Page last updated: 2024-12-05

isovaleric acid

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

Description

Isovaleric acid, also known as 3-methylbutanoic acid, is a branched-chain fatty acid with a pungent odor. It is a colorless liquid that is found naturally in various plants and animals. Isovaleric acid has been studied for its potential applications in various fields, including medicine, cosmetics, and food production.

In the medical field, isovaleric acid is a precursor to the synthesis of valproic acid, an anticonvulsant drug used to treat epilepsy. It has also been investigated for its potential role in the treatment of other neurological disorders, such as Alzheimer's disease and Parkinson's disease.

In the cosmetic industry, isovaleric acid is used as a fragrance ingredient due to its pleasant odor. It is also used as a flavoring agent in the food industry, particularly in the production of cheese and dairy products.

Isovaleric acid is also a byproduct of the metabolism of leucine, an essential amino acid. Elevated levels of isovaleric acid in the blood can indicate a genetic disorder known as isovaleric acidemia, a rare metabolic disease that can lead to developmental delays and neurological problems. This makes the study of isovaleric acid in the medical field important for understanding the underlying causes of such diseases and developing potential treatments.'

isovaleric acid: structure [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

isovaleric acid : A C5, branched-chain saturated fatty acid. [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 CID10430
CHEMBL ID568737
CHEBI ID28484
SCHEMBL ID43436
MeSH IDM0051879

Synonyms (104)

Synonym
3-methylbuttersaeure
3-methyl-n-butyric acid
isovaleriansaeure
CHEBI:28484 ,
isopropylacetic acid
nsc62783
acetic acid, isopropyl-
.beta.-methylbutyric acid
butyric acid, 3-methyl-
wln: qv1y1&1
delphinic acid
nsc-62783
3-methylbutyric acid
3-methylbutyrate
isovalerianic
isopentanoic acid
beta-methylbutyric acid
isovaleric acid (natural)
nsc 62783
ai3-24132
brn 1098522
fema number: 3102
hsdb 629
kyselina isovalerova [czech]
isobutyl formic acid
isobutylformic acid
einecs 207-975-3
fema no. 3102
IVA ,
butanoic acid, 3-methyl-
inchi=1/c5h10o2/c1-4(2)3-5(6)7/h4h,3h2,1-2h3,(h,6,7
isopropylacetate
3-methylbutanoic acid
isovaleric acid
C08262
503-74-2
isovaleric acid, >=99%, fcc, fg
isovaleric acid, natural, >=98%, fg
DB03750
isovalerianic acid
LMFA01020181
3-methyl-butanoic acid
isovaleric acid, 99%
butanoic acid, 3-methyl-, (r)-
3,4-diisovaleryl adrenaline
BMSE000373
CHEMBL568737
M0182
AKOS000119861
NCGC00249082-01
92634-50-9
cas-503-74-2
NCGC00259153-01
tox21_201604
dtxcid309182
dtxsid5029182 ,
3-methyl-butyric acid
methylbutanoic acid
35915-22-1
STL146358
ec 207-975-3
1br7x184l5 ,
4-02-00-00895 (beilstein handbook reference)
unii-1br7x184l5
kyselina isovalerova
FT-0627533
isovaleric acid [hsdb]
isovaleric acid [mi]
isovaleric acid [fcc]
isovaleric acid [mart.]
isovaleric acid [fhfi]
delphinic-acid
isovaleric acid [who-dd]
S6287
3-methyl butyric acid
iso-valeric acid
methyl butanoic acid
BBL027399
SCHEMBL43436
isovaleric acid sodium salt (salt/mix)
iso-c4h9cooh
STR08356
1219805-32-9
mfcd00002726
J-522594
F2191-0067
isovaleric acid, analytical standard
3-methylbutyric acid: isopropyl-acetic acid
b-methylbutyrate
b-methylbutyric acid
3-methylbutyric acid: isopropyl-acetate
CS-W013696
HY-W012980
Q415536
3-methylbutyric-2,2-d2 acid
BCP32116
3-methylbutanoic acid;3-methylbutyric acid;isopentanoic acid
AMY40214
D78213
3-methylbutanoicacid
EN300-19718
3-methyl-d3-butyric--d4 acid
Z104474910
isovaleric acid (mart.)

