Rupatadine

CHEMBL91397 Phase 4 ได้รับการอนุมัติ Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
416.0 g/mol
LogP
5.8
Phase
4

Rupatadine is a second-generation antihistamine with dual H1 receptor antagonist and platelet-activating factor (PAF) receptor antagonist activity, used for the treatment of allergic rhinitis and chronic urticaria, with some investigation in rheumatoid arthritis-related pruritus. By blocking both histamine H1 receptors and PAF receptors, it provides broader anti-allergic and anti-inflammatory effects than selective antihistamines. It has low sedation potential due to limited CNS penetration.

น้ำหนักโมเลกุล

416.0000 g/mol

LogP

5.80

TPSA

29.00 Ų

Lipinski RO5

ผ่าน

ด้านการรักษา

กลไกการออกฤทธิ์

Competitively binds to its target receptor without activating it, blocking the natural ligand from binding and preventing receptor-mediated signaling.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

กลไก

Competitively binds to its target receptor without activating it, blocking the natural ligand from binding and preventing receptor-mediated signaling.

โครงสร้าง 2 มิติ

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SMILES

Cc1cncc(CN2CCC(=C3c4ccc(Cl)cc4CCc4cccnc43)CC2)c1

InChI

InChI=1S/C26H26ClN3/c1-18-13-19(16-28-15-18)17-30-11-8-20(9-12-30)25-24-7-6-23(27)14-22(24)5-4-21-3-2-10-29-26(21)25/h2-3,6-7,10,13-16H,4-5,8-9,11-12,17H2,1H3

Molecular Formula

C26H26ClN3

HBD / HBA

- / 3

พันธะที่หมุนได้

2

อะตอมหนัก

30

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.

คำถามที่พบบ่อย

Rupatadine is a second-generation antihistamine with dual H1 receptor antagonist and platelet-activating factor (PAF) receptor antagonist activity, used for the treatment of allergic rhinitis and chronic urticaria, with some investigation in rheumatoid arthritis-related pruritus. By blocking both histamine H1 receptors and PAF receptors, it provides broader anti-allergic and anti-inflammatory effects than selective antihistamines. It has low sedation potential due to limited CNS penetration.

Competitively binds to its target receptor without activating it, blocking the natural ligand from binding and preventing receptor-mediated signaling.

Yes, Rupatadine 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). CHEMBL91397. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 133017. Chemical information database.

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

ข้อจำกัดความรับผิดชอบทางการแพทย์

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.