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

Details

Stereochemistry ACHIRAL
Molecular Formula C19H21NS
Molecular Weight 295.442
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PIZOTYLINE

SMILES

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

InChI

InChIKey=FIADGNVRKBPQEU-UHFFFAOYSA-N
InChI=1S/C19H21NS/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

HIDE SMILES / InChI

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
Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
5 ng/mL
1 mg single, oral
dose: 1 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
PIZOTYLINE plasma
Homo sapiens
population: UNKNOWN
age: ADULT
sex: UNKNOWN
food status: UNKNOWN
14 ng/mL
1 mg 3 times / day steady-state, oral
dose: 1 mg
route of administration: Oral
experiment type: STEADY-STATE
co-administered:
PIZOTYLINE plasma
Homo sapiens
population: UNKNOWN
age: ADULT
sex: UNKNOWN
food status: UNKNOWN
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
23 h
1 mg single, oral
dose: 1 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
PIZOTYLINE plasma
Homo sapiens
population: UNKNOWN
age: ADULT
sex: UNKNOWN
food status: UNKNOWN
Funbound

Funbound

ValueDoseCo-administeredAnalytePopulation
9%
1 mg single, oral
dose: 1 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
PIZOTYLINE plasma
Homo sapiens
population: UNKNOWN
age: ADULT
sex: UNKNOWN
food status: UNKNOWN
Doses

Doses

DosePopulationAdverse events​
0.5 mg 3 times / day multiple, oral
Studied dose
Dose: 0.5 mg, 3 times / day
Route: oral
Route: multiple
Dose: 0.5 mg, 3 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
Disc. AE: Weight gain, Sleepiness...
AEs leading to
discontinuation/dose reduction:
Weight gain
Sleepiness
Sources:
1 mg 3 times / day multiple, oral
Studied dose
Dose: 1 mg, 3 times / day
Route: oral
Route: multiple
Dose: 1 mg, 3 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
Disc. AE: Weight gain, Depression...
AEs leading to
discontinuation/dose reduction:
Weight gain (11.1%)
Depression (7.4%)
Hunger abnormal (3.7%)
Confusion (3.7%)
Sources:
AEs

AEs

AESignificanceDosePopulation
Sleepiness Disc. AE
0.5 mg 3 times / day multiple, oral
Studied dose
Dose: 0.5 mg, 3 times / day
Route: oral
Route: multiple
Dose: 0.5 mg, 3 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
Weight gain Disc. AE
0.5 mg 3 times / day multiple, oral
Studied dose
Dose: 0.5 mg, 3 times / day
Route: oral
Route: multiple
Dose: 0.5 mg, 3 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
Weight gain 11.1%
Disc. AE
1 mg 3 times / day multiple, oral
Studied dose
Dose: 1 mg, 3 times / day
Route: oral
Route: multiple
Dose: 1 mg, 3 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
Confusion 3.7%
Disc. AE
1 mg 3 times / day multiple, oral
Studied dose
Dose: 1 mg, 3 times / day
Route: oral
Route: multiple
Dose: 1 mg, 3 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
Hunger abnormal 3.7%
Disc. AE
1 mg 3 times / day multiple, oral
Studied dose
Dose: 1 mg, 3 times / day
Route: oral
Route: multiple
Dose: 1 mg, 3 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
Depression 7.4%
Disc. AE
1 mg 3 times / day multiple, oral
Studied dose
Dose: 1 mg, 3 times / day
Route: oral
Route: multiple
Dose: 1 mg, 3 times / day
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
Overview

OverviewOther

Other InhibitorOther SubstrateOther Inducer







Drug as perpetrator​

Drug as perpetrator​

TargetModalityActivityMetaboliteClinical evidence
no [IC50 >10 uM]
no [IC50 >10 uM]
no [IC50 >10 uM]
no
yes [Activation 28.1838 uM]
yes [IC50 1.2589 uM]
yes [IC50 3.9811 uM]
Drug as victimTox targets

