U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C4H6O5
Molecular Weight 134.0874
Optical Activity ( - )
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MALIC ACID, L-

SMILES

O[C@@H](CC(O)=O)C(O)=O

InChI

InChIKey=BJEPYKJPYRNKOW-REOHCLBHSA-N
InChI=1S/C4H6O5/c5-2(4(8)9)1-3(6)7/h2,5H,1H2,(H,6,7)(H,8,9)/t2-/m0/s1

HIDE SMILES / InChI

Molecular Formula C4H6O5
Molecular Weight 134.0874
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

L-Malic acid is a tart-tasting organic dicarboxylic acid that plays a role in many sour or tart foods. L-Malic acid is the naturally occurring form, whereas a mixture of L- and D-malic acid is produced synthetically. In humans, L-malic acid is both derived from food sources and synthesized in the body through the citric acid cycle or Krebs cycle which takes place in the mitochondria. L-Malate's importance to the production of energy in the body during both aerobic and anaerobic conditions is well established. Under aerobic conditions, the oxidation of L-malate to oxaloacetate provides reducing equivalents to the mitochondria through the malate-aspartate redox shuttle. During anaerobic conditions, where a buildup of excess of reducing equivalents inhibits glycolysis, L-malic acid's simultaneous reduction to succinate and oxidation to oxaloacetate is capable of removing the accumulating reducing equivalents. This allows L-malic acid to reverse hypoxia's inhibition of glycolysis and energy production. In studies on rats it has been found that only tissue malate is depleted following exhaustive physical activity. Notably, the administration of malic acid to rats has been shown to elevate mitochondrial malate and increase mitochondrial respiration and energy production. L-Malic acid is the source of extreme tartness in United States-produced confectionery, the so-called extreme candy. It is also used with or in place of the less sour citric acid in sour sweets. These sweets are sometimes labeled with a warning stating that excessive consumption can cause irritation of the mouth. The quantitative determination of L-malic acid is especially important in the manufacture of wine, beer, bread, fruit and vegetable products, as well as in cosmetics and pharmaceuticals. It is one of the most important fruit acids, and has the highest concentration of all acids in wine. In the wine industry, the level of L-malic acid is monitored, along with L-lactic acid, during malolactic fermentation. Malic acid is approved for use as a food additive in the EU, US and Australia and New Zealand. Malic acid, when added to food products, is denoted by E number E296.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Curative
ACERBINE

Approved Use

Acerbine solution is suitable for the treatment of superficial skin injuries, such as burns, scalds, sunburn, wounds and abrasions.
PubMed

PubMed

TitleDatePubMed
Variation of isoenzyme and RAPD patterns in Candida albicans morphological mutants with altered colony ultrastructure.
2001
Metabolic regulation of pH in plant cells: role of cytoplasmic pH in defense reaction and secondary metabolism.
2001
Assays of lipogenic enzymes.
2001
Peroxisome proliferator perfluorodecanoic acid alters glutathione and related enzymes.
2001
Survey of normal appearing mouse strain which lacks malic enzyme and Nad+-linked glycerol phosphate dehydrogenase: normal pancreatic beta cell function, but abnormal metabolite pattern in skeletal muscle.
2001 Apr
Single-cell dissection and microdroplet chemistry.
2001 Apr
Reevaluating the free-ion activity model of trace metal toxicity toward higher plants: experimental evidence with copper and zinc.
2001 Apr
Phlebotomine sandflies in Venezuela. V. Review of the genus Brumptomyia (Diptera: Psychodidae), with description of the female of Brumptomyia devenanzii, re-description of the male and isozymatic profile.
2001 Apr
In vivo and in vitro effects of prolactin and growth hormone on lipid metabolism in a teleost, Anabas testudineus (Bloch).
2001 Apr
FlhD/FlhC-regulated promoters analyzed by gene array and lacZ gene fusions.
2001 Apr 1
Effect of an antidiabetic extract of Catharanthus roseus on enzymic activities in streptozotocin induced diabetic rats.
2001 Aug
Carbohydrate deprivation reduces NADPH-production in fish liver but not in adipose tissue.
2001 Aug
Characterization of a novel complex from halophilic archaebacteria, which displays chaperone-like activities in vitro.
2001 Aug 10
Structural analyses of a malate dehydrogenase with a variable active site.
2001 Aug 17
Substrate and cofactor binding to fluorescently labeled cytoplasmic malate dehydrogenase.
2001 Feb 9
[Lactate and malate dehydrogenase activity in the sterlet and Russian sturgeon under conditions of the widespread muscular pathology].
2001 Jan-Feb
Malo-ethanolic fermentation in grape must by recombinant strains of Saccharomyces cerevisiae.
2001 Jul
Thyroid hormone--sympathetic interaction and adaptive thermogenesis are thyroid hormone receptor isoform--specific.
2001 Jul
Massive sequence comparisons as a help in annotating genomic sequences.
2001 Jul
Altered expression and function of mitochondrial beta-oxidation enzymes in juvenile intrauterine-growth-retarded rat skeletal muscle.
2001 Jul
Relationships between inhibition constants, inhibitor concentrations for 50% inhibition and types of inhibition: new ways of analysing data.
2001 Jul 1
pH-dependent investigations of vanadium(V)-peroxo-malate complexes from aqueous solutions. In search of biologically relevant vanadium(V)-peroxo species.
2001 Jul 16
Metabolic flux analysis for succinic acid production by recombinant Escherichia coli with amplified malic enzyme activity.
2001 Jul 20
Transcriptome meets metabolome: hierarchical and metabolic regulation of the glycolytic pathway.
2001 Jul 6
Tungstate Uptake by a highly specific ABC transporter in Eubacterium acidaminophilum.
2001 Jul 6
The first examples of (S)-2-hydroxyacid dehydrogenases catalyzing the transfer of the pro-4S hydrogen of NADH are found in the archaea.
2001 Jul 9
The effect of nucleotides and mitochondrial chaperonin 10 on the structure and chaperone activity of mitochondrial chaperonin 60.
2001 Jun
Two-dimensional electrophoresis and characterization of antigens from Paracoccidioides brasiliensis.
2001 Jun
Inducible and constitutive expression using new plasmid and integrative expression vectors for Thermus sp.
2001 Jun
Aluminum speciation studies in biological fluids. Part 7. A quantitative investigation of aluminum(III)-malate complex equilibria and their potential implications for aluminum metabolism and toxicity.
2001 Jun
Oral almotriptan vs. oral sumatriptan in the abortive treatment of migraine: a double-blind, randomized, parallel-group, optimum-dose comparison.
2001 Jun
Energetic determinants of tyrosine phosphorylation of focal adhesion proteins during hypoxia/reoxygenation of kidney proximal tubules.
2001 Jun
A pre-genetic study of the isoforms of malic enzyme associated with lipid accumulation in Mucor circinelloides.
2001 Jun
An NMR and enzyme study of the carbon metabolism of Neisseria meningitidis.
2001 Jun
What controls the outer mitochondrial membrane permeability for ADP: facts for and against the role of oncotic pressure.
2001 Jun 1
Myoadenylate deaminase deficiency does not affect muscle anaplerosis during exhaustive exercise in humans.
2001 Jun 15
Histochemical study of acute and chronic intraperitoneal nicotine effects on several glycolytic and Krebs cycle dehydrogenase activities in the frontoparietal cortex and subcortical nuclei of the rat brain.
2001 Jun 15
An NMR-based metabonomic approach to the investigation of coelomic fluid biochemistry in earthworms under toxic stress.
2001 Jun 29
Relationship between NADP-specific isocitrate dehydrogenase and glutathione peroxidase in aging rat skeletal muscle.
2001 Mar
Myxothiazol induces H(2)O(2) production from mitochondrial respiratory chain.
2001 Mar 2
[Properties of gluconeogenesis enzymes from flatworms].
2001 Mar-Apr
Production of beta-thujaplicin in Cupressus lusitanica suspension cultures fed with organic acids and monoterpenes.
2001 May
Induction of a peroxisomal malate dehydrogenase isoform in liver of starved rats.
2001 May
Partial amino acid catabolism leading to the formation of alanine in Periophthalmodon schlosseri (mudskipper): a strategy that facilitates the use of amino acids as an energy source during locomotory activity on land.
2001 May
Aluminum activates a citrate-permeable anion channel in the aluminum-sensitive zone of the maize root apex. A comparison between an aluminum- sensitive and an aluminum-resistant cultivar.
2001 May
Oxyconformity in the intertidal worm Sipunculus nudus: the mitochondrial background and energetic consequences.
2001 May
Relationship between allozyme genotype and sensitivity to stressors in the western mosquitofish Gambusia affinis detected for elevated temperature but not mercury.
2001 May
Total synthesis of (-)-rosmarinecine by intramolecular cycloaddition of (S)-malic acid derived pyrroline N-oxide.
2001 May 3
Tricarboxylic acid cycle enzymes of the ectomycorrhizal basidiomycete, Suillus bovinus.
2001 May-Jun
Assimilation of D-malate by Rhodobacter capsulatus E1F1.
2001 Sep
Patents

