Cevimeline

CHEMBL168815 Phase 4 Đã phê duyệt 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.

Khối lượng phân tử

199,3200 g/mol

LogP

1,50

TPSA

37,80 Ų

Lipinski RO5

Đạt

Cơ chế tác dụng

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

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Cơ chế

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

Cấu trúc 2D

SVG PNG

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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

Liên kết có thể quay

0

Nguyên tử nặng

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.

Câu hỏi thường gặp

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.

Tuyên bố miễn trách y tế

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.