Page last updated: 2024-12-05

6-dehydrotestosterone

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

Description

6-dehydrotestosterone (6-DHT) is a potent androgen that is a metabolite of testosterone. It is synthesized by the enzyme 5α-reductase, which converts testosterone to dihydrotestosterone (DHT), and then by the enzyme 3β-hydroxysteroid dehydrogenase, which converts DHT to 6-DHT. 6-DHT is a potent agonist of the androgen receptor, and it has been shown to have a variety of effects, including promoting muscle growth, masculinization, and prostate growth. 6-DHT is studied because of its potential role in male pattern baldness and prostate cancer. It is also being investigated as a potential therapeutic agent for a variety of conditions, including hypogonadism, muscle wasting, and osteoporosis.'

6-dehydrotestosterone : A 17beta-hydroxy steroid that is testosterone that contains an additional double bond between positions 6 and 7. [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 SourceID
PubMed CID17209
CHEBI ID29117
SCHEMBL ID3364701
MeSH IDM0081084

Synonyms (39)

Synonym
delta(sup 6)-testosterone
6,7-dehydrotestosterone
nsc 75560
androsta-4,6-dien-3-one, 17-hydroxy-, (17beta)-
(17-beta)-17-hydroxyandrosta-4,6-dien-3-one
(17beta)-17-hydroxyandrosta-4,6-dien-3-one
einecs 219-623-6
androsta-4,6-dien-3-one, 17-beta-hydroxy-
androsta-4,6-dien-17-beta-ol-3-one
androsta-4,6-dien-3-one, 17-hydroxy-, (17-beta)-
6-dehydrotestosterone
6,7-didehydrotestosterone
CHEBI:29117
17beta-hydroxyandrosta-4,6-dien-3-one
nsc-75560
nsc75560
2484-30-2
androsta-4, 17-hydroxy-, (17.beta.)-
(8r,9s,10r,13s,14s,17s)-17-hydroxy-10,13-dimethyl-1,2,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-one
SCHEMBL3364701
LMST02020082
17-hydroxy-4,6-androstadiene-3-one
delta(6)-testosterone
4p45k0o2lx ,
unii-4p45k0o2lx
2352-19-4
17b-hydroxy-4,6-androstadiene-3-one
17-hydroxyandrosta-4,6-dien-3-one #
UMDCOKNNLDEKJB-DYKIIFRCSA-N
17beta-hydroxyandrosta-4,6-dien-3-one (?6-testosterone)
.delta.6-testosterone
testosterone impurity i [ep impurity]
Q27109951
6-dehydrotestosterone acetate
(8r,9s,10r,13s,14s,17s)-17-hydroxy-10,13-dimethyl-1,2,8,9,10,11,12,13,14,15,16,17-dodecahydro-3h-cyclopenta[a]phenanthren-3-one
A903335
(1s,3as,3br,9ar,9bs,11as)-1-hydroxy-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,7h,8h,9h,9ah,9bh,10h,11h,11ah-cyclopenta[a]phenanthren-7-one
17?-hydroxyandrosta-4,6-dien-3-one (?6-testosterone)
DTXSID801043247
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (3)

ClassDescription
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.
enoneAn alpha,beta-unsaturated ketone of general formula R(1)R(2)C=CR(3)-C(=O)R(4) (R(4) =/= H) in which the C=O function is conjugated to a C=C double bond at the alpha,beta position.
[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 (14)

TimeframeStudies, This Drug (%)All Drugs %
pre-19909 (64.29)18.7374
1990's4 (28.57)18.2507
2000's0 (0.00)29.6817
2010's1 (7.14)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: 11.43

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

MetricThis Compound (vs All)
Research Demand Index11.43 (24.57)
Research Supply Index2.77 (2.92)
Research Growth Index4.20 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (11.43)

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%
Other15 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]