Page last updated: 2024-11-12
3'-hydroxystanozolol
Description
Research Excerpts
Clinical Trials
Roles
Classes
Pathways
Study Profile
Bioassays
Related Drugs
Related Conditions
Protein Interactions
Research Growth
Market Indicators
Description
3'-hydroxystanozolol: structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]
Cross-References
| ID Source | ID |
|---|---|
| PubMed CID | 14299601 |
| CHEBI ID | 192613 |
| MeSH ID | M0386713 |
Synonyms (19)
| Synonym |
|---|
| 3'-hydroxystanazolol |
| 3'-hydroxystanozolol |
| 125709-39-9 |
| CHEBI:192613 |
| (1s,2s,10s,13r,14s,17s,18s)-17-hydroxy-2,17,18-trimethyl-6,7-diazapentacyclo[11.7.0.02,10.04,8.014,18]icos-4(8)-en-5-one |
| 3-hydroxy-stanozolol |
| DTXSID50558682 |
| (1s,2s,10s,13r,14s,17s,18s)-17-hydroxy-2,17,18-trimethyl-6,7-diazapentacyclo[11.7.0.0^{2,10}.0^{4,8}.0^{14,18}]icos-4(8)-en-5-one |
| (5.alpha.,17.beta.)-1',2'-dihydro-17-hydroxy-17-methyl-5'h-androst-2-eno(3,2-c)pyrazol-5'-one |
| (5alpha,17beta)-1',2'-dihydro-17-hydroxy-17-methyl-5'h-androst-2-eno(3,2-c)pyrazol-5'-one |
| 2295-92-3 |
| 01AEG6W4Y9 , |
| 5'h-androst-2-eno(3,2-c)pyrazol-5'-one, 1',2'-dihydro-17-hydroxy-17-methyl-, (5.alpha.,17.beta.)- |
| 5'h-androst-2-eno(3,2-c)pyrazol-5'-one, 1',2'-dihydro-17-hydroxy-17-methyl-, (5alpha,17beta)- |
| unii-01aeg6w4y9 |
| (5 ,17 )-1',2'-dihydro-17-hydroxy-17-methyl-5'h-androst-2-eno[3,2-c]pyrazol-5'-one |
| 3-hydroxystanozolol |
| Q27231420 |
| PD061119 |
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]
Drug Classes (1)
| Class | Description |
|---|---|
| steroid | Any of naturally occurring compounds and synthetic analogues, based on the cyclopenta[a]phenanthrene carbon skeleton, partially or completely hydrogenated; there are usually methyl groups at C-10 and C-13, and often an alkyl group at C-17. By extension, one or more bond scissions, ring expansions and/or ring contractions of the skeleton may have occurred. Natural steroids are derived biogenetically from squalene which is a triterpene. |
| [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 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 4 (57.14) | 29.6817 |
| 2010's | 3 (42.86) | 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: 17.43
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.
| This Compound (17.43) All Compounds (24.57) |
Study Types
| Publication Type | This drug (%) | All Drugs (%) |
|---|---|---|
| Trials | 0 (0.00%) | 5.53% |
| Reviews | 0 (0.00%) | 6.00% |
| Case Studies | 1 (12.50%) | 4.05% |
| Observational | 0 (0.00%) | 0.25% |
| Other | 7 (87.50%) | 84.16% |
| [information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] | ||