Home Cart Sign in  
Chemical Structure| 127373-66-4 Chemical Structure| 127373-66-4

Structure of Sivelestat
CAS No.: 127373-66-4

Chemical Structure| 127373-66-4

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

Sivelestat is a competitive inhibitor of human neutrophil elastase(IC50 = 44 nM and Ki=200 nM) and also inhibits leukocyte elastase obtained from rabbit, rat, hamster and mouse.

Synonyms: ONO5046; LY544349; EI546

4.5 *For Research Use Only !

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

US Stock

Global Stock

In Stock
{[ item.pr_size ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

  • {[ item.pr_size ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of Sivelestat

CAS No. :127373-66-4
Formula : C20H22N2O7S
M.W : 434.46
SMILES Code : O=C(O)CNC(C1=CC=CC=C1NS(=O)(C2=CC=C(OC(C(C)(C)C)=O)C=C2)=O)=O
Synonyms :
ONO5046; LY544349; EI546
MDL No. :MFCD00889071
InChI Key :BTGNGJJLZOIYID-UHFFFAOYSA-N
Pubchem ID :107706

Safety of Sivelestat

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Isoform Comparison

Biological Activity

In Vitro:

Cell Line
Concentration Treated Time Description References
Human umbilical vein endothelial cells (HUVECs) 20 μM 12 hours Sivelestat reversed NET-induced endothelial damage and inflammatory responses. PMC7075277
Mouse peritoneal exudate cells (PECs) macrophages 0.5 µg/mL 16 hours To evaluate the effect of NE on the expression of inflammatory cytokines and CXC chemokines. Results showed that the expression of all examined genes was significantly increased in NE-treated macrophages. PMC10177873
Rat intestinal epithelial cells 100 μM 24 hours To investigate the effect of Sivelestat on ZO-1 expression, results showed Sivelestat attenuated NE-induced ZO-1 reduction PMC9014170
Human neutrophils 10 μM 4 hours Sivelestat significantly inhibited the release of extracellular DNA and neutrophil elastase from PMA-activated neutrophils, indicating effective inhibition of NET formation. PMC7075277
Primary CD34+ MDS cells 300 µg/ml 72 hours Inhibited HMGB1 protein expression, reduced cell expansion and colony-forming capacity PMC6800136
MDS-L cells 300 µg/ml 72 hours Inhibited HMGB1 protein expression, reduced cell expansion and colony-forming capacity PMC6800136

