Page last updated: 2024-11-06

2-(hydroxymethyl)anthraquinone

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

Description

2-(hydroxymethyl)anthraquinone: structure given in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID87014
CHEMBL ID21049
CHEBI ID28649
SCHEMBL ID41511
MeSH IDM0209010

Synonyms (34)

Synonym
brn 2120452
ccris 3522
anthraquinone, 2-(hydroxymethyl)-
einecs 241-274-3
9,10-anthracenedione, 2-(hydroxymethyl)-
2-(hydroxymethyl)-9,10-anthraquinone
2-(hydroxymethyl)anthracene-9,10-dione
CHEBI:28649 ,
2-(hydroxymethyl)anthraquinone
17241-59-7
2-hydroxymethylanthraquinone
anthraquinone-2-methanol
2-(hydroxymethyl)anthraquinone, 97%
CHEMBL21049
2-hydroxymethyl-anthraquinone
A811412
4-08-00-02607 (beilstein handbook reference)
FT-0608819
AKOS015856505
2-hydroxymethyl-9,10-anthracenedione
SCHEMBL41511
2-hydroxymethyl-9,10-anthraquinone
2-(hydroxymethyl)anthra-9,10-quinone #
mfcd00001236
DTXSID10169278
AS-63881
2-(hydroxymethyl)-9,10-dihydroanthracene-9,10-dione
CS-0131104
HY-N7502
J-010816
9,10-anthracenedione,2-(hydroxymethyl)
BCP24351
Q27103810
PD167284
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (1)

RoleDescription
metaboliteAny intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
[role information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Drug Classes (1)

ClassDescription
anthraquinone
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Bioassays (6)

Assay IDTitleYearJournalArticle
AID1867248Antibacterial activity against multidrug resistant Helicobacter pylori JRES00015 assessed as bacterial growth inhibition incubated for 3 days by broth microdilution method
AID1867247Antibacterial activity against multidrug resistant Helicobacter pylori HP159 assessed as bacterial growth inhibition incubated for 3 days by broth microdilution method
AID67634Compound is measured for surviving fractions of EMT6 tumor cells treated in culture with (0.50 uM) concentration for 1 hr under aerobic condition.1980Journal of medicinal chemistry, Nov, Volume: 23, Issue:11
2-Methylanthraquinone derivatives as potential bioreductive alkylating agents.
AID1867246Antibacterial activity against multidrug resistant Helicobacter pylori G27 assessed as bacterial growth inhibition incubated for 3 days by broth microdilution method
AID231332Ratio of toxicity in areobic conditions to hypoxic condition of EMT6 cells1980Journal of medicinal chemistry, Nov, Volume: 23, Issue:11
2-Methylanthraquinone derivatives as potential bioreductive alkylating agents.
AID67635Compound is measured for surviving fractions of EMT6 tumor cells treated in culture with (0.50 uM) concentration for 1 hr under hypoxic condition.1980Journal of medicinal chemistry, Nov, Volume: 23, Issue:11
2-Methylanthraquinone derivatives as potential bioreductive alkylating agents.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (5)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901 (20.00)18.7374
1990's1 (20.00)18.2507
2000's1 (20.00)29.6817
2010's1 (20.00)24.3611
2020's1 (20.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 17.90

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 moderate demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index17.90 (24.57)
Research Supply Index1.79 (2.92)
Research Growth Index4.51 (4.65)
Search Engine Demand Index10.37 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (17.90)

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%
Other5 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]