Author/Authors :
Hiroshi Fukushima، نويسنده , , Akira Hiratate، نويسنده , , Masato Takahashi، نويسنده , , Ayako Mikami، نويسنده , , Masako Saito-Hori، نويسنده , , Eiji Munetomo، نويسنده , , Kiyokazu Kitano، نويسنده , , Sumi Chonan، نويسنده , , Hidetaka Saito، نويسنده , , Akio Suzuki، نويسنده , , Yuji Takaoka، نويسنده , , Koji Yamamoto، نويسنده ,
Abstract :
Dipeptidyl peptidase IV (DPP-IV) inhibitors are promising antidiabetic drugs, and several drugs are in the developmental stage. We previously reported that the introduction of fluorine to the 4-position of 2-cyanopyrrolidine enhanced the DPP-IV inhibitory effect. In the present report, we examined the structure–activity relationship (SAR) of 2-cyano-4-fluoropyrrolidine with N-substituted glycine at the 1-position. We report the identification of a potent and stable DPP-IV inhibitor (TS-021) with a long-term persistent plasma drug concentration and a potent antihyperglycemic activity.
Keywords :
TS-021 , Dipeptidyl peptidase IV , Fluoropyrrolidine , Diabetes