Page last updated: 2024-12-07

3,7,12-trihydroxycoprostanic acid

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 CID122166
CHEBI ID89753
SCHEMBL ID1490655
MeSH IDM0044745

Synonyms (22)

Synonym
3alpha,7alpha,12alpha-trihydroxycoprostanic acid
(3alpha,5beta,7alpha,12alpha)-3,7,12-trihydroxycholestane-5-carboxylic acid
3,7,12-trihydroxycoprostanic acid
3,7,12-trihydroxycoprostanate
5-thca
863-39-8
trihydroxycoprostanoic acid
(3r,5r,7r,8r,9s,10r,12s,13r,14s,17r)-3,7,12-trihydroxy-10,13-dimethyl-17-[(2r)-6-methylheptan-2-yl]-1,2,3,4,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthrene-5-carboxylic acid
SCHEMBL1490655
CHEBI:89753
(3alpha,5beta,7alpha,12alpha)-3,7,12-trihydroxycholestane-5-carboxylate
3alpha,7alpha,12alpha-trihydroxycoprostanate
(3a,5b,7a,12a)-3,7,12-trihydroxy-cholestane-5-carboxylate
tryhydroxycoprostanic acid
tryhydroxycoprostanate
(3a,5b,7a,12a)-3,7,12-trihydroxy-cholestane-5-carboxylic acid
Q27161941
DTXSID801186225
8ZJG7M7XQT
cholestane-5-carboxylic acid, 3,7,12-trihydroxy-, (3alpha,5beta,7alpha,12alpha)-
3,7,12-trihydroxycholestane-5-carboxylic acid, (3alpha,5beta,7alpha,12alpha)-
(3alpha,5beta,7alpha,12alpha)-3,7,12-trihydroxy-cholestane-5-carboxylic acid
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (1)

RoleDescription
human metaboliteAny mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
[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 (5)

ClassDescription
12alpha-hydroxy steroid
3alpha-hydroxy steroidA 3-hydroxy steroid in which the 3-hydroxy substituent is in the alpha-position.
7alpha-hydroxy steroidA 7-hydroxy steroid in which the hydroxy group at position 7 has an alpha-configuration.
hydroxy monocarboxylic acidAny monocarboxylic acid which also contains a separate (alcoholic or phenolic) hydroxy substituent.
cholestanoic acidAny steroid acid based on a cholestane skeleton.
[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 (31)

TimeframeStudies, This Drug (%)All Drugs %
pre-199018 (58.06)18.7374
1990's13 (41.94)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: 10.93

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 Index10.93 (24.57)
Research Supply Index3.47 (2.92)
Research Growth Index4.40 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (10.93)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies5 (16.13%)4.05%
Observational0 (0.00%)0.25%
Other26 (83.87%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]