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Details

Stereochemistry ABSOLUTE
Molecular Formula C4H5NO4.K.H
Molecular Weight 171.193
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of POTASSIUM ASPARTATE ANHYDROUS

SMILES

[H+].[K+].N[C@@H](CC([O-])=O)C([O-])=O

InChI

InChIKey=TXXVQZSTAVIHFD-DKWTVANSSA-M
InChI=1S/C4H7NO4.K/c5-2(4(8)9)1-3(6)7;/h2H,1,5H2,(H,6,7)(H,8,9);/q;+1/p-1/t2-;/m0./s1

HIDE SMILES / InChI

Molecular Formula K
Molecular Weight 39.0983
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula H
Molecular Weight 1.0079
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C4H5NO4
Molecular Weight 131.0868
Charge -2
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Description
Curator's Comment: description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/15703381 | https://www.ncbi.nlm.nih.gov/pubmed/3814227 | https://www.ncbi.nlm.nih.gov/pubmed/16061593

Disodium aspartate is used in organic biosynthesis.

CNS Activity

Curator's Comment: Aspartic acid is produced in the brain and acts as endogenous neurotransmitter.

Originator

Curator's Comment: Aspartic acid was first discovered in 1827 by Auguste-Arthur Plisson and Étienne Ossian Henry by hydrolysis of asparagine, which had been isolated from asparagus juice in 1806

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: Q7L266
Gene ID: 80150.0
Gene Symbol: ASRGL1
Target Organism: Homo sapiens (Human)
18.4 µM [EC50]
Target ID: P08236
Gene ID: 2990.0
Gene Symbol: GUSB
Target Organism: Homo sapiens (Human)
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
Doses

Doses

DosePopulationAdverse events​
6 g 1 times / day multiple, oral
Highest studied dose
Dose: 6 g, 1 times / day
Route: oral
Route: multiple
Dose: 6 g, 1 times / day
Sources:
healthy, 22.4 ± 2.6 years
n = 10
Health Status: healthy
Age Group: 22.4 ± 2.6 years
Sex: M
Population Size: 10
Sources:
Overview

Overview

CYP3A4CYP2C9CYP2D6hERG

OverviewOther

Other InhibitorOther SubstrateOther Inducer







Drug as perpetrator​

Drug as perpetrator​

TargetModalityActivityMetaboliteClinical evidence
no
Drug as victim
PubMed

PubMed

TitleDatePubMed
L-amino acid sensing by the extracellular Ca2+-sensing receptor.
2000 Apr 25
Characterization of the protective effects of melatonin and related indoles against alpha-naphthylisothiocyanate-induced liver injury in rats.
2001
Protective effect of allopurinol on hepatic energy metabolism in ischemic and reperfused rat liver.
2001 Feb
Comparison of clinical, virologic and pathologic features in patients with acute hepatitis B and C.
2001 Feb
Endotoxin clearance and its relation to hepatic and renal disturbances in rats with liver cirrhosis.
2001 Feb
Extracellular amino acid levels measured with intracerebral microdialysis in the model of posttraumatic epilepsy induced by intracortical iron injection.
2001 Feb
Molecular mechanism of action at estrogen receptor alpha of a new clinically relevant antiestrogen (GW7604) related to tamoxifen.
2001 Feb
Central infusions of the recombinant human prolactin receptor antagonist, S179D-PRL, delay the onset of maternal behavior in steroid-primed, nulliparous female rats.
2001 Feb
DNA-protein crosslinks induced by nickel compounds in isolated rat lymphocytes: role of reactive oxygen species and specific amino acids.
2001 Feb 1
Evidence for glutamate receptor mediated transmission at mechanoreceptors in the skin.
2001 Feb 12
Phosphorylation-induced change of the oligomerization state of alpha B-crystallin.
2001 Feb 16
A novel osteopontin-like protein is expressed in the trout ovary during ovulation.
2001 Feb 2
DNA recognition by the methyl-CpG binding domain of MeCP2.
2001 Feb 2
Quantitative analysis of immunogold labeling indicates low levels and non-vesicular localization of L-aspartate in rat primary afferent terminals.
2001 Feb 5
Maintenance of primary murine hepatocyte functions in multicomponent polymer capsules--in vitro cryopreservation studies.
2001 Jan
Characterization of peptide substrates and viral enzyme that affect the cleavage site specificity of the human spumaretrovirus proteinase.
2001 Jan
Structure activity relationship of antiproliferative N-acyl-aspartic acid dimethyl ester. 2. Variation of the aspartyl moiety.
2001 Jan
Use of intraosseous blood for repeated hematologic and biochemical analyses in healthy pigs.
2001 Jan
Chloroplast genetic engineering.
2001 Jan
Oxygen free radical generation in healthy blood donors and cardiac patients: the protective effect of allopurinol.
2001 Jan
Leukocyte filtration in the early reperfusion phase on cardiopulmonary bypass reduces myocardial injury.
2001 Jan
Elevation of hepatic transaminases after enoxaparin use: case report and review of unfractionated and low-molecular-weight heparin-induced hepatotoxicity.
2001 Jan
The effect of amino acid-modifying reagents on chloroplast protein import and the formation of early import intermediates.
2001 Jan
A comparison of the effect of nitroparacetamol and paracetamol on liver injury.
2001 Jan
Effect of early arterialization of the porcine liver allograft on reperfusion injury, hepatocellular injury, and endothelial cell dysfunction.
2001 Jan
Microdialysis study of amino acid neurotransmitters in the spinal dorsal horn of patients undergoing microsurgical dorsal root entry zone lesioning. Technical note.
2001 Jan
Pregnancy complicated by pre-eclampsia-eclampsia with HELLP syndrome.
2001 Jan
alpha(2)-Adrenoceptor agonists inhibit vitreal glutamate and aspartate accumulation and preserve retinal function after transient ischemia.
2001 Jan
GYGD pore motifs in neighbouring potassium channel subunits interact to determine ion selectivity.
2001 Jan 1
The single pore residue Asp542 determines Ca2+ permeation and Mg2+ block of the epithelial Ca2+ channel.
2001 Jan 12
Propylene glycol toxicosis in a llama.
2001 Jan 15
Strain is more important than electrostatic interaction in controlling the pKa of the catalytic group in aspartate aminotransferase.
2001 Jan 16
The effect of ketamine hydrochloride anesthesia on basal and N-methyl-D,L-aspartate induced plasma prolactin secretion in the adult male rhesus monkey.
2001 Jan 19
Three-dimensional structure of Erwinia chrysanthemi pectin methylesterase reveals a novel esterase active site.
2001 Jan 26
Positive and negative strands of HCV-RNA in sera and peripheral blood mononuclear cells of chronically hemodialyzed patients.
2001 Jan-Feb
Vitamin B12 and hepatic enzyme serum levels correlate in male alcohol-dependent patients.
2001 Jan-Feb
Characterization, amino acid sequence and evolution of edema-inducing, basic phospholipase A2 from Trimeresurus flavoviridis venom.
2001 Jul
Serum hyaluronic acid as an early prognostic marker in biliary atresia.
2001 Mar
Recruitment, activation and retention of caspases-9 and -3 by Apaf-1 apoptosome and associated XIAP complexes.
2001 Mar 1
In vivo evidence for accelerated generation of hydroxyl radicals in liver of Long-Evans Cinnamon (LEC) rats with acute hepatitis.
2001 Mar 1
Differential effects of endomorphin-1 and -2 on amphetamine sensitization: neurochemical and behavioral aspects.
2001 Mar 1
The N-terminal segment of recombinant porcine fructose-1,6-bisphosphatase participates in the allosteric regulation of catalysis.
2001 Mar 2
Crystal structure of Lyme disease antigen outer surface protein C from Borrelia burgdorferi.
2001 Mar 30
Pathobiochemical mechanisms involved in the control of the disease caused by Trypanosoma congolense in African grey duiker (Sylvicapra grimmia).
2001 Mar 5
Patents

