Sivelestat
CAS No. 127373-66-4
Sivelestat( EI-546 | LY-544349 | ONO-5046 )
Catalog No. M11143 CAS No. 127373-66-4
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
Size | Price / USD | Stock | Quantity |
5MG | 38 | In Stock |
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10MG | 55 | In Stock |
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25MG | 99 | In Stock |
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50MG | 189 | In Stock |
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100MG | 284 | In Stock |
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200MG | 471 | In Stock |
|
500MG | 753 | In Stock |
|
1G | Get Quote | In Stock |
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Biological Information
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Product NameSivelestat
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NoteResearch use only, not for human use.
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Brief DescriptionA potent, specific and competitive inhibitor of human neutrophil elastase with IC50 of 44 nM.
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DescriptionA 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.Other Indication Approved(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.
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In Vitro——
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In VivoAnimal 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.
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SynonymsEI-546 | LY-544349 | ONO-5046
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PathwayMetabolic Enzyme/Protease
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TargetElastase
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Recptorneutrophilelastase
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Research AreaOther Indications
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IndicationOther Disease
Chemical Information
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CAS Number127373-66-4
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Formula Weight434.4629
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Molecular FormulaC20H22N2O7S
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Purity>98% (HPLC)
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Solubility10 mM in DMSO
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SMILESCC(C)(C)C(=O)OC1=CC=C(C=C1)S(=O)(=O)NC2=CC=CC=C2C(=O)NCC(=O)O
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Chemical NamePropanoic acid, 2,2-dimethyl-, 4-[[[2-[[(carboxymethyl)amino]carbonyl]phenyl]amino]sulfonyl]phenyl ester
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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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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