Literature DB >> 22853995

4-Substituted boro-proline dipeptides: synthesis, characterization, and dipeptidyl peptidase IV, 8, and 9 activities.

Wengen Wu1, Yuxin Liu, Lawrence J Milo, Ying Shu, Peng Zhao, Youhua Li, Iwona Woznica, Gengli Yu, David G Sanford, Yuhong Zhou, Sarah E Poplawski, Beth A Connolly, James L Sudmeier, William W Bachovchin, Jack H Lai.   

Abstract

The boroProline-based dipeptidyl boronic acids were among the first DPP-IV inhibitors identified, and remain the most potent known. We introduced various substitutions at the 4-position of the boroProline ring regioselectively and stereoselectively, and incorporated these aminoboronic acids into a series of 4-substituted boroPro-based dipeptides. Among these dipeptidyl boronic acids, Arg-(4S)-boroHyp (4q) was the most potent inhibitor of DPP-IV, DPP8 and DPP9, while (4S)-Hyp-(4R)-boroHyp (4o) exhibited the most selectivity for DPP-IV over DPP8 and DPP9.
Copyright © 2012 Elsevier Ltd. All rights reserved.

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Year:  2012        PMID: 22853995     DOI: 10.1016/j.bmcl.2012.07.033

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  1 in total

1.  Targeted inactivation of dipeptidyl peptidase 9 enzymatic activity causes mouse neonate lethality.

Authors:  Margaret G Gall; Yiqian Chen; Ana Julia Vieira de Ribeiro; Hui Zhang; Charles G Bailey; Derek S Spielman; Denise M T Yu; Mark D Gorrell
Journal:  PLoS One       Date:  2013-11-06       Impact factor: 3.240

  1 in total

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