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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
FlhD/FlhC-regulated promoters analyzed by gene array and lacZ gene fusions.
2001 Apr 1
Contribution of cryofixation and freeze-substitution to analytical microscopy: a study of Tritrichomonas foetus hydrogenosomes.
2001 Apr 1
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
High level expression of C4-specific NADP-malic enzyme in leaves and impairment of photoautotrophic growth in a C3 plant, rice.
2001 Feb
Exercise and ovarian steroid hormones: their effects on mitochondrial respiration.
2001 Feb 16
Azospirillum doebereinerae sp. nov., a nitrogen-fixing bacterium associated with the C4-grass Miscanthus.
2001 Jan
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
Poly-beta-hydroxybutyrate metabolism is affected by changes in respiratory enzymatic activities due to cold stress in two psychrotrophic strains of Rhizobium.
2001 Jan
A new locus for autosomal dominant dilated cardiomyopathy identified on chromosome 6q12-q16.
2001 Jan
Study of an enzyme membrane reactor with immobilized fumarase for production of L-malic acid.
2001 Jan 5
Thyroid hormone--sympathetic interaction and adaptive thermogenesis are thyroid hormone receptor isoform--specific.
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
Transcriptome meets metabolome: hierarchical and metabolic regulation of the glycolytic pathway.
2001 Jul 6
The effect of nucleotides and mitochondrial chaperonin 10 on the structure and chaperone activity of mitochondrial chaperonin 60.
2001 Jun
Oral almotriptan vs. oral sumatriptan in the abortive treatment of migraine: a double-blind, randomized, parallel-group, optimum-dose comparison.
2001 Jun
The homeodomain proteins PBX and MEIS1 are accessory factors that enhance thyroid hormone regulation of the malic enzyme gene in hepatocytes.
2001 Jun 29
Methyl pyruvate initiates membrane depolarization and insulin release by metabolic factors other than ATP.
2001 Mar 1
Identification of the human mitochondrial oxodicarboxylate carrier. Bacterial expression, reconstitution, functional characterization, tissue distribution, and chromosomal location.
2001 Mar 16
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
Relationship between allozyme genotype and sensitivity to stressors in the western mosquitofish Gambusia affinis detected for elevated temperature but not mercury.
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
Enzymatic computing.
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 Sat Dec 16 18:06:15 GMT 2023
Edited
by admin
on Sat Dec 16 18:06:15 GMT 2023
Record UNII
LUX2V74GAA
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LYSINE MALATE
Common Name English
LYSINE MALATE [JAN]
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 Sat Dec 16 18:06:15 GMT 2023 , Edited by admin on Sat Dec 16 18:06:15 GMT 2023
PRIMARY
PUBCHEM
71749819
Created by admin on Sat Dec 16 18:06:15 GMT 2023 , Edited by admin on Sat Dec 16 18:06:15 GMT 2023
PRIMARY
EPA CompTox
DTXSID90992102
Created by admin on Sat Dec 16 18:06:15 GMT 2023 , Edited by admin on Sat Dec 16 18:06:15 GMT 2023
PRIMARY
FDA UNII
LUX2V74GAA
Created by admin on Sat Dec 16 18:06:15 GMT 2023 , Edited by admin on Sat Dec 16 18:06:15 GMT 2023
PRIMARY
CAS
71555-10-7
Created by admin on Sat Dec 16 18:06:15 GMT 2023 , Edited by admin on Sat Dec 16 18:06:15 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
PARENT -> SALT/SOLVATE