Alogliptin
From Wikipedia, the free encyclopedia
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Alogliptin
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| Systematic (IUPAC) name | |
| 2-({6-[(3R)-3-aminopiperidin-1-yl]-3-methyl-2,4-dioxo- 3,4-dihydropyrimidin-1(2H)-yl}methyl)benzonitrile |
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| Identifiers | |
| CAS number | |
| ATC code | ? |
| PubChem | |
| Chemical data | |
| Formula | C18H21N5O2 |
| Mol. mass | 339.39 g/mol |
| SMILES | & |
| Pharmacokinetic data | |
| Bioavailability | ? |
| Metabolism | ? |
| Half life | ? |
| Excretion | ? |
| Therapeutic considerations | |
| Pregnancy cat. |
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| Legal status | |
| Routes | Oral |
Alogliptin (codenamed SYR-322) is an investigational anti-diabetic drug in the DPP-4 inhibitor class,[1] being developed by Takeda Pharmaceutical Company. Takeda has submitted a New Drug Application for alogliptin to the U.S. Food and Drug Administration, after positive results from Phase III clinical trials.[2]
[edit] References
- ^ Feng J, Zhang Z, Wallace MB, et al (2007). "Discovery of alogliptin: a potent, selective, bioavailable, and efficacious inhibitor of dipeptidyl peptidase IV". J. Med. Chem. 50 (10): 2297–300. doi:. PMID 17441705.
- ^ Takeda Pharmaceutical Company (January 4, 2008). "Takeda Submits New Drug Application for Alogliptin (SYR-322) in the U.S.". Press release. Retrieved on 2008-01-09.
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