Page last updated: 2024-12-08
2-hydroxy-1,4-benzoquinone
Description
2-hydroxy-1,4-benzoquinone: formed by the reaction of benzoquinone with hydrogen peroxide; structure given in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]
hydroxyquinone : Any quinone in which one or more of the carbons making up the quinone moiety is substituted by a hydroxy group. [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]
2-hydroxy-1,4-benzoquinone : The simplest member of the class of 2-hydroxy-1,4-benzoquinones, that is 1,4-benzoquinone in which a single hydrogen is replaced by a hydroxy group. [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]
Cross-References
| ID Source | ID |
|---|
| PubMed CID | 151011 |
| CHEBI ID | 18400 |
| SCHEMBL ID | 221723 |
| SCHEMBL ID | 8663010 |
| MeSH ID | M0152947 |
Synonyms (20)
| Synonym |
|---|
| 2-hydroxycyclohexa-2,5-diene-1,4-dione |
| CHEBI:18400 |
| 2-hydroxy-p-benzoquinone |
| hydroxy-p-benzoquinone |
| 2-hydroxy-2,5-cyclohexadiene-1,4-dione |
| 2-hydroxy-1,4-benzoquinone |
| 2474-72-8 |
| hydroxybenzoquinone , |
| C07103 |
| unii-c7i5hv2jfi |
| c7i5hv2jfi , |
| 2,5-cyclohexadiene-1,4-dione, 2-hydroxy- |
| hydroxy-1,4-benzoquinone |
| SCHEMBL221723 |
| hydroxyquinone [vandf] |
| hydroxyquinone |
| SCHEMBL8663010 |
| DTXSID60179468 |
| 4-hydroxy-o-benzochinon |
| Q5955500 |
Roles (1)
| Role | Description |
|---|
| mouse metabolite | Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus). |
| [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)
| Class | Description |
|---|
| monohydroxy-1,4-benzoquinones | Any 1,4-benzoquinone carrying a single hydroxy substituent. |
| [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] |
Research
Studies (7)
| Timeframe | Studies, This Drug (%) | All Drugs % |
|---|
| pre-1990 | 3 (42.86) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (28.57) | 29.6817 |
| 2010's | 2 (28.57) | 24.3611 |
| 2020's | 0 (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: 19.87
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.
| Metric | This Compound (vs All) |
|---|
| Research Demand Index | 19.87 (24.57) | | Research Supply Index | 2.08 (2.92) | | Research Growth Index | 4.32 (4.65) | | Search Engine Demand Index | 15.26 (26.88) | | Search Engine Supply Index | 2.00 (0.95) |
| |
Study Types
| Publication Type | This drug (%) | All Drugs (%) |
|---|
| Trials | 0 (0.00%) | 5.53% |
| Reviews | 0 (0.00%) | 6.00% |
| Case Studies | 0 (0.00%) | 4.05% |
| Observational | 0 (0.00%) | 0.25% |
| Other | 7 (100.00%) | 84.16% |
| [information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |