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Details

Stereochemistry ABSOLUTE
Molecular Formula C6H14N2O2.C4H6O5
Molecular Weight 280.275
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LYSINE MALATE

SMILES

O[C@@H](CC(O)=O)C(O)=O.NCCCC[C@H](N)C(O)=O

InChI

InChIKey=NWZSZGALRFJKBT-KNIFDHDWSA-N
InChI=1S/C6H14N2O2.C4H6O5/c7-4-2-1-3-5(8)6(9)10;5-2(4(8)9)1-3(6)7/h5H,1-4,7-8H2,(H,9,10);2,5H,1H2,(H,6,7)(H,8,9)/t5-;2-/m00/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

Molecular Formula C6H14N2O2
Molecular Weight 146.1876
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
Assays of lipogenic 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
Differential gene expression in the small intestines of wildtype and W/W(V) mice.
2001 Apr
Effect of an antidiabetic extract of Catharanthus roseus on enzymic activities in streptozotocin induced diabetic rats.
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
Alteration of the specificity of malate dehydrogenase by chemical modulation of an active site arginine.
2001 Aug 17
Chaperone function of mutant versions of alpha A- and alpha B-crystallin prepared to pinpoint chaperone binding sites.
2001 Feb
NADP-malic enzyme from plants: a ubiquitous enzyme involved in different metabolic pathways.
2001 Feb 9
Computerized analysis of cytochemical reactions for dehydrogenases and oxygraphic studies as methods to evaluate the function of the mitochondrial sheath in rat spermatozoa.
2001 Jan
Iron-induced changes in pyruvate metabolism of Tritrichomonas foetus and involvement of iron in expression of hydrogenosomal proteins.
2001 Jan
Technical advance: reduction of Fe(III)-chelates by mesophyll leaf disks of sugar beet. Multi-component origin and effects of Fe deficiency.
2001 Jan
Acetate as a carbon source for hydrogen production by photosynthetic bacteria.
2001 Jan 23
Cat8 and Sip4 mediate regulated transcriptional activation of the yeast malate dehydrogenase gene MDH2 by three carbon source-responsive promoter elements.
2001 Jan 30
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
Ergosteroids IV: synthesis and biological activity of steroid glucuronosides, ethers, and alkylcarbonates.
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
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
Two-dimensional electrophoresis and characterization of antigens from Paracoccidioides brasiliensis.
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
The homeodomain proteins PBX and MEIS1 are accessory factors that enhance thyroid hormone regulation of the malic enzyme gene in hepatocytes.
2001 Jun 29
Relationship between NADP-specific isocitrate dehydrogenase and glutathione peroxidase in aging rat skeletal muscle.
2001 Mar
A study into the role of L-aspartic acid on the metabolism of L-malic acid and D-glucose by Oenococcus oeni.
2001 Mar
Methyl pyruvate initiates membrane depolarization and insulin release by metabolic factors other than ATP.
2001 Mar 1
Dysfunctional mitochondrial respiration in the wobbler mouse brain.
2001 Mar 16
[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
New phenolic constituents from the fruit juice of Phyllanthus emblica.
2001 May
Magnesium ameliorates aluminum rhizotoxicity in soybean by increasing citric acid production and exudation by roots.
2001 May
Amide hydrogen exchange shows that malate dehydrogenase is a folded monomer at pH 5.
2001 May
High frequency of cytolytic T lymphocytes directed against a tumor-specific mutated antigen detectable with HLA tetramers in the blood of a lung carcinoma patient with long survival.
2001 May 1
Total synthesis of (-)-rosmarinecine by intramolecular cycloaddition of (S)-malic acid derived pyrroline N-oxide.
2001 May 3
Determination of organic acids and inorganic anions in wine by isotachophoresis on a planar chip.
2001 May 4
Enzymatic computing.
2001 May-Jun
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 Wed Apr 02 10:06:24 GMT 2025
Edited
by admin
on Wed Apr 02 10:06:24 GMT 2025
Record UNII
LUX2V74GAA
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LYSINE MALATE [JAN]
Preferred Name English
LYSINE MALATE
Common Name English
Lysine malate [WHO-DD]
Common Name English
L-LYSINE, (S)-HYDROXYBUTANEDIOATE (1:1)
Systematic Name English
L-LYSINE, (2S)-2-HYDROXYBUTANEDIOATE (1:1)
Systematic Name English
Code System Code Type Description
SMS_ID
100000127144
Created by admin on Wed Apr 02 10:06:24 GMT 2025 , Edited by admin on Wed Apr 02 10:06:24 GMT 2025
PRIMARY
PUBCHEM
71749819
Created by admin on Wed Apr 02 10:06:24 GMT 2025 , Edited by admin on Wed Apr 02 10:06:24 GMT 2025
PRIMARY
EPA CompTox
DTXSID90992102
Created by admin on Wed Apr 02 10:06:24 GMT 2025 , Edited by admin on Wed Apr 02 10:06:24 GMT 2025
PRIMARY
FDA UNII
LUX2V74GAA
Created by admin on Wed Apr 02 10:06:24 GMT 2025 , Edited by admin on Wed Apr 02 10:06:24 GMT 2025
PRIMARY
CAS
71555-10-7
Created by admin on Wed Apr 02 10:06:24 GMT 2025 , Edited by admin on Wed Apr 02 10:06:24 GMT 2025
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
PARENT -> SALT/SOLVATE