Glycyl-L-glutamine hydrate - ≥97%(HPLC) , CAS No.172669-64-6

CAS: 172669-64-6 Cat. No.: G167882 Formula: C₇H₁₃N₃O₄ · H₂O Peso molecolare: 221.21

GRADE & PURITY ≥97%(HPLC)

Synonyms

BCP13679 | UNII-668A00JUHO | (S)-5-Amino-2-(2-aminoacetamido)-5-oxopentanoic acid hydrate | AC-4720 | Glycyl-L-glutamine hydrate | Gly-gln | Glycyl-L-Glutamine (hydrate) | Glycyl-L-glutamine xhydrate | Glycyl-L-glutamine monohydrate | L-Glutamine, N2-glyc

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Panoramica

Glycyl-glutamine (gly-gln) is a dipeptide that is used as a substitute for glutamine in cell culture. Higher cell yields are obtained when this dipeptide is used instead of glutamine, where gly-gln affects substrate utilization and metabolism. Cell growth is higher as the concentrations of this dipeptide remain high, due to lower peptidase affinity.

Heat-stable substitute for glutamine in mammalian cell culture media.

Specifications

Sinonimi

BCP13679 | UNII-668A00JUHO | (S)-5-Amino-2-(2-aminoacetamido)-5-oxopentanoic acid hydrate | AC-4720 | Glycyl-L-glutamine hydrate | Gly-gln | Glycyl-L-Glutamine (hydrate) | Glycyl-L-glutamine xhydrate | Glycyl-L-glutamine monohydrate | L-Glutamine, N2-glyc

Specifiche e purezza

≥97%(HPLC)

Applicazione

As a heat-stable substitute for glutamine in mammalian cell culture medium.

Condizioni di conservazione di stoccaggio

Store at -20°C

Spedito in

Ice chest + Ice pads

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Purezza

≥97%(HPLC)

Nomi e identificatori

Pubchem Sid

504769842

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504769842

Sorrisi canonici

O.NCC(=O)N[C@@H](CCC(N)=O)C(O)=O

IUPAC Name

(2S)-5-amino-2-[(2-aminoacetyl)amino]-5-oxopentanoic acid;hydrate

InChIKey

KLFWVRQACSYLOH-WCCKRBBISA-N

INCHI

1S/C7H13N3O4.H2O/c8-3-6(12)10-4(7(13)14)1-2-5(9)11;/h4H,1-3,8H2,(H2,9,11)(H,10,12)(H,13,14);1H2/t4-;/m0./s1

Isomeri SMILES

C(CC(=O)N)[C@@H](C(=O)O)NC(=O)CN.O

CAS alternativo

13115-71-4

Peso molecolare

221.21

Reaxy-Rn

7395534

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=7395534&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Classe Carboxylic acids and derivatives
      • Subclass Amino acids, peptides, and analogues
        • Level5 Peptides
          • Level6 Dipeptides

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Classe: Carboxylic acids and derivatives
• Subclass: Amino acids, peptides, and analogues
• Intermediate Tree Nodes: Peptides
• Direct Parent: Dipeptides
• Alternative Parents: Glutamine and derivatives N-acyl-L-glutamines Alpha amino acid amides Fatty amides Fatty acids and conjugates Secondary carboxylic acid amides Primary carboxylic acid amides Amino acids Monocarboxylic acids and derivatives Carboxylic acids Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Alpha-dipeptide - Glutamine or derivatives - N-acyl-alpha-amino acid - N-acyl-alpha amino acid or derivatives - N-acyl-l-alpha-amino acid - N-acyl-l-glutamine - Alpha-amino acid amide - Alpha-amino acid or derivatives - Fatty acyl - Fatty acid - Fatty amide - Amino acid - Carboxamide group - Secondary carboxylic acid amide - Primary carboxylic acid amide - Amino acid or derivatives - Monocarboxylic acid or derivatives - Carboxylic acid - Organic nitrogen compound - Organonitrogen compound - Primary aliphatic amine - Organooxygen compound - Primary amine - Hydrocarbon derivative - Carbonyl group - Organic oxide - Amine - Organic oxygen compound - Aliphatic acyclic compound
• Descrizione: 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: 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

Proprietà chimiche e fisiche

• Rotazione specifica [α]: -5.0 to -8.0 deg(C=3, 1mol/L HCl)
• Peso molecolare: 221.210 g/mol
• Hydrogen Bond Donor Count: 5
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 6
• Exact Mass: 221.101 Da
• Monoisotopic Mass: 221.101 Da
• Topological Polar Surface Area: 137.000 Ų
• Heavy Atom Count: 15
• Formal Charge: 0
• Complexity: 241.000
• 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: 2

XLogP3