U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C19H21NS.ClH
Molecular Weight 331.903
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PIZOTIFEN HYDROCHLORIDE

SMILES

Cl.CN1CCC(CC1)=C2C3=C(CCC4=CC=CC=C24)SC=C3

InChI

InChIKey=INPORWDLYCTBBN-UHFFFAOYSA-N
InChI=1S/C19H21NS.ClH/c1-20-11-8-15(9-12-20)19-16-5-3-2-4-14(16)6-7-18-17(19)10-13-21-18;/h2-5,10,13H,6-9,11-12H2,1H3;1H

HIDE SMILES / InChI

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C19H21NS
Molecular Weight 295.442
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description
Curator's Comment: description was created based on several sources, including https://www.drugs.com/uk/sanomigran-1-5mg-tablets-leaflet.html | https://www.drugs.com/uk/pizotifen-0-5mg-tablets-leaflet.html | https://www.ncbi.nlm.nih.gov/pubmed/24189186

Pizotifen (INN) or pizotyline (USAN), trade name Sandomigran, is a benzocycloheptene-based drug used as a medicine, primarily as a preventative to reduce the frequency of recurrent migraine headaches. Pizotifen is a serotonin antagonist acting mainly at the 5-HT2A and 5HT2C receptors. It also has some activity as an antihistamine as well as some anticholinergic activity. The main medical use for pizotifen is for the prevention of vascular headache including migraine and cluster headache. Pizotifen is one of a range of medications used for this purpose, other options include propranolol, topiramate, valproic acid and amitriptyline. While pizotifen is reasonably effective, its use is limited by side effects, principally drowsiness and weight gain, and it is usually not the first choice medicine for preventing migraines, instead being used as an alternative when other drugs have failed to be effective. It is not effective in relieving migraine attacks once in progress. Pizotifen has also been reported as highly effective in a severe case of erythromelalgia, a rare neurovascular disease that is sometimes refractory to the other drugs named above. Side effects include sedation, dry mouth, drowsiness, increased appetite and weight gain. Occasionally it may cause nausea, headaches, or dizziness. In rare cases, anxiety, aggression and depression may also occur. Pizotifen is well absorbed from the gastro-intestinal tract, peak plasma concentrations occurring approximately 5 hours after oral administration. The absorption of pizotifen is fast (absorption half life 0.5 to 0.8 hours) and nearly complete (80%). Over 90% is bound to plasma proteins. Pizotifen undergoes extensive metabolism. Over half of a dose is excreted in the urine, chiefly as metabolites; a significant proportion is excreted in the faeces. The primary metabolite of pizotifen (N-glucuronide conjugate) has a long elimination half-life of about 23 hours.

Originator

Sources: Bollettino - Societa Italiana di Biologia Sperimentale Volume 42, Issue 17, Pages 1097-100, Journal, 1966

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Sandomigran

Approved Use

Unknown
Primary
Sandomigran

Approved Use

Unknown
Primary
Sandomigran

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Effects of chronic treatment with antidepressants on aggressiveness induced by clonidine in mice.
1982
Arterial complications of migraine treatment with methysergide and parenteral ergotamine.
1982 Jul 24
The role of the central serotonergic system in pilocarpine-induced seizures: receptor mechanisms.
1989 Nov
Agonist activity of antimigraine drugs at recombinant human 5-HT1A receptors: potential implications for prophylactic and acute therapy.
1997 Jun
Central pathways for cough in man--unanswered questions.
2002
Cyclic vomiting syndrome in Thai children.
2002 Aug
Migraine and Raynaud phenomenon: possible late complications of Kawasaki disease.
2002 Mar
Hypotension caused by extracorporeal circulation: serotonin from pump-activated platelets triggers nitric oxide release.
2002 Nov 12
Systematic review of treatments for recurrent abdominal pain.
2003 Jan
French guidelines for the diagnosis and management of migraine in adults and children.
2004 Aug
Determination of ketotifen in human plasma by LC-MS.
2004 Jan 27
Do pizotifen or propranolol reduce the frequency of migraine headache?
2004 Jul
Topiramate in migraine prevention: evidence-based medicine from clinical trials.
2004 Oct
Use of intravenous midazolam and clonidine in cyclical vomiting syndrome: a case report.
2005 Jan
Anticipatory nausea in cyclical vomiting.
2005 Mar 24
Pizotyline effectively attenuates the stimulus effects of N-methyl-3,4-methylenedioxyamphetamine (MDMA).
2005 Oct
Weight variations in the prophylactic therapy of primary headaches: 6-month follow-up.
2005 Sep
Management of migraine in Australian general practice.
2007 Aug 6
Pediatric migraine: pharmacologic agents for prophylaxis.
2007 Jul
Stages of motor output reorganization after hemispheric stroke suggested by longitudinal studies of cortical physiology.
2008 Aug
Pharmacological interventions for recurrent abdominal pain (RAP) and irritable bowel syndrome (IBS) in childhood.
2008 Jan 23
Drug use in children: cohort study in three European countries.
2008 Nov 24
Optimizing prophylactic treatment of migraine: Subtypes and patient matching.
2008 Oct
What happens to new-onset headache in children that present to primary care? A case-cohort study using electronic primary care records.
2009 Dec
Treatment of primary headache in children: a multicenter hospital-based study in France.
2009 Dec
5-Hydroxytryptamine Receptor Subtypes and their Modulators with Therapeutic Potentials.
2009 Jun
Recent concepts on cyclic vomiting syndrome in children.
2010 Apr
Prophylaxis of migraine headache.
2010 Apr 20
New methods for diagnosis and treatment of vestibular diseases.
2010 Aug 9
Patents

