Page last updated: 2024-11-07

4-hydroxyvaleric acid

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

4-Hydroxyvaleric acid, also known as γ-hydroxyvaleric acid, is a naturally occurring hydroxycarboxylic acid found in various plants and microorganisms. It has been reported to exhibit antioxidant activity, potentially contributing to its role in plant defense mechanisms. The synthesis of 4-hydroxyvaleric acid has been investigated using various methods, including enzymatic and chemical approaches. One notable study explored the production of 4-hydroxyvaleric acid through the fermentation of glucose by the bacterium Lactobacillus plantarum. This compound has also been studied for its potential applications in the pharmaceutical and cosmetic industries. Research is ongoing to explore its therapeutic properties and potential benefits for human health.'

Cross-References

ID SourceID
PubMed CID114539
CHEMBL ID169219
CHEBI ID180192
SCHEMBL ID27394
MeSH IDM0443726

Synonyms (27)

Synonym
4-hydroxypentanoic acid
CHEBI:180192
13532-37-1
LMFA01050009
4-hydroxy-valeric acid
4-hydroxy-pentanoic acid
4-hydroxyvaleric acid
CHEMBL169219
EN300-69020
unii-58b139q3rl
einecs 236-884-1
58b139q3rl ,
gamma-hydroxyvaleric acid
pentanoic acid, 4-hydroxy-
AKOS008148154
SCHEMBL27394
.gamma.-methyl-.gamma.-hydroxybutyric acid
.gamma.-hydroxyvaleric acid
valeric acid, 4-hydroxy-
FMHKPLXYWVCLME-UHFFFAOYSA-N
Q5520261
(rs)-4-hydroxyvaleric acid
DTXSID60928958
CS-0278525
4-hydroxypentanoicacid
PD121665
Z838959470
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
hydroxy fatty acidAny fatty acid carrying one or more hydroxy substituents.
[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
AID71719Binding affinity towards [3H]-GHB binding site at 10 uM1988Journal of medicinal chemistry, May, Volume: 31, Issue:5
Analogues of gamma-hydroxybutyric acid. Synthesis and binding studies.
AID71718Binding affinity towards [3H]-GHB binding site at 1 uM1988Journal of medicinal chemistry, May, Volume: 31, Issue:5
Analogues of gamma-hydroxybutyric acid. Synthesis and binding studies.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (12)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901 (8.33)18.7374
1990's0 (0.00)18.2507
2000's2 (16.67)29.6817
2010's8 (66.67)24.3611
2020's1 (8.33)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 40.14

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

MetricThis Compound (vs All)
Research Demand Index40.14 (24.57)
Research Supply Index2.71 (2.92)
Research Growth Index4.71 (4.65)
Search Engine Demand Index56.30 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (40.14)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials1 (7.69%)5.53%
Reviews0 (0.00%)6.00%
Case Studies1 (7.69%)4.05%
Observational0 (0.00%)0.25%
Other11 (84.62%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]