The following articles (labelled with PubMed ID or TBD) are for your review
| PMID | Data | Article Title | Organization |
|---|
| 23886684 |
36 |
Synthesis of quaternarya-amino acid-based arginase inhibitors via the Ugi reaction. |
Institutes For Pharmaceutical Discovery |
| 23453840 |
32 |
2-Substituted-2-amino-6-boronohexanoic acids as arginase inhibitors. |
Institutes For Pharmaceutical Discovery |
| 23472952 |
35 |
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 |
| 21728378 |
9 |
Binding ofa,a-disubstituted amino acids to arginase suggests new avenues for inhibitor design. |
Drexel University |
| 29914772 |
4 |
Rational design of novel irreversible inhibitors for human arginase. |
Brown University |
| 17441705 |
28 |
Discovery of alogliptin: a potent, selective, bioavailable, and efficacious inhibitor of dipeptidyl peptidase IV. |
Takeda Pharmaceutical |
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