Dabigatran
An anticoagulant that directly inhibits thrombin, a key protein in the blood clotting process. It is used to prevent blood clots and strokes in certain patients.
Peso Molecular
471,5100 g/mol
LogP
1,70
TPSA
150,00 Ų
Regra dos 5 de Lipinski
Aprovado
Áreas Terapêuticas
Classes de Medicamentos
Mecanismo de Ação
Direct thrombin (Factor IIa) inhibitor.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Direct thrombin (Factor IIa) inhibitor.
Estrutura 2D
Cite this structure
Embed this structure
SMILES
CN1C2=C(C=C(C=C2)C(=O)N(CCC(=O)O)C3=CC=CC=N3)N=C1CNC4=CC=C(C=C4)C(=N)N
InChI
InChI=1S/C25H25N7O3/c1-31-20-10-7-17(25(35)32(13-11-23(33)34)21-4-2-3-12-28-21)14-19(20)30-22(31)15-29-18-8-5-16(6-9-18)24(26)27/h2-10,12,14,29H,11,13,15H2,1H3,(H3,26,27)(H,33,34)
Molecular Formula
C25H25N7O3
HBD / HBA
4 / 7
Ligações Rotacionáveis
9
Átomos Pesados
35
Ibuprofen with dabigatran increases GI bleeding risk through additive effects; dabigatran itself carries a higher inherent GI bleeding risk than other DOACs.
Diltiazem increases dabigatran plasma levels through P-glycoprotein inhibition, potentially raising bleeding risk without a change in INR (dabigatran has no INR to monitor).
Cyclosporine dramatically increases dabigatran exposure through P-gp inhibition, raising the risk of serious or life-threatening bleeding.
Low-dose aspirin combined with dabigatran increases bleeding risk; clinical evidence suggests a 2-fold increase in major bleeding events.
No side effects recorded
Side effect data is not yet available for this drug.
Perguntas frequentes
An anticoagulant that directly inhibits thrombin, a key protein in the blood clotting process. It is used to prevent blood clots and strokes in certain patients.
Direct thrombin (Factor IIa) inhibitor.
Key pharmacokinetic parameters for Dabigatran: Half-life: 12-17 hours.
Yes, Dabigatran is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
Related Drugs
References & Data Sources
- PubChem — National Center for Biotechnology Information (NCBI). CID 216210. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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