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Elastase

Elastase is a serine protease that catalyzes not only the hydrolysis of peptide bonds of proteins but also the hydrolysis of amides and esters. Although it has similar functions as trypsin and chymotrypsin, elastase preferentially targets the protein elastin catalyzing cleavage at its neutral sites. Two major types of elastase have been identified, including pancreatic elastase and neutrophil elastase (PMN). While he pancreatic elastase is produced initially as an inactive protein requiring the activation by trypsin in the duodenum; PMN is found in relatively high levels in the azurophilic granules of circulating leukocytes and neutrophils. Both types of elastase exhibit similar activities but differ in substrate specificity and inhibitor profile.

Products for  Elastase

  1. Cat.No. Product Name Information
  2. GC11847 (Z-Ala-Ala-Ala-Ala)2Rh110 fluorogenic elastase substrate (Z-Ala-Ala-Ala-Ala)2Rh110  Chemical Structure
  3. GC32016 AE-3763 AE-3763 is a peptide-based human neutrophil elastase inhibitor with an IC50 of 29 nM. AE-3763  Chemical Structure
  4. GC14785 Alvelestat NE inhibitor Alvelestat  Chemical Structure
  5. GC13487 ARP 100 A selective inhibitor of MMP-2 ARP 100  Chemical Structure
  6. GC12088 BAY-678 HNE inhibitor BAY-678  Chemical Structure
  7. GC35476 BAY-678 racemate BAY-678 racemate is a racemate of BAY-678. BAY-678 racemate  Chemical Structure
  8. GC31564 BAY-85-8501 BAY-85-8501 is a selective, reversible and potent inhibitor of Human Neutrophil Elastase (HNE), with an IC50 of 65 pM. BAY-85-8501  Chemical Structure
  9. GC35884 DMP 777 DMP 777 is a potent, selective, and orally active human leukocyte elastase (HLE) inhibitor. DMP 777  Chemical Structure
  10. GC61744 FK706 FK706 is a potent, slow-binding and competitive inhibitor of human neutrophil elastase with an IC50 of 83 nM and a Ki of 4.2 nM. FK706  Chemical Structure
  11. GC60858 Freselestat quarterhydrate Freselestat quarterhydrate (ONO-6818 quarterhydrate) is a potent and orally active neutrophil elastase inhibitor with a Ki of 12.2 nM. Freselestat quarterhydrate  Chemical Structure
  12. GC11615 GW311616 inhibitor of human neutrophil elastase(HNE) GW311616  Chemical Structure
  13. GC13851 GW311616 hydrochloride

    HNE inhibitor

    GW311616 hydrochloride  Chemical Structure
  14. GC31494 Lodelaben (SC-39026) Lodelaben (SC-39026) is a human neutrophil elastase inhibitor with an IC50 and Ki of 0.5 and 1.5 μM, respectively. Lodelaben (SC-39026)  Chemical Structure
  15. GC11981 Neutrophil Elastase Inhibitor

    neutrophil elastase inhibitor

    Neutrophil Elastase Inhibitor  Chemical Structure
  16. GC50225 ONO 6818 ONO 6818 (ONO-6818) is a potent and orally active neutrophil elastase inhibitor with a Ki of 12.2 nM. ONO 6818  Chemical Structure
  17. GC37618 Secologanoside Secologanoside is a triterpenoid isolated from Poraqueiba sericea, weakly inhibits elastase with an IC50 of 164 μg/mL. Secologanoside  Chemical Structure
  18. GC16724 Sivelestat (ONO-5046) Sivelestat (ONO-5046) (EI546) is a competitive inhibitor of human neutrophil elastase, with an IC50 of 44 nM and a Ki of 200 nM. Sivelestat (ONO-5046) (EI546) has the potential for the study of acute lung injury/acute respiratory distress syndrome or disseminated intravascular coagulation in COVID-19. Sivelestat (ONO-5046)  Chemical Structure
  19. GC17247 Sivelestat sodium salt An inhibitor of neutrophil elastase Sivelestat sodium salt  Chemical Structure
  20. GC10672 SSR 69071 A potent inhibitor of neutrophil elastase SSR 69071  Chemical Structure
  21. GC32628 ZD-0892 ZD-0892 is a selective and potent inhibitor of a neutrophil elastase with Kis of 6.7 and 200 nM for human neutrophil elastase and porcine pancreatic elastase, respectively. ZD-0892  Chemical Structure
  22. GC32005 ZD8321 ZD8321 is a potent inhibitor of human Neutrophil elastase (NE) with a Ki of 13±1.7 nM. ZD8321  Chemical Structure

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