Patents

Sample Use Guides

Apply Acerbine solution (malic acid, salicylic acid, benzoic acid) to the wound or damaged skin two or more times daily or moisten the dressing again. Once scar formation begins, one application a day is generally sufficient.
Route of Administration: Topical
Of various yeasts tested in the conversion of fumaric to L-malic acid, Saccharomyces bayanus had the highest activity of fumarase. Cells permeabilized with 0.2% (w/v) CTAB for 5 min gave maximum enzyme activity. Under non-growth conditions, fumarase activity in the permeabilized cells was four times higher (271 U/g) than that of the intact cells (67 U/g). The proposed mathematical model for the batch production of L-malic acid was validated at different initial fumaric acid concentrations. The average conversion of fumaric acid was up to 82% and gave 21, 40, 83 and 175 mM L-malic acid from respectively, 25, 50, 100 and 210 mM: fumaric acid.
Substance Class Chemical
Created
by admin
on Fri Dec 16 15:57:11 UTC 2022
Edited
by admin
on Fri Dec 16 15:57:11 UTC 2022
Record UNII
J3TZF807X5
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MALIC ACID, L-
II  
Common Name English
HYDROXYBUTANEDIOIC ACID, (-)-
Common Name English
(-)-MALIC ACID
Systematic Name English
HYDROXYSUCCINNIC ACID (-)
Common Name English
L-malic acid [WHO-DD]
Common Name English
(-)-HYDROXYSUCCINIC ACID
Systematic Name English
BUTANEDIOIC ACID, 2-HYDROXY-, (2S)-
Common Name English
L-MALIC ACID [FHFI]
Common Name English
NSC-9232
Code English
FEMA NO. 2655
Code English
L-MALIC ACID
FHFI   WHO-DD  
Common Name English
MALIC ACID [HSDB]
Common Name English
APPLE ACID
Common Name English
MALIC ACID, L- [II]
Common Name English
MALIC ACID L-(-)-FORM [MI]
Common Name English
L-MALATE
Common Name English
MALIC ACID L-(-)-FORM
MI  
Common Name English
Classification Tree Code System Code
DSLD 2323 (Number of products:281)
Created by admin on Fri Dec 16 15:57:11 UTC 2022 , Edited by admin on Fri Dec 16 15:57:11 UTC 2022
JECFA EVALUATION (-)-MALIC ACID
Created by admin on Fri Dec 16 15:57:11 UTC 2022 , Edited by admin on Fri Dec 16 15:57:11 UTC 2022
Code System Code Type Description
DAILYMED
J3TZF807X5
Created by admin on Fri Dec 16 15:57:11 UTC 2022 , Edited by admin on Fri Dec 16 15:57:11 UTC 2022
PRIMARY
CHEBI
15589
Created by admin on Fri Dec 16 15:57:11 UTC 2022 , Edited by admin on Fri Dec 16 15:57:11 UTC 2022
PRIMARY
NCI_THESAURUS
C45678
Created by admin on Fri Dec 16 15:57:11 UTC 2022 , Edited by admin on Fri Dec 16 15:57:11 UTC 2022
CONCEPT Industrial Aid
PUBCHEM
222656
Created by admin on Fri Dec 16 15:57:11 UTC 2022 , Edited by admin on Fri Dec 16 15:57:11 UTC 2022
PRIMARY
NSC
9232
Created by admin on Fri Dec 16 15:57:11 UTC 2022 , Edited by admin on Fri Dec 16 15:57:11 UTC 2022
PRIMARY
CHEBI
6650
Created by admin on Fri Dec 16 15:57:11 UTC 2022 , Edited by admin on Fri Dec 16 15:57:11 UTC 2022
PRIMARY
EPA CompTox
DTXSID30273987
Created by admin on Fri Dec 16 15:57:11 UTC 2022 , Edited by admin on Fri Dec 16 15:57:11 UTC 2022
PRIMARY
CHEBI
30797
Created by admin on Fri Dec 16 15:57:11 UTC 2022 , Edited by admin on Fri Dec 16 15:57:11 UTC 2022
PRIMARY
NCI_THESAURUS
C84394
Created by admin on Fri Dec 16 15:57:11 UTC 2022 , Edited by admin on Fri Dec 16 15:57:11 UTC 2022
PRIMARY
EVMPD
SUB38365
Created by admin on Fri Dec 16 15:57:11 UTC 2022 , Edited by admin on Fri Dec 16 15:57:11 UTC 2022
PRIMARY
RXCUI
1427053
Created by admin on Fri Dec 16 15:57:11 UTC 2022 , Edited by admin on Fri Dec 16 15:57:11 UTC 2022
PRIMARY RxNorm
FDA UNII
J3TZF807X5
Created by admin on Fri Dec 16 15:57:11 UTC 2022 , Edited by admin on Fri Dec 16 15:57:11 UTC 2022
PRIMARY
ECHA (EC/EINECS)
202-601-5
Created by admin on Fri Dec 16 15:57:11 UTC 2022 , Edited by admin on Fri Dec 16 15:57:11 UTC 2022
PRIMARY
CAS
97-67-6
Created by admin on Fri Dec 16 15:57:11 UTC 2022 , Edited by admin on Fri Dec 16 15:57:11 UTC 2022
PRIMARY
MERCK INDEX
M7041
Created by admin on Fri Dec 16 15:57:11 UTC 2022 , Edited by admin on Fri Dec 16 15:57:11 UTC 2022
PRIMARY Merck Index
Related Record Type Details
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT