Glu-Glu - ≥98% , CAS No.3929-61-1

CAS: 3929-61-1 Cat. No.: G121400 Fórmula: C₁₀H₁₆N₂O₇ Peso molecular: 276.24

GRADE & PURITY ≥98%

Synonyms

glutamyl glutamic acid | alpha-glutamylglutamic acid | H-GLU-GLU-OH | HY-W016012 | EE dipeptide | E-E Dipeptide | H-L-Glu-L-Glu-OH | Q-102197 | N-L-alpha-Glutamyl-L-glutamic acid | Glu(Glu) | Dipotassium glutamyl-glutamate | glutamylglutamate | AKOS027320

Storage

Store at -20°C,Argon charged

Shipped In

Ice chest + Ice pads

Descripción general

Application

(S)-2-((S)-2-Amino-4-carboxybutanamido)pentanedioic Acid is an amino acid derivative that is used in a variety of settings, including polypeptide synthesis. It has been used in the preparation of pharmaceuticals (using polypeptides) towards the treatment of diabetes and obesity.

Specifications

Sinónimos

glutamyl glutamic acid | alpha-glutamylglutamic acid | H-GLU-GLU-OH | HY-W016012 | EE dipeptide | E-E Dipeptide | H-L-Glu-L-Glu-OH | Q-102197 | N-L-alpha-Glutamyl-L-glutamic acid | Glu(Glu) | Dipotassium glutamyl-glutamate | glutamylglutamate | AKOS027320

Especificaciones y pureza

≥98%

Mecanismos bioquímicos y fisiológicos

Glu-Glu is a small anionic dipeptides that may be used in physicochemical analysis of conformations states and protonation patterns.

Condiciones de almacenamiento de almacenamiento

Store at -20°C,Argon charged

Enviado en

Ice chest + Ice pads

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Pureza

≥98%

Nombres e identificadores

Pubchem Sid

508816574

Sonrisas canónicas

C(CC(=O)O)C(C(=O)NC(CCC(=O)O)C(=O)O)N

IUPAC Name

(2S)-2-[[(2S)-2-amino-4-carboxybutanoyl]amino]pentanedioic acid

InChIKey

KOSRFJWDECSPRO-WDSKDSINSA-N

INCHI

1S/C10H16N2O7/c11-5(1-3-7(13)14)9(17)12-6(10(18)19)2-4-8(15)16/h5-6H,1-4,11H2,(H,12,17)(H,13,14)(H,15,16)(H,18,19)/t5-,6-/m0/s1

Isómeros SMILES

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

WGK Alemania

3

Peso molecular

276.24

Reaxy-Rn

1729672

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1729672&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 Peptides
          • Level6 Dipeptides

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Clase: Carboxylic acids and derivatives
• Subclass: Amino acids, peptides, and analogues
• Intermediate Tree Nodes: Peptides
• Direct Parent: Dipeptides
• Alternative Parents: Glutamic acid and derivatives N-acyl-L-alpha-amino acids Alpha amino acid amides Tricarboxylic acids and derivatives Amino fatty acids N-acyl amines Secondary carboxylic acid amides Amino acids Carboxylic acids Organopnictogen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Alpha-dipeptide - Glutamic acid or derivatives - N-acyl-alpha-amino acid - N-acyl-alpha amino acid or derivatives - N-acyl-l-alpha-amino acid - Alpha-amino acid amide - Alpha-amino acid or derivatives - Tricarboxylic acid or derivatives - Amino fatty acid - Fatty acyl - Fatty amide - N-acyl-amine - Amino acid - Secondary carboxylic acid amide - Amino acid or derivatives - Carboxamide group - Carboxylic acid - Organic nitrogen compound - Organonitrogen compound - Primary aliphatic amine - Organooxygen compound - Primary amine - Hydrocarbon derivative - Carbonyl group - Organic oxide - Organopnictogen compound - Amine - Organic oxygen compound - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as dipeptides. These are organic compounds containing a sequence of exactly two alpha-amino acids joined by a peptide bond.
• External Descriptors: dipeptide

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

Objetivos asociados (humanos)

FOLH1 Tclin Glutamate carboxypeptidase II (711 Activities)

Discover Target: FOLH1

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

SLC15A1 Tchem Oligopeptide transporter small intestine isoform (922 Activities)

Discover Target: SLC15A1

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

Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: Aqueous Acid (Slightly), DMSO (Slightly, Heated, Sonicated)
• Sensibilidad: Moisture sensitive
• Peso molecular: 276.240 g/mol
• XLogP3: -5.100
• Hydrogen Bond Donor Count: 5
• Hydrogen Bond Acceptor Count: 8
• Rotatable Bond Count: 9
• Exact Mass: 276.096 Da
• Monoisotopic Mass: 276.096 Da
• Topological Polar Surface Area: 167.000 Ų
• Heavy Atom Count: 19
• Formal Charge: 0
• Complexity: 369.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 2
• 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