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Details

Stereochemistry RACEMIC
Molecular Formula C5H7NO4.Na.H.2H2O
Molecular Weight 205.1416
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MONOSODIUM DL-GLUTAMATE DIHYDRATE

SMILES

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

InChI

InChIKey=HOYBDRIVSZUNOP-UHFFFAOYSA-M
InChI=1S/C5H9NO4.Na.2H2O/c6-3(5(9)10)1-2-4(7)8;;;/h3H,1-2,6H2,(H,7,8)(H,9,10);;2*1H2/q;+1;;/p-1

HIDE SMILES / InChI

Molecular Formula C5H9NO4
Molecular Weight 147.1293
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Molecular Formula H2O
Molecular Weight 18.0153
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula Na
Molecular Weight 22.98976928
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

D,L-Glutamic acid is a mixture of naturally occurring proteinogenic L-glutamic acid and non-proteinogenic D-glutamic acid. D,L-Glutamic acid is used to study mechanisms of crystal formation and self-assembly on surfaces and copolymer development. D-Glutamic acid is a component of bacterial peptidoglycans, produced by glutamate racemase.

Approval Year

PubMed

PubMed

TitleDatePubMed
Structure-activity relationship study of first selective inhibitor of excitatory amino acid transporter subtype 1: 2-Amino-4-(4-methoxyphenyl)-7-(naphthalen-1-yl)-5-oxo-5,6,7,8-tetrahydro-4H-chromene-3-carbonitrile (UCPH-101).
2010-10-14
Analysis of Monosodium l-Glutamate in Food Products by High-Performance Thin Layer Chromatography.
2010-07
Self-assembly of (S)-glutamic acid on Ag(100): a combined LT-STM and ab initio investigation.
2010-05-18
RNA polymerase activity and specific RNA structure are required for efficient HCV replication in cultured cells.
2010-04-29
Taste preference and nerve response to 5'-inosine monophosphate are enhanced by glutathione in mice.
2009-11
On the importance of ribose orientation in the substrate activation of the coenzyme B12-dependent mutases.
2009-08-24
The glutamate receptor GluR5 agonist (S)-2-amino-3-(3-hydroxy-7,8-dihydro-6H-cyclohepta[d]isoxazol-4-yl)propionic acid and the 8-methyl analogue: synthesis, molecular pharmacology, and biostructural characterization.
2009-08-13
Excitatory amino acid transporters as potential drug targets.
2009-06
Glutamic acid adsorbed on Ag(110): direct and indirect molecular interactions.
2009-05-06
Expression of the pgsB encoding the poly-gamma-DL-glutamate synthetase of Bacillus subtilis (natto).
2009-05
Dancing of the second aromatic residue around the 6,8-diazabicyclo[3.2.2]nonane framework: influence on sigma receptor affinity and cytotoxicity.
2009-04-09
Relationships between the structure of 6-allyl-6,8-diazabicyclo[3.2.2]nonane derivatives and their sigma receptor affinity and cytotoxic activity.
2009-01-15
Chemo-enzymatic synthesis of (2S,4R)-2-amino-4-(3-(2,2-diphenylethylamino)-3-oxopropyl)pentanedioic acid: a novel selective inhibitor of human excitatory amino acid transporter subtype 2.
2008-07-24
Synthesis of bicyclic sigma receptor ligands with cytotoxic activity.
2007-11-29
Synthesis of bridged piperazines with sigma receptor affinity.
2007-10
Partial agonism and antagonism of the ionotropic glutamate receptor iGLuR5: structures of the ligand-binding core in complex with domoic acid and 2-amino-3-[5-tert-butyl-3-(phosphonomethoxy)-4-isoxazolyl]propionic acid.
2007-08-31
Response properties of the pharyngeal branch of the glossopharyngeal nerve for umami taste in mice and rats.
2007-04-24
Toward an improved understanding of the glutamate mutase system.
2007-02-14
Glutamatergic autoinhibition of quantal release augments the early phase of releases after a depolarization pulse.
2006-05
The structure of a mixed GluR2 ligand-binding core dimer in complex with (S)-glutamate and the antagonist (S)-NS1209.
2006-04-07
Electroreductive intramolecular coupling of aromatic imino esters: is four-membered cyclization much more favorable than six-membered cyclization?
2006-03-30
Functional characterisation of homomeric ionotropic glutamate receptors GluR1-GluR6 in a fluorescence-based high throughput screening assay.
2006-02
Rational design and enantioselective synthesis of (1R,4S,5R,6S)-3-azabicyclo[3.3.0]octane-4,6-dicarboxylic acid - a novel inhibitor at human glutamate transporter subtypes 1, 2, and 3.
