| Name | (2R)-1-{2-[(3R)-pyrrolidin-3-ylamino]-acetyl}-pyrrolidine-2-boronic acid mono-L-tartrate salt |
|---|---|
| Synonyms |
L-tartrate salt of (2R)-1-{7-[(9R)-pyrrolidin-9-ylamino]-acetyl}-pyrrolidine-2-boronic acid
dutogliptin |
| Description | Dutogliptin tartrate (PHX-1149) is an orally available, potent, and selective dipeptidyl peptidase-4 (DPP4) inhibitor for the treatment of type 2 diabetes mellitus. |
|---|---|
| Related Catalog | |
| Target |
DPP4[1] |
| In Vivo | Dutogliptin exhibits low plasma protein binding (11%) and is rapidly absorbed with a Tmax of 3-4 h and a half-life of 10-13 h. Dutogliptin is metabolically stable and does not inhibit or induce the activity of major CYP450s[2]. |
| References |
| Molecular Formula | C14H26BN3O9 |
|---|---|
| Molecular Weight | 391.18200 |
| Exact Mass | 391.17600 |
| PSA | 199.89000 |