L-Methionine sulfoxide - ≥98% , CAS No.3226-65-1

CAS: 3226-65-1 Cat. No.: L134616 Molecular Weight: 165.21 Beilstein Registry Number: 4129939 EC Number: 221-758-0

GRADE & PURITY ≥98%

Synonyms

(2S)-2-amino-4-methylsulfinyl-butyric acid | Q27102175 | CHEBI:17016 | (2S)-2-azanyl-4-methylsulfinyl-butanoic acid | L-methionine sulfoxide | alpha-amino-gamma-(methylsulfinyl)-Butyric acid | L-Methionine, S-oxide | 4-METHYLBENZENECARBONYL CHLORIDE | met

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Overview

L-Methionine sulfoxide can be used as a substrate to study the specificity and kinetics of various methionine sulfoxide reductases.
A structural analog of glutamate.

Specifications

Synonyms

(2S)-2-amino-4-methylsulfinyl-butyric acid | Q27102175 | CHEBI:17016 | (2S)-2-azanyl-4-methylsulfinyl-butanoic acid | L-methionine sulfoxide | alpha-amino-gamma-(methylsulfinyl)-Butyric acid | L-Methionine, S-oxide | 4-METHYLBENZENECARBONYL CHLORIDE | met

Specifications & Purity

≥98%

Biochemical and Physiological Mechanisms

L-Methionine sulfoxide, a structural analog of glutamate, may be used as a substrate to study the specificity and kinetics of various methionine sulfoxide reductase(s).

Storage

Store at 2-8°C, Argon charged

Shipped In

Wet ice

This product requires cold chain shipping. Ground and other economy services are not available.

Purity

≥98%

Names and Identifiers

• Pubchem Sid: 504757434
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504757434
• Canonical Smiles: CS(=O)CCC(C(=O)O)N
• IUPAC Name: (2S)-2-amino-4-methylsulfinylbutanoic acid
• InChIKey: QEFRNWWLZKMPFJ-YGVKFDHGSA-N
• INCHI: 1S/C5H11NO3S/c1-10(9)3-2-4(6)5(7)8/h4H,2-3,6H2,1H3,(H,7,8)/t4-,10?/m0/s1
• Isomeric SMILES: CS(=O)CC[C@@H](C(=O)O)N
• WGK Germany: 3
• Molecular Weight: 165.21
• Beilstein: 4129939
• Reaxy-Rn: 2206690
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2206690&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Class Carboxylic acids and derivatives
      • Subclass Amino acids, peptides, and analogues
        • Level5 Amino acids and derivatives
          • Level6 Alpha amino acids and derivatives
            • Level7 Alpha amino acids
              • Level8 L-alpha-amino acids

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Class: Carboxylic acids and derivatives
• Subclass: Amino acids, peptides, and analogues
• Intermediate Tree Nodes: Amino acids and derivatives - Alpha amino acids and derivatives - Alpha amino acids
• Direct Parent: L-alpha-amino acids
• Alternative Parents: Thia fatty acids Sulfoxides Amino acids Sulfinyl compounds Monocarboxylic acids and derivatives Carboxylic acids Organopnictogen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: L-alpha-amino acid - Thia fatty acid - Fatty acid - Fatty acyl - Sulfoxide - Amino acid - Carboxylic acid - Monocarboxylic acid or derivatives - Sulfinyl compound - Carbonyl group - Organic oxygen compound - Organic nitrogen compound - Primary amine - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Amine - Primary aliphatic amine - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as l-alpha-amino acids. These are alpha amino acids which have the L-configuration of the alpha-carbon atom.
• External Descriptors: methionine S-oxide

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

Associated Targets(non-human)

Ggt1 Gamma-glutamyltranspeptidase 1 (36 Activities)

Discover Target: Ggt1

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

Mechanisms of Action

Chemical and Physical Properties

• Sensitivity: Air Sensitive,Heat Sensitive,Hygroscopic
• Melt Point(°C): 255 °C
• Molecular Weight: 165.210 g/mol
• XLogP3: -4.100
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 4
• Exact Mass: 165.046 Da
• Monoisotopic Mass: 165.046 Da
• Topological Polar Surface Area: 99.600 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 148.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 1
• 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: 1