108708-25-4

Z-Pro-Pro-CHO Chemical Structure
108708-25-4

Chemical Structure

Z-Pro-Pro-CHO

  • CAS No.: 108708-25-4
  • Formula:C18H22N2O4
  • Molecular Weight:330.38

IUPAC Name: benzyl 2-(2-formylpyrrolidine-1-carbonyl)pyrrolidine-1-carboxylate

InChIKey: ORZXYSPOAVJYRU-UHFFFAOYSA-N

SMILES: O=C(N1C(C(N2C(C=O)CCC2)=O)CCC1)OCC3=CC=CC=C3

Biological Activity: Z-Pro-Pro-CHO is a potent inhibitor of prolyl oligopeptidase (POP), with extremely high affinity for human prolyl oligopeptidase (HsPOP) (IC50=0.012 μM), and it also effectively inhibits the activity of Schistosoma mansoni prolyl oligopeptidase (SmPOP) (IC50=0.16 μM). Z-Pro-Pro-CHO does not block the phosphorylation of ERK or the production of TNF-α or IFN-γ in immune cells from presensitized mice, nor does it induce harmful phenotypes in cultured Schistosoma mansoni schistosomula. Z-Pro-Pro-CHO only partially inhibits epithelial cell wound healing at extremely high concentrations. Z-Pro-Pro-CHO finds wide application in studies related to schistosomiasis[1][2][3].

Cat. No. Product Name Purity Description Pricing
HY-134454
Z-Pro-Pro-CHO 98.03% Z-Pro-Pro-CHO is a potent inhibitor of prolyl oligopeptidase (POP), with extremely high affinity for human prolyl oligopeptidase (HsPOP) (IC50=0.012 μM), and it also effectively inhibits the activity of Schistosoma mansoni prolyl oligopeptidase (SmPOP) (IC50=0.16 μM). Z-Pro-Pro-CHO does not block the phosphorylation of ERK or the production of TNF-α or IFN-γ in immune cells from presensitized mice, nor does it induce harmful phenotypes in cultured Schistosoma mansoni schistosomula. Z-Pro-Pro-CHO only partially inhibits epithelial cell wound healing at extremely high concentrations. Z-Pro-Pro-CHO finds wide application in studies related to schistosomiasis.
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