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
Mice Liver ischemia-reperfusion injury model Intravenous injection 0.2 mg/kg per hour From anesthesia induction to postoperative day 1 Sivelestat mitigated liver ischemia-reperfusion injury by inhibiting neutrophil elastase activity, evidenced by reduced serum ALT and AST levels PMC10036740
Sprague-Dawley rats Acute lung injury model induced by fat embolism Lung perfusate 10 μg/g lung weight Single administration, observed for 3 hours Sivelestat significantly attenuated the acute lung injury caused by fat embolism, including the increases in lung weight/body weight ratio, lung weight gain, exhaled NO, protein concentration in bronchoalveolar lavage fluid, pulmonary arterial pressure, and microvascular permeability. Additionally, Sivelestat reduced the activities of neutrophil elastase, myeloperoxidase, malondialdehyde, and phospholipase A2, and decreased the levels of nitrate/nitrite, methyl guanidine, tumor necrosis factor α, and interleukin-1β. PMC3265425
Sprague-Dawley rats Hindlimb ischemia-reperfusion injury model Intravenous injection or intramuscular injection 15 or 60 mg/kg bw/d Once daily for 7 days Sivelestat at 15 mg/kg bw/d improved hindlimb perfusion, promoted angiogenesis, reduced muscle fibrosis, and enhanced motor function by eliminating NETs; while local injection at 60 mg/kg bw/d had adverse effects on tissue repair PMC9961174
Mice Acute liver failure model Intraperitoneal injection 150 mg/kg Single dose, 24 hours before ALF induction Sivelestat pretreatment significantly attenuated D-GalN/LPS-induced liver necrosis and hepatocellular damage, reduced serum ALT and AST levels, and decreased neutrophil infiltration in the liver. PMC9307949
Mice AAT-KO mouse model Intraperitoneal injection 2 mg/mouse twice daily Twice daily, until day 1 postinfection Sivelestat significantly reduced bacterial loads in AAT-KO mice after S. pneumoniae infection and protected alveolar collectin SP-D from NE-dependent degradation. PMC7934856
BALB/c mice APAP-induced acute liver injury model Intraperitoneal injection 200 mg/kg Single dose at 30 min, 3 h, or 5 h after APAP challenge To evaluate the protective effect of Sivelestat on APAP-induced acute liver injury. Results showed that Sivelestat treatment significantly improved survival, reduced serum transaminase elevation and hepatic necrosis, and decreased intrahepatic neutrophil infiltration and NOS-II expression. PMC10177873
C57BL/6 mice Partial inferior vena cava ligation (pIVCL) model Subcutaneous injection 30 mg/kg Three times a week for six weeks To investigate the effect of Sivelestat on pIVCL-induced portal hypertension, results showed that Sivelestat reduced portal pressure and fibrin formation. PMC6581607
NSG mice MDS-L cell transplantation model Intraperitoneal injection 5 mg/kg Once daily for 7 days Reduced MDS-L cell engraftment in the bone marrow, inhibited MDS cell expansion PMC6800136
BALB/c mice LPS-induced endotoxic shock model Intraperitoneal injection 50 mg/kg Single dose, observed for 18 hours Nanoparticle-mediated delivery of sivelestat effectively inhibited NET formation, decreased the clinical signs of lung injury, reduced NE and other proinflammatory cytokines in serum, and rescued animals against endotoxic shock. PMC7075277
Mice FFD-induced MASH model Intraperitoneal injection 50 mg/kg Three times a week, for 6 weeks Sivelestat significantly reduced the MoKC proportion, liver steatosis, inflammation and fibrosis in mice PMC11873038
C57BL/6J mice Renal ischemia-reperfusion injury model Intravenous injection 50 mg/kg Single dose Pretreatment with sivelestat significantly reduced renal Neutrophil elastase (NE), serum creatinine, and blood urea nitrogen levels after renal ischemia-reperfusion. Sivelestat also reduced histological damage and cell apoptosis in kidneys following ischemia-reperfusion injury (IRI). Additionally, sivelestat administration decreased the mRNA expression levels of interleukin 6 (IL-6), Macrophage inflammatory protein-2 (MIP-2), monocyte chemoattractant protein-1 (MCP-1), and tumor necrosis factor (TNF)-α in the kidneys during IRI. The kidney tissues of the SI group showed significantly reduced TLR4, Myd88, and NF-κB p-p65 protein expression levels compared to the I group (all P<0.05). PMC11466837
Sprague-Dawley (SD) rats Cecal ligation and puncture (CLP)-induced sepsis model Intraperitoneal injection 50 mg/kg Single dose, observed for 24 hours To evaluate the effects of Sivelestat on survival rate, gut microbiome, and metabolite profiles in septic rats. Results showed that Sivelestat significantly improved the survival rate of septic rats (80% vs 50%) and ameliorated gut microbiota composition and metabolite profiles. PMC8965314
ApoE-/- mice High-fat high-cholesterol diet-induced atherosclerosis model Intraperitoneal injection 50 mg/kg/day Once daily for 8 weeks To investigate the effect of Sivelestat on atherosclerosis, results showed Sivelestat attenuated atherosclerotic phenotypes, including decreasing toxic lipid accumulation, vascular monocyte infiltration, and inflammatory cytokines PMC9014170
Sprague-Dawley rats Cecal ligation and puncture (CLP)-induced sepsis model Intraperitoneal injection 50 or 100 mg/kg Immediately after surgery, observed up to 108 hours To evaluate the protective effects of Sivelestat on sepsis-related acute kidney injury. Results showed that Sivelestat improved the survival rate of septic rats, restored mean arterial pressure and glomerular filtration rate, inhibited the increase in serum blood urea nitrogen and neutrophil gelatinase-associated lipocalin levels, and reduced the production of inflammatory mediators and macrophage infiltration. PMC4990314

Clinical Trial:

NCT Number Conditions Phases Recruitment Completion Date Locations
NCT00036062 Respiratory Distress Syndrome,... More >> Adult|Acute Lung Injury Less << PHASE1|PHASE2 COMPLETED 2025-12-02 Birmingham, Alabama, United St... More >>ates|Phoenix, Arizona, United States|Tucson, Arizona, United States|Orange, California, United States|Sacramento, California, United States|San Diego, California, United States|Denver, Colorado, United States|Englewood, Colorado, United States|New Haven, Connecticut, United States|Washington, District of Columbia, United States|Bay Pines, Florida, United States|Clearwater, Florida, United States|Ft. Lauderdale, Florida, United States|Augusta, Georgia, United States|Austell, Georgia, United States|Chicago, Illinois, United States|Elk Grove Village, Illinois, United States|Maywood, Illinois, United States|North Chicago, Illinois, United States|Indianapolis, Indiana, United States|Des Moines, Iowa, United States|Kansas City, Kansas, United States|Lexington, Kentucky, United States|Louisville, Kentucky, United States|Baton Rouge, Louisiana, United States|Lake Charles, Louisiana, United States|Shreveport, Louisiana, United States|Portland, Maine, United States|Baltimore, Maryland, United States|Silver Spring, Maryland, United States|Towson, Maryland, United States|Boston, Massachusetts, United States|Detroit, Michigan, United States|Kalamazoo, Michigan, United States|St. Louis, Missouri, United States|Camden, New Jersey, United States|Hackensack, New Jersey, United States|Holmdel, New Jersey, United States|Bronx, New York, United States|Buffalo, New York, United States|Elmhurst, New York, United States|Manhasset, New York, United States|Mineola, New York, United States|New York, New York, United States|Rochester, New York, United States|Greensboro, North Carolina, United States|Winston-Salem, North Carolina, United States|Akron, Ohio, United States|Cincinnati, Ohio, United States|Toledo, Ohio, United States|Portland, Oregon, United States|Allentown, Pennsylvania, United States|Hershey, Pennsylvania, United States|Philadelphia, Pennsylvania, United States|Pittsburgh, Pennsylvania, United States|Providence, Rhode Island, United States|Sioux Falls, South Dakota, United States|Memphis, Tennessee, United States|Nashville, Tennessee, United States|Houston, Texas, United States|Irving, Texas, United States|Lubbock, Texas, United States|San Antonio, Texas, United States|Newport News, Virginia, United States|Morgantown, West Virginia, United States|Garran, Australian Capital Territory, Australia|Camperdown, New South Wales, Australia|Kingswood, New South Wales, Australia|Kogarah, New South Wales, Australia|St. Leonards, New South Wales, Australia|Wentworthville, New South Wales, Australia|SouthPort, Queensland, Australia|Adelaide, South Australia, Australia|Bedford Park, South Australia, Australia|Woodville, South Australia, Australia|Heidelberg, Victoria, Australia|Parkville, Victoria, Australia|Prahran, Victoria, Australia|Fremantle, Western Australia, Australia|Perth, Western Australia, Australia|Aaist, Belgium|Antwerpen, Belgium|Arion, Belgium|Braine L' Alleud, Belgium|Brugge, Belgium|Brussels, Belgium|Gent, Belgium|Liege, Belgium|Edmonton, Alberta, Canada|Vancouver, British Columbia, Canada|Winnipeg, Manitoba, Canada|Halifax, Nova Scotia, Canada|Hamilton, Ontario, Canada|Toronto, Ontario, Canada|Windsor, Ontario, Canada|Montreal, Quebec, Canada|Sherbrooke, Quebec, Canada|Christchurch, Canterbury, New Zealand|Auckland, New Zealand|Hastings, New Zealand|Wellington, New Zealand|Manresa, Barcelona, Spain|Sabadell, Barcelona, Spain|Getafe, Madrid, Spain|El Palmar, Murcia, Spain|Badajoz, Spain|Barcelona, Spain|Madrid, Spain|Murcia, Spain|Palma De Mallorca, Spain Less <<

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.30mL

0.46mL

0.23mL

11.51mL

2.30mL

1.15mL

23.02mL

4.60mL

2.30mL

Dissolving Methods
Please choose the appropriate dissolution scheme according to your animal administration guide.For the following dissolution schemes, clear stock solution should be prepared according to in vitro experiments, and then cosolvent should be added in turn:

in order to ensure the reliability of the experimental results, the clarified stock solution can be properly preserved according to the storage conditions; The working fluid for in vivo experiment is recommended to be prepared now and used on the same day;

The percentage shown in front of the following solvent refers to the volume ratio of the solvent in the final solution; If precipitation or precipitation occurs in the preparation process, it can be assisted by heating and/or ultrasound.
Protocol 1
Protocol 2

References

 

Historical Records

Categories