Page last updated: 2024-12-10

11-dehydrocorticosterone

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

Description

## 11-Dehydrocorticosterone: An Important Research Molecule

11-Dehydrocorticosterone (11-DHC) is a steroid hormone that plays a crucial role in various physiological processes. It is a precursor to corticosterone, a major stress hormone in rodents, and has been shown to have its own unique biological effects.

Here's why 11-DHC is important for research:

**1. Understanding Stress Response:**

* 11-DHC is a key intermediate in the biosynthesis of corticosterone, a hormone involved in the body's stress response.
* Studying 11-DHC helps researchers understand how stress affects the body at the molecular level.

**2. Exploring Anti-Inflammatory Effects:**

* 11-DHC has been shown to possess anti-inflammatory properties in various studies.
* Research exploring 11-DHC's anti-inflammatory mechanisms could lead to new drug development for inflammatory diseases.

**3. Potential Therapeutic Applications:**

* 11-DHC's role in regulating blood pressure and cardiovascular function is being investigated.
* Research into these potential therapeutic applications could lead to treatments for hypertension and other cardiovascular disorders.

**4. Investigating Neuroprotective Effects:**

* Studies suggest 11-DHC may have neuroprotective effects, potentially playing a role in protecting neurons from damage.
* Further research could explore 11-DHC's potential as a therapeutic agent for neurological diseases.

**5. Examining Its Role in Energy Metabolism:**

* 11-DHC has been shown to influence energy metabolism, potentially affecting glucose levels and lipid metabolism.
* Studying this aspect could offer insights into the complex interplay between stress, hormones, and energy regulation.

**6. Understanding Its Effects on Brain Function:**

* 11-DHC can cross the blood-brain barrier, potentially affecting brain function and behavior.
* Research into 11-DHC's effects on the brain could lead to a deeper understanding of its role in cognitive processes and mental health.

**7. Developing New Diagnostic Tools:**

* 11-DHC levels can be measured in various biological samples, providing potential biomarkers for various health conditions.
* Further research could lead to the development of new diagnostic tools for diseases related to stress, inflammation, or metabolic disorders.

**Overall, 11-DHC is a multifaceted molecule with significant potential for research and therapeutic applications. Continued research into its various biological effects and potential therapeutic uses is critical for advancing our understanding of physiology and developing new treatments for various diseases.**

11-dehydrocorticosterone : An 11-oxo steroid that is corticosterone in which the hydroxy substituent at the 11beta position has been oxidised to give the corresponding ketone. [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 CID5311364
CHEMBL ID3244489
CHEBI ID78600
SCHEMBL ID141610
MeSH IDM0044588

Synonyms (39)

Synonym
dehydrocortocicosterone
dehydrocorticosterone
cortisone, 17-deoxy-
corticosterone, 11-dehydro-
11-dehydrocorticosteron
21-hydroxypregn-4-ene-3,11-20-trione
nsc-9702
kendall's compound a
11-oxo-11-deoxycorticosterone
17-deoxycortisone
corticosterone, dehydro-
11-dehydrocorticosterone
72-23-1
(8s,9s,10r,13s,14s,17s)-17-(2-hydroxyacetyl)-10,13-dimethyl-2,6,7,8,9,12,14,15,16,17-decahydro-1h-cyclopenta[a]phenanthrene-3,11-dione
21-hydroxypregn-4-ene-3,11,20-trione
fo4v44a3g3 ,
pregn-4-ene-3,11,20-trione, 21-hydroxy-
nsc 9702
einecs 200-776-2
unii-fo4v44a3g3
11-dehydrocorticosterone [mi]
17-(1-keto-2-hydroxyethyl)-.delta.4-androsten-3,11-dione
dehydrocorticosteron
.delta.4-pregnen-21-ol-3,11,20-trione
dehydrocorticosteron [who-dd]
CHEMBL3244489
SCHEMBL141610
17-(1-keto-2-hydroxyethyl)-delta(4)androsten-3,11-dione
4-pregnen-21-ol- 3,11,20-trione
delta(4)-pregnen-21-ol-3,11,20-trione
11-dhc
CHEBI:78600 ,
FUFLCEKSBBHCMO-KJQYFISQSA-N
4-pregnen-21-ol-3,11,20-trione
4QF7
Q27105083
MS-25291
HY-113447
PD133479

Research Excerpts

Bioavailability

ExcerptReferenceRelevance
" It is hypothesized that once corticosterone reaches the site of inflammation, the enzymes 11beta-hydroxysteroid dehydrogenases (11betaHSDs) can influence bioavailability by interconverting corticosterone and the inert metabolite 11-dehydrocorticosterone."( 11beta-hydroxysteroid dehydrogenases are regulated during the pulmonary granulomatous response to the mycobacterial glycolipid trehalose-6,6'-dimycolate.
Abbott, AN; Actor, JK; Guidry, TV; Hunter, RL; Kling, MA; Thomas, AM; Welsh, KJ, 2009
)
0.54

Dosage Studied

ExcerptRelevanceReference
"The concurrent administration of compound E at a daily dosage of 2 mg."( The mechanism of action of 17-hydroxy-11-dehydrocorticosterone (compound E) and of the adrenocorticotropic hormone in experimental hypersensitivity in rabbits.
GERMUTH, FG; OTTINGER, B; OYAMA, J, 1951
)
0.5
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (2)

RoleDescription
human metaboliteAny mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
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 (6)

ClassDescription
21-hydroxy steroid
3-oxo-Delta(4) steroidA 3-oxo steroid conjugated to a C=C double bond at the alpha,beta position.
20-oxo steroidAn oxo steroid carrying an oxo group at position 20.
11-oxo steroidAny oxo steroid that has an oxo substituent at position 11.
corticosteroidA natural or synthetic analogue of the hormones secreted by the adrenal gland.
primary alpha-hydroxy ketoneAn alpha-hydroxy ketone in which the carbonyl group and the hydroxy group are linked by a -CH2 (methylene) group.
[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]

Bioassays (2)

Assay IDTitleYearJournalArticle
AID1132664Glucocorticoid activity in sc dosed bilaterally adrenalectomized rat assessed as glycogen deposition in liver administered for 5 days relative to cortisol1978Journal of medicinal chemistry, May, Volume: 21, Issue:5
A Fujita--Ban structure--activity analysis of 44 steroids.
AID977611Experimentally measured binding affinity data (Kd) for protein-ligand complexes derived from PDB2015Biochimica et biophysica acta, Apr, Volume: 1854, Issue:4
Structures and binding studies of the complexes of phospholipase A2 with five inhibitors.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (157)

TimeframeStudies, This Drug (%)All Drugs %
pre-199048 (30.57)18.7374
1990's52 (33.12)18.2507
2000's34 (21.66)29.6817
2010's20 (12.74)24.3611
2020's3 (1.91)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 22.61

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 Index22.61 (24.57)
Research Supply Index5.12 (2.92)
Research Growth Index4.39 (4.65)
Search Engine Demand Index26.67 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (22.61)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials1 (0.61%)5.53%
Reviews3 (1.82%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other161 (97.58%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]