Alogliptin Benzoate

CHEMBL227529 Phase 4 Disetujui Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
461.5 g/mol
LogP
Phase
4

The benzoate salt form of alogliptin, a DPP-4 inhibitor used to improve blood sugar control in type 2 diabetes by prolonging the action of incretin hormones that stimulate insulin release after meals. This formulation provides predictable oral absorption and once-daily dosing convenience.

Berat Molekul

461,5000 g/mol

TPSA

131,00 Ų

Area Terapeutik

Mekanisme Kerja

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)

Mekanisme

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.

Struktur 2D

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SMILES

Cn1c(=O)cc(N2CCC[C@@H](N)C2)n(Cc2ccccc2C#N)c1=O.O=C(O)c1ccccc1

InChI

InChI=1S/C18H21N5O2.C7H6O2/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;8-7(9)6-4-2-1-3-5-6/h2-3,5-6,9,15H,4,7-8,11-12,20H2,1H3;1-5H,(H,8,9)/t15-;/m1./s1

Molecular Formula

C25H27N5O4

HBD / HBA

2 / 7

Ikatan yang Dapat Dirotasi

4

Atom Berat

34

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.

Pertanyaan yang Sering Diajukan

The benzoate salt form of alogliptin, a DPP-4 inhibitor used to improve blood sugar control in type 2 diabetes by prolonging the action of incretin hormones that stimulate insulin release after meals. This formulation provides predictable oral absorption and once-daily dosing convenience.

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 Benzoate is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.

{# References & Data Sources section for drug detail pages. Renders standard pharmacological database links plus the drug's data_sources field. #}

References & Data Sources

  • ChEMBL — European Bioinformatics Institute (EBI). CHEMBL227529. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 16088021. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.

Penyangkalan Medis

This content is for educational and informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider before making medication decisions.

Data sources: ChEMBL, PubChem, DailyMed.