Sodium (±)-10-Camphorsulfonate

CAS : 34850-66-3

Ref. 3D-JBA85066

Informations sur le produit

• Nom: Sodium (±)-10-Camphorsulfonate
• Synonymes: (7,7-Dimethyl-2-Oxo-Norbornan-1-Yl)Methylsulfonyloxysodium, 10-Camphorsulfonic acid sodium salt, Bicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, sodium salt, Bicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, sodium salt (1:1), Camphor Sulfonic Acid, Camphor-W-sulphonic acid sodium, P-camphor-10-sulfonic acid sodium salt, Sodium (7,7-Dimethyl-2-Oxobicyclo[2.2.1]Hept-1-Yl)Methanesulfonate, Sodium (±)-7,7-Dimethyl-2-Oxobicyclo[2,2,1]Heptane-1-Methanesulphonate, Sodium 2-Oxobornane-10-Sulphonate, Sodium <span class="text-smallcaps">D</smallcap><smallcap>L</span>-camphorsulfonate, Sodium Camphor Sulfonate, Sodium Camphorsulfonate, Sodium Camphorsulphonate, Sodium dl-10-camphorsulfonate, Sodium (+)-10-camphorsulfonate, Was 22, sodium [(1S,4S)-7,7-dimethyl-2-oxobicyclo[2.2.1]hept-1-yl]methanesulfonate
• CAS: 34850-66-3

Description

Sodium (±)-10-Camphorsulfonate is a drug that has been shown to be effective against a variety of bacteria including Pseudomonas aeruginosa, Staphylococcus aureus, and Escherichia coli. It inhibits the growth of bacteria by binding to the active site of bacterial DNA gyrase and topoisomerase IV enzyme. The reaction yield for this compound is high, with an average reaction time of 10 minutes under certain conditions. Sodium (±)-10-Camphorsulfonate has been shown to be more efficacious than gabexate in inhibiting the development of influenza virus in vitro. This drug also has anti-inflammatory properties, which may be due to its ability to inhibit prostaglandin synthesis.

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 254.28 g/mol
• Formule: C₁₀H₁₅NaO₄S
• Degré de pureté: Min. 95%