cyclizine
{{Short description|Medication for motion sickness or vertigo}}
{{Use dmy dates|date=January 2020}}
{{Drugbox
| Watchedfields = changed
| verifiedrevid = 458445801
| IUPAC_name = 1-benzhydryl-4-methyl-piperazine
| image = Cyclizine2DCSD.svg
| image_class = skin-invert-image
| width = 150px
| image2 = Cyclizine_3d_balls.png
| image_class2 = bg-transparent
| width2 = 125px
| tradename = Marezine, Valoid, Nausicalm, others
| Drugs.com = {{drugs.com|CDI|cyclizine}}
| pregnancy_AU = A
| legal_AU = S3
| legal_UK = P
| legal_US = OTC
| legal_status = OTC (Netherlands)
| routes_of_administration = By mouth, IM, IV
| bioavailability =
| metabolism = N-demethylated to inactive norcyclizine{{cite web|title=DrugBank: Cyclizine. Pharmacology: metabolism|url=http://www.drugbank.ca/drugs/DB01176|website=DrugBank Database|access-date=5 January 2016|url-status=live|archive-url=https://web.archive.org/web/20160130173806/http://www.drugbank.ca/drugs/DB01176|archive-date=30 January 2016}}
| elimination_half-life = 20 hours
| excretion =
| IUPHAR_ligand = 7151
| CAS_number_Ref = {{cascite|correct|??}}
| CAS_number = 82-92-8
| ATC_prefix = R06
| ATC_suffix = AE03
| PubChem = 6726
| DrugBank_Ref = {{drugbankcite|correct|drugbank}}
| DrugBank = DB01176
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID = 6470
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII = QRW9FCR9P2
| KEGG_Ref = {{keggcite|correct|kegg}}
| KEGG = D03621
| ChEBI_Ref = {{ebicite|correct|EBI}}
| ChEBI = 3994
| ChEMBL_Ref = {{ebicite|correct|EBI}}
| ChEMBL = 648
| C=18 | H=22 | N=2
| SMILES = CN(CC1)CCN1C(C2=CC=CC=C2)C3=CC=CC=C3
| StdInChI_Ref = {{stdinchicite|correct|chemspider}}
| StdInChI = 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
| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
| StdInChIKey = UVKZSORBKUEBAZ-UHFFFAOYSA-N
}}
Cyclizine, sold under a number of brand names, is a medication used to treat and prevent nausea, vomiting and dizziness due to motion sickness or vertigo. It may also be used for nausea after general anaesthesia or that which developed from opioid use.{{cite web|title=Cyclizine 50mg Tablets - Summary of Product Characteristics (SPC) - (eMC)|url=https://www.medicines.org.uk/emc/medicine/27036|website=www.medicines.org.uk|access-date=13 December 2016|date=27 March 2015|url-status=live|archive-url=https://web.archive.org/web/20161220173557/https://www.medicines.org.uk/emc/medicine/27036|archive-date=20 December 2016}}{{cite book | vauthors = Feldman M, Friedman LS, Brandt LJ |title=Sleisenger and Fordtran's Gastrointestinal and Liver Disease: Pathophysiology, Diagnosis, Management |date=2015 |publisher=Elsevier Health Sciences |isbn=9781455749898 |page=218 |url= https://books.google.com/books?id=4CMJBgAAQBAJ&pg=PA218 |url-status=live|archive-url= https://web.archive.org/web/20161220102552/https://books.google.ca/books?id=4CMJBgAAQBAJ&pg=PA218 |archive-date=2016-12-20 }} It is taken by mouth, in the rectum, or injected into a vein.{{cite book | vauthors = ((World Health Organization)) | title = World Health Organization model list of essential medicines: 21st list 2019 | year = 2019 | hdl = 10665/325771 | author-link = World Health Organization | publisher = World Health Organization | location = Geneva | id = WHO/MVP/EMP/IAU/2019.06. License: CC BY-NC-SA 3.0 IGO }}
Common side effects include sleepiness, dry mouth, constipation, and trouble with vision. More serious side effects include low blood pressure and urinary retention.{{cite web|title=Cyclizine Side Effects in Detail - Drugs.com|url=https://www.drugs.com/sfx/cyclizine-side-effects.html|website=www.drugs.com|access-date=13 December 2016|url-status=live|archive-url=https://web.archive.org/web/20161221001454/https://www.drugs.com/sfx/cyclizine-side-effects.html|archive-date=21 December 2016}} It is not generally recommended in young children or those with glaucoma. Cyclizine appears to be safe during pregnancy but has not been well studied.{{cite web|title=Cyclizine Use During Pregnancy {{!}} Drugs.com|url=https://www.drugs.com/pregnancy/cyclizine.html|website=www.drugs.com|access-date=13 December 2016|url-status=live|archive-url=https://web.archive.org/web/20161221001234/https://www.drugs.com/pregnancy/cyclizine.html|archive-date=21 December 2016}} It is in the anticholinergic and antihistamine family of medications.
