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Details

Stereochemistry ACHIRAL
Molecular Formula C26H28N2.C10H11ClO3
Molecular Weight 583.159
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of CINNARIZINE CLOFIBRATE

SMILES

CC(C)(OC1=CC=C(Cl)C=C1)C(O)=O.C(\C=C\C2=CC=CC=C2)N3CCN(CC3)C(C4=CC=CC=C4)C5=CC=CC=C5

InChI

InChIKey=GNQQJMWZCJAUJT-RSGUCCNWSA-N
InChI=1S/C26H28N2.C10H11ClO3/c1-4-11-23(12-5-1)13-10-18-27-19-21-28(22-20-27)26(24-14-6-2-7-15-24)25-16-8-3-9-17-25;1-10(2,9(12)13)14-8-5-3-7(11)4-6-8/h1-17,26H,18-22H2;3-6H,1-2H3,(H,12,13)/b13-10+;

HIDE SMILES / InChI

Description
Curator's Comment: Description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/2015612

Cinnarizine is a piperazine derivative with antihistaminic, antiserotonergic, antidopaminergic, and calcium channel-blocking activities. It inhibits calcium translocation across the vestibular sensory cells in the ampullae and maintains endolymph flow by preventing constriction of the stria vascularis. It is currently used for the treatment of nausea, vomiting, and vertigo caused by Meniere’s disease and other vestibular disorders. Cinnarizine is also used for prevention and treatment of motion sickness. Chronic use of cinnarizine may induce extrapyramidal symptoms.

Originator

Curator's Comment: reference retrieved from https://www.ncbi.nlm.nih.gov/pubmed/26051684 # Janssen Pharmaceutical

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Preventing
STUGERON

Approved Use

Cinnarizine helps symptoms caused by balance or movement problems. Cinnarizine tablets are used to control travel sickness, and for problems with balance (such as Ménières disease) to treat symptoms of feeling dizzy or lightheaded, ringing in the ears, feeling sick (nausea) and being sick (vomiting).
Preventing
STUGERON

Approved Use

Cinnarizine helps symptoms caused by balance or movement problems. Cinnarizine tablets are used to control travel sickness, and for problems with balance (such as Ménières disease) to treat symptoms of feeling dizzy or lightheaded, ringing in the ears, feeling sick (nausea) and being sick (vomiting).
PubMed

PubMed

TitleDatePubMed
Anticonvulsive properties of cinnarizine and flunarizine in rats and mice.
1975 Sep
Protective effect of creatinol O-phosphate (COP) on ventricular fibrillation and death induced by intravenous CaCl2 in mice.
1979
Flunarizine- and cinnarizine-induced extrapyramidal reactions.
1987 May
Aggravation of Parkinson's disease by cinnarizine.
1988 Jan
Parkinsonism, tremor, and depression induced by cinnarizine and flunarizine.
1988 Sep 17
Movement disorders and depression due to flunarizine and cinnarizine.
1989
Extrapyramidal and depressive side reactions with flunarizine and cinarizine.
1989 Feb
Cholestasis associated with cinnarizine.
1990 Dec 1
Cinnarizine-induced parkinsonism in primates.
1992 Apr
Calcium-entry blockers-induced parkinsonism: possible role of inherited susceptibility.
1992 Spring
Effects of the combination of ketoconazole and calcium channel antagonists against Candida albicans in vitro.
1993 Jul
Possible pharmacokinetic and pharmacodynamic factors affecting parkinsonism inducement by cinnarizine and flunarizine.
1995 Nov 9
A long-term follow-up study of cinnarizine- and flunarizine-induced parkinsonism.
1997 Jan
Subacute cutaneous lupus erythematosus associated with cinnarizine and thiethylperazine therapy.
1998
[Drug-induced parkinsonism. Clinical aspects compared with Parkinson disease].
1998 Jul
Etiology of parkinsonism in a Brazilian movement disorders clinic.
1998 Jun
Cinnarizine-induced parkinsonism: ten years later.
1998 May
Cinnarizine-induced cholestasis.
1999 Mar
[Akathisia, parkinsonism and depression induced by cinnarizine: a case report].
1999 May 1-15
Quantitative prediction of catalepsy induced by amoxapine, cinnarizine and cyclophosphamide in mice.
2000 May
Treatment of vertigo due to acute unilateral vestibular loss with a fixed combination of cinnarizine and dimenhydrinate: a double-blind, randomized, parallel-group clinical study.
2004 Jun
Parkinsonism and other movement disorders in outpatients in chronic use of cinnarizine and flunarizine.
2004 Sep
Effects of cinnarizine, a calcium antagonist that produces human parkinsonism, in parkin knock out mice.
2005 Aug
Tardive blepharospasm associated with cinnarizine use.
2006 Jul-Aug
[Parkinsonism due to the medication].
2009
Interference with bile salt export pump function is a susceptibility factor for human liver injury in drug development.
2010 Dec
A cell protection screen reveals potent inhibitors of multiple stages of the hepatitis C virus life cycle.
2010 Feb 23
The differential diagnoses of parkinsonism: findings from a cohort of 1528 patients and a 10 years comparison in tertiary movement disorders clinics.
2010 Jun
A multifactorial approach to hepatobiliary transporter assessment enables improved therapeutic compound development.
2013 Nov
Patents

