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Details

Stereochemistry ABSOLUTE
Molecular Formula C3H5O3
Molecular Weight 89.07
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge -1

SHOW SMILES / InChI
Structure of LACTATE ION, L-

SMILES

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

InChI

InChIKey=JVTAAEKCZFNVCJ-REOHCLBHSA-M
InChI=1S/C3H6O3/c1-2(4)3(5)6/h2,4H,1H3,(H,5,6)/p-1/t2-/m0/s1

HIDE SMILES / InChI

Molecular Formula C3H6O3
Molecular Weight 90.0779
Charge 0
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
High resolution 1H n.m.r. studies of vertebrate blood and plasma.
1983 Jun 1
Lactate- and isoproterenol-induced panic attacks in panic disorder patients and controls.
1988 Feb
Cloning of a lactate dehydrogenase gene from Clostridium acetobutylicum B643 and expression in Escherichia coli.
1990 Dec
Malignant ventricular tachycardia during propafenone treatment in a child with junctional automatic tachycardia: effectiveness of intravenous molar sodium lactate.
1991 May
Physiology and pathophysiology of organic acids in cerebrospinal fluid.
1993
Lactate and pyruvate concentrations in capillary blood from newborns.
1994 Sep
Intracellular flux analysis applied to the effect of dissolved oxygen on hybridomas.
1995 Dec
Standardized method for high-resolution 1H-NMR of cerebrospinal fluid.
1995 May
Abnormal substrate levels that depend upon mitochondrial function in cerebrospinal fluid from Alzheimer patients.
1998
Paraquat-induced renal injury studied by 1H nuclear magnetic resonance spectroscopy of urine.
1998 Jun
L-lactic acid as a mosquito (Diptera: Culicidae) repellent on human and mouse skin.
2001 Jan
Optimisation of media and cultivation conditions for L(+)(S)-lactic acid production by Lactobacillus casei NRRL B-441.
2001 Jul
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 Jul
The 12,13-diol cyclization approach for a truly stereocontrolled total synthesis of epothilone B and the synthesis of a conformationally restrained analogue.
2001 May 18
Diastereomeric salts of lactic acid and 1-phenylethylamine, their structures and relative stabilities.
2002 Dec
Asymmetric intramolecular [2 + 2] photocycloadditions: alpha- and beta-hydroxy acids as chiral tether groups.
2002 Feb 22
Asymmetric total synthesis of (+)-brefeldin A from (S)-lactate by triple chirality transfer process and nitrile oxide cycloaddition.
2002 Feb 8
1H and (13)C NMR spectroscopic analysis of human saliva.
2002 Jun
RIO: analyzing proteomes by automated phylogenomics using resampled inference of orthologs.
2002 May 16
Synthesis of optically active atropisomeric anilide derivatives through diastereoselective N-allylation with a chiral Pd-pi-allyl catalyst.
2003 Dec 12
The absolute configuration of 1-carboxyethyl substituents on common hexoses by circular dichroism.
2003 Jan 2
Asymmetric intermolecular C-H functionalization of benzyl silyl ethers mediated by chiral auxiliary-based aryldiazoacetates and chiral dirhodium catalysts.
2005 Dec 23
Dynamic simulation of red blood cell metabolism and its application to the analysis of a pathological condition.
2005 May 9
Automated no-carrier-added synthesis of [1-11C]-labeled D- and L-enantiomers of lactic acid.
2006 Dec
Plasma concentrations and urinary excretion of purine bases (uric acid, hypoxanthine, and xanthine) and oxypurinol after rigorous exercise.
2006 Jan
Remote ischaemic preconditioning protects against cardiopulmonary bypass-induced tissue injury: a preclinical study.
2006 Oct
Physiological and behavioral effects of naloxone and lactate in normal volunteers with relevance to the pathophysiology of panic disorder.
2007 Jan 15
Non-Hodgkin's lymphomas: immunologic prognostic studies.
2007 Jul
Role of GPR81 in lactate-mediated reduction of adipose lipolysis.
2008 Dec 19
Facile alcoholysis of L-lactide catalysed by Group 1 and 2 metal complexes.
2008 Jun 21
Design of a "new motif" with beta-amino acids and alpha-aminoxy acids: synthesis of hybrid peptides with 12/10-helix.
2008 May 16
Examination of the biological role of the alpha(2-->6)-linked sialic acid in gangliosides binding to the myelin-associated glycoprotein (MAG).
2009 Feb 26
Lactate inhibits lipolysis in fat cells through activation of an orphan G-protein-coupled receptor, GPR81.
2009 Jan 30
Serum amyloid A as a prognostic marker in melanoma identified by proteomic profiling.
2009 May 1
Characterization of a diverse secretome generated by the mouse preimplantation embryo in vitro.
2010 Jun 23
Perioperative chronic use of statins and the risk of muscle complaints in patients undergoing knee and hip endoprosthesis surgery.
2010 Mar
Screening β-arrestin recruitment for the identification of natural ligands for orphan G-protein-coupled receptors.
2013 Jun
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
by admin
on Sat Dec 16 09:48:30 GMT 2023
Edited
by admin
on Sat Dec 16 09:48:30 GMT 2023
Record UNII
435SSH7H89
Record Status Validated (UNII)
Record Version
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Name Type Language
LACTATE ION, L-
Common Name English
LACTIC ACID, ION(1-), L-
Systematic Name English
(S)-(+)-LACTATE ION
Common Name English
PROPANOIC ACID, 2-HYDROXY-, ION(1-), (2S)-
Systematic Name English
L-LACTATE ION
Common Name English
L-LACTATE
Common Name English
LACTATE, (S)-
Systematic Name English
Code System Code Type Description
CHEBI
16651
Created by admin on Sat Dec 16 09:48:31 GMT 2023 , Edited by admin on Sat Dec 16 09:48:31 GMT 2023
PRIMARY
CAS
1977-17-9
Created by admin on Sat Dec 16 09:48:31 GMT 2023 , Edited by admin on Sat Dec 16 09:48:31 GMT 2023
SUPERSEDED
CAS
4305-71-9
Created by admin on Sat Dec 16 09:48:31 GMT 2023 , Edited by admin on Sat Dec 16 09:48:31 GMT 2023
SUPERSEDED
EPA CompTox
DTXSID801018949
Created by admin on Sat Dec 16 09:48:31 GMT 2023 , Edited by admin on Sat Dec 16 09:48:31 GMT 2023
PRIMARY
FDA UNII
435SSH7H89
Created by admin on Sat Dec 16 09:48:31 GMT 2023 , Edited by admin on Sat Dec 16 09:48:31 GMT 2023
PRIMARY
RXCUI
1427172
Created by admin on Sat Dec 16 09:48:31 GMT 2023 , Edited by admin on Sat Dec 16 09:48:31 GMT 2023
PRIMARY
PUBCHEM
5460161
Created by admin on Sat Dec 16 09:48:31 GMT 2023 , Edited by admin on Sat Dec 16 09:48:31 GMT 2023
PRIMARY
CAS
72-08-2
Created by admin on Sat Dec 16 09:48:31 GMT 2023 , Edited by admin on Sat Dec 16 09:48:31 GMT 2023
PRIMARY
CAS
148182-33-6
Created by admin on Sat Dec 16 09:48:31 GMT 2023 , Edited by admin on Sat Dec 16 09:48:31 GMT 2023
SUPERSEDED
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