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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 SourceID
PubMed CID14299601
CHEBI ID192613
MeSH IDM0386713

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)

ClassDescription
steroidAny 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)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's4 (57.14)29.6817
2010's3 (42.86)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: 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.

MetricThis Compound (vs All)
Research Demand Index17.43 (24.57)
Research Supply Index2.20 (2.92)
Research Growth Index4.44 (4.65)
Search Engine Demand Index10.37 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (17.43)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies1 (12.50%)4.05%
Observational0 (0.00%)0.25%
Other7 (87.50%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]