D-Glutamic acid - Moligand™, ≥98% , CAS No.6893-26-1

Name: D-Glutamic acid - Moligand™, ≥98% , CAS No.6893-26-1
Brand: Aladdin Scientific
SKU: G100444
Availability: InStock

CAS: 6893-26-1 Cat. No.: G100444 Formule: C₅H₉NO₄ Poids moléculaire: 147.13 Beilstein Registry Number: 1723800 Numéro CE: 230-000-8

22 Citations COA

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D-Glutamic acid - Moligand™, ≥98% CAS No(6893-26-1) G100444 by Aladdin Scientific

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DISPONIBLE À COMMANDE

QUALITÉ & PURETÉ Moligand™ ? ≥98%

Synonyms

Storage

Room temperature

Shipped In

Normal

Fiche de spécifications

Vue d’ensemble Spécifications Noms et identifiants Documentation Données avancées Taxonomic Classification Structure 3D Cibles associées (humaines) Cibles associées (non humaines) Mécanismes d'action Certificats (CoA, COO, BSE/TSE et tableau d'analyse) Propriétés chimiques et physiques FAQ et articles Citations of This Product Calculateurs de solution Avis

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Pourquoi cette qualité

Moligand™, ≥98% Moligand™ pour les flux de travail chromatographiques et analytiques sensibles nécessitant une interférence de ligne de base minimale.

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Stockage & expédition

Room temperature Expédition Normal. Consultez le COA spécifique au lot pour les spécifications exactes.

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Documents qualité

SDS, COA, fiche technique et fiche de spécifications disponibles au téléchargement. COA spécifique au lot accessible via la recherche par numéro de lot.

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Preuve documentaire

Cité dans 22 publications à comité de lecture couvrant la chromatographie, la synthèse organique et les réactions de couplage croisé.

Vue d’ensemble

D-Glutamic acid is an essential constituent of the bacterial peptidoglycan structure. It is added to UDP-N-acetylmuramyl-L-alanine (UDP-MurNAc-L-alanine) by the enzyme D-glutamic acid-adding enzyme (murD). This is, then, incorporated into the peptidoglycan precursor. Peptidoglycan makes up the cell walls of Gram-positive and -negative bacteria. The conversion of L-glutamate to D-glutamate by glutamate racemase (GR) enzyme is an essential step in the synthesis of peptidoglycan.

application：

D-Glutamic acid acts as a superior to alpha ketoglutarate. It helps in the growth of Lactobacillus arabinosus. It can inhibit the IgE binding to peanut allergens. It is widely used in pharmaceuticals and foods.

Spécifications

Synonymes

Spécifications et pureté

Moligand™, ≥98%

Mécanismes biochimiques et physiologiques

Excitatory amino acid acting at NMDA receptors; less active than the L-isomer.L-isomeralso available.

Conditions de stockage de stockage

Room temperature

Expédié en

Normal

Grade

Moligand™

Pureté

≥98%

Noms et identifiants

Pubchem Sid

488182816

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/488182816

Sourires canoniques

C(CC(=O)O)C(C(=O)O)N

IUPAC Name

(2R)-2-aminopentanedioic acid

InChIKey

WHUUTDBJXJRKMK-GSVOUGTGSA-N

INCHI

1S/C5H9NO4/c6-3(5(9)10)1-2-4(7)8/h3H,1-2,6H2,(H,7,8)(H,9,10)/t3-/m1/s1

Isomères SMILES

C(CC(=O)O)[C@H](C(=O)O)N

WGK Allemagne

Poids moléculaire

147.13

Beilstein

1723800

Reaxy-Rn

1723799

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1723799&ln=

Documentation

📋 Fiche de données de sécurité (FDS)

Document complet couvrant les dangers, la manipulation, le stockage et la conformité réglementaire.

<<<<<<< HEAD Télécharger la SDS → ======= Télécharger la SDS → >>>>>>> release248-p3

✅ Certificat d'analyse (COA)

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📊 Fiche technique

Résumé de référence rapide des spécifications et applications du produit.

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🔬 Fiche de spécifications

Attributs de qualité complets et critères d'acceptation pour cette qualité.

