sulfates de dextran - 100 kDa LS , CAS No.9011-18-1

CAS: 9011-18-1 Cat. No.: D397464 Numéro CE: 618-471-1 PubChem CID: 2337

QUALITÉ & PURETÉ 100 kDa LS

Synonyms

4-aminobenzoic acid-ethyl ester | Anaesthesinum | Benzoak | ETHYL4-AMINOBENZOATE | Norcaine | Norcainum | Aethoform | Anesthin | Bensokain | HSDB 7225 | BENZOCAINE [USP MONOGRAPH] | CAS-94-09-7 | Acide benzoïque, 4-amino-, ester éthylique | Chiggerex | Et

Storage

Stocker à 2-8°C, chargé d'argon, desséché

Shipped In

Glace humide

Vue d’ensemble

Description du produit：

Les sulfates de dextran sont produits par sulfatation de fractions de dextran sélectionnées.

Le sulfate de dextran est fourni sous forme de sel de sodium et est stabilisé par une petite addition de sels de phosphate. Un certificat d'analyse est fourni avec chaque lot. La gamme de poids moléculaire, la teneur en soufre, l'humidité, etc. sont soigneusement contrôlées.

Structure du Dextran

Le dextran est un polysaccharide dérivé de la bactérie Leuconostoc mesenteroides B512F et consiste en un glucane linéaire α-D-(1 - 6) avec une faible teneur (environ 5 %) en chaînes latérales liées au carbone 3 du glucose. Le sulfate de dextran est un dérivé sulfaté de la fraction de dextran sélectionnée. La teneur en sulfate de nos sulfates de dextran faiblement sulfatés se situe entre 8 et 13 %.

Applications

Le sulfate de dextran possède un large éventail de domaines d'application et de propriétés. En voici quelques exemples

Agent anticoagulant dans les milieux cellulaires

Précipitation sélective des lipoprotéines

Accélération de l'hybridation de l'ADN.

Libération de l'ADN des complexes ADN-histones

Inhibition de la liaison de l'ARNt aux ribosomes

Inhibition des ribonucléases

Propriétés antivirales

Utilisé en cosmétique pour ses propriétés anti-inflammatoires et la rétention osmotique de l'eau

Séparation des micro-organismes et des macromolécules

Adjuvant dans les vaccins

Études de la perméabilité des membranes

Spécifications

Synonymes

4-aminobenzoic acid-ethyl ester | Anaesthesinum | Benzoak | ETHYL4-AMINOBENZOATE | Norcaine | Norcainum | Aethoform | Anesthin | Bensokain | HSDB 7225 | BENZOCAINE [USP MONOGRAPH] | CAS-94-09-7 | Acide benzoïque, 4-amino-, ester éthylique | Chiggerex | Et

Spécifications et pureté

100 kDa LS

Conditions de stockage de stockage

Stocker à 2-8°C, chargé d'argon, desséché

Expédié en

Glace humide

Propriétés du produit

ALogP

1.9

Noms et identifiants

IUPAC Name

ethyl 4-aminobenzoate

InChIKey

BLFLLBZGZJTVJG-UHFFFAOYSA-N

INCHI

1S/C9H11NO2/c1-2-12-9(11)7-3-5-8(10)6-4-7/h3-6H,2,10H2,1H3

Isomères SMILES

CCOC(=O)C1=CC=C(C=C1)N

WGK Allemagne

2

RTECS

HH9290000

PubChem CID

2337

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Classe Benzene and substituted derivatives
      • Subclass Benzoic acids and derivatives

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: Benzene and substituted derivatives
• Subclass: Benzoic acids and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Benzoic acid esters
• Alternative Parents: Aminobenzoic acids and derivatives Benzoyl derivatives Aniline and substituted anilines Carboxylic acid esters Amino acids and derivatives Monocarboxylic acids and derivatives Primary amines Organopnictogen compounds Organooxygen compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Aminobenzoic acid or derivatives - Benzoate ester - Benzoyl - Aniline or substituted anilines - Amino acid or derivatives - Carboxylic acid ester - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Amine - Organonitrogen compound - Organooxygen compound - Primary amine - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Aromatic homomonocyclic compound
• Description: This compound belongs to the class of organic compounds known as benzoic acid esters. These are ester derivatives of benzoic acid.
• External Descriptors: substituted aniline - benzoate ester

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

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CA2 Tclin Carbonic anhydrase II (17698 Activities)

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ESR1 Tclin Estrogen receptor alpha (17718 Activities)

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HMGCR Tclin HMG-CoA reductase (2475 Activities)

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ADRB1 Tclin Beta-1 adrenergic receptor (6630 Activities)

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Mécanismes d'action

Propriétés chimiques et physiques

• Solubilité: readily soluble in water
• Sensibilité: Moisture sensitive
• Rotation spécifique [α]: 93° (C=6,H2O)
• Poids moléculaire: 165.190 g/mol
• XLogP3: 1.900
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 165.079 Da
• Monoisotopic Mass: 165.079 Da
• Topological Polar Surface Area: 52.300 Ų
• Heavy Atom Count: 12
• Formal Charge: 0
• Complexity: 151.000
• 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