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Details

Stereochemistry ABSOLUTE
Molecular Formula C3H5O3.Na
Molecular Weight 112.0598
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SODIUM LACTATE, L-

SMILES

[Na+].C[C@H](O)C([O-])=O

InChI

InChIKey=NGSFWBMYFKHRBD-DKWTVANSSA-M
InChI=1S/C3H6O3.Na/c1-2(4)3(5)6;/h2,4H,1H3,(H,5,6);/q;+1/p-1/t2-;/m0./s1

HIDE SMILES / InChI

Molecular Formula Na
Molecular Weight 22.98976928
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C3H5O3
Molecular Weight 89.07
Charge -1
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Lactic Acid, L- (L-lactic acid, L-lactate) is the levorotatory isomer of lactic acid, the biologically active isoform in humans. Lactic acid or lactate is produced during fermentation from pyruvate by lactate dehydrogenase. Lactate dehydrogenase is isomer-specific so that production and metabolism of D-lactate require D-LDH and L-lactate requires L-LDH. Mammalian cells only contain L-LDH so that in humans the lactate produced is almost exclusively L-lactate. Carbohydrate-fermenting bacterial species (e.g. lactobacillus spp) have by contrast both enzymes and therefore the capacity to produce both D-lactate and L-lactate. L-lactic acid is the primary agonist of hydroxycarboxylic acid receptor 1 (HCA1), which is a Gi/o-coupled G protein-coupled receptor (GPCR). Poly-L-lactic acid is an absorbable, semi-permanent, injectable implant that can be used to restore volume and stimulate collagen formation gradually. It is FDA-approved for the correction of facial fat loss associated with antiretroviral therapy-induced lipoatrophy in HIV patients. It is FDA-approved for use in immunocompetent people for the correction of nasolabial fold deficiencies and other facial wrinkles. It has been used off-label to enhance the cheeks, hands, neck, thighs, gluteal enhancement and chest wall deformities, such as pectus excavatum or thoracic deformities secondary to surgical procedures.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: Q9BXC0
Gene ID: 27198.0
Gene Symbol: HCAR1
Target Organism: Homo sapiens (Human)
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Palliative
PRISMASOL

Approved Use

PRISMASOL solution is indicated as a replacement solution in Continuous Renal Replacement Therapy (CRRT) and in case of drug poisoning when CRRT is used to remove dialyzable substances.

Launch Date

2006
PubMed

PubMed

TitleDatePubMed
Screening β-arrestin recruitment for the identification of natural ligands for orphan G-protein-coupled receptors.
2013-06
Characterization of a diverse secretome generated by the mouse preimplantation embryo in vitro.
2010-06-23
An autocrine lactate loop mediates insulin-dependent inhibition of lipolysis through GPR81.
2010-04-07
Perioperative chronic use of statins and the risk of muscle complaints in patients undergoing knee and hip endoprosthesis surgery.
2010-03
Studies on the biodegradation of fosfomycin: growth of Rhizobium huakuii PMY1 on possible intermediates synthesised chemically.
2009-05-07
Serum amyloid A as a prognostic marker in melanoma identified by proteomic profiling.
2009-05-01
Overcoming extractability hurdles of a 14C labeled taxane analogue milataxel and its metabolite from xenograft mouse tumor and brain tissues.
2009-04-05
Examination of the biological role of the alpha(2-->6)-linked sialic acid in gangliosides binding to the myelin-associated glycoprotein (MAG).
2009-02-26
Lactate inhibits lipolysis in fat cells through activation of an orphan G-protein-coupled receptor, GPR81.
2009-01-30
Role of GPR81 in lactate-mediated reduction of adipose lipolysis.
2008-12-19
Facile alcoholysis of L-lactide catalysed by Group 1 and 2 metal complexes.
2008-06-21
Design of a "new motif" with beta-amino acids and alpha-aminoxy acids: synthesis of hybrid peptides with 12/10-helix.
2008-05-16
Non-Hodgkin's lymphomas: immunologic prognostic studies.
2007-07
Physiological and behavioral effects of naloxone and lactate in normal volunteers with relevance to the pathophysiology of panic disorder.
2007-01-15
Automated no-carrier-added synthesis of [1-11C]-labeled D- and L-enantiomers of lactic acid.
2006-12
Remote ischaemic preconditioning protects against cardiopulmonary bypass-induced tissue injury: a preclinical study.
2006-10
Plasma concentrations and urinary excretion of purine bases (uric acid, hypoxanthine, and xanthine) and oxypurinol after rigorous exercise.
2006-01
Asymmetric intermolecular C-H functionalization of benzyl silyl ethers mediated by chiral auxiliary-based aryldiazoacetates and chiral dirhodium catalysts.
2005-12-23
Proton MR CSF analysis and a new software as predictors for the differentiation of meningitis in children.
2005-06
Dynamic simulation of red blood cell metabolism and its application to the analysis of a pathological condition.
2005-05-09
In vivo and in vitro nuclear magnetic resonance spectroscopy as a tool for investigating hepatobiliary disease: a review of H and P MRS applications.
2005-04
Synthesis of optically active atropisomeric anilide derivatives through diastereoselective N-allylation with a chiral Pd-pi-allyl catalyst.
2003-12-12
Structure of the O-polysaccharide of Proteus penneri 28 and Proteus vulgaris O31 and classification of P. penneri 26 and 28 in Proteus serogroup O31.
2003-10-24
The absolute configuration of 1-carboxyethyl substituents on common hexoses by circular dichroism.
2003-01-02
Diastereomeric salts of lactic acid and 1-phenylethylamine, their structures and relative stabilities.
2002-12
1H and (13)C NMR spectroscopic analysis of human saliva.
2002-06
RIO: analyzing proteomes by automated phylogenomics using resampled inference of orthologs.
2002-05-16
Asymmetric intramolecular [2 + 2] photocycloadditions: alpha- and beta-hydroxy acids as chiral tether groups.
2002-02-22
Asymmetric total synthesis of (+)-brefeldin A from (S)-lactate by triple chirality transfer process and nitrile oxide cycloaddition.
2002-02-08
Optimisation of media and cultivation conditions for L(+)(S)-lactic acid production by Lactobacillus casei NRRL B-441.
2001-07
A double-blind, randomized, placebo-controlled pilot study to investigate the effects of finasteride combined with a biodegradable self-reinforced poly L-lactic acid spiral stent in patients with urinary retention caused by bladder outlet obstruction from benign prostatic hyperplasia.
2001-07
The 12,13-diol cyclization approach for a truly stereocontrolled total synthesis of epothilone B and the synthesis of a conformationally restrained analogue.
2001-05-18
L-lactic acid as a mosquito (Diptera: Culicidae) repellent on human and mouse skin.
2001-01
Paraquat-induced renal injury studied by 1H nuclear magnetic resonance spectroscopy of urine.
1998-06
Abnormal substrate levels that depend upon mitochondrial function in cerebrospinal fluid from Alzheimer patients.
1998
Intracellular flux analysis applied to the effect of dissolved oxygen on hybridomas.
1995-12
Standardized method for high-resolution 1H-NMR of cerebrospinal fluid.
1995-05
Lactate and pyruvate concentrations in capillary blood from newborns.
1994-09
Physiology and pathophysiology of organic acids in cerebrospinal fluid.
1993
1H NMR characterization of normal human cerebrospinal fluid and the detection of methylmalonic acid in a vitamin B12 deficient patient.
1991-08
Malignant ventricular tachycardia during propafenone treatment in a child with junctional automatic tachycardia: effectiveness of intravenous molar sodium lactate.
1991-05
Cloning of a lactate dehydrogenase gene from Clostridium acetobutylicum B643 and expression in Escherichia coli.
1990-12
Lactate- and isoproterenol-induced panic attacks in panic disorder patients and controls.
1988-02
High resolution 1H n.m.r. studies of vertebrate blood and plasma.
1983-06-01
Patents