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Données avancées

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic acids and derivatives
  - Classe Carboxylic acids and derivatives
    - Subclass Amino acids, peptides, and analogues
      - Level5 Amino acids and derivatives
        Level6 Alpha amino acids and derivatives
        Level7 Glutamic acid and derivatives

Kingdom	Organic compounds
Superclass	Organic acids and derivatives
Classe	Carboxylic acids and derivatives
Subclass	Amino acids, peptides, and analogues
Intermediate Tree Nodes	Amino acids and derivatives - Alpha amino acids and derivatives
Direct Parent	Glutamic acid and derivatives
Alternative Parents	D-alpha-amino acids Amino fatty acids Dicarboxylic acids and derivatives Amino acids Carboxylic acids Organopnictogen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds
Molecular Framework	Aliphatic acyclic compounds
Substituents	Glutamic acid or derivatives - Alpha-amino acid - D-alpha-amino acid - Amino fatty acid - Dicarboxylic acid or derivatives - Fatty acid - Fatty acyl - Amino acid - Carboxylic acid - Organic oxide - Primary amine - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Organopnictogen compound - Carbonyl group - Organic oxygen compound - Amine - Organic nitrogen compound - Hydrocarbon derivative - Aliphatic acyclic compound
Description	This compound belongs to the class of organic compounds known as glutamic acid and derivatives. These are compounds containing glutamic acid or a derivative thereof resulting from reaction of glutamic acid at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.
External Descriptors	Other amino acids
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Structure 3D

Cibles associées (humaines)

CA2 Tclin Carbonic anhydrase II (17698 Activities)

Discover Target: CA2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)

Discover Target: CHRM1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

GRM3 Tchem Metabotropic glutamate receptor 3 (732 Activities)

Discover Target: GRM3

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CA1 Tclin Carbonic anhydrase I (13240 Activities)

Discover Target: CA1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

GRM4 Tchem Metabotropic glutamate receptor 4 (2320 Activities)

Discover Target: GRM4

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

GRM6 Tchem Metabotropic glutamate receptor 6 (361 Activities)

Discover Target: GRM6

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

GRM1 Tchem Metabotropic glutamate receptor 1 (2309 Activities)

Discover Target: GRM1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

GRM5 Tchem Metabotropic glutamate receptor 5 (5733 Activities)

Discover Target: GRM5

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CYP2D6 Tclin Cytochrome P450 2D6 (33882 Activities)

Discover Target: CYP2D6

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SLC1A3 Tchem Excitatory amino acid transporter 1 (586 Activities)

Discover Target: SLC1A3

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CYP1A2 Tchem Cytochrome P450 1A2 (26471 Activities)

Discover Target: CYP1A2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CYP2C9 Tchem Cytochrome P450 2C9 (32119 Activities)

Discover Target: CYP2C9

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CYP2C19 Tchem Cytochrome P450 2C19 (29246 Activities)

Discover Target: CYP2C19

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)

Discover Target: CYP3A4

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

THP-1 (11052 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

APEX1 Tchem DNA-(apurinic or apyrimidinic site) lyase (38016 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

USP1 Tchem Ubiquitin carboxyl-terminal hydrolase 1 (22556 Activities)

Discover Target: USP1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

FTO Tchem Alpha-ketoglutarate-dependent dioxygenase FTO (473 Activities)

Discover Target: FTO

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Cibles associées (non humaines)

Grm2 Metabotropic glutamate receptor 2 (1326 Activities)

Discover Target: Grm2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Pkm Pyruvate kinase isozymes M1/M2 (66 Activities)

Discover Target: Pkm

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Grm7 Metabotropic glutamate receptor 7 (580 Activities)

Discover Target: Grm7

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

murI Glutamate racemase (2 Activities)

Discover Target: murI

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Rattus norvegicus (775804 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

lef Anthrax lethal factor (7585 Activities)

Discover Target: lef

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ffp 4'-phosphopantetheinyl transferase ffp (24982 Activities)

Discover Target: ffp

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Gria2 Glutamate receptor ionotropic, AMPA (2103 Activities)

Discover Target: Gria2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Grik1 Glutamate receptor ionotropic, kainate (722 Activities)

Discover Target: Grik1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mécanismes d'action

Certificats (CoA, COO, BSE/TSE et tableau d'analyse)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

