Page last updated: 2024-12-08

19-hydroxytestosterone

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

Cross-References

ID SourceID
PubMed CID150968
CHEBI ID798
SCHEMBL ID1331839
MeSH IDM0111021

Synonyms (27)

Synonym
LMST02020070
CHEBI:798
2126-37-6
nsc77799
nsc-77799
C05294 ,
17beta,19-dihydroxyandrost-4-en-3-one
19-hydroxytestosterone ,
(8r,9s,10s,13s,14s,17s)-17-hydroxy-10-(hydroxymethyl)-13-methyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one
unii-4gs1h36r0u
nsc 77799
androst-4-en-3-one, 17,19-dihydroxy-, (17beta)-
4gs1h36r0u ,
SCHEMBL1331839
androst-4-en-3-one, 17,19-dihydroxy-, (17.beta.)-
17.beta.,19-dihydroxyandrost-4-ene-3-one
androst-4-en-3-one, 17.beta.,19-dihydroxy-
17.beta.,19-dihydroxyandrost-4-en-3-one
4-androstene-17.beta.,19-diol-3-one
17beta, 19-dihydroxyandrost-4-en-3-one
17beta, 19-dihydroxy-4-androsten-3-one
17beta,19-dihydroxy-4-androsten-3-one
4-androsten-17.beta.,19-diol-3-one
17,19-dihydroxyandrost-4-en-3-one #
w hydroxy testosterone
Q27105361
DTXSID801314363
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (1)

RoleDescription
mouse metaboliteAny 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 (3)

ClassDescription
19-hydroxy steroid
3-oxo-Delta(4) steroidA 3-oxo steroid conjugated to a C=C double bond at the alpha,beta position.
17beta-hydroxy steroidA 17-hydroxy steroid in which the hydroxy group at position 17 has a beta-configuration.
[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]

Pathways (1)

PathwayProteinsCompounds
estradiol biosynthesis II18

Research

Studies (4)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901 (25.00)18.7374
1990's3 (75.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)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: 18.15

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 Index18.15 (24.57)
Research Supply Index1.79 (2.92)
Research Growth Index4.76 (4.65)
Search Engine Demand Index10.37 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (18.15)

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]