L-Leucine- β-naphthylamide - ≥98%, used for L-Leucine β-naphthylamide has been used as a substrate: to measure the activity of aminopeptidase in Escherichia coli to evaluate the enzyme activity of cathepsin H from rabbit skeletal muscles in the proteolyti

CAS: 732-85-4 Cat. No.: L354305 Summenformel: C₁₆H₂₀N₂O Molekulargewicht: 256.34 EG-Nummer: 211-990-0

GRADE & PURITY ≥98%

Synonyms

Leucine-beta-naphthylamide | L-leucine 2-naphthylamide | L-Leucyl-.beta.-naphthylamide hydrochloride (Salt/Mix) | Pentanamide,2-amino-4-methyl-N-2-naphthalenyl-,(2S)- | 2-Amino-4-methyl-N-(2-naphthyl)pentanamide | DTXSID20993920 | EINECS 211-990-0 | URACI

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Übersicht

Substrate for aminopeptidase M

Specifications

Synonyme

Leucine-beta-naphthylamide | L-leucine 2-naphthylamide | L-Leucyl-.beta.-naphthylamide hydrochloride (Salt/Mix) | Pentanamide,2-amino-4-methyl-N-2-naphthalenyl-,(2S)- | 2-Amino-4-methyl-N-(2-naphthyl)pentanamide | DTXSID20993920 | EINECS 211-990-0 | URACI

Spezifikationen & Reinheit

≥98%

Anmeldung

L-Leucine β-naphthylamide has been used as a substrate: to measure the activity of aminopeptidase in Escherichia coli to evaluate the enzyme activity of cathepsin H from rabbit skeletal muscles in the proteolytic assay of L-Leucine aminopeptidase

Storage

Store at -20°C

Verschickt in

Ice chest + Ice pads

Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.

Reinheit

≥98%

Namen und Kennungen

Kanonisches Lächeln

CC(C)CC(C(=O)NC1=CC2=CC=CC=C2C=C1)N

IUPAC Name

(2S)-2-amino-4-methyl-N-naphthalen-2-ylpentanamide

InChIKey

JWHURRLUBVMKOT-HNNXBMFYSA-N

INCHI

1S/C16H20N2O/c1-11(2)9-15(17)16(19)18-14-8-7-12-5-3-4-6-13(12)10-14/h3-8,10-11,15H,9,17H2,1-2H3,(H,18,19)/t15-/m0/s1

Isomere SMILES

CC(C)C[C@@H](C(=O)NC1=CC2=CC=CC=C2C=C1)N

Molekulargewicht

256.34

Reaxy-Rn

2216069

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2216069&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Klasse Naphthalenes

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Klasse: Naphthalenes
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Naphthalenes
• Alternative Parents: Propargyl-type 1,3-dipolar organic compounds Carboximidic acids Organopnictogen compounds Organooxygen compounds Monoalkylamines Hydrocarbon derivatives
• Molecular Framework: Aromatic homopolycyclic compounds
• Substituents: Naphthalene - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carboximidic acid derivative - Carboximidic acid - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Amine - Aromatic homopolycyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as naphthalenes. These are compounds containing a naphthalene moiety, which consists of two fused benzene rings.
• 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

Wirkungsmechanismen

Chemische und physikalische Eigenschaften

• Molekulargewicht: 256.339 g/mol
• XLogP3: 3.200
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 4
• Exact Mass: 256.158 Da
• Monoisotopic Mass: 256.158 Da
• Topological Polar Surface Area: 55.100 Ų
• Heavy Atom Count: 19
• Formal Charge: 0
• Complexity: 303.000
• 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