Ulinastatin
CAS No. 80449-31-6
Ulinastatin( Bikunin | Mingin | Miraclid | Trypsin inhibitor UTI | Urinary trypsin inhibitor 1 | Urinastatin )
Catalog No. M24803 CAS No. 80449-31-6
Ulinastatin is a multivalent Kunitz-type serine protease inhibitor with anti-inflammatory properties.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 10MG | 39 | In Stock |
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| 25MG | 82 | In Stock |
|
| 50MG | 127 | In Stock |
|
| 100MG | 207 | In Stock |
|
| 200MG | 306 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameUlinastatin
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NoteResearch use only, not for human use.
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Brief DescriptionUlinastatin is a multivalent Kunitz-type serine protease inhibitor with anti-inflammatory properties.
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DescriptionUlinastatin is a multivalent Kunitz-type serine protease inhibitor with anti-inflammatory properties.
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In VitroWestern Blot Analysis Cell Line:Human lung epithelial BEAS-2B cells Concentration:500 U, 2500 U, 5000 U Incubation Time:24 hours Result:Markedly attenuated TLR4 expression and NF-κB activation in LPS-stimulated BEAS-2B cells.
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In VivoAnimal Model:Male C57BL/6 mice (8-10 weeks old, 18-22 g)Dosage:10000 U/kg Administration:i.v.; twice (1 h before and 6 h after LPS treatment)Result:Significantly protected animals from LPS-induced ALI.
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SynonymsBikunin | Mingin | Miraclid | Trypsin inhibitor UTI | Urinary trypsin inhibitor 1 | Urinastatin
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PathwayOthers
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TargetOther Targets
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RecptorKunitz-type serine protease
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Research Area——
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Indication——
Chemical Information
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CAS Number80449-31-6
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Formula Weight——
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Molecular Formula——
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Purity>98% (HPLC)
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SolubilityIn Vitro:?H2O : 10 mg/mL
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SMILES——
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Chemical Name——
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.Nakahama H , Kuribayashi K , Sugita M , et al. Cytoprotective effect of ulinastatin, a Kunitz-type protease inhibitor, on hypoxic injury in L2 cells treated with antimycin A via stabilization of lysosomal fragility.[J]. Pulmonary Pharmacology & Therapeutics, 1999, 12(1):1-6.
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