Cevimeline

CHEMBL168815 Phase 4 Onaylandı Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
199.3 g/mol
LogP
1.5
Phase
4

A cholinergic agonist that stimulates muscarinic M3 receptors in exocrine glands, increasing saliva and tear production. It is indicated for the treatment of dry mouth in patients with Sjögren's syndrome. Common side effects reflect its muscarinic stimulation and include sweating, nausea, and urinary frequency.

Moleküler Ağırlık

199,3200 g/mol

LogP

1,50

TPSA

37,80 Ų

Lipinski RO5

Geçer

Etki Mekanizması

Competitively blocks muscarinic acetylcholine receptors, reducing parasympathetic nervous system activity. Effects include decreased secretions, bronchodilation, and relaxation of smooth muscle.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mekanizma

Competitively blocks muscarinic acetylcholine receptors, reducing parasympathetic nervous system activity. Effects include decreased secretions, bronchodilation, and relaxation of smooth muscle.

2D Yapı

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SMILES

CC1OC2(CS1)CN1CCC2CC1

InChI

InChI=1S/C10H17NOS/c1-8-12-10(7-13-8)6-11-4-2-9(10)3-5-11/h8-9H,2-7H2,1H3

Molecular Formula

C10H17NOS

HBD / HBA

- / 3

Döndürülebilir Bağlar

0

Ağır Atomlar

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.

Sıkça Sorulan Sorular

A cholinergic agonist that stimulates muscarinic M3 receptors in exocrine glands, increasing saliva and tear production. It is indicated for the treatment of dry mouth in patients with Sjögren's syndrome. Common side effects reflect its muscarinic stimulation and include sweating, nausea, and urinary frequency.

Competitively blocks muscarinic acetylcholine receptors, reducing parasympathetic nervous system activity. Effects include decreased secretions, bronchodilation, and relaxation of smooth muscle.

Yes, Cevimeline 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). CHEMBL168815. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 25137844. Chemical information database.

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

Tıbbi Sorumluluk Reddi

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.