GRADE & PURITY ≥98%

Synonyms

alanine-2-naphthylamide | Q27162483 | L-alanine-2-naphthylamide | L-alanine2-naphthylamide | L-Alanine-b-naphthylamide | H-ALA-BETANA | alanine beta-naphthylamide | (2S)-2-amino-N-(naphthalen-2-yl)propanamide | (S)-2-Amino-N-(2-naphthyl)propionamide | DTX

Storage

Store at 2-8°C

Shipped In

Wet ice

Overview

L-alanine β-naphthamide has been used to determine the activity of alanine aminopeptidase (AAP) in blood samples. It can also be used as a fluorescent substrate to determine the activity of neutral aminopeptidase (APN) in cultured human and mouse chondrocytes.

Specifications

Synonyms

alanine-2-naphthylamide | Q27162483 | L-alanine-2-naphthylamide | L-alanine2-naphthylamide | L-Alanine-b-naphthylamide | H-ALA-BETANA | alanine beta-naphthylamide | (2S)-2-amino-N-(naphthalen-2-yl)propanamide | (S)-2-Amino-N-(2-naphthyl)propionamide | DTX

Specifications & Purity

≥98%

Storage

Store at 2-8°C

Shipped In

Wet ice

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

Purity

≥98%

Names and Identifiers

• Canonical Smiles: C[C@H](N)C(=O)Nc1ccc2ccccc2c1
• IUPAC Name: (2S)-2-amino-N-naphthalen-2-ylpropanamide
• InChIKey: RQHPADKWNYTHOH-VIFPVBQESA-N
• INCHI: 1S/C13H14N2O/c1-9(14)13(16)15-12-7-6-10-4-2-3-5-11(10)8-12/h2-9H,14H2,1H3,(H,15,16)/t9-/m0/s1
• Isomeric SMILES: C[C@@H](C(=O)NC1=CC2=CC=CC=C2C=C1)N
• Molecular Weight: 214.26

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 acid amides

• 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
• Direct Parent: Alpha amino acid amides
• Alternative Parents: Alanine and derivatives Naphthalenes N-arylamides Secondary carboxylic acid amides Organopnictogen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aromatic homopolycyclic compounds
• Substituents: Alpha-amino acid amide - Alanine or derivatives - Naphthalene - N-arylamide - Benzenoid - Carboxamide group - Secondary carboxylic acid amide - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Primary amine - Organooxygen compound - Organonitrogen compound - Organopnictogen compound - Primary aliphatic amine - Organic oxygen compound - Carbonyl group - Amine - Aromatic homopolycyclic compound
• Description: This compound belongs to the class of organic compounds known as alpha amino acid amides. These are amide derivatives of alpha amino acids.
• 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

• Solubility: Soluble in ethanol
• Melt Point(°C): 100-101° C
• Molecular Weight: 214.260 g/mol
• XLogP3: 1.800
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 214.111 Da
• Monoisotopic Mass: 214.111 Da
• Topological Polar Surface Area: 55.100 Ų
• Heavy Atom Count: 16
• Formal Charge: 0
• Complexity: 254.000
• 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