129229-82-9Relevant academic research and scientific papers
Specific and irreversible cyclopeptide inhibitors of dipeptidyl peptidase IV activity of the T-cell activation antigen CD26
Nguyen, Coralie,Blan, Julià,Mazaleyrat, Jean-Paul,Krust, Bernard,Callebaut, Christian,Jacotot, Etienne,Hovanessian, Ara G.,Wakselman, Michel
, p. 2100 - 2110 (2007/10/03)
The dipeptidyl peptidase IV (DPP IV) activity of CD26 is Characterized by its post-prolinecleaving capacity that plays an important but not yet understood role in biological processes. Here we describe a new family of specific and irreversible inhibitors
Cyclic peptides as selective substrates and suicide substrate precursors of trypsin-like proteinases
Bogetto, Nicole,Vilain, Anne-Cecile,Montagne, Jean-Jacques,Reboud-Ravaux, Michele,Mazaleyrat, Jean-Paul,et al.
, p. 152 - 166 (2007/10/02)
Cyclopeptides of general formula c1-aB(CH2X)-Gly4>, in which P1 is arginine or lysine and aB(CH2X) an ortho- or meta-aminobenzoic acid residue substituted in the para position to the nitrogen atom by a methyl (X=H), a phenoxymethyl
Inhibitors of HIV-1 proteinase. Substrate analogues containing substituted aminobenzoic acids as proline mimics
Xie, J.,Mazaleyrat, J. P.,Savrda, J.,Wakselman, M.
, p. 642 - 654 (2007/10/02)
A series of linear peptides that are simplified analogues of the sequence around the p17-p24 cleavage site of the Pr55gag human immunodeficiency virus polyprotein, were prepared by solution peptide synthesis, as potential inhibitors
Cyclopeptidic inactivators for chymotrypsin-like proteinases
Wakselman,Mazaleyrat,Xie,Montagne,Vilain,Reboud-Ravaux
, p. 699 - 707 (2007/10/02)
Cyclopeptides containing a functionalized meta-aminobenzoic acid residue (m-aB[CH2X] with X = OC6H5, OAc, Br, Cl) linked to a tetraglycyl-phenylalanyl sequence, have been synthesized in solution. A phenyl ether group has b
