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Sivelestat sodium

HCID 66739009
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Grundinformationen

CAS
201677-61-4
Standard-SMILES
CC(C)(C)C(=O)Oc1ccc(S(=O)(=O)Nc2ccccc2C(=O)NCC(=O)O)cc1.O.[Na]
Summenformel
C20H25N2NaO8S
Durchschnittliche Molmasse
476,48 g/mol

Namen und Bezeichner

Bevorzugter Name
Sivelestat sodium
Englischer Name
Sivelestat sodium
Summenformel
C20H25N2NaO8S
Molmasse
476.48

Namen und Synonyme

SIVELESTAT SODIUM TETRAHYDRATESIVELESTAT SODIUM HYDRATEElaspolSvelestat sodiumSivelestat sodiumSivelestat(anhydrous)EI546 sodium tetrahydrateONO5046 sodium tetrahydrateSiverus sodium tetrahydrateSivelestat sodium Impurity A

Datenbank-Bezeichner

CAS
201677-61-4
PubChem CID
66739009

Eigenschaften

Physikochemische Eigenschaften

storage temp.
Sealed in dry,Room Temperature
Löslichkeit
Soluble in DMSO (up to 20 mg/ml).
Aggregatzustand
White solid.
Farbe
White
Stabilität
1 year · Stable for 1 year from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 2 months
InChIKey
YMOIFFHCERRYCO-UHFFFAOYSA-N
SMILES
C(C1C=CC=CC=1NS(C1C=CC(OC(=O)C(C)(C)C)=CC=1)(=O)=O)(=O)NCC(=O)O.[NaH].O
CAS Datenbank
201677 · 201677-61-4(CAS DataBase Reference)

Sicherheit und Regulatorisches

Sicherheitsangaben dienen nur zur Orientierung und ersetzen weder das Sicherheitsdatenblatt (SDB) des Lieferanten noch geltende Vorschriften oder eine fachliche Bewertung.

Sicherheitsdaten

hs_code
2935909099

Chemie und Industrie

Anwendungen · 2 Einträge

BeschreibungSivelestat is an acyl enzyme inhibitor of neutrophil elastase, developed as an injectable formulation for the treatment of acute lung injury associated with systemic inflammatory response syndrome. A neutrophil predominant inflammation associated with excessive release of human neutrophil elastase (HNE) from azurophilic granules is capable of damaging both the lung parenchymal cells and the extracellular matrix allowing an alveolar capillary barrier disruption. Sivelestat is a sulfonanilide-containing pivaloyloxy benzene derivative prepared in a three step synthesis. This agent acts as a reversible and selective inhibitor of HNE with an lG.0 value of 0.044 PM. Sivelestat has exhibited potent protective effects against various causes of lung injuries in animal models. In an acid-induced acute lung injury model in conscious hamster, administration of sivelestat for 48 h following HCI instillation, dose-dependently reduced mortality and significantly improved the protein levels in bronchoalveolar lavage fluids and pulmonary artery pressure. In a similar study, the agent inhibited the endotoxin-induced acute lung dysfunctions (marked elevation of pulmonary vascular permeability, leukocyte migration, hemorrhage and parenchymal injury) in different animal species. Moreover, in a cardiopulmonary bypass model in dog, sivelestat ameliorated the respiratory index and interstitial-intra-alveolar edema. Sivelestat has a relatively poor bioavailability, due to an extensive first-pass metabolism and is easily hydrolyzed in vitro to an inactive metabolite. In two animal species, the half-life time was approximately 5-7 min. Clinical trials have shown that treatment with the agent improves respiratory function and facilitates early removal of patients from mechanical ventilation. However, in the last clinical study, conducted by Eli Lilly in patients with acute lung injury, no difference in mortality and safety was seen between sivelestat and placebo.

VerwendenTreatment of acute lung injury; acute respiratory distress syndrome (elastase inhibitor).

Anbieter100 Anbieter

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