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[3] DPP-4 is a dipeptidase that selectively binds substrates that contain proline at the P1-position, thus many DPP-4 inhibitors have 5-membered heterocyclic rings that mimic proline, e } : CS1 maint: deprecated archival service (link) Current Topics in Medicinal Chemistry , 7 (6): 597608, doi:10.2174/156802607780090993, PMID 17352680 Current Topics in Medicinal Chemistry , 7 (6): 557568, doi:10.2174/156802607780091028, PMID 17352677 1 2 3 "Dipeptidyl Peptidase-IV Inhibitors: Pharmacological Profile and Clinical Use", Clinical Diabetes , 26 (2): 5357, doi:10.2337/diaclin.26.2.53, retrieved 29 July 2013 Bioorganic & Medicinal Chemistry Letters , 17 (20): 56385642, doi:10.1016/j.bmcl.2007.07.081, PMID 17822893 Bioorganic & Medicinal Chemistry Letters , 15 (21): 47704773, doi:10.1016/j.bmcl.2005.07.026, PMID 16115768 Current Topics in Medicinal Chemistry , 7 (6): 569578, doi:10.2174/156802607780091073, PMID 17352678 1 2 Diabetologia , 50 (1 Supp): S362S363, doi:10.1007/s00125-007-0809-7, PMID 17710465, ProQuest 213848837 (registration required) Journal of Medicinal Chemistry , 50 (10): 22972300, doi:10.1021/jm070104l, PMID 17441705 FDA Continues Review of Takeda's New Drug Application for Alogliptin (SYR-322), a DPP- 4 agent for Type 2 Diabetes , retrieved 29 July 2013
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Understanding where they fit helps make informed decisions
The current evidence is based on its known biological mechanisms and promising results from animal studies on nerve injury, inflammation, and tissue repair
