122624-57-1Relevant articles and documents
Phosphinic peptide matrix metalloproteinase-9 inhibitors by solid-phase synthesis using a building block approach
Buchardt, Jens,Ferreras, Mercedes,Krog-Jensen, Christian,Delaisse, Jean-Marie,Foged, Niels Taekker,Meldal, Morten
, p. 2877 - 2884 (1999)
The solid-phase synthesis of an array of different pseudopeptides containing a phosphinic glycine-leucine moiety (-GΨ{P(O)OH-CH2}L-)[1] is described. The resulting pseudopeptides were shown to act as matrix metalloproteinase-9 (MMP-9
Synthesis of phosphorus isosters of β-amyloid peptides fragments
Dmitriev,Ragulin
, p. 2091 - 2098 (2015/11/02)
We have developed a synthetic route to pseudo dipeptides, analogs of certain fragments of β-amyloid peptides (products of the APP protein hydrolysis). These compounds can be used for preparation of phosphinic acidic oligopeptides representing the peptide sequence of the β-amyloid but containing the phosphorus isoster peptide fragment. Synthesis of pseudo ornityl-glutamate, pseudo arginyl-glutamate, pseudo glycyl-leucine, and pseudo isoleucyl-glycine via amino- and amidoalkylation of phosphonic acids containing the structural isoster of the corresponding amino acid is described.