Research Excerpts

Overview

Isovaleric acid (IVA) is a 5-carbon branched-chain fatty acid present in fermented foods and produced in the colon by bacterial fermentation of leucine. It is an unusual fatty acid that is important for echolocation and hearing in acoustic tissues of some odontocetes. Its functional significance in blubber is unknown.

ExcerptReferenceRelevance
"Isovaleric acid (IVA) is a 5-carbon branched-chain fatty acid present in fermented foods and produced in the colon by bacterial fermentation of leucine. "( Branched Short-Chain Fatty Acid Isovaleric Acid Causes Colonic Smooth Muscle Relaxation via cAMP/PKA Pathway.
Blakeney, BA; Crowe, MS; Grider, JR; Mahavadi, S; Murthy, KS, 2019
)
2.24
"Isovaleric acidaemia is a rare inherited organic acidaemia associated with a characteristic odour in affected patients. "( A novel duplication at the putative DNA polymerase alpha arrest site and a founder mutation in Chinese in the IVD gene underlie isovaleric acidaemia.
Chan, AY; Lai, CK; Lam, CW; Lee, HH; Lee, RS; Siu, TS; Yuen, YP, 2010
)
2.01
"Isovaleric acidemia is a rare autosomal recessive inborn error of leucine metabolism. "( Chronic intermittent form of isovaleric acidemia mimicking diabetic ketoacidosis.
Cayonu, N; Erdem, E; Uysalol, E; Yildirmak, ZY, 2010
)
2.09
"Isovaleric acid (iso5:0) is an unusual fatty acid that is important for echolocation and hearing in acoustic tissues of some odontocetes, but its functional significance in blubber is unknown. "( High concentrations of isovaleric acid in the fats of odontocetes: variation and patterns of accumulation in blubber vs. stability in the melon.
Iverson, SJ; Koopman, HN; Read, AJ, 2003
)
2.07
"Isovaleric acidemia is a rare autosomal recessive inborn error of leucine catabolism caused by deficiency of isovaleryl coenzyme A dehydrogenase. "( Acute metabolic decompensation in an adult patient with isovaleric acidemia.
Feinstein, JA; O'Brien, K, 2003
)
2.01
"Isovaleric acidaemia is an inborn error of leucine metabolism due to deficiency of isovaleryl-CoA dehydrogenase, which results in accumulation of isovaleric acid in body fluids. "( Isovaleric acidaemia: cranial CT and MRI findings.
Acun, C; Aktuglu, C; Aydin, K; Demirel, F; Sogut, A; Tomac, N; Tomsac, N, 2004
)
3.21
"Isovaleric acidemia (IVA) is an inborn error of leucine metabolism that can cause significant morbidity and mortality. "( A common mutation is associated with a mild, potentially asymptomatic phenotype in patients with isovaleric acidemia diagnosed by newborn screening.
Berry, SA; Burton, BK; Edland, SD; Ensenauer, R; Grünert, S; Hahn, S; Huey, JC; Koch, HG; Marquardt, I; Matern, D; Rinaldo, P; Santer, R; Sass, JO; Vockley, J; Willard, JM, 2004
)
1.98
"Isovaleric acidemia (IVA) is an autosomal recessive inborn error of leucine metabolism caused by a deficiency of the mitochondrial enzyme isovaleryl-CoA dehydrogenase (IVD) resulting in the accumulation of derivatives of isovaleryl-CoA. "( Isovaleric acidemia: new aspects of genetic and phenotypic heterogeneity.
Ensenauer, R; Vockley, J, 2006
)
3.22
"Isovaleric acidemia (IVA) is an autosomal recessive inborn error of the leucine metabolism that is caused by a deficiency of isovaleryl-CoA dehydrogenase (IVD). "( Different spectrum of mutations of isovaleryl-CoA dehydrogenase (IVD) gene in Korean patients with isovaleric acidemia.
Ki, CS; Kim, ND; Lee, DH; Lee, YK; Lee, YW; Vockley, J,
)
1.79
"Isovaleric acidemia (IVA) is an inborn error of leucine metabolism, resulting in an accumulation of isovaleric acid in the body fluids. "( Cerebellar hemorrhage complicating isovaleric acidemia: a case report.
Burton, BK; Challa, VR; Fischer, AQ; McLean, WT, 1981
)
1.98
"Isovaleric acidemia (IVA) is a recessive disorder caused by a deficiency of isovaleryl-CoA dehydrogenase (IVD). "( Exon skipping in IVD RNA processing in isovaleric acidemia caused by point mutations in the coding region of the IVD gene.
Anderson, BD; Liu, W; Rogan, PK; Seelan, RS; Smith, DI; Vockley, J; Willard, J, 2000
)
2.02
"Isovaleric acidemia is a rare inborn error of metabolism caused by a deficiency of isovaleryl-CoA dehydrogenase (IVD), a nucleus-encoded, homotetrameric, mitochondrial flavoenzyme that catalyzes the conversion of isovaleryl-CoA to 3-methylcrotonyl-CoA. "( Mitochondrial import and processing of wild type and type III mutant isovaleryl-CoA dehydrogenase.
Vockley, J; Volchenboum, SL, 2000
)
1.75
"Isovaleric acidemia (IVA) is an inborn error of leucine metabolism and is caused by a genetically determined deficiency of isovaleryl-CoA dehydrogenase (IVD), a mitochondrial matrix enzyme. "( Molecular characterization of four different classes of mutations in the isovaleryl-CoA dehydrogenase gene responsible for isovaleric acidemia.
Parimoo, B; Tanaka, K; Vockley, J, 1991
)
1.93
"Isovaleric acidemia is a disorder of leucine metabolism caused by a deficiency of isovaleryl-CoA dehydrogenase. "( Isovaleryl-CoA dehydrogenase activity in isovaleric acidemia fibroblasts using an improved tritium release assay.
Hyman, DB; Tanaka, K, 1986
)
1.98