Tox targets

TargetModalityActivityMetaboliteClinical evidence
PubMed

PubMed

TitleDatePubMed
Validation and application of reversed phase high-performance liquid chromatographic method for quantification of pizotifen malate in pharmaceutical solid dosage formulations.
2010-10
New methods for diagnosis and treatment of vestibular diseases.
2010-08-09
Fulminant hepatitis possibly related to pizotifen therapy.
2010-06-24
P3MC: a double blind parallel group randomised placebo controlled trial of Propranolol and Pizotifen in preventing migraine in children.
2010-06-16
Prescribing for migraine with the focus on selective 5HT1-receptor agonists: a pharmacy database analysis.
2010-05
Prophylaxis of migraine headache.
2010-04-20
Recent concepts on cyclic vomiting syndrome in children.
2010-04
Cluster headache.
2010-02-09
Potential contribution of prescription practices to the emergence and spread of chloroquine resistance in south-west Nigeria: caution in the use of artemisinin combination therapy.
2009-12-30
What happens to new-onset headache in children that present to primary care? A case-cohort study using electronic primary care records.
2009-12
Treatment of primary headache in children: a multicenter hospital-based study in France.
2009-12
5-Hydroxytryptamine Receptor Subtypes and their Modulators with Therapeutic Potentials.
2009-06
Migraine headache in children.
2009-01-13
Prophylaxis of migraine: general principles and patient acceptance.
2008-12
Drug use in children: cohort study in three European countries.
2008-11-24
Optimizing prophylactic treatment of migraine: Subtypes and patient matching.
2008-10
Stages of motor output reorganization after hemispheric stroke suggested by longitudinal studies of cortical physiology.
2008-08
Cluster headache.
2008-07-23
Weight gain with pizotifen therapy.
2008-07
Pizotifen relieves acute migraine symptoms.
2008-03-01
Cluster headache.
2008-02-15
Pharmacological interventions for recurrent abdominal pain (RAP) and irritable bowel syndrome (IBS) in childhood.
2008-01-23
Update on the prophylaxis of migraine.
2008-01
[Confusional syndrome caused by pizotifen].
2007-10-19
Migraine associated vertigo.
2007-09
Management of migraine in Australian general practice.
2007-08-06
Pediatric migraine: pharmacologic agents for prophylaxis.
2007-07
Recommendations for the management of migraine in paediatric patients.
2007-04
The Effect of Paroxetine on the Reduction of Migraine Frequency is Independent of Its Anxiolytic Effect.
2006-12
Evaluation of guided imagery as treatment for recurrent abdominal pain in children: a randomized controlled trial.
2006-11-08
Pharmacological prevention of migraine: to be considered case by case.
2006-10
Anatomical alterations of the visual motion processing network in migraine with and without aura.
2006-10
Topiramate in the prevention of migraine: a review of its efficacy, tolerability, and acceptability.
2006-09
Topiramate for migraine prophylaxis.
2006-08
Which therapy for which patient?
2006-05
Potential vascular alpha1-adrenoceptor blocking properties of an array of 5-HT receptor ligands in the rat.
2006-03-27
Adult abdominal migraine: a new syndrome or sporadic feature of migraine headache? A case report.
2006-01
Cyclic Vomiting Syndrome in 41 adults: the illness, the patients, and problems of management.
2005-12-21
Raynaud phenomena and migraine in two children: inclusion within a family of related disorders.
2005-12
Pizotyline effectively attenuates the stimulus effects of N-methyl-3,4-methylenedioxyamphetamine (MDMA).
2005-10
Weight variations in the prophylactic therapy of primary headaches: 6-month follow-up.
2005-09
Anticipatory nausea in cyclical vomiting.
2005-03-24
Serotonin2C receptor blockade and thermoregulation during exercise in the heat.
2005-03
Use of intravenous midazolam and clonidine in cyclical vomiting syndrome: a case report.
2005-01
Practice parameter: pharmacological treatment of migraine headache in children and adolescents: report of the American Academy of Neurology Quality Standards Subcommittee and the Practice Committee of the Child Neurology Society.
2004-12-28
Agonist activity of antimigraine drugs at recombinant human 5-HT1A receptors: potential implications for prophylactic and acute therapy.