Sample Use Guides

Facial fat loss (lipoatrophy) Sculptra (Poly-L-lactic acid): Intradermal or SubQ: ~0.05-0.2 mL per individual injection depending on technique used; ~20 injections may be needed per cheek. Treatment should be individualized. Separate treatments by ≥2 weeks. Typical course involves 3-6 treatments. Supplemental injections may be needed. Do not overfill contour deficiency. For patients with severe facial fat loss, the average treatment requires ~1 vial per cheek area per treatment.
Route of Administration: Other
Substance Class Chemical
Created
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on Mon Mar 31 17:50:34 GMT 2025
Edited
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on Mon Mar 31 17:50:34 GMT 2025
Record UNII
P2Y1C6M9PS
Record Status Validated (UNII)
Record Version
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Name Type Language
SODIUM LACTATE, L-
II  
Common Name English
(S)-2-HYDROXYPROPANOIC ACID MONOSODIUM SALT
Preferred Name English
SODIUM (S)-LACTATE SOLUTION
Common Name English
SODIUM (S)-LACTATE SOLUTION [EP MONOGRAPH]
Common Name English
SODIUM L-LACTATE [JAN]
Common Name English
SODIUM L-LACTATE
Common Name English
SODIUM-L-LACTATE
Common Name English
Sodium L-lactate [WHO-DD]
Common Name English
SODIUM (S)-LACTATE
Systematic Name English
SODIUM LACTATE, (S)-
Common Name English
SODIUM LACTATE, L- [II]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29730
Created by admin on Mon Mar 31 17:50:34 GMT 2025 , Edited by admin on Mon Mar 31 17:50:34 GMT 2025
Code System Code Type Description
EVMPD
SUB36522
Created by admin on Mon Mar 31 17:50:34 GMT 2025 , Edited by admin on Mon Mar 31 17:50:34 GMT 2025
PRIMARY
CAS
867-56-1
Created by admin on Mon Mar 31 17:50:34 GMT 2025 , Edited by admin on Mon Mar 31 17:50:34 GMT 2025
PRIMARY
EPA CompTox
DTXSID5052830
Created by admin on Mon Mar 31 17:50:34 GMT 2025 , Edited by admin on Mon Mar 31 17:50:34 GMT 2025
PRIMARY
DAILYMED
P2Y1C6M9PS
Created by admin on Mon Mar 31 17:50:34 GMT 2025 , Edited by admin on Mon Mar 31 17:50:34 GMT 2025
PRIMARY
NCI_THESAURUS
C61944
Created by admin on Mon Mar 31 17:50:34 GMT 2025 , Edited by admin on Mon Mar 31 17:50:34 GMT 2025
PRIMARY
SMS_ID
100000128870
Created by admin on Mon Mar 31 17:50:34 GMT 2025 , Edited by admin on Mon Mar 31 17:50:34 GMT 2025
PRIMARY
PUBCHEM
23664767
Created by admin on Mon Mar 31 17:50:34 GMT 2025 , Edited by admin on Mon Mar 31 17:50:34 GMT 2025
PRIMARY
FDA UNII
P2Y1C6M9PS
Created by admin on Mon Mar 31 17:50:34 GMT 2025 , Edited by admin on Mon Mar 31 17:50:34 GMT 2025
PRIMARY
ECHA (EC/EINECS)
212-762-3
Created by admin on Mon Mar 31 17:50:34 GMT 2025 , Edited by admin on Mon Mar 31 17:50:34 GMT 2025
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE