N-Heptanoyl-DL-homoserine lactone - ≥97% , CAS No.106983-26-0

CAS: 106983-26-0 Cat. No.: N464430 Peso molecular: 213.27

GRADE & PURITY ≥97%

Synonyms

N-(2-oxooxolan-3-yl)heptanamide | 82FBC7F8-02FF-4811-BF33-57EA6A9E9A17 | DTXSID30407866 | N-(2-Oxotetrahydrofuran-3-yl)heptanamide | Heptanamide, N-(tetrahydro-2-oxo-3-furanyl)- | N-Heptanoyl-DL-homoserine lactone | MFCD01862914 | N-Heptanoyl-DL-homoserin

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Descripción general

Description

Application test: Induces violacein expression in aChromobacterium violaceummutant usually not able to produce homoserine lactones.

Specifications

Sinónimos

N-(2-oxooxolan-3-yl)heptanamide | 82FBC7F8-02FF-4811-BF33-57EA6A9E9A17 | DTXSID30407866 | N-(2-Oxotetrahydrofuran-3-yl)heptanamide | Heptanamide, N-(tetrahydro-2-oxo-3-furanyl)- | N-Heptanoyl-DL-homoserine lactone | MFCD01862914 | N-Heptanoyl-DL-homoserin

Especificaciones y pureza

≥97%

Mecanismos bioquímicos y fisiológicos

N-庚酰-DL-高丝氨酸内酯 (C7HSL) 是一类高丝氨酸内酯，包括；N-辛酰-高丝氨酸内酯 (N-C8-HSL)、N-癸酰-DL-高丝氨酸内酯 (N-C10-HSL)、N-（3-氧癸酰）高丝氨酸-L-内酯 (3-oxo-C10 HSL)、N-（3-氧十二酰）高丝氨酸-L-内酯 (3-oxo-C12-HSL)、N-（3-氧十四酰）-L-高丝氨酸内酯 (3-oxo-C14-HSL)、N-（3-羟基癸酰）-L-高丝氨酸内酯，N-（3-羟基辛酰）-L-高丝氨酸内酯参与细菌群体感应过程。这些N-酰基-高丝氨酸内

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

≥97%

Nombres e identificadores

• Sonrisas canónicas: CCCCCCC(=O)NC1CCOC1=O
• IUPAC Name: N-(2-oxooxolan-3-yl)heptanamide
• InChIKey: FTMZLSDESAOPSZ-UHFFFAOYSA-N
• INCHI: 1S/C11H19NO3/c1-2-3-4-5-6-10(13)12-9-7-8-15-11(9)14/h9H,2-8H2,1H3,(H,12,13)
• Isómeros SMILES: CCCCCCC(=O)NC1CCOC1=O
• Peso molecular: 213.27
• Reaxy-Rn: 10162518
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=10162518&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 Amino acids and derivatives
          • Level6 Alpha amino acids and derivatives
            • Level7 N-acyl-alpha amino acids and derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Clase: Carboxylic acids and derivatives
• Subclass: Amino acids, peptides, and analogues
• Intermediate Tree Nodes: Amino acids and derivatives - Alpha amino acids and derivatives
• Direct Parent: N-acyl-alpha amino acids and derivatives
• Alternative Parents: Alpha amino acid esters Acyl homoserine lactones N-acyl amines Gamma butyrolactones Oxolanes Secondary carboxylic acid amides Carboxylic acid esters Oxacyclic compounds Monocarboxylic acids and derivatives Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: Alpha-amino acid ester - N-acyl-alpha amino acid or derivatives - Acyl-homoserine lactone - Fatty amide - Gamma butyrolactone - Fatty acyl - N-acyl-amine - Oxolane - Carboxamide group - Carboxylic acid ester - Lactone - Secondary carboxylic acid amide - Oxacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Carbonyl group - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Aliphatic heteromonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as n-acyl-alpha amino acids and derivatives. These are compounds containing an alpha amino acid (or a derivative thereof) which bears an acyl group at its terminal nitrogen 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

Objetivos asociados (no humanos)

Staphylococcus aureus (210822 Activities)

Explore this target

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

Bacillus subtilis (32866 Activities)

Explore this target

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

Mecanismos de acción

Propiedades químicas y físicas

• Sensibilidad: Moisture sensitive
• Punto de inflamación (°F): Not applicable
• Punto de inflamación (°C): Not applicable
• Peso molecular: 213.270 g/mol
• XLogP3: 2.100
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 6
• Exact Mass: 213.136 Da
• Monoisotopic Mass: 213.136 Da
• Topological Polar Surface Area: 55.400 Ų
• Heavy Atom Count: 15
• Formal Charge: 0
• Complexity: 228.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• 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