Alogliptin
A DPP-4 inhibitor that enhances the body's natural incretin hormones to stimulate insulin secretion and reduce glucagon release in response to meals, lowering blood sugar in adults with type 2 diabetes. It has cardiovascular safety data showing it does not increase the risk of heart failure.
आणविक भार
339.4000 g/mol
LogP
0.60
TPSA
93.70 Ų
लिपिंस्की RO5
उत्तीर्ण
चिकित्सीय क्षेत्र
क्रिया का तंत्र
Inhibits dipeptidyl peptidase-4, the enzyme that rapidly degrades incretin hormones (GLP-1 and GIP). This prolongs incretin activity, stimulating glucose-dependent insulin secretion and suppressing glucagon release.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Inhibits dipeptidyl peptidase-4, the enzyme that rapidly degrades incretin hormones (GLP-1 and GIP). This prolongs incretin activity, stimulating glucose-dependent insulin secretion and suppressing glucagon release.
2D संरचना
Cite this structure
Embed this structure
SMILES
Cn1c(=O)cc(N2CCC[C@@H](N)C2)n(Cc2ccccc2C#N)c1=O
InChI
InChI=1S/C18H21N5O2/c1-21-17(24)9-16(22-8-4-7-15(20)12-22)23(18(21)25)11-14-6-3-2-5-13(14)10-19/h2-3,5-6,9,15H,4,7-8,11-12,20H2,1H3/t15-/m1/s1
Molecular Formula
C18H21N5O2
HBD / HBA
1 / 5
घूर्णनीय बंधन
3
भारी परमाणु
25
No targets recorded
Target interaction data is not yet available for this drug.
No interactions recorded
Drug interaction data is not yet available for this compound.
No side effects recorded
Side effect data is not yet available for this drug.
अक्सर पूछे जाने वाले प्रश्न
A DPP-4 inhibitor that enhances the body's natural incretin hormones to stimulate insulin secretion and reduce glucagon release in response to meals, lowering blood sugar in adults with type 2 diabetes. It has cardiovascular safety data showing it does not increase the risk of heart failure.
Inhibits dipeptidyl peptidase-4, the enzyme that rapidly degrades incretin hormones (GLP-1 and GIP). This prolongs incretin activity, stimulating glucose-dependent insulin secretion and suppressing glucagon release.
Yes, Alogliptin is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL376359. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 11450633. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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