Cinnarizine
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Cinnarizine
structure -
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CAS No:
298-57-7
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Formula:
C26H28N2
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Chemical Name:
Cinnarizine
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Synonyms:
Piperazine,1-(diphenylmethyl)-4-(3-phenyl-2-propen-1-yl)-;Piperazine,1-cinnamyl-4-(diphenylmethyl)-;Piperazine,1-(diphenylmethyl)-4-(3-phenyl-2-propenyl)-;1-(Diphenylmethyl)-4-(3-phenyl-2-propen-1-yl)piperazine;R 516;R 1575;N-Benzhydryl-N′-cinnamylpiperazine;1-Cinnamyl-4-(diphenylmethyl)piperazine;Cinnarizine;Dimitronal;1-Diphenylmethyl-4-cinnamoylpiperazine;Marisan;Midronal;Mitronal;Stugeron;Glanil;Labyrin;Dimitron;Stutgeron;Stutgin;Toliman;Folcodal;Sepan;1-Benzhydryl-4-cinnamylpiperazine;Lazeta;1-Cinnamyl-4-benzhydrylpiperazine;1-(3-Phenylallyl)-4-(diphenylmethyl)piperazine;Artate;Cinazyn;Apotomin;Corathiem;Cinaperazine;Katoseran;Giganten;Cerepar;Spaderizine;Cinnageron;Cerebolan;Hilactan;Cinnipirine;Denapol;Eglen;Carecin;Cinnacet;Sedatromin;Ixterol;Siptazin;Aplactan;Olamin;516MD;Processine;Aplexal;Cinarizine;Vergo;Stunarone
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Categories:
Active Pharmaceutical Ingredients > Circulatory System Drugs
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CAS No:
Description
Cinnarizine is an antihistamine and a calcium channel blocker, promote cerebral blood flow, used to treat cerebral apoplexy, post-trauma cerebral symptoms, and cerebral arteriosclerosis.
Characteristics
6.5
5.8
white powder
1.13 g/cm3
120.2 °C
505.8°C at 760 mmHg
229.8±14.6 °C
1.626
soluble in chloroform at 50mg/ml
Refrigerator
2.35E-10mmHg at 25°C
LD50 oral in rat: > 6500mg/kg
Cinnarizine Use and Manufacturing
General procedure: General procedure for amination of allylic alcoholsAllylic alcohols 1 (0.4 mmol), Pd(Xantphos)Cl2 (0.02 mmol, 5 molpercent), amines 2(0.6 mmol) and 2-PrOH (1.5 mL) were added to a 25 mL flame-dried Young-typetube under nitrogen atmosphere. The mixture was stirred at room temperature for 12hrs. After concentrated under reduced pressure, the residue was purified by flashcolumn chromatography on silica gel and eluted with EtOAc/PE (1/100-1/1) to affordthe desired product 3.General procedure: Benzyltriphenyl phosphonium chloride (17.9 mmol) (prepared according to thereported procedure [31]) was added to a solution of 4a–c (17.0 mmol) in dichloromethane (50 ml) under N2 atmosphere. The mixture was cooled to 5 °C and t-BuOK (41.3 mmol) was added under stirring. After completion, the reaction mixture was quenched into water (100 ml). The organic layer was separated, dried over anhydrous sodium sulfate, and concentrated under vacuum to obtain crude material 5a–c. The crude was then subjected to column purification over SiO2 using EtOAc/hexane as an eluent to afford 1a–c[25] and 6a–c in pure form.
For the treatment of vertigo/meniere's disease, nausea and vomiting, motion sickness and also useful for vestibular symptoms of other origins.
Drug Function and Efficacy
Extract from the above information
Registered Holders
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FDC LTD
Active
United States
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Jinyao Pharmaceutical Co., Ltd.
Active
China
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Shanghai Modern Hasen (Shangqiu) Pharmaceutical Co., Ltd.
Active
China
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