Sample Use Guides

Stugeron® 15 mg tablets Cinnarizine For travel sickness Adults and children over 12 years old: • 2 tablets 2 hours before travelling then • 1 tablet every 8 hours during the journey Children aged 5 – 12 years old: • 1 tablet 2 hours before travelling then • ½ a tablet every 8 hours during the journey For problems with balance Adults and children over 12 years old: • 2 tablets 3 times a day Children aged 5-12 years old: • 1 tablet 3 times a day
Route of Administration: Oral
In Vitro Use Guide
10 uM cinnarizine prevented histamine-induced rat mesangial cell and glomerular contraction.
Name Type Language
CINNARIZINE CLOFIBRATE
INN  
INN  
Official Name English
cinnarizine clofibrate [INN]
Common Name English
2-(P-CHLOROPHENOXY)-2-METHYLPROPIONIC ACID COMPOUND WITH (E)-1-CINNAMYL-4-(DIPHENYLMETHYL)PIPERAZINE (1:1)
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C270
Created by admin on Fri Dec 15 16:13:39 GMT 2023 , Edited by admin on Fri Dec 15 16:13:39 GMT 2023
Code System Code Type Description
SMS_ID
100000081048
Created by admin on Fri Dec 15 16:13:39 GMT 2023 , Edited by admin on Fri Dec 15 16:13:39 GMT 2023
PRIMARY
EVMPD
SUB06303MIG
Created by admin on Fri Dec 15 16:13:39 GMT 2023 , Edited by admin on Fri Dec 15 16:13:39 GMT 2023
PRIMARY
PUBCHEM
6436096
Created by admin on Fri Dec 15 16:13:39 GMT 2023 , Edited by admin on Fri Dec 15 16:13:39 GMT 2023
PRIMARY
CAS
60763-49-7
Created by admin on Fri Dec 15 16:13:39 GMT 2023 , Edited by admin on Fri Dec 15 16:13:39 GMT 2023
PRIMARY
INN
4272
Created by admin on Fri Dec 15 16:13:39 GMT 2023 , Edited by admin on Fri Dec 15 16:13:39 GMT 2023
PRIMARY
FDA UNII
8RJ419895I
Created by admin on Fri Dec 15 16:13:39 GMT 2023 , Edited by admin on Fri Dec 15 16:13:39 GMT 2023
PRIMARY
NCI_THESAURUS
C87470
Created by admin on Fri Dec 15 16:13:39 GMT 2023 , Edited by admin on Fri Dec 15 16:13:39 GMT 2023
PRIMARY