Discovery of beta-aminoacyl containing thiazolidine derivatives as potent and selective dipeptidyl peptidase IV inhibitors

Cited 14 time in webofscience Cited 0 time in scopus
  • Hit : 551
  • Download : 1
A series of beta-aminoacyl containing thiazolidine derivatives was synthesized and evaluated for their ability to inhibit DPP-IV. Several thiazolidine derivatives with an acid moiety were found to be potent DPP-IV inhibitors. Among them, compound 2da is the most active in this series with an IC(50) value of 1 nM, and it showed excellent selectivity over DPP-IV related enzymes including DPP-2, DPP-8, and DPP-9. Compound 2da is chemically and metabolically stable, and showed no CYP inhibition, hERG binding or cytotoxicity. Compound 2db, an ester prodrug of 2da, showed good in vivo DPP-IV inhibition after oral administration in rat and dog models. (C) 2011 Elsevier Ltd. All rights reserved.
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Issue Date
2011-03
Language
English
Article Type
Article
Keywords

GLUCAGON-LIKE PEPTIDE-1; BIOLOGICAL EVALUATION; GLUCOSE-TOLERANCE; DESIGN

Citation

BIOORGANIC MEDICINAL CHEMISTRY LETTERS, v.21, no.5, pp.1366 - 1370

ISSN
0960-894X
DOI
10.1016/j.bmcl.2011.01.041
URI
http://hdl.handle.net/10203/94911
Appears in Collection
CH-Journal Papers(저널논문)
Files in This Item
This item is cited by other documents in WoS
⊙ Detail Information in WoSⓡ Click to see webofscience_button
⊙ Cited 14 items in WoS Click to see citing articles in records_button

qr_code

  • mendeley

    citeulike


rss_1.0 rss_2.0 atom_1.0