Page last updated: 2024-11-06

allotetrahydrocortisol

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

Description

allotetrahydrocortisol: RN given refers to (3alpha,5alpha,11beta)-isomer [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID92748
CHEBI ID89627
SCHEMBL ID5609666
MeSH IDM0049046

Synonyms (72)

Synonym
allopregnane-3.alpha.,17.alpha.,21-tetrol-20-one
compound f, allotetrahydro-
wintersteiner's compound d
allocortisol, tetrahydro-
nsc86469
.alpha.-thf
nsc-86469
302-91-0
allotetrahydrocortisol
cortisol, allotetrahydro-
athf
5.alpha.-tetrahydrocortisol
3.alpha.,5.alpha.-tetrahydrocortisol
allo-tetrahydrocortisol
pregnan-20-one,11,17,21-tetrahydroxy-, (3.alpha.,5.alpha.,11.beta.)-
allotetrahydrocompound f
kendall's compound c
tetrahydroallocortisol
5.alpha.-pregnan-20-one,11.beta.,17,21-tetrahydroxy-
allo-3.alpha.-tetrahydrocortisol
reichstein's substance c
5a-tetrahydrocortisol
LMST02030200
2-hydroxy-1-[(3r,5s,8s,9s,10s,11s,13s,14s,17r)-3,11,17-trihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,14,15,16-tetradecahydrocyclopenta[a]phenanthren-17-yl]ethanone
allopregnane-3alpha,11beta,17alpha,21-tetrol-20-one
5alpha-tetrahydrocortisol
pregnan-20-one, 3,11,17,21-tetrahydroxy-, (3alpha,5alpha,11beta)-
3-alpha,11-beta,17-alpha,21-tetrahydroxy-5-alpha-pregnan-20-one
a30u7u312e ,
3alpha,5alpha-tetrahydrocortisol
allo-3alpha-tetrahydrocortisol
alpha-thf
nsc 86469
einecs 206-131-1
5alpha-pregnan-20-one, 3alpha,11beta,17,21-tetrahydroxy-
unii-a30u7u312e
allo-3|a-tetrahydro cortisol
allopregnane-3.alpha.,11.beta.,17.alpha.,21-tetrol-20-one
pregnan-20-one, 3,11,17,21-tetrahydroxy-, (3.alpha.,5.alpha.,11.beta.)-
(3.alpha.,5.alpha.,11.beta.)-3,11,17,21-tetrahydroxypregnan-20-one
3.alpha.-allotetrahydrocortisol
3.alpha.,11.beta.,17,21-tetrahydroxy-20-oxo-5.alpha.-pregnane
3.alpha.,11.beta.,17,21-tetrahydroxy-5.alpha.-pregnan-20-one
17-(1-keto-2-hydroxyethyl)androstane-3,11,17-triol
allopregnane-3.alpha.,11.beta.,17.alpha.,21-tetrol-20-one [mi]
SCHEMBL5609666
CHEBI:89627
AODPIQQILQLWGS-FDSHTENPSA-N
5a-pregnane-3a,11b,17a,21-tetrol-20-one
allotetrahydro-cortisol
tetrahydro-allocortisol
5a-pregnane-3a,11b,17a,21-tetraol-20-one
allo-3a-tetrahydrocortisol
3alpha, 5alpha-tetrahydrocortisol
allotetrahydro-compound f
3a,11b,17,21-tetrahydroxy-5a-pregnan-20-one
allopregnane-3a,11b,21-tetrol-20-one
3a,11b,17a,21-tetrahydroxy-5a-pregnan-20-one
a-thf
3a,5a-tetrahydrocortisol
allopregnane-3a,11b,17a,21-tetrol-20-one
3a-allotetrahydrocortisol
Q27161825
3,11,17,21-tetrahydroxypregnan-20-one
allo-3alpha-tetrahydro cortisol
DTXSID80861575
2-hydroxy-1-((3r,8s,9s,10s,11s,13s,14s,17r)-3,11,17-trihydroxy-10,13-dimethylhexadecahydro-1h-cyclopenta[a]phenanthren-17-yl)ethanone
HY-113215
CS-0059329
allo-3?-tetrahydro cortisol
PD126220
AKOS040740675

Research Excerpts

Bioavailability

ExcerptReferenceRelevance
" The aim of this study was to determine whether in major depression changes in the activity patterns of local modulators of glucocorticoid action might contribute to an increase in cortisol bioavailability and if they change during antidepressant treatment and clinical response."( Cortisol metabolism in depressed patients and healthy controls.
Deuschle, M; Frankhauser, P; Gilles, M; Hamann, B; Kopf, D; Lederbogen, F; Lewicka, S; Onken, V; Römer, B; Schilling, C, 2009
)
0.35
" These changes suggest an increase in cortisol bioavailability within tissues."( Cortisol metabolism in depressed patients and healthy controls.
Deuschle, M; Frankhauser, P; Gilles, M; Hamann, B; Kopf, D; Lederbogen, F; Lewicka, S; Onken, V; Römer, B; Schilling, C, 2009
)
0.35
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
corticosteroid hormoneAny of a class of steroid hormones that are produced in the adrenal cortex.
[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
Glucocorticoid biosynthesis1411

Research

Studies (38)

TimeframeStudies, This Drug (%)All Drugs %
pre-199012 (31.58)18.7374
1990's7 (18.42)18.2507
2000's10 (26.32)29.6817
2010's9 (23.68)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: 10.73

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 Index10.73 (24.57)
Research Supply Index3.71 (2.92)
Research Growth Index4.44 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (10.73)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials1 (2.56%)5.53%
Reviews0 (0.00%)6.00%
Case Studies5 (12.82%)4.05%
Observational0 (0.00%)0.25%
Other33 (84.62%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]