Sample Use Guides

Aspartic acid is a nutrient component found in animal and vegetable sources. In clinical trials to alleviate opioid abstinence it was administered orally.
Route of Administration: Oral
Activation of recombinant NMDA receptors was measured using two-electrode voltage clamp. Current and voltage electrodes were made from thin-walled borosilicate glass using a PP-830 electrode puller and when filled with 3 M KCl, possessed resistances of between 0.5 and 1.5 MΩ. Oocytes were voltage-clamped at potentials of -40 mV. Aspartate was able to activate wild type NR1/NR2A NMDA receptors with EC50 of 18.4 uM.
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:50:31 GMT 2023
Edited
by admin
on Fri Dec 15 17:50:31 GMT 2023
Record UNII
E9VW2509NH
Record Status Validated (UNII)
Record Version
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Name Type Language
POTASSIUM ASPARTATE ANHYDROUS
Common Name English
POTASSIUM L-ASPARTATE [JAN]
Common Name English
L-ASPARTIC ACID, MONOPOTASSIUM SALT
Common Name English
L-ASPARTIC ACID, POTASSIUM SALT (1:1)
Common Name English
POTASSIUM L-ASPARTATE
JAN  
Systematic Name English
POTASSIUM HYDROGEN ASPARTATE
Systematic Name English
MONOPOTASSIUM ASPARTATE
Systematic Name English
L-ASPARTIC ACID MONOPOTASSIUM SALT
Common Name English
ASPARTIC ACID MONOPOTASSIUM SALT
Common Name English
MONOPOTASSIUM ASPARTATE ANHYDROUS
Common Name English
L-ASPARTIC ACID POTASSIUM SALT
Common Name English
MONOPOTASSIUM L-ASPARTATE
Systematic Name English
ASPARTIC ACID, MONOPOTASSIUM SALT, L-
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID70273966
Created by admin on Fri Dec 15 17:50:31 GMT 2023 , Edited by admin on Fri Dec 15 17:50:31 GMT 2023
PRIMARY
CAS
1115-63-5
Created by admin on Fri Dec 15 17:50:31 GMT 2023 , Edited by admin on Fri Dec 15 17:50:31 GMT 2023
PRIMARY
FDA UNII
E9VW2509NH
Created by admin on Fri Dec 15 17:50:31 GMT 2023 , Edited by admin on Fri Dec 15 17:50:31 GMT 2023
PRIMARY
EVMPD
SUB14982MIG
Created by admin on Fri Dec 15 17:50:31 GMT 2023 , Edited by admin on Fri Dec 15 17:50:31 GMT 2023
PRIMARY
EVMPD
SUB129951
Created by admin on Fri Dec 15 17:50:31 GMT 2023 , Edited by admin on Fri Dec 15 17:50:31 GMT 2023
PRIMARY
SMS_ID
100000088528
Created by admin on Fri Dec 15 17:50:31 GMT 2023 , Edited by admin on Fri Dec 15 17:50:31 GMT 2023
PRIMARY
PUBCHEM
23672742
Created by admin on Fri Dec 15 17:50:31 GMT 2023 , Edited by admin on Fri Dec 15 17:50:31 GMT 2023
PRIMARY
ECHA (EC/EINECS)
214-226-4
Created by admin on Fri Dec 15 17:50:31 GMT 2023 , Edited by admin on Fri Dec 15 17:50:31 GMT 2023
PRIMARY
Related Record Type Details
SOLVATE->ANHYDROUS
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY