| Literature DB >> 18556198 |
Sebastiaan Van Goethem1, Pieter Van der Veken, Véronique Dubois, Anna Soroka, Anne-Marie Lambeir, Xin Chen, Achiel Haemers, Simon Scharpé, Ingrid De Meester, Koen Augustyns.
Abstract
To obtain selective and potent inhibitors of dipeptidyl peptidases 8 and 9, we synthesized a series of substituted isoindolines as modified analogs of allo-Ile-isoindoline, the reference DPP8/9 inhibitor. The influence of phenyl substituents and different P2 residues on the inhibitors' affinity toward other DPPs and more specifically, their potential to discriminate between DPP8 and DPP9 will be discussed. Within this series compound 8j was shown to be a potent and selective inhibitor of DPP8/9 with low activity toward DPP II.Entities:
Mesh:
Substances:
Year: 2008 PMID: 18556198 DOI: 10.1016/j.bmcl.2008.05.079
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823