Dosage Studied

ExcerptRelevanceReference
" In addition a dose-response effect of alanine was observed."( Alanine decreases the protein requirements of infants with inborn errors of amino acid metabolism.
Algert, S; Kelts, DG; Nyhan, WL; Prodanos, C; Wolff, JA, 1985
)
0.27
" All odorants tested were found to stimulate cAMP accumulation, and the dose-response curves were multiphasic, with less stimulation seen at higher concentrations."( Calcium modulates the rapid kinetics of the odorant-induced cyclic AMP signal in rat olfactory cilia.
Borisy, FF; Jaworsky, DE; Matsuzaki, O; Ronnett, GV, 1995
)
0.29
" The treatments were: control (without isovalerate), low isovalerate (LIV), medium isovalerate (MIV) and high isovalerate (HIV) dosage of isovalerate at 100, 200 and 300 mg isovalerate per kg dry matter (DM) intake respectively."( Effects of isovalerate on ruminal fermentation, urinary excretion of purine derivatives and digestibility in steers.
Dong, KH; Huang, YX; Liu, Q; Wang, C; Wang, H; Yang, WZ; Zhang, SL, 2009
)
0.35
" Identification of organic chemical compounds extracted from eggs was performed using GC-MS and chemicals were tested in the same behavioral assays in a dose-response manner."( The egg and larval pheromone dodecanoic acid mediates density-dependent oviposition of Phlebotomus papatasi.
Apperson, CS; Hatano, E; Kowacich, D; Ponnusamy, L; Schal, C; Shymanovich, T; Wasserberg, G, 2020
)
0.56
" Pentadecanoic acid induced significant oviposition stimulation, especially when dosed at 10 ppm."( Behavioural and antennal responses of Aedes aegypti (l.) (Diptera: Culicidae) gravid females to chemical cues from conspecific larvae.
Boullis, A; Delannay, C; Héry, L; Mulatier, M; Vega-Rúa, A; Verheggen, F, 2021
)
0.62
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (2)

RoleDescription
plant metaboliteAny eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
mammalian metaboliteAny animal metabolite produced during a metabolic reaction in mammals.
[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 (3)

ClassDescription
short-chain fatty acidAn aliphatic monocarboxylic acid with a chain length of less than C6. If any non-hydrocarbon substituent is present, the compound is not normally regarded as a short-chain fatty acid.
methylbutyric acidA methyl-branched fatty acid comprising a butyric acid core carrying a single methyl substituent.
branched-chain saturated fatty acidAny saturated fatty acid with a carbon side-chain or isopropyl termination.
[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
Olfactory Signaling Pathway8028
Valine Biosynthesis912
Sensory Perception21568
Leucine, isoleucine and valine metabolism2470

