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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This product is a controlled substance and not for sale in your territory.

This product is not for sale in your territory.

This compound is listed in the SVHC (Substances of Very High Concern) candidate list of ECHA (European Chemicals Agency).

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References