Sivelestat sodium

CAS No. 150374-95-1

Sivelestat sodium( EI-546 | LY-544349 | ONO-5046 )

Catalog No. M12093 CAS No. 150374-95-1

A potent, specific and competitive inhibitor of human neutrophil elastase with IC50 of 44 nM.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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Biological Information

  • Product Name
    Sivelestat sodium
  • Note
    Research use only, not for human use.
  • Brief Description
    A potent, specific and competitive inhibitor of human neutrophil elastase with IC50 of 44 nM.
  • Description
    A potent, specific and competitive inhibitor of human neutrophil elastase with IC50 of 44 nM; also inhibits leukocyte elastase obtained from rabbit, rat, hamster and mouse, do not inhibit trypsin, thrombin, plasmin, plasma kallikrein, pancreas kallikrein, chymotrypsin and cathepsin G (>10 uM); attenuates LPS-induced acute lung inflammation in the hamster.
  • In Vitro
    Sivelestat (ONO-5046) does not inhibit trypsin, thrombin, plasmin, plasma kallikrein, pancreas kallikrein, chymotrypsin and cathepsin G even at 100 μM.Sivelestat (ONO-5046) exhibits IC50 values of 44 nM, 36 nM, 19 nM, 37 nM and 49 nM for human, rabbit, rat, hamster and mouse neutrophil elastase, respectively.
  • In Vivo
    Sivelestat (ONO-5046, 0.021-2.1 mg/kg, intratracheally) suppresses lung hemorrhage in hamster (ID50 = 82 pg/kg) by intratracheal administration and increase of skin capillary permeability in guinea pig (ID50 = 9.6 mg/kg) by intravenous administration, both of which are induced by human neutrophil elastase.Sivelestat (10 mg/kg, infusion via the tail vein) ameliorates lung injury after hemorrhagic shock in rats.Sivelestat (15, 60 mg/kg, ip) prevents ischemia–reperfusion injury in the rat bladder. Animal Model:Male Golden hamsters, weighing 90 to 110 g.Dosage:0.021-2.1 mg/kg.Administration:Intratracheally five min before HNE injection.Result:Significantly and dosedependently suppressed the lung hemorrhage.Animal Model:Male Sprague-Dawley rats weighing 350-400 g.Dosage:10 mg/kg.Administration:Continuous infusion via the tail vein at 10 mg/kg/h for 60 min during the resuscitation phase.Result:Greatly suppressed lung injury, as revealed by the reduced histological damage.Significantly ameliorated HSR-induced lung injury.Markedly decreased the levels of TNF-α and iNOS gene.Animal Model:Male Sprague Dawley rats, 8 weeks old and weighing 250-320 g.Dosage:15 mg/kg or 60 mg/kg.Administration:IP.Result:Decreased the blood flow in the bladder during reperfusion phase compared to the IR group.
  • Synonyms
    EI-546 | LY-544349 | ONO-5046
  • Pathway
    Metabolic Enzyme/Protease
  • Target
    Elastase
  • Recptor
    Elastase
  • Research Area
    Other Indications
  • Indication
    Other Disease

Chemical Information

  • CAS Number
    150374-95-1
  • Formula Weight
    456.4447
  • Molecular Formula
    C20H21N2NaO7S
  • Purity
    >98% (HPLC)
  • Solubility
    10 mM in DMSO
  • SMILES
    CC(C)(C)C(=O)OC1=CC=C(C=C1)S(=O)(=O)NC2=CC=CC=C2C(=O)NCC(=O)[O-].[Na+]
  • Chemical Name
    Propanoic acid, 2,2-dimethyl-, 4-[[[2-[[(carboxymethyl)amino]carbonyl]phenyl]amino]sulfonyl]phenyl ester, sodium salt (1:1)

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Kawabata K, et al. Biochem Biophys Res Commun. 1991 Jun 14;177(2):814-20. 2. Yasui S, et al. Eur Respir J. 1995 Aug;8(8):1293-9. 3. Sakamaki F, et al. Am J Respir Crit Care Med. 1996 Jan;153(1):391-7.
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