Rasagiline

CHEMBL887 Phase 4 승인됨 Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
171.2 g/mol
LogP
1.8
Phase
4

A MAO-B inhibitor used to treat Parkinson's disease, either alone in early stages or combined with levodopa in more advanced disease, by increasing dopamine levels in the brain. It may also have neuroprotective properties that could slow disease progression.

분자량

171.2400 g/mol

LogP

1.80

TPSA

12.00 Ų

리핀스키 5의 법칙

통과

치료 영역

Pharmacokinetics (PK)

Pharmacodynamics (PD)

2D 구조

SVG PNG

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SMILES

C#CCN[C@@H]1CCc2ccccc21

InChI

InChI=1S/C12H13N/c1-2-9-13-12-8-7-10-5-3-4-6-11(10)12/h1,3-6,12-13H,7-9H2/t12-/m1/s1

Molecular Formula

C12H13N

HBD / HBA

1 / 1

회전 가능 결합

2

무거운 원자

13

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.

자주 묻는 질문

A MAO-B inhibitor used to treat Parkinson's disease, either alone in early stages or combined with levodopa in more advanced disease, by increasing dopamine levels in the brain. It may also have neuroprotective properties that could slow disease progression.

Yes, Rasagiline 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). CHEMBL887. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 3052776. Chemical information database.

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

의학적 면책조항

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.