Eslicarbazepine Acetate
This anticonvulsant is converted in the body to eslicarbazepine, which blocks sodium channels in neurons to reduce abnormal electrical activity in the brain. It is used as an add-on treatment for partial-onset seizures.
Molekularmasse
296,3200 g/mol
LogP
2,00
TPSA
72,60 Ų
Lipinski-Regel der Fünf
Bestanden
Therapeutische Bereiche
Wirkmechanismus
Selectively blocks angiotensin II type 1 (AT1) receptors, preventing the vasoconstrictive and aldosterone-secreting effects of angiotensin II. This results in vasodilation, reduced sodium retention, and decreased blood pressure.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Selectively blocks angiotensin II type 1 (AT1) receptors, preventing the vasoconstrictive and aldosterone-secreting effects of angiotensin II. This results in vasodilation, reduced sodium retention, and decreased blood pressure.
2D-Struktur
Cite this structure
Embed this structure
SMILES
CC(=O)O[C@H]1Cc2ccccc2N(C(N)=O)c2ccccc21
InChI
InChI=1S/C17H16N2O3/c1-11(20)22-16-10-12-6-2-4-8-14(12)19(17(18)21)15-9-5-3-7-13(15)16/h2-9,16H,10H2,1H3,(H2,18,21)/t16-/m0/s1
Molecular Formula
C17H16N2O3
HBD / HBA
1 / 3
Rotierbare Bindungen
2
Schwere Atome
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.
Häufig gestellte Fragen
This anticonvulsant is converted in the body to eslicarbazepine, which blocks sodium channels in neurons to reduce abnormal electrical activity in the brain. It is used as an add-on treatment for partial-onset seizures.
Selectively blocks angiotensin II type 1 (AT1) receptors, preventing the vasoconstrictive and aldosterone-secreting effects of angiotensin II. This results in vasodilation, reduced sodium retention, and decreased blood pressure.
Yes, Eslicarbazepine Acetate 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). CHEMBL87992. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 179344. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
Medizinischer Haftungsausschluss
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.
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