Buclizine

CHEMBL1201271 Phase 4 Одобрено Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
433.0 g/mol
LogP
7.1
Phase
4

An antihistamine with antiemetic, antivertigo, and mild anxiolytic properties, used to treat motion sickness, vertigo, and nausea. It acts by blocking histamine and muscarinic receptors in the central nervous system. It is also used as an appetite stimulant in some formulations.

Молекулярная масса

433,0000 g/mol

LogP

7,10

TPSA

6,50 Ų

Правило пяти Липинского

Соответствует

Механизм действия

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)

Механизм

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 Структура

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SMILES

CC(C)(C)c1ccc(CN2CCN(C(c3ccccc3)c3ccc(Cl)cc3)CC2)cc1

InChI

InChI=1S/C28H33ClN2/c1-28(2,3)25-13-9-22(10-14-25)21-30-17-19-31(20-18-30)27(23-7-5-4-6-8-23)24-11-15-26(29)16-12-24/h4-16,27H,17-21H2,1-3H3

Molecular Formula

C28H33ClN2

HBD / HBA

- / 2

Вращаемые Связи

6

Тяжёлые Атомы

31

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.

Часто задаваемые вопросы

An antihistamine with antiemetic, antivertigo, and mild anxiolytic properties, used to treat motion sickness, vertigo, and nausea. It acts by blocking histamine and muscarinic receptors in the central nervous system. It is also used as an appetite stimulant in some formulations.

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, Buclizine 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). CHEMBL1201271. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 6729. Chemical information database.

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

Медицинский отказ от ответственности

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.