Ácido DL-glutámico monohidratado - para cultivo celular, ≥98% , CAS No.19285-83-7

CAS: 19285-83-7 Cat. No.: G111548 Peso molecular: 165.14

GRADE & PURITY for Cell culture, ≥98%

Synonyms

SCHEMBL910049 | OZDAOHVKBFBBMZ-UHFFFAOYSA-N | AKOS022174795 | MFCD00150703 | AMY16018 | 2-azanylpentanedioic acid hydrate | HMS1571C03 | DTXCID1029095 | DL-GlutamicAcidMonohydrate | NCGC00260356-01 | FT-0625463 | 2-aminopentanedioic acid;hydrate | (+/-)-2

Storage

Room temperature

Shipped In

Normal

Descripción general

El ácido DL-glutámico monohidratado es un neurotransmisor aminoácido excitador que actúa como agonista en los receptores glutamatérgicos kainato, NMDA, AMPA y metabotrópicos. El ácido L-glutámico es un aminoácido proteinogénico que se incorpora a las proteínas siguiendo las instrucciones del código genético. Es una mezcla de isómeros D y L del ácido glutámico.
Un agonista de los receptores glutamatérgicos

Specifications

Sinónimos

SCHEMBL910049 | OZDAOHVKBFBBMZ-UHFFFAOYSA-N | AKOS022174795 | MFCD00150703 | AMY16018 | 2-azanylpentanedioic acid hydrate | HMS1571C03 | DTXCID1029095 | DL-GlutamicAcidMonohydrate | NCGC00260356-01 | FT-0625463 | 2-aminopentanedioic acid;hydrate | (+/-)-2

Especificaciones y pureza

para cultivo celular, ≥98%

Mecanismos bioquímicos y fisiológicos

Neurotransmisor aminoácido excitador agonista de los receptores glutamatérgicos kainato, NMDA, AMPA y metabotrópicos.

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Grado

for Cell culture

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 504768400
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504768400
• Sonrisas canónicas: C(CC(=O)O)C(C(=O)O)N.O
• IUPAC Name: 2-aminopentanedioic acid;hydrate
• InChIKey: OZDAOHVKBFBBMZ-UHFFFAOYSA-N
• INCHI: 1S/C5H9NO4.H2O/c6-3(5(9)10)1-2-4(7)8;/h3H,1-2,6H2,(H,7,8)(H,9,10);1H2
• Isómeros SMILES: C(CC(=O)O)C(C(=O)O)N.O
• Peso molecular: 165.14
• Reaxy-Rn: 4155097
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4155097&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Clase 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
• Clase: 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: 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 - 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
• Descripción: 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: Not available

Data sources

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

Propiedades químicas y físicas

• Solubilidad: 1 M HCl: 100 mg/mL, clear, colorless
• Sensibilidad: Moisture sensitive.
• Punto de fusión (°C): 197-199°C
• Peso molecular: 165.140 g/mol
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 4
• Exact Mass: 165.064 Da
• Monoisotopic Mass: 165.064 Da
• Topological Polar Surface Area: 102.000 Ų
• Heavy Atom Count: 11
• Formal Charge: 0
• Complexity: 145.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 1
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 2

XLogP3

Referencias

1. Yan Tang, Xiaohan Xia, Zhenqi Zhu, Xun Zhang, Bin Yang.  (2024)  Terahertz spectroscopic study of the dehydration process and hydrogen bonding network of DL-glutamic acid and its monohydrate.  JOURNAL OF MOLECULAR STRUCTURE,      [PMID:] [10.1016/j.molstruc.2024.138610]

2. Mei Lin, Wei Bingjie, Liu Chunyan, Zhao Mengting, Cui Tian, Wei Xiangyang.  (2025)  Polyvinylpyrrolidone-stabilized ultra-small Fe3O4 nanoparticles-functionalized graphene oxide with synergistically enhanced peroxidase-like activity for glutathione colorimetric determination in rat serum.  MICROCHIMICA ACTA,  192  (4): (1-11).  [PMID:40131482] [10.1007/s00604-025-07044-w]