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Buclizine

Catalog No. DB00354 Name DrugBank
CAS Number 82-95-1 Website http://www.ualberta.ca/
M. F. C28H33ClN2 Telephone (780) 492-3111
M. W. 433.02802 Fax (780) 492-1071
Purity Email david.wishart@ualberta.ca
Storage Chembase ID: 238

SYNONYMS

IUPAC name
1-[(4-tert-butylphenyl)methyl]-4-[(4-chlorophenyl)(phenyl)methyl]piperazine
IUPAC Traditional name
buclizine
Brand Name
Aphilan R
Histabuticine
Longifene
Hitabutyzyne
Bucladin
Histabutizine
Buclifen
Buclina
Buclodin
Histabutyzine
Histabutyzine Hydrochloride
Posdel
Postafen
Softran
Aphilan-R Base
Bucladin-S
Histabutyzine Dihydrochloride
Vibazine
Synonyms
Buclizine Dihydrochloride
Buclizinum [INN-Latin]
Buclizina [INN-Spanish]
Buclizine Hydrochloride
Histabutyzine Dihydrochloride
Vibazine Hydrochloride

DATABASE IDS

PubChem SID 46507608
PubChem CID 6729
CAS Number 82-95-1

PROPERTIES

Hydrophobicity(logP) 7.1

DETAILS

Description (English)
Item Information
Drug Groups approved
Description Buclizine is an antihistamine of the piperazine derivative family. [Wikipedia]
Indication For prevention and treatment of nausea, vomiting, and dizziness associated with motion sickness and vertigo (dizziness caused by other medical problems).
Pharmacology Buclizine is a piperazine-derivative antihistamine used as an antivertigo/antiemetic agent. Buclizine is used in the prevention and treatment of nausea, vomiting, and dizziness associated with motion sickness. Additionally, it has been used in the management of vertigo in diseases affecting the vestibular apparatus. Although the mechanism by which buclizine exerts its antiemetic and antivertigo effects has not been fully elucidated, its central anticholinergic properties are partially responsible. The drug depresses labyrinth excitability and vestibular stimulation, and it may affect the medullary chemoreceptor trigger zone. It also possesses anticholinergic, antihistaminic, central nervous system depressant, and local anesthetic effects.
Affected Organisms
Humans and other mammals
Biotransformation Hepatic.
Absorption Rapidly absorbed following oral administration.
External Links
Wikipedia

REFERENCES