoxantrone is used to treat several types of cancer, including breast cancer, leukemia, lymphoma, and prostate cancer. Researchers are investigating its potential effectiveness against other cancers and exploring new ways to administer it.
* **Side effects and drug resistance:** Like many other chemotherapy drugs, mitoxantrone has side effects. Researchers are working to understand the mechanism behind these side effects and develop strategies to minimize them. They are also investigating ways to overcome drug resistance that may develop in cancer cells over time.
* **Potential for drug development:** Mitoxantrone's unique structure and mechanism of action have inspired the development of new anthracenedione-based drugs with improved effectiveness and fewer side effects.

**In summary,** Mitoxantrone is a crucial molecule in cancer research due to its clinical importance, unique mechanism of action, and potential for development of new anti-cancer therapies. Ongoing research aims to improve its effectiveness, reduce its side effects, and explore its applications in new treatment regimens.

1-hydroxy-5,8-bis(2-((2-hydroxyethyl)amino)ethylamino)-9,10-anthracenedione: structure given in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID133411
CHEMBL ID106847
SCHEMBL ID3273264
MeSH IDM0116690

Synonyms (16)

Synonym
9,10-anthracenedione, 5-hydroxy-1,4-bis((2-((2-hydroxyethyl)amino)ethyl)amino)-
1,4-bis((2-((2-hydroxyethyl)amino)ethyl)amino)-5-hydroxy-9,10-anthracenedione
1-hydroxy-5,8-bis(2-((2-hydroxyethyl)amino)ethylamino)-9,10-anthracenedione
80189-44-2
mhaq
amentantrone
CHEMBL106847
5-hydroxy-1,4-bis[2-(2-hydroxyethylamino)ethylamino]anthracene-9,10-dione
1-hydroxy-5,8-bis(((2-((2-hydroxyethyl)amino)ethyl)amino))-9,10-anthracenedione
niosh/cb5749300
anthraquinone, 1,4-bis(2-(2-hydroxyethylamino)ethylamino)-8-hydroxy-
1,4-bis(2-(2-hydroxyethylamino)ethylamino)-8-hydroxyanthraquinone
CB57493000 ,
DTXSID20230145
SCHEMBL3273264
5-hydroxy-1,4-bis((2-((2-hydroxyethyl)amino)ethyl)amino)anthracene-9,10-dione
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (7)

Assay IDTitleYearJournalArticle
AID88359Effective concentration against cell growth of HeLa cell line by 50%1996Journal of medicinal chemistry, Aug-02, Volume: 39, Issue:16
Peptidyl anthraquinones as potential antineoplastic drugs: synthesis, DNA binding, redox cycling, and biological activity.
AID98039Effective concentration against cell growth of L1210 cell line by 50%1996Journal of medicinal chemistry, Aug-02, Volume: 39, Issue:16
Peptidyl anthraquinones as potential antineoplastic drugs: synthesis, DNA binding, redox cycling, and biological activity.
AID87614In vitro cytotoxic activity against HeLaS3 cells in tissue culture was determined1990Journal of medicinal chemistry, Jan, Volume: 33, Issue:1
5-[(Aminoalkyl)amino]imidazo[4,5,1-de]acridin-6-ones as a novel class of antineoplastic agents. Synthesis and biological activity.
AID24663Exclusion parameter (base pairs)1996Journal of medicinal chemistry, Aug-02, Volume: 39, Issue:16
Peptidyl anthraquinones as potential antineoplastic drugs: synthesis, DNA binding, redox cycling, and biological activity.
AID151960In vivo antitumor activity was determined against P 388 leukemia cells implanted (ip) in BDF1 mice at a dose of 12.5 mg/kg (3 cures)1990Journal of medicinal chemistry, Jan, Volume: 33, Issue:1
5-[(Aminoalkyl)amino]imidazo[4,5,1-de]acridin-6-ones as a novel class of antineoplastic agents. Synthesis and biological activity.
AID82830Effective concentration against cell growth of HL60 cell line by 50%1996Journal of medicinal chemistry, Aug-02, Volume: 39, Issue:16
Peptidyl anthraquinones as potential antineoplastic drugs: synthesis, DNA binding, redox cycling, and biological activity.
AID54649Intrinsic Binding constant of compound to DNA at pH 7 and 25 Centigrade1996Journal of medicinal chemistry, Aug-02, Volume: 39, Issue:16
Peptidyl anthraquinones as potential antineoplastic drugs: synthesis, DNA binding, redox cycling, and biological activity.
[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-19901 (16.67)18.7374
1990's2 (33.33)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's3 (50.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 12.67

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 Index12.67 (24.57)
Research Supply Index1.95 (2.92)
Research Growth Index4.62 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (12.67)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other6 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]