Patents

Sample Use Guides

1.5mg daily (one 1.5mg tablet at night or 0.5mg tablets three times daily).
Route of Administration: Oral
HEK293-EBNA cell was used as the gene transferring cell. Cultured HEK293-EBNA cells expressing human 5-HT2B receptor were washed with PBS(-). The cells were scraped in the presence of PBS(-), and the cells were recovered by centrifugation (1000 rpm, 10 min, 4 OC). They were homogenized using Polytron (PTA 10-TS) in the presence of 5 mM Tris-HCl (pH 7.4) buffer and centrifuged (40,000 xg. 10 min, 4 OC). They were suspended using a homogenizer in the presence of 50 mM Tris–HCl (pH 7.4) buffer. They were subjected to centrifugation (40,000 xg, 10 min, 4 OC), suspended in 50 mM Tris–HCl (pH 7.4) and stored at 80 0C. A total volume of 500 mkL containing 50 mM Tris–HCl–4 mM CaCl2 (pH 7.4) buffer, the human 5-HT2B receptor expressing HEK293-EBNA cell membrane preparation and a radio ligand [3H] Mesulergine (3.1 TBq/mmol) was incubated at 25 OC for 1 h. The Pizotifen was dissolved in 100% DMSO and diluted to respective concentrations.
Substance Class Chemical
Created
by admin
on Sat Dec 16 01:25:46 GMT 2023
Edited
by admin
on Sat Dec 16 01:25:46 GMT 2023
Record UNII
MKZ19G896I
Record Status Validated (UNII)
Record Version
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Name Type Language
PIZOTIFEN HYDROCHLORIDE
WHO-DD  
Common Name English
Pizotifen hydrochloride [WHO-DD]
Common Name English
PIZOTYLINE HYDROCHLORIDE [MI]
Common Name English
PIZOTYLINE HYDROCHLORIDE
MI  
Common Name English
NSC-291564
Code English
PIPERIDINE, 4-(9,10-DIHYDRO-4H-BENZO(4,5)CYCLOHEPTA(1,2-B)THIEN-4-YLIDENE)-1-METHYL-, HYDROCHLORIDE (1:1)
Systematic Name English
Code System Code Type Description
EVMPD
SUB03886MIG
Created by admin on Sat Dec 16 01:25:46 GMT 2023 , Edited by admin on Sat Dec 16 01:25:46 GMT 2023
PRIMARY
CAS
73391-87-4
Created by admin on Sat Dec 16 01:25:46 GMT 2023 , Edited by admin on Sat Dec 16 01:25:46 GMT 2023
PRIMARY
PUBCHEM
3056070
Created by admin on Sat Dec 16 01:25:46 GMT 2023 , Edited by admin on Sat Dec 16 01:25:46 GMT 2023
PRIMARY
MERCK INDEX
m8899
Created by admin on Sat Dec 16 01:25:46 GMT 2023 , Edited by admin on Sat Dec 16 01:25:46 GMT 2023
PRIMARY Merck Index
EPA CompTox
DTXSID60223632
Created by admin on Sat Dec 16 01:25:46 GMT 2023 , Edited by admin on Sat Dec 16 01:25:46 GMT 2023
PRIMARY
NSC
291564
Created by admin on Sat Dec 16 01:25:46 GMT 2023 , Edited by admin on Sat Dec 16 01:25:46 GMT 2023
PRIMARY
SMS_ID
100000085316
Created by admin on Sat Dec 16 01:25:46 GMT 2023 , Edited by admin on Sat Dec 16 01:25:46 GMT 2023
PRIMARY
FDA UNII
MKZ19G896I
Created by admin on Sat Dec 16 01:25:46 GMT 2023 , Edited by admin on Sat Dec 16 01:25:46 GMT 2023
PRIMARY
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