Protein Targets (8)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
nuclear receptor subfamily 1, group I, member 3Homo sapiens (human)Potency45.33520.001022.650876.6163AID1224838; AID1224839; AID1224893
retinoic acid nuclear receptor alpha variant 1Homo sapiens (human)Potency11.27180.003041.611522,387.1992AID1159552; AID1159555
retinoid X nuclear receptor alphaHomo sapiens (human)Potency8.74180.000817.505159.3239AID1159527; AID1159531
estrogen-related nuclear receptor alphaHomo sapiens (human)Potency3.54150.001530.607315,848.9004AID1224841; AID1259401
pregnane X nuclear receptorHomo sapiens (human)Potency59.76550.005428.02631,258.9301AID1346982
nuclear factor erythroid 2-related factor 2 isoform 1Homo sapiens (human)Potency53.26600.000627.21521,122.0200AID743202; AID743219
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Inhibition Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Solute carrier family 22 member 20Mus musculus (house mouse)Ki32.32971.10006.67899.1201AID360149
Solute carrier family 22 member 6Mus musculus (house mouse)Ki2,339.61500.40745.02179.4000AID360150
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (7)

Assay IDTitleYearJournalArticle
AID1347086qHTS for Inhibitors of the Functional Ribonucleoprotein Complex (vRNP) of Lymphocytic Choriomeningitis Arenaviruses (LCMV): LCMV Primary Screen - GLuc reporter signal2020Antiviral research, 01, Volume: 173A cell-based, infectious-free, platform to identify inhibitors of lassa virus ribonucleoprotein (vRNP) activity.
AID1347082qHTS for Inhibitors of the Functional Ribonucleoprotein Complex (vRNP) of Lassa (LASV) Arenavirus: LASV Primary Screen - GLuc reporter signal2020Antiviral research, 01, Volume: 173A cell-based, infectious-free, platform to identify inhibitors of lassa virus ribonucleoprotein (vRNP) activity.
AID1347083qHTS for Inhibitors of the Functional Ribonucleoprotein Complex (vRNP) of Lassa (LASV) Arenavirus: Viability assay - alamar blue signal for LASV Primary Screen2020Antiviral research, 01, Volume: 173A cell-based, infectious-free, platform to identify inhibitors of lassa virus ribonucleoprotein (vRNP) activity.
AID360150Inhibition of mouse Oat1-mediated [3H]PAH uptake in Xenopus oocytes after 1 hr2007The Journal of biological chemistry, Aug-17, Volume: 282, Issue:33
Structural variation governs substrate specificity for organic anion transporter (OAT) homologs. Potential remote sensing by OAT family members.
AID360151Ratio of pKi for mouse Oat1 expressed in Xenopus oocytes to pKi for mouse Oat6 expressed in Xenopus oocytes2007The Journal of biological chemistry, Aug-17, Volume: 282, Issue:33
Structural variation governs substrate specificity for organic anion transporter (OAT) homologs. Potential remote sensing by OAT family members.
AID360149Inhibition of mouse Oat6-mediated [3H]ES uptake in Xenopus oocytes after 1 hr2007The Journal of biological chemistry, Aug-17, Volume: 282, Issue:33
Structural variation governs substrate specificity for organic anion transporter (OAT) homologs. Potential remote sensing by OAT family members.
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.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (288)

TimeframeStudies, This Drug (%)All Drugs %
pre-199088 (30.56)18.7374
1990's50 (17.36)18.2507
2000's82 (28.47)29.6817
2010's48 (16.67)24.3611
2020's20 (6.94)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 62.89

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

MetricThis Compound (vs All)
Research Demand Index62.89 (24.57)
Research Supply Index5.74 (2.92)
Research Growth Index4.53 (4.65)
Search Engine Demand Index105.17 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (62.89)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials3 (0.98%)5.53%
Reviews12 (3.92%)6.00%
Case Studies49 (16.01%)4.05%
Observational0 (0.00%)0.25%
Other242 (79.08%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]