Paper

Tree Display

AceDB Schema

XML Display

Feedback

Paper Report for: Feng_2007_J.Med.Chem_50_2297

Reference

Title: Discovery of alogliptin: a potent, selective, bioavailable, and efficacious inhibitor of dipeptidyl peptidase IV
Feng J, Zhang Z, Wallace MB, Stafford JA, Kaldor SW, Kassel DB, Navre M, Shi L, Skene RJ and Gwaltney SL, 2nd <4 more author(s)>
Ref: Journal of Medicinal Chemistry, 50:2297, 2007 : PubMed

        



Related information

Gene_Locus| human-DPP4
Structure in RCSB-PDB | 2ONC
Structure in ESTHER | 2ONC
Inhibitor | Alogliptin,


Citations formats

Feng J, Zhang Z, Wallace MB, Stafford JA, Kaldor SW, Kassel DB, Navre M, Shi L, Skene RJ, Asakawa T, Takeuchi K, Xu R, Webb DR, Gwaltney SL, 2nd (2007)
Discovery of alogliptin: a potent, selective, bioavailable, and efficacious inhibitor of dipeptidyl peptidase IV
Journal of Medicinal Chemistry 50: 2297-300

Feng J, Zhang Z, Wallace MB, Stafford JA, Kaldor SW, Kassel DB, Navre M, Shi L, Skene RJ, Asakawa T, Takeuchi K, Xu R, Webb DR, Gwaltney SL, 2nd (2007)
Journal of Medicinal Chemistry 50: 2297-300



Send your questions or comments to :
Mail to: Nicolas Lenfant, Thierry Hotelier, Yves Bourne, Pascale Marchot and Arnaud Chatonnet.
Please cite: Lenfant 2013 Nucleic.Acids.Res. or Marchot Chatonnet 2012 Prot.Pept Lett.
For technical information about these pages see:
ESTHER Home Page and ACEDB Home Page
AcePerl Lincoln Stein Home Page
webmaster

Acknowledgements and disclaimer