| Literature DB >> 12238937 |
Erik A A Wallén1, Johannes A M Christiaans, Markus M Forsberg, Jarkko I Venäläinen, Pekka T Männistö, Jukka Gynther.
Abstract
New dicarboxylic acid bis(L-prolyl-pyrrolidine) amides were synthesized, and their inhibitory activity against prolyl oligopeptidase from pig brain was tested in vitro. As compared with earlier described prolyl oligopeptidase inhibitors, these new compounds have in common an L-prolyl-pyrrolidine moiety, but the typical lipophilic acyl end group is replaced by another L-prolyl-pyrrolidine moiety connected symmetrically with a short dicarboxylic acid linker. These compounds are a new type of peptidomimetic prolyl oligopeptidase inhibitor.Entities:
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Year: 2002 PMID: 12238937 DOI: 10.1021/jm020966g
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446