896459-74-8Relevant academic research and scientific papers
Synthesis and SAR of azolopyrimidines as potent and selective dipeptidyl peptidase-4 (DPP4) inhibitors for type 2 diabetes
Brigance, Robert P.,Meng, Wei,Fura, Aberra,Harrity, Thomas,Wang, Aiying,Zahler, Robert,Kirby, Mark S.,Hamann, Lawrence G.
body text, p. 4395 - 4398 (2010/09/18)
Several pyrazolo-, triazolo-, and imidazolopyrimidines were synthesized and evaluated as inhibitors of DPP4. Of these three classes of compounds, the imidazolopyrimidines displayed the greatest potency and demonstrated excellent selectivity over the other
Dihydropyrazolopyrimidine Inhibitors of KV1.5 (IKur)
Vaccaro, Wayne,Huynh, Tram,Lloyd, John,Atwal, Karnail,Finlay, Heather J.,Levesque, Paul,Conder, Mary Lee,Jenkins-West, Tonya,Shi, Hong,Sun, Lucy
experimental part, p. 6381 - 6385 (2009/09/06)
A series of dihydropyrazolopyrimidine inhibitors of KV1.5 (IKur) have been identified. The synthesis, structure-activity relationships and selectivity against several other ion channels are described.
