Page last updated: 2024-12-07

19-norandrostenedione

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

Description

19-norandrostenedione is a synthetic steroid hormone that is structurally similar to testosterone. It's important to understand that **19-norandrostenedione is not testosterone** and it does not directly convert to testosterone in the body.

Here's why it's important for research:

* **Potential therapeutic applications:** 19-norandrostenedione has been investigated for potential therapeutic applications in conditions like:
* **Muscle wasting:** Studies have explored its use in conditions like HIV/AIDS-related muscle wasting due to its potential to promote muscle growth.
* **Osteoporosis:** Research has explored its potential role in increasing bone mineral density and preventing bone loss.
* **Hormone replacement therapy:** Some studies have looked into its potential use in hormone replacement therapy, especially in women experiencing menopause.
* **Understanding steroid metabolism:** Studying 19-norandrostenedione helps researchers understand the complex pathways of steroid hormone metabolism in the body, including how different steroids are synthesized and metabolized.
* **Development of new drugs:** Research on 19-norandrostenedione has helped identify potential targets for drug development, particularly in the areas of muscle growth, bone health, and hormone regulation.

**However, it's crucial to note:**

* **Safety concerns:** 19-norandrostenedione has been linked to potential side effects, including liver damage, increased risk of blood clots, and masculinizing effects in women.
* **Limited clinical evidence:** While research has explored its potential, there is limited clinical evidence to support its safety and efficacy for any specific therapeutic application.
* **Regulation:** 19-norandrostenedione is often marketed as a dietary supplement, but its sale and use are regulated in many countries due to safety concerns.

**In summary:** 19-norandrostenedione is a synthetic steroid hormone that is being studied for potential therapeutic uses. However, its safety and efficacy are not fully established, and further research is needed before it can be widely used for medical purposes.

19-norandrostenedione: structure [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID92834
CHEBI ID34187
SCHEMBL ID868884
MeSH IDM0043593

Synonyms (44)

Synonym
(+)-19-norandrost-4-ene-3,17-dione
estr-4-ene-3,17-dione
nsc12164
19-norandrostenedione
nsc-12164
.delta.4-estrene-3,17-dione
delta4-estrene-3,17-dione
delta,4-estrene-3,17-dione
DB01434
(8r,9s,10r,13s,14s)-13-methyl-1,2,6,7,8,9,10,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthrene-3,17-dione
19-norandrost-4-ene-3,17-dione
d-19-norandrost-4-ene-3,17-dione
3,17-dioxo-19-norandrost-4-ene
u90987pvu5 ,
nordione
(+)-estr-4-ene-3,17-dione
nsc 12164
einecs 211-995-8
unii-u90987pvu5
AKOS015896166
(+)-19-norandrost-4-en-3,17-dione
4-oestrendione
4-oestren-3,17-dione
4-norendione
norethisterone impurity b [ep impurity]
19-norandrost-4-en-3,17-dione
4-norendion
19-nor-4-androstene-3,17-dione
19-nor-4-androstene-3,17-dion
norethisterone acetate impurity j [ep impurity]
SCHEMBL868884
estra-4-ene-3,17-dione
estra4-ene-3,17-dione
CHEBI:34187
Q-102802
19-nor-androstene-4-ene-3,17-dione
19-norandrost-4-en-3,17-dione (8.beta.,9.alpha.,10.beta.)
norandrostenedione (19-norandrost-4-ene-3,17-dione)
norandrostenedione (19-norandrost-4-ene-3,17-dione) 1.0 mg/ml in acetonitrile
DTXSID50862392
Q4557695
estra-4-en-3,17-dione(19-nor ad)
(3as,3br,9ar,9bs,11as)-11a-methyl-1h,2h,3h,3ah,3bh,4h,5h,7h,8h,9h,9ah,9bh,10h,11h,11ah-cyclopenta[a]phenanthrene-1,7-dione
PD008864

Research Excerpts

Bioavailability

ExcerptReferenceRelevance
" This may be due to a slower rate of absorption and/or a reduced diuresis, resulting in a longer period for the metabolites to accumulate in the urine."( Influence of delivery mode on the urinary excretion of nandrolone metabolites.
Dunster, PM; Grace, PB; Houghton, E; Judkins, C; Maughan, RJ; Watson, P, 2010
)
0.36

Dosage Studied

ExcerptRelevanceReference
" The dose-response of DHT was biphasic in the presence and absence of FSH, such that progesterone production in the presence of 8 micrograms/ml DHT was similar to basal progesterone production."( Comparative effects of androgens and catecholestrogens on progesterone production by porcine granulosa cells.
Hammond, JM; Spicer, LJ, 1988
)
0.27
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
3-oxo steroidAny oxo steroid where an oxo substituent is located at position 3.
[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 (41)

TimeframeStudies, This Drug (%)All Drugs %
pre-199011 (26.83)18.7374
1990's7 (17.07)18.2507
2000's18 (43.90)29.6817
2010's4 (9.76)24.3611
2020's1 (2.44)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 27.94

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 Index27.94 (24.57)
Research Supply Index3.95 (2.92)
Research Growth Index4.54 (4.65)
Search Engine Demand Index48.33 (26.88)
Search Engine Supply Index3.26 (0.95)

This Compound (27.94)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials8 (18.60%)5.53%
Reviews1 (2.33%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other34 (79.07%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]