Cyclizine was discovered in 1947.{{cite book| vauthors = Williams P |title=The story of the Wellcome Trust : unlocking Sir Henry's legacy to medical research|date=2010|publisher=JJG|location=Hindringham|isbn=9781899163922|page=14|url=https://books.google.com/books?id=yjcgAQAAMAAJ&q=Cyclizine+discovery+1947|url-status=live|archive-url=https://web.archive.org/web/20161220102538/https://books.google.ca/books?id=yjcgAQAAMAAJ&q=Cyclizine+discovery+1947|archive-date=2016-12-20}} It is on the World Health Organization's List of Essential Medicines.{{cite book | vauthors = ((World Health Organization)) | title = World Health Organization model list of essential medicines: 22nd list (2021) | year = 2021 | hdl = 10665/345533 | author-link = World Health Organization | publisher = World Health Organization | location = Geneva | id = WHO/MHP/HPS/EML/2021.02 | hdl-access=free }} In the United States it is available over the counter.{{cite web|title=Cyclizine: Indications, Side Effects, Warnings - Drugs.com|url=https://www.drugs.com/cdi/cyclizine.html|website=www.drugs.com|access-date=13 December 2016|url-status=live|archive-url=https://web.archive.org/web/20161221001637/https://www.drugs.com/cdi/cyclizine.html|archive-date=21 December 2016}}
Medical uses
Primary uses include nausea, vomiting and dizziness associated with motion sickness, vertigo and post-operatively following administration of general anesthesia and opioids. It is sometimes given in hyperemesis gravidarum, although the manufacturer advises that it be avoided in pregnancy. Off-license use often occurs with specialists in hospitals to treat inpatients who have become severely dehydrated in pregnancy. An off-label use is as an opioid/opiate potentiator.{{cite web|url=http://www.medicines.org.uk/EMC/medicine/14672/SPC/Valoid+Tablets/|title=Valoid Tablets by Amdipharm|work=Electronic Medicines Compendium|publisher=Datapharm|url-status=dead|archive-url=https://web.archive.org/web/20160304051657/http://www.medicines.org.uk/EMC/medicine/14672/SPC/Valoid+Tablets/|archive-date=2016-03-04|access-date=2011-10-01}}
The drug Diconal is a combination of cyclizine and the opioid dipipanone.{{cite web|url=http://emc.medicines.org.uk/emc/assets/c/html/DisplayDoc.asp?DocumentID=15199|title=Diconal Tablets by Amdipharm|work=Electronic Medicines Compendium|publisher=Datapharm|url-status=dead|archive-url=https://web.archive.org/web/20080401052533/http://emc.medicines.org.uk/emc/assets/c/html/displaydoc.asp?documentid=15199|archive-date=2008-04-01|access-date=2008-08-05}} Dipipanone is a schedule I controlled substance in the US.{{cite web | title=Conversion Factors for Controlled Substances | website=DEA Diversion Control Division | url=https://www.deadiversion.usdoj.gov/quotas/conv_factor/index.html | access-date=26 March 2020}}
Contraindications
Its antimuscarinic action warrants caution in patients with prostatic hypertrophy, urinary retention, or angle-closure glaucoma. Liver disease exacerbates its sedative effects.
Adverse effects
Common (over 10%) — Drowsiness, dry mouth.
Uncommon (1% to 10%) — Headache, psychomotor impairment, dermatitis, and antimuscarinic effects such as diplopia (double vision), tachycardia, constipation, urinary retention and gastro-intestinal disturbances.
Rare (less than 1%) — Hypersensitivity reactions (bronchospasm, angioedema, anaphylaxis, rashes and photosensitivity reactions), extrapyramidal effects, dizziness, confusion, depression, sleep disturbances, tremor, liver dysfunction, and hallucinations.
Pharmacology
Cyclizine is a piperazine derivative with histamine H1-receptor antagonist (antihistamine) activity. The precise mechanism of action in inhibiting the symptoms of motion sickness is not well understood. It may have effects directly on the vestibular system and on the chemoreceptor trigger zone. Cyclizine exerts a central anticholinergic (antimuscarinic) action.
Synthesis
Cyclizine may be prepared by the Eschweiler–Clarke methylation of diphenylmethylpiperazine or by reaction of benzhydryl bromide with 1-methylpiperazine in acetonitrile to form the hydrobromide salt of the drug.
History
Cyclizine was developed in the American division of pharmacy company Burroughs Wellcome (today GlaxoSmithKline) during a research study involving many drugs of the antihistamine group. Cyclizine was quickly clinically found as a potent and long-acting antiemetic. The company named the substance – or more precisely cyclizine's hydrochloride form which it usually appears in – "marezine hydrochloride" and started to sell it in the United States under trade name Marezine. Selling was begun in France under trade name Marzine in 1965.
