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Details

Stereochemistry ACHIRAL
Molecular Formula C19H21NS.C4H4O4
Molecular Weight 411.514
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of PIZOTYLINE MALEATE

SMILES

OC(=O)\C=C/C(O)=O.CN1CCC(CC1)=C2C3=C(CCC4=C2C=CC=C4)SC=C3

InChI

InChIKey=GGYSHFFKUHGBIK-BTJKTKAUSA-N
InChI=1S/C19H21NS.C4H4O4/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;5-3(6)1-2-4(7)8/h2-5,10,13H,6-9,11-12H2,1H3;1-2H,(H,5,6)(H,7,8)/b;2-1-

HIDE SMILES / InChI

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
Comparative trial of serotonin antagonists in the management of migraine.
1970 May 9
Paroxysmal hemicrania and cluster headache: two discrete entities or is there an overlap?
2002 Dec
[Critical ischaemia of the limbs and localized livedo in a case of ergotism].
2002 Jan 25
[Current views on migraine and anti-migraine preparations].
2003
Agomelatine(S 20098) antagonizes the penile erections induced by the stimulation of 5-HT2C receptors in Wistar rats.
2003 Oct
Determination of ketotifen in human plasma by LC-MS.
2004 Jan 27
Cyclic Vomiting Syndrome in 41 adults: the illness, the patients, and problems of management.
2005 Dec 21
Update on the prophylaxis of migraine.
2008 Jan
Prophylaxis of migraine headache.
2010 Apr 20
Cluster headache.
2010 Feb 9
P3MC: a double blind parallel group randomised placebo controlled trial of Propranolol and Pizotifen in preventing migraine in children.
2010 Jun 16
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.
Name Type Language
PIZOTYLINE MALEATE
Common Name English
PIZOTIFEN HYDROGEN MALEATE
Common Name English
PIPERIDINE, 4-(9,10-DIHYDRO-4H-BENZO(4,5)CYCLOHEPTA(1,2-B)THIEN-4-YLIDENE)-1-METHYL-, (Z)-2-BUTENEDIOATE (1:1)
Systematic Name English
PIZOTIFEN MALEATE
WHO-DD  
Common Name English
Pizotifen Maleate [WHO-DD]
Common Name English
PIPERIDINE, 4-(9,10-DIHYDRO-4H-BENZO(4,5)CYCLOHEPTA(1,2-B)THIEN-4-YLIDENE)-1-METHYL-, (2Z)-2-BUTENEDIOATE (1:1)
Systematic Name English
Code System Code Type Description
ECHA (EC/EINECS)
246-204-5
Created by admin on Fri Dec 15 15:18:51 GMT 2023 , Edited by admin on Fri Dec 15 15:18:51 GMT 2023
PRIMARY
PUBCHEM
6439699
Created by admin on Fri Dec 15 15:18:51 GMT 2023 , Edited by admin on Fri Dec 15 15:18:51 GMT 2023
PRIMARY
CAS
24359-22-6
Created by admin on Fri Dec 15 15:18:51 GMT 2023 , Edited by admin on Fri Dec 15 15:18:51 GMT 2023
PRIMARY
EVMPD
SUB03887MIG
Created by admin on Fri Dec 15 15:18:51 GMT 2023 , Edited by admin on Fri Dec 15 15:18:51 GMT 2023
PRIMARY
FDA UNII
2S5E7G70SZ
Created by admin on Fri Dec 15 15:18:51 GMT 2023 , Edited by admin on Fri Dec 15 15:18:51 GMT 2023
PRIMARY
SMS_ID
100000085335
Created by admin on Fri Dec 15 15:18:51 GMT 2023 , Edited by admin on Fri Dec 15 15:18:51 GMT 2023
PRIMARY
CHEBI
50214
Created by admin on Fri Dec 15 15:18:51 GMT 2023 , Edited by admin on Fri Dec 15 15:18:51 GMT 2023
PRIMARY