1997-06
The role of the central serotonergic system in pilocarpine-induced seizures: receptor mechanisms.
1989-11
Arterial complications of migraine treatment with methysergide and parenteral ergotamine.
1982-07-24
Effects of chronic treatment with antidepressants on aggressiveness induced by clonidine in mice.
1982
Comparative trial of serotonin antagonists in the management of migraine.
1970-05-09
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 Mon Mar 31 18:40:14 GMT 2025
Edited
by admin
on Mon Mar 31 18:40:14 GMT 2025
Record UNII
0BY8440V3N
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PIZOTYLINE
MI   USAN  
USAN  
Official Name English
PIZOTIFEN
INN   MART.   WHO-DD  
INN  
Preferred Name English
PIZOTIFEN [MART.]
Common Name English
BC-105
Code English
Pizotifen [WHO-DD]
Common Name English
PIZOTYLINE [USAN]
Common Name English
PIZOTYLINE [MI]
Common Name English
SANDOMIGRAN
Brand Name English
PIPERIDINE, 4-(9,10-DIHYDRO-4H-BENZO(4,5)CYCLOHEPTA(1,2-B)THIEN-4-YLIDENE)-1-METHYL-
Systematic Name English
4-(9,10-Dihydro-4H-benzo[4,5]cyclohepta[1,2-b]thien-4-ylidene)-1-methylpiperidine
Systematic Name English
pizotifen [INN]
Common Name English
Classification Tree Code System Code
WHO-ATC N02CX01
Created by admin on Mon Mar 31 18:40:14 GMT 2025 , Edited by admin on Mon Mar 31 18:40:14 GMT 2025
NCI_THESAURUS C66885
Created by admin on Mon Mar 31 18:40:14 GMT 2025 , Edited by admin on Mon Mar 31 18:40:14 GMT 2025
WHO-VATC QN02CX01
Created by admin on Mon Mar 31 18:40:14 GMT 2025 , Edited by admin on Mon Mar 31 18:40:14 GMT 2025
Code System Code Type Description
IUPHAR
93
Created by admin on Mon Mar 31 18:40:14 GMT 2025 , Edited by admin on Mon Mar 31 18:40:14 GMT 2025
PRIMARY
SMS_ID
100000092611
Created by admin on Mon Mar 31 18:40:14 GMT 2025 , Edited by admin on Mon Mar 31 18:40:14 GMT 2025
PRIMARY
DRUG BANK
DB06153
Created by admin on Mon Mar 31 18:40:14 GMT 2025 , Edited by admin on Mon Mar 31 18:40:14 GMT 2025
PRIMARY
CHEBI
50213
Created by admin on Mon Mar 31 18:40:14 GMT 2025 , Edited by admin on Mon Mar 31 18:40:14 GMT 2025
PRIMARY
MESH
D010918
Created by admin on Mon Mar 31 18:40:14 GMT 2025 , Edited by admin on Mon Mar 31 18:40:14 GMT 2025
PRIMARY
PUBCHEM
27400
Created by admin on Mon Mar 31 18:40:14 GMT 2025 , Edited by admin on Mon Mar 31 18:40:14 GMT 2025
PRIMARY
RXCUI
8373
Created by admin on Mon Mar 31 18:40:14 GMT 2025 , Edited by admin on Mon Mar 31 18:40:14 GMT 2025
PRIMARY RxNorm
NCI_THESAURUS
C87214
Created by admin on Mon Mar 31 18:40:14 GMT 2025 , Edited by admin on Mon Mar 31 18:40:14 GMT 2025
PRIMARY
DRUG CENTRAL
2220
Created by admin on Mon Mar 31 18:40:14 GMT 2025 , Edited by admin on Mon Mar 31 18:40:14 GMT 2025
PRIMARY
WIKIPEDIA
PIZOTIFEN
Created by admin on Mon Mar 31 18:40:14 GMT 2025 , Edited by admin on Mon Mar 31 18:40:14 GMT 2025
PRIMARY
EPA CompTox
DTXSID6023490
Created by admin on Mon Mar 31 18:40:14 GMT 2025 , Edited by admin on Mon Mar 31 18:40:14 GMT 2025
PRIMARY
CHEBI
50212
Created by admin on Mon Mar 31 18:40:14 GMT 2025 , Edited by admin on Mon Mar 31 18:40:14 GMT 2025
PRIMARY
CAS
15574-96-6
Created by admin on Mon Mar 31 18:40:14 GMT 2025 , Edited by admin on Mon Mar 31 18:40:14 GMT 2025
PRIMARY
ECHA (EC/EINECS)
239-632-9
Created by admin on Mon Mar 31 18:40:14 GMT 2025 , Edited by admin on Mon Mar 31 18:40:14 GMT 2025
PRIMARY
EVMPD
SUB09954MIG
Created by admin on Mon Mar 31 18:40:14 GMT 2025 , Edited by admin on Mon Mar 31 18:40:14 GMT 2025
PRIMARY
INN
2693
Created by admin on Mon Mar 31 18:40:14 GMT 2025 , Edited by admin on Mon Mar 31 18:40:14 GMT 2025
PRIMARY
MERCK INDEX
m8899
Created by admin on Mon Mar 31 18:40:14 GMT 2025 , Edited by admin on Mon Mar 31 18:40:14 GMT 2025
PRIMARY Merck Index
FDA UNII
0BY8440V3N
Created by admin on Mon Mar 31 18:40:14 GMT 2025 , Edited by admin on Mon Mar 31 18:40:14 GMT 2025
PRIMARY
ChEMBL
CHEMBL294951
Created by admin on Mon Mar 31 18:40:14 GMT 2025 , Edited by admin on Mon Mar 31 18:40:14 GMT 2025
PRIMARY
Related Record Type Details
TARGET -> INHIBITOR
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
TARGET -> INHIBITOR
Related Record Type Details
ACTIVE MOIETY