N-Acetyl-S-(carbamoylethyl)-L-cysteine-d3Copied to clipboard(AAMA-d3) - Moligand™,≥95 atom% D,≥95% , CAS No.81690-92-8(Unlabelled)

CAS: 81690-92-8(Unlabelled) Cat. No.: N648466 Molecular Weight: 237.29

GRADE & PURITY Moligand™, ≥95 atom% D,≥95%

Synonyms

(2R)-3-(3-amino-3-oxopropyl)sulfanyl-2-[(2,2,2-trideuterioacetyl)amino]propanoic acid | AAMA-d3 | N-(Acetyl-d3)-S-(3-aMino-3-oxopropyl)-L-cysteine | N-Acetyl-S-(carbaMoylethyl)-L-cysteine-d3 | D3-N-Acetyl-S-(carbamoylethyl)-L-cysteine

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Overview

N-Acetyl-S-(carbamoylethyl)-L-cysteine-d 3 is the deuterium labeled N-Acetyl-S-(carbamoylethyl)-L-cysteine.

In Vitro

Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs. MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Specifications

Synonyms

(2R)-3-(3-amino-3-oxopropyl)sulfanyl-2-[(2, 2, 2-trideuterioacetyl)amino]propanoic acid | AAMA-d3 | N-(Acetyl-d3)-S-(3-aMino-3-oxopropyl)-L-cysteine | N-Acetyl-S-(carbaMoylethyl)-L-cysteine-d3 | D3-N-Acetyl-S-(carbamoylethyl)-L-cysteine

Specifications & Purity

Moligand™, ≥95 atom% D, ≥95%

Biochemical and Physiological Mechanisms

N-Acetyl-S-(carbamoylethyl)-L-cysteine-d 3 is the deuterium labeled N-Acetyl-S-(carbamoylethyl)-L-cysteine.

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.

Grade

Moligand™

Purity

≥95 atom% D, ≥95%

Names and Identifiers

• Canonical Smiles: NC(CCSC[C@H](NC(C([2H])([2H])[2H])=O)C(O)=O)=O
• IUPAC Name: (2R)-3-(3-amino-3-oxopropyl)sulfanyl-2-[(2,2,2-trideuterioacetyl)amino]propanoic acid
• InChIKey: GGBCHNJZQQEQRX-FYFSCIFKSA-N
• INCHI: 1S/C8H14N2O4S/c1-5(11)10-6(8(13)14)4-15-3-2-7(9)12/h6H,2-4H2,1H3,(H2,9,12)(H,10,11)(H,13,14)/t6-/m0/s1/i1D3
• Molecular Weight: 237.29

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 N-acyl-alpha amino acids and derivatives
              • Level8 N-acyl-alpha amino acids
                • Level9 N-acyl-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 - N-acyl-alpha amino acids and derivatives - N-acyl-alpha amino acids
• Direct Parent: N-acyl-L-alpha-amino acids
• Alternative Parents: Cysteine and derivatives Fatty acids and conjugates Acetamides Secondary carboxylic acid amides Primary carboxylic acid amides Sulfenyl compounds Monocarboxylic acids and derivatives Dialkylthioethers Carboxylic acids Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: N-acyl-l-alpha-amino acid - Cysteine or derivatives - Fatty acid - Acetamide - Carboxamide group - Primary carboxylic acid amide - Secondary carboxylic acid amide - Carboxylic acid - Monocarboxylic acid or derivatives - Thioether - Sulfenyl compound - Dialkylthioether - Organic oxygen compound - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organic oxide - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as n-acyl-l-alpha-amino acids. These are n-acylated alpha amino acids which have the L-configuration of the alpha-carbon atom.
• 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

Chemical and Physical Properties

• Sensitivity: Moisture sensitive