Dapagliflozin

CHEMBL429910 Phase 4 Aprobado Small molecule
Half-Life
12.9 hours
Bioavailability
Protein Binding
Molecular Weight
408.9 g/mol
LogP
2.3
Phase
4

An SGLT2 inhibitor that lowers blood sugar by blocking glucose reabsorption in the kidney, causing excess glucose to be excreted in urine, and has additional benefits for heart failure and chronic kidney disease regardless of diabetes status. It also promotes modest weight loss and blood pressure reduction.

Peso molecular

408,8730 g/mol

LogP

2,30

TPSA

99,40 Ų

Regla de cinco de Lipinski

Cumple

Áreas terapéuticas

Clases de fármacos

Mecanismo de acción

Selective SGLT2 inhibitor reducing renal glucose and sodium reabsorption.

Pharmacokinetics (PK)

Half-Life 12.9 hours

Pharmacodynamics (PD)

Mecanismo

Selective SGLT2 inhibitor reducing renal glucose and sodium reabsorption.

Estructura 2D

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SMILES

CCOc1ccc(Cc2cc([C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)ccc2Cl)cc1

InChI

InChI=1S/C21H25ClO6/c1-2-27-15-6-3-12(4-7-15)9-14-10-13(5-8-16(14)22)21-20(26)19(25)18(24)17(11-23)28-21/h3-8,10,17-21,23-26H,2,9,11H2,1H3/t17-,18-,19+,20-,21+/m1/s1

Molecular Formula

C21H25ClO6

HBD / HBA

4 / 6

Enlaces Rotables

6

Átomos Pesados

28

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.

Preguntas frecuentes

An SGLT2 inhibitor that lowers blood sugar by blocking glucose reabsorption in the kidney, causing excess glucose to be excreted in urine, and has additional benefits for heart failure and chronic kidney disease regardless of diabetes status. It also promotes modest weight loss and blood pressure reduction.

Selective SGLT2 inhibitor reducing renal glucose and sodium reabsorption.

Key pharmacokinetic parameters for Dapagliflozin: Half-life: 12.9 hours.

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

Related Drugs

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References & Data Sources

  • ChEMBL — European Bioinformatics Institute (EBI). CHEMBL429910. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 9887712. Chemical information database.

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

Aviso médico

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.