2006-01-12
Investigating the mechanism of chiral surface reactions: the interaction of methylacetoacetate with (S)-glutamic Acid modified Ni{111}.
2006-01-03
Azetidinic amino acids: stereocontrolled synthesis and pharmacological characterization as ligands for glutamate receptors and transporters.
2005-11-07
A binding site tyrosine shapes desensitization kinetics and agonist potency at GluR2. A mutagenic, kinetic, and crystallographic study.
2005-10-21
Molecular ordering and adsorbate induced faceting in the Ag{110}-(S)-glutamic acid system.
2005-10-11
Transport of thalidomide by the human intestinal caco-2 monolayers.
2005-07-14
Molecular modeling directed synthesis of a bicyclic analogue of the delta opioid receptor agonist SNC 80.
2005-06
Exploring the GluR2 ligand-binding core in complex with the bicyclical AMPA analogue (S)-4-AHCP.
2005-04
Crystal structure of the kainate receptor GluR5 ligand-binding core in complex with (S)-glutamate.
2005-02-14
Voltammetric studies of Zn and Fe complexes of EDTA: evidence for the push mechanism.
2005-02
Stereoselective inhibition of glutamate carboxypeptidase by organophosphorus derivatives of glutamic acid.
2004-11-15
Stereospecific activity of two glutamate analogs.
2004-11
Umami taste responses are mediated by alpha-transducin and alpha-gustducin.
2004-09-01
Synthesis, theoretical and structural analyses, and enantiopharmacology of 3-carboxy homologs of AMPA.
2004-08
Betaxanthin formation and free amino acids in hairy roots of Beta vulgaris var. lutea depending on nutrient medium and glutamate or glutamine feeding.
2004-05
Highly diastereoselective synthesis of trans-2,5-disubstituted tetrahydrofurans.
2004-04-30
Antifreeze activities of poly(gamma-glutamic acid) produced by Bacillus licheniformis.
2003-10
Nutritional requirements of Pochonia chlamydospora and ARF18, fungal parasites of nematode eggs.
2003-05
Rational design, synthesis, and pharmacological evaluation of 2-azanorbornane-3-exo,5-endo-dicarboxylic acid: a novel conformationally restricted glutamic acid analogue.
2003-02-21
Synthesis and structure-activity relationship studies of novel 2-diarylethyl substituted (2-carboxycycloprop-1-yl)glycines as high-affinity group II metabotropic glutamate receptor ligands.
2003-01-17
Anandamide uptake by synaptosomes from human, mouse and rat brain: inhibition by glutamine and glutamate.
2002-09-03
Biochemistry and molecular genetics of poly-gamma-glutamate synthesis.
2002-06
Calcium diglutamate improves taste characteristics of lower-salt soup.
2002-06
Selective antagonists at group I metabotropic glutamate receptors: synthesis and molecular pharmacology of 4-aryl-3-isoxazolol amino acids.
2002-02-14
Novel 1-hydroxyazole bioisosteres of glutamic acid. Synthesis, protolytic properties, and pharmacology.
2002-01-03
The AMPA receptor binding site: focus on agonists and competitive antagonists.
2002
Interconversion of (S)-glutamate and (2S,3S)-3-methylaspartate: a distinctive B(12)-dependent carbon-skeleton rearrangement.
2001-08-22
Resolution, configurational assignment, and enantiopharmacology at glutamate receptors of 2-amino-3-(3-carboxy-5-methyl-4-isoxazolyl)propionic acid (ACPA) and demethyl-ACPA.
2001
Substance Class Chemical
Created
by admin
on Tue Apr 01 18:33:38 GMT 2025
Edited
by admin
on Tue Apr 01 18:33:38 GMT 2025
Record UNII
0QJS788KX5
Record Status Validated (UNII)
Record Version
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Name Type Language
MONOSODIUM DL-GLUTAMATE DIHYDRATE
Systematic Name English
GLUTAMIC ACID, MONOSODIUM SALT, DIHYDRATE
Preferred Name English
SODIUM DL-GLUTAMATE DIHYDRATE
Systematic Name English
DL-GLUTAMIC ACID, MONOSODIUM SALT, DIHYDRATE
Systematic Name English
Code System Code Type Description
FDA UNII
0QJS788KX5
Created by admin on Tue Apr 01 18:33:38 GMT 2025 , Edited by admin on Tue Apr 01 18:33:38 GMT 2025
PRIMARY
CAS
66905-08-6
Created by admin on Tue Apr 01 18:33:38 GMT 2025 , Edited by admin on Tue Apr 01 18:33:38 GMT 2025
PRIMARY
PUBCHEM
131953542
Created by admin on Tue Apr 01 18:33:38 GMT 2025 , Edited by admin on Tue Apr 01 18:33:38 GMT 2025
PRIMARY
Related Record Type Details
ANHYDROUS->SOLVATE