PMID

Data

Article Title

Organization

Synthesis of quaternarya-amino acid-based arginase inhibitors via the Ugi reaction.

Institutes For Pharmaceutical Discovery

2-Substituted-2-amino-6-boronohexanoic acids as arginase inhibitors.

Institutes For Pharmaceutical Discovery

Discovery of (R)-2-amino-6-borono-2-(2-(piperidin-1-yl)ethyl)hexanoic acid and congeners as highly potent inhibitors of human arginases I and II for treatment of myocardial reperfusion injury.

Institutes For Pharmaceutical Discovery

Binding ofa,a-disubstituted amino acids to arginase suggests new avenues for inhibitor design.

Drexel University

Rational design of novel irreversible inhibitors for human arginase.

Brown University

Discovery of alogliptin: a potent, selective, bioavailable, and efficacious inhibitor of dipeptidyl peptidase IV.

Takeda Pharmaceutical