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Discovery of alogliptin: a potent, selective, bioavailable, and efficacious inhibitor of dipeptidyl peptidase IV
- Source :
- Journal of medicinal chemistry. 50(10)
- Publication Year :
- 2007
-
Abstract
- Alogliptin is a potent, selective inhibitor of the serine protease dipeptidyl peptidase IV (DPP-4). Herein, we describe the structure-based design and optimization of alogliptin and related quinazolinone-based DPP-4 inhibitors. Following an oral dose, these noncovalent inhibitors provide sustained reduction of plasma DPP-4 activity and a lowering of blood glucose in animal models of diabetes. Alogliptin is currently undergoing phase III trials in patients with type 2 diabetes.
- Subjects :
- Blood Glucose
Models, Molecular
ERG1 Potassium Channel
animal structures
Dipeptidyl Peptidase 4
Alogliptin Benzoate
Type 2 diabetes
Pyrimidinones
Pharmacology
In Vitro Techniques
Dipeptidyl peptidase
Diabetes Mellitus, Experimental
chemistry.chemical_compound
Mice
Structure-Activity Relationship
Dogs
Pharmacokinetics
Piperidines
Diabetes mellitus
Drug Discovery
medicine
Animals
Cytochrome P-450 Enzyme Inhibitors
Humans
Hypoglycemic Agents
Rats, Wistar
Uracil
Quinazolinone
Quinazolinones
Serine protease
Dipeptidyl-Peptidase IV Inhibitors
Binding Sites
biology
Haplorhini
Glucose Tolerance Test
medicine.disease
Ether-A-Go-Go Potassium Channels
Rats
chemistry
Biochemistry
biology.protein
Microsomes, Liver
Molecular Medicine
Female
Alogliptin
Subjects
Details
- ISSN :
- 00222623
- Volume :
- 50
- Issue :
- 10
- Database :
- OpenAIRE
- Journal :
- Journal of medicinal chemistry
- Accession number :
- edsair.doi.dedup.....17c687f8eb619d6b2740935381cb9b80