Vildagliptin

CHEMBL142703 Phase 4 Onaylandı Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
303.4 g/mol
LogP
0.9
Phase
4

Vildagliptin is a dipeptidyl peptidase-4 (DPP-4) inhibitor that prevents the enzymatic degradation of incretin hormones GLP-1 and GIP, prolonging their physiological effects of glucose-dependent insulin secretion stimulation and glucagon suppression to improve glycemic control in type 2 diabetes. It is used as monotherapy or in combination with metformin, sulfonylureas, or insulin for type 2 diabetes management. DPP-4 inhibition provides glucose-dependent hypoglycemic effects with low risk of hypoglycemia.

Moleküler Ağırlık

303,4000 g/mol

LogP

0,90

TPSA

76,40 Ų

Lipinski RO5

Geçer

Terapötik Alanlar

Pharmacokinetics (PK)

Pharmacodynamics (PD)

2D Yapı

SVG PNG

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SMILES

N#C[C@@H]1CCCN1C(=O)CNC12CC3CC(CC(O)(C3)C1)C2

InChI

InChI=1S/C17H25N3O2/c18-9-14-2-1-3-20(14)15(21)10-19-16-5-12-4-13(6-16)8-17(22,7-12)11-16/h12-14,19,22H,1-8,10-11H2/t12?,13?,14-,16?,17?/m0/s1

Molecular Formula

C17H25N3O2

HBD / HBA

2 / 4

Döndürülebilir Bağlar

3

Ağır Atomlar

22

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.

Sıkça Sorulan Sorular

Vildagliptin is a dipeptidyl peptidase-4 (DPP-4) inhibitor that prevents the enzymatic degradation of incretin hormones GLP-1 and GIP, prolonging their physiological effects of glucose-dependent insulin secretion stimulation and glucagon suppression to improve glycemic control in type 2 diabetes. It is used as monotherapy or in combination with metformin, sulfonylureas, or insulin for type 2 diabetes management. DPP-4 inhibition provides glucose-dependent hypoglycemic effects with low risk of hypoglycemia.

Yes, Vildagliptin 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). CHEMBL142703. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 6918537. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.

Tıbbi Sorumluluk Reddi

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.