DAUDA - ≥98% , CAS No.73025-02-2

CAS: 73025-02-2 Cat. No.: D351182 Fórmula: C₂₃H₃₄N₂O₄S Peso molecular: 434.59 Número EC: 634-721-2

CALIDAD & PUREZA ≥98%

Synonyms

11-(5-(dimethylamino)naphthalene-1-sulfonamido)undecanoic acid | 11-[[5-(dimethylamino)naphthalen-1-yl]sulonylamino]undecanoic acid | DAUDA | SCHEMBL591663 | Undecanoic acid, 11-(((5-(dimethylamino)-1-naphthalenyl)sulfonyl)amino)- | 11-[5-(Dimethylamino)-

Storage

Protected from light,Store at -20°C

Shipped In

Ice chest + Ice pads

Descripción general

DAUDA is an environment-sensitive fluorescent fatty acid analogue that alters its intensities and fluorescent emission spectra on entry into binding proteins. DAUDA has been used to determine the relative affinity of natural fatty acids for polymorphs of the|Schistosoma mansoni|Sm14 fatty acid-binding protein.

Especificaciones

Sinónimos

11-(5-(dimethylamino)naphthalene-1-sulfonamido)undecanoic acid | 11-[[5-(dimethylamino)naphthalen-1-yl]sulonylamino]undecanoic acid | DAUDA | SCHEMBL591663 | Undecanoic acid, 11-(((5-(dimethylamino)-1-naphthalenyl)sulfonyl)amino)- | 11-[5-(Dimethylamino)-

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Protected from light,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.

Tipo de acción

INHIBITOR

Pureza

≥98%

Nombres e identificadores

Pubchem Sid

504756858

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504756858

Sonrisas canónicas

CN(C)C1=CC=CC2=C1C=CC=C2S(=O)(=O)NCCCCCCCCCCC(=O)O

IUPAC Name

11-[[5-(dimethylamino)naphthalen-1-yl]sulfonylamino]undecanoic acid

InChIKey

CEPGVMDMVJGHFQ-UHFFFAOYSA-N

INCHI

1S/C23H34N2O4S/c1-25(2)21-15-11-14-20-19(21)13-12-16-22(20)30(28,29)24-18-10-8-6-4-3-5-7-9-17-23(26)27/h11-16,24H,3-10,17-18H2,1-2H3,(H,26,27)

Isómeros SMILES

CN(C)C1=CC=CC2=C1C=CC=C2S(=O)(=O)NCCCCCCCCCCC(=O)O

Peso molecular

434.59

Reaxy-Rn

8946533

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=8946533&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Clase Naphthalenes
      • Subclass Naphthalene sulfonic acids and derivatives

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Clase: Naphthalenes
• Subclass: Naphthalene sulfonic acids and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: 1-naphthalene sulfonic acids and derivatives
• Alternative Parents: 1-naphthalene sulfonamides Medium-chain fatty acids Dialkylarylamines Organosulfonamides Aminosulfonyl compounds Amino acids Monocarboxylic acids and derivatives Carboxylic acids Organopnictogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aromatic homopolycyclic compounds
• Substituents: 1-naphthalene sulfonic acid or derivatives - Naphthalene sulfonamide - 1-naphthalene sulfonamide - Tertiary aliphatic/aromatic amine - Medium-chain fatty acid - Dialkylarylamine - Organosulfonic acid amide - Fatty acyl - Fatty acid - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Aminosulfonyl compound - Amino acid or derivatives - Amino acid - Tertiary amine - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Carbonyl group - Amine - Hydrocarbon derivative - Aromatic homopolycyclic compound
• Descripción: This compound belongs to the class of organic compounds known as 1-naphthalene sulfonic acids and derivatives. These are organic aromatic compounds that contain a naphthalene moiety that carries a sulfonic acid group (or a derivative thereof) at the 1-position. Naphthalene is a bicyclic compound that is made up of two fused benzene ring.
• 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

Propiedades químicas y físicas

• Solubilidad: DMF：25 mg / ml, DMSO：25 mg / ml, Ethanol: 30 mg / ml, Ethanol: PBS (pH 7.2) (1:1): 0.5 mg / ml
• Sensibilidad: Light sensitive
• Peso molecular: 434.600 g/mol
• XLogP3: 5.700
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 14
• Exact Mass: 434.224 Da
• Monoisotopic Mass: 434.224 Da
• Topological Polar Surface Area: 95.100 Ų
• Heavy Atom Count: 30
• Formal Charge: 0
• Complexity: 603.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• 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