Page last updated: 2024-11-05

2-hydroxybutyric acid

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

Description

2-Hydroxybutyric acid, also known as α-hydroxybutyric acid, is a naturally occurring organic compound. It is a chiral molecule, existing in two enantiomeric forms: (R)-2-hydroxybutyric acid and (S)-2-hydroxybutyric acid. It is a four-carbon monocarboxylic acid with a hydroxyl group attached to the second carbon atom. It plays a role in various metabolic pathways and is involved in the biosynthesis of amino acids and other important biomolecules. The racemic mixture of (R)- and (S)-2-hydroxybutyric acid is a common by-product of industrial fermentations and can be used as a chiral building block in the synthesis of pharmaceuticals and other fine chemicals. Research into 2-hydroxybutyric acid focuses on its role in metabolism, its potential therapeutic applications, and its environmental impact.'

2-hydroxybutyric acid: RN given refers to cpd without isomeric designation [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

hydroxybutyric acid : Any compound comprising a butyric acid core carrying at least one hydroxy substituent. [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]

2-hydroxybutyric acid : A hydroxybutyric acid having a single hydroxyl group located at position 2; urinary secretion of 2-hydroxybutyric acid is increased with alcohol ingestion or vigorous physical exercise and is associated with lactic acidosis and ketoacidosis in humans and diabetes in animals. [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 CID11266
CHEMBL ID567588
CHEBI ID1148
SCHEMBL ID6963
MeSH IDM0099087

Synonyms (60)

Synonym
alpha-hydroxybutyrate
alpha-hydroxy-n-butyric acid
nsc 6495
butanoic acid, 2-hydroxy-
butyric acid, 2-hydroxy-
.alpha.-hydroxy-n-butyric acid
nsc6495
nsc-6495
.alpha.-hydroxybutyric acid
565-70-8
alpha-hydroxybutyric acid
CHEBI:1148 ,
600-15-7
alpha-hydroxybutanoic acid
2-hydroxybutyric acid
2-hydroxybutanoic acid ,
LMFA01050004
2-hydroxy-butanoic acid
(+/-)alpha-hydoxy butyric acid
BC3EA1BE-590C-48AC-ACE7-8989B8E96BFC
2-hydroxy-butyric acid anion
CHEMBL567588
dl-2-hydroxybutyric acid
H0227
AKOS000121162
hydroxybutyric acid
unii-o0adr0i4h5
einecs 209-985-3
o0adr0i4h5 ,
(1)-2-hydroxybutyric acid
FT-0625392
FT-0649270
(rs)-2-hydroxybutyric acid
butanoic acid, 2-hydroxy-, (+/-)-
dl-2-hydroxybutanoic acid
S6119
AKOS016053528
SCHEMBL6963
2-hydroxy-butyric acid
(+/-)-2-hydroxybutanoic acid
ethylglycolic acid
dl-2-hydroxy-n-butyric acid
DTXSID8041903
alpha-hydroxy butyric acid
2-hydroxybutanoic acid, aldrichcpr
mfcd00070502
D90822
Q3288610
SY066872
FT-0773381
BCP33336
(r)-alpha-hydroxybutyric acid
HY-113381
CS-0062339
SB44876
SB44466
-hydroxybutyric acid
SY234828
EN300-27738
Z246073650
[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).
algal metaboliteAny eukaryotic metabolite produced during a metabolic reaction in algae including unicellular organisms like chlorella and diatoms to multicellular organisms like giant kelps and brown algae.
[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 (2)

ClassDescription
hydroxybutyric acidAny compound comprising a butyric acid core carrying at least one hydroxy substituent.
2-hydroxy monocarboxylic acid
[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 (4)

PathwayProteinsCompounds
Propanoate Metabolism1837
Malonic Aciduria1837
Methylmalonic Aciduria Due to Cobalamin-Related Disorders1837
Malonyl-CoA Decarboxylase Deficiency1837

Protein Targets (1)

Other Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Biological Processes (4)

Processvia Protein(s)Taxonomy
lactate transmembrane transportMonocarboxylate transporter 4Homo sapiens (human)
pyruvate catabolic processMonocarboxylate transporter 4Homo sapiens (human)
pyruvate transmembrane transportMonocarboxylate transporter 4Homo sapiens (human)
monocarboxylic acid transportMonocarboxylate transporter 4Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Molecular Functions (5)

Processvia Protein(s)Taxonomy
RNA bindingMonocarboxylate transporter 4Homo sapiens (human)
protein bindingMonocarboxylate transporter 4Homo sapiens (human)
monocarboxylic acid transmembrane transporter activityMonocarboxylate transporter 4Homo sapiens (human)
lactate:proton symporter activityMonocarboxylate transporter 4Homo sapiens (human)
pyruvate transmembrane transporter activityMonocarboxylate transporter 4Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Ceullar Components (6)

Processvia Protein(s)Taxonomy
plasma membraneMonocarboxylate transporter 4Homo sapiens (human)
membraneMonocarboxylate transporter 4Homo sapiens (human)
basolateral plasma membraneMonocarboxylate transporter 4Homo sapiens (human)
apical plasma membraneMonocarboxylate transporter 4Homo sapiens (human)
lateral plasma membraneMonocarboxylate transporter 4Homo sapiens (human)
nuclear membraneMonocarboxylate transporter 4Homo sapiens (human)
plasma membraneMonocarboxylate transporter 4Homo sapiens (human)
basolateral plasma membraneMonocarboxylate transporter 4Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (5)

Assay IDTitleYearJournalArticle
AID447578Inhibition of HDAC in human Hela cells nuclear extracts assessed as residual activity at 500 uM by fluorimetric assay2009Bioorganic & medicinal chemistry, Jul-15, Volume: 17, Issue:14
Molecular modifications on carboxylic acid derivatives as potent histone deacetylase inhibitors: Activity and docking studies.
AID682143TP_TRANSPORTER: inhibition of pyruvate uptake in Xenopus laevis oocytes1998The Journal of biological chemistry, Oct-30, Volume: 273, Issue:44
Human monocarboxylate transporter 2 (MCT2) is a high affinity pyruvate transporter.
AID95754Protein interaction energy by using binding affinity towards human L-xylulose reductase enzyme2003Bioorganic & medicinal chemistry letters, Apr-17, Volume: 13, Issue:8
Structure-based design of inhibitors of human L-xylulose reductase modelled into the active site of the enzyme.
AID681140TP_TRANSPORTER: uptake in Xenopus laevis oocytes2000The Journal of physiology, Dec-01, Volume: 529 Pt 2Characterisation of human monocarboxylate transporter 4 substantiates its role in lactic acid efflux from skeletal muscle.
AID681374TP_TRANSPORTER: inhibition of pyruvate uptake in Xenopus laevis oocytes1998The Journal of biological chemistry, Oct-30, Volume: 273, Issue:44
Human monocarboxylate transporter 2 (MCT2) is a high affinity pyruvate transporter.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (89)

TimeframeStudies, This Drug (%)All Drugs %
pre-199018 (20.22)18.7374
1990's12 (13.48)18.2507
2000's12 (13.48)29.6817
2010's38 (42.70)24.3611
2020's9 (10.11)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 47.28

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 Index47.28 (24.57)
Research Supply Index4.54 (2.92)
Research Growth Index4.95 (4.65)
Search Engine Demand Index71.39 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (47.28)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials3 (3.33%)5.53%
Reviews2 (2.22%)6.00%
Case Studies2 (2.22%)4.05%
Observational1 (1.11%)0.25%
Other82 (91.11%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]