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36 results found

Lot Number	Certificate Type	Date	Article
J2222328	Certificate of Analysis	Jul 30, 2026	G100444
H2525511	Certificate of Analysis	Jun 12, 2025	G100444
H2525510	Certificate of Analysis	Jun 12, 2025	G100444
H2525509	Certificate of Analysis	Jun 12, 2025	G100444
H2525508	Certificate of Analysis	Jun 12, 2025	G100444
H2525367	Certificate of Analysis	Jun 12, 2025	G100444
G2609050	Certificate of Analysis	Jun 12, 2025	G100444
G2609049	Certificate of Analysis	Jun 12, 2025	G100444
G2609048	Certificate of Analysis	Jun 12, 2025	G100444
L2031127	Certificate of Analysis	Oct 14, 2024	G100444
I2411359	Certificate of Analysis	Sep 02, 2024	G100444
I2411358	Certificate of Analysis	Sep 02, 2024	G100444
I2411357	Certificate of Analysis	Sep 02, 2024	G100444
I2411356	Certificate of Analysis	Sep 02, 2024	G100444
I2411355	Certificate of Analysis	Sep 02, 2024	G100444
E2411269	Certificate of Analysis	Mar 21, 2024	G100444
G2321358	Certificate of Analysis	Jun 30, 2023	G100444
C2605165	Certificate of Analysis	Jun 30, 2023	G100444
G2321350	Certificate of Analysis	Jun 30, 2023	G100444
G2321286	Certificate of Analysis	Jun 30, 2023	G100444
G2321427	Certificate of Analysis	Jun 30, 2023	G100444
G2321382	Certificate of Analysis	Jun 30, 2023	G100444
G2321381	Certificate of Analysis	Jun 30, 2023	G100444
G2321365	Certificate of Analysis	Jun 30, 2023	G100444
J2222358	Certificate of Analysis	Jul 04, 2022	G100444
J2222354	Certificate of Analysis	Jul 04, 2022	G100444
J2222345	Certificate of Analysis	Jul 04, 2022	G100444
J2222326	Certificate of Analysis	Jul 04, 2022	G100444
B2309083	Certificate of Analysis	Jul 04, 2022	G100444
J2222325	Certificate of Analysis	Jul 04, 2022	G100444
D2319408	Certificate of Analysis	Jul 04, 2022	G100444
F2218030	Certificate of Analysis	Jun 22, 2022	G100444
E2223102	Certificate of Analysis	Feb 26, 2022	G100444
E2223103	Certificate of Analysis	Feb 26, 2022	G100444
E2223104	Certificate of Analysis	Feb 26, 2022	G100444
E2223106	Certificate of Analysis	Feb 26, 2022	G100444

Propriétés chimiques et physiques

Solubilité	Soluble in water, slightly soluble in ethanol, insoluble in ether
Rotation spécifique [α]	-30.0 to -33.0 deg(C=5, HCl(1+5))
Point de fusion (°C)	200-202°C
Poids moléculaire	147.130 g/mol
XLogP3	-3.700
Hydrogen Bond Donor Count	3
Hydrogen Bond Acceptor Count	5
Rotatable Bond Count	4
Exact Mass	147.053 Da
Monoisotopic Mass	147.053 Da
Topological Polar Surface Area	101.000 Å²
Heavy Atom Count	10
Formal Charge	0
Complexity	145.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	1
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

FAQ et articles

Synthesis and Metabolism of Glutamate and GABA: Core Mechanisms of Neurotransmitters

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Building Blocks Amino acids Vitamins GABA Metabolites Neurotransmitters Glutamate Glutamate/GABA metabolism Neural signaling pathways

Moisturizing Mechanism of Polyglutamic Acid: From the γ-Glutamyl Structure to Hydration Networks and Surface Film-Forming Behavior

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

cosmetics Polyglutamic Acid

Citations of This Product

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📚 Citations par application

Other applications13

Electrochemistry & battery electrolyte7

Organic synthesis — reaction medium9

Extraction & workup solvent5

Drug / compound screening1

Crystallization & recrystallization1

Spectroscopy sample preparation3

Chromatography (HPLC / GC / TLC)1

Film coating1

Nanoparticle / material biocompatibility1

Voir les 22 citations →

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