L-Methionylglycine - ≥98% , CAS No.14486-03-4

CAS: 14486-03-4 Cat. No.: M121443 Peso molecular: 206.26 Número EC: 238-487-9

GRADE & PURITY ≥98%

Synonyms

DS-14534 | AKOS010405233 | CHEBI:73611 | L-Methionylglycine | L-Methionyl-glycine | EN300-881949 | NSC19173 | QXOHLNCNYLGICT-YFKPBYRVSA-N | 5-Chloroisatoic anhydride, 97% | 2-[[(2S)-2-Azaniumyl-4-methylsulfanylbutanoyl]amino]acetate | L-Methionylglycine (

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Specifications

Sinónimos

DS-14534 | AKOS010405233 | CHEBI:73611 | L-Methionylglycine | L-Methionyl-glycine | EN300-881949 | NSC19173 | QXOHLNCNYLGICT-YFKPBYRVSA-N | 5-Chloroisatoic anhydride, 97% | 2-[[(2S)-2-Azaniumyl-4-methylsulfanylbutanoyl]amino]acetate | L-Methionylglycine (

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Store at -20°C

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: 504764437
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504764437
• Sonrisas canónicas: CSCCC(C(=O)NCC(=O)O)N
• IUPAC Name: 2-[[(2S)-2-amino-4-methylsulfanylbutanoyl]amino]acetic acid
• InChIKey: QXOHLNCNYLGICT-YFKPBYRVSA-N
• INCHI: 1S/C7H14N2O3S/c1-13-3-2-5(8)7(12)9-4-6(10)11/h5H,2-4,8H2,1H3,(H,9,12)(H,10,11)/t5-/m0/s1
• Isómeros SMILES: CSCC[C@@H](C(=O)NCC(=O)O)N
• WGK Alemania: 3
• Peso molecular: 206.26
• Reaxy-Rn: 1726611
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1726611&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: Methionine and derivatives N-acyl-alpha amino acids Alpha amino acid amides N-acyl amines Secondary carboxylic acid amides Amino acids Carboxylic acid salts Sulfenyl compounds Carboxylic acids Dialkylthioethers Monocarboxylic acids and derivatives Hydrocarbon derivatives Carbonyl compounds Organopnictogen compounds Organic salts Monoalkylamines Organic zwitterions Organic oxides
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Alpha-dipeptide - Methionine or derivatives - N-acyl-alpha-amino acid - N-acyl-alpha amino acid or derivatives - Alpha-amino acid amide - Alpha-amino acid or derivatives - Fatty acyl - Fatty amide - N-acyl-amine - Amino acid or derivatives - Carboxamide group - Amino acid - Carboxylic acid salt - Secondary carboxylic acid amide - Carboxylic acid - Monocarboxylic acid or derivatives - Dialkylthioether - Sulfenyl compound - Thioether - Amine - Organic zwitterion - Organic oxygen compound - Organic nitrogen compound - Primary aliphatic amine - Organic salt - Hydrocarbon derivative - Organic oxide - Carbonyl group - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Primary amine - Organopnictogen 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)

ACE Tclin Angiotensin-converting enzyme (1423 Activities)

Discover Target: ACE

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

Mecanismos de acción

Propiedades químicas y físicas

• Rotación específica [α]: +85 +/- 2 (C=2,In water at 25°C )
• Punto de fusión (°C): 212°C(lit.)
• Peso molecular: 206.270 g/mol
• XLogP3: -3.000
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 6
• Exact Mass: 206.073 Da
• Monoisotopic Mass: 206.073 Da
• Topological Polar Surface Area: 118.000 Ų
• Heavy Atom Count: 13
• Formal Charge: 0
• Complexity: 187.000
• 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