{{cite book | url = https://books.google.com/books?id=Cb6BOkj9fK4C&pg=404 | title = Drug discovery: a history | vauthors = Sneader W | publisher = John Wiley & Sons | year = 2005 | page = 404 | isbn = 0-471-89979-8 | url-status = live | archive-url = https://web.archive.org/web/20170910174226/https://books.google.com/books?id=Cb6BOkj9fK4C&pg=404 | archive-date = 2017-09-10 }}
{{cite book | url = https://books.google.com/books?id=X2EyLsG4bcUC&pg=406 | title = Pharmaceutical manufacturing encyclopedia | vauthors = Sittig M | publisher = William Andrew | year = 1988 | page = 406 | isbn = 0-8155-1144-2 | url-status = live | archive-url = https://web.archive.org/web/20170910174226/https://books.google.com/books?id=X2EyLsG4bcUC&pg=406 | archive-date = 2017-09-10 }}
The substance received more credit when NASA chose it as a space antiemetic for the first crewed Moon flight. Cyclizine was introduced to many countries as a common antiemetic. It is an over-the-counter drug in many countries because it has been well tolerated, although it has not been studied much.{{cite book | vauthors = Rajoo SG | veditors = Lobo M | work = Barts & The London NHS Trust | chapter-url = http://www.drugs.smd.qmul.ac.uk/drugs/html5/Anti-emetics/AN-FEF54A37-6289-402B-E208-9284E183608A.html | title = Anti-emetics - Metoclopramide, Domperidone, Ondansetron, Cyclizine. | chapter = Introduction |access-date=2015-03-09 |url-status=live |archive-url=https://web.archive.org/web/20150402111754/http://www.drugs.smd.qmul.ac.uk/drugs/html5/Anti-emetics/AN-FEF54A37-6289-402B-E208-9284E183608A.html |archive-date=2015-04-02 }}
Society and culture
Some people using methadone recreationally combine cyclizine with their methadone dose, a combination that is known to produce strong psychoactive effects.{{cite journal | vauthors = Ruben SM, McLean PC, Melville J | title = Cyclizine abuse among a group of opiate dependents receiving methadone | journal = British Journal of Addiction | volume = 84 | issue = 8 | pages = 929–34 | date = August 1989 | pmid = 2775912 | doi = 10.1111/j.1360-0443.1989.tb00766.x }}
It has also been used recreationally for its anticholinergic effects to induce hallucinations.{{cite journal | vauthors = Bassett KE, Schunk JE, Crouch BI | title = Cyclizine abuse by teenagers in Utah | journal = The American Journal of Emergency Medicine | volume = 14 | issue = 5 | pages = 472–4 | date = September 1996 | pmid = 8765114 | doi = 10.1016/S0735-6757(96)90156-4 }}
It has been used illegally in greyhound racing to sabotage a dog's performance.Conor Ryan for The Independent. June 20, 2013 [http://www.irishexaminer.com/ireland/igb-left-with-250k-bill-after-dog-doping-case-234547.html IGB left with €250k bill after dog doping case] {{webarchive|url=https://web.archive.org/web/20160304000528/http://www.irishexaminer.com/ireland/igb-left-with-250k-bill-after-dog-doping-case-234547.html |date=2016-03-04 }}
=Names=
As cyclizine hydrochloride tablets and cyclizine lactate solution for intramuscular or intravenous injection (brand names: Valoid in UK and South Africa and Marezine, Marzine and Emoquil in US). Cyclizine was marketed as Bonine for Kids in the US, but was discontinued in 2012, and replaced with meclizine.
{{ cite web
| url = http://www.bonine.com/bonine_kids.php
| title = Bonine for Kids
| publisher = Insight Pharmaceuticals
| url-status = dead
| archive-url = https://web.archive.org/web/20100917221933/http://bonine.com/bonine_kids.php
| archive-date = 2010-09-17
}}
Cyclizine derivatives
class="wikitable" style="margin-left:auto; margin-right:auto; text-align:center;" |
colspan="3" | Structural comparison of cyclizine and related H1 antagonists{{cite book|title=Foye's Principles of Medicinal Chemistry|date=2013|publisher=Wolters Kluwer Health / Lippincott Williams & Wilkins|isbn=978-1-60913-345-0 |edition=7th|location=Philadelphia|page=1056 | vauthors = Lemke TL, Williams DA, Roche VF, Zito SW }} |
---|
colspan="3" | File:Cyclizine derivatives backbone.svg |
Compound
! R1 ! R2 |
Cyclizine
| H | CH3 |
Chlorcyclizine
| Cl | CH3 |
Meclizine
| Cl |
Buclizine
| Cl |
Oxatomide
| H |
Hydroxyzine
| Cl |
Cetirizine
| Cl |
See also
References
{{Reflist}}
External links
- {{cite web| url = https://druginfo.nlm.nih.gov/drugportal/name/cyclizine | publisher = U.S. National Library of Medicine| work = Drug Information Portal| title = Cyclizine }}
{{Antihistamines}}
{{Hallucinogens}}
{{Acetylcholine receptor modulators}}
{{Histamine receptor modulators}}
{{Piperazines}}
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Category:H1 receptor antagonists
Category:Wikipedia medicine articles ready to translate