(R)-2-((6-(3-aminopiperidin-1-yl)-3-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)methyl)benzonitrile; Nesina; SYR-322; SYR 322
Description
Alogliptin Benzoate is the benzoate salt form of alogliptin, a selective, orally bioavailable, pyrimidinedione-based inhibitor of dipeptidyl peptidase 4 (DPP-4), with hypoglycemic activity. In addition to its effect on glucose levels, alogliptin may inhibit inflammatory responses by preventing the toll-like receptor 4 (TLR-4)-mediated formation of proinflammatory cytokines.Alogliptin benzoate is a benzoate salt obtained by combining equimolar amounts of alogliptin and benzoic acid. Used for treatment of type 2 diabetes. It has a role as an EC 3.4.14.5 (dipeptidyl-peptidase IV) inhibitor and a hypoglycemic agent. It contains an alogliptin(1+).
Physical & Chemical Properties
Molecular FormulaC25H27N5O4
Density:g/cm³
Boiling Point:671.2°C
Solubility:
Slightly soluble in water, ethanol and ethyl acetate; soluble in chloroform, DMSO and methanol (with mild heating).
Molecular Weight:461.52g/mol
Flash Point:359.7°C
Melting Point:180–182°C
Uses
As a therapeutic drug for type 2 diabetes, it improves glycemic control in patients when used in combination with diet and exercise.It inhibits DPP-4, prolongs the action duration of glucagon-like peptide-1 (GLP-1) in vivo, promotes insulin secretion, and suppresses glucagon release.