Cyclizine

CHEMBL648 Phase 4 承認済み Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
266.4 g/mol
LogP
3.6
Phase
4

An antihistamine with antiemetic and anticholinergic properties used to prevent and treat nausea, vomiting, and motion sickness. It acts centrally in the vomiting center of the brain and is used perioperatively and for vertigo.

分子量

266.4000 g/mol

LogP

3.60

TPSA

6.50 Ų

リピンスキーの五則

適合

治療領域

作用機序

Competitively blocks histamine H1 receptors on effector cells, preventing histamine-mediated vasodilation, increased vascular permeability, bronchoconstriction, and pruritus. First-generation agents also cross the blood-brain barrier, causing sedation.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

機序

Competitively blocks histamine H1 receptors on effector cells, preventing histamine-mediated vasodilation, increased vascular permeability, bronchoconstriction, and pruritus. First-generation agents also cross the blood-brain barrier, causing sedation.

2D構造

SVG PNG

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SMILES

CN1CCN(C(c2ccccc2)c2ccccc2)CC1

InChI

InChI=1S/C18H22N2/c1-19-12-14-20(15-13-19)18(16-8-4-2-5-9-16)17-10-6-3-7-11-17/h2-11,18H,12-15H2,1H3

Molecular Formula

C18H22N2

HBD / HBA

- / 2

回転可能結合数

3

重原子数

20

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.

よくある質問

An antihistamine with antiemetic and anticholinergic properties used to prevent and treat nausea, vomiting, and motion sickness. It acts centrally in the vomiting center of the brain and is used perioperatively and for vertigo.

Competitively blocks histamine H1 receptors on effector cells, preventing histamine-mediated vasodilation, increased vascular permeability, bronchoconstriction, and pruritus. First-generation agents also cross the blood-brain barrier, causing sedation.

Yes, Cyclizine 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). CHEMBL648. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 6726. Chemical information database.

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

医学的免責事項

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.