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

Details

Stereochemistry ACHIRAL
Molecular Formula C21H21NO2
Molecular Weight 319.3969
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of OXETORONE

SMILES

CN(C)CCC=C1C2=C(COC3=C1C=CC=C3)C4=C(O2)C=CC=C4

InChI

InChIKey=VZVRZTZPHOHSCK-UHFFFAOYSA-N
InChI=1S/C21H21NO2/c1-22(2)13-7-10-17-15-8-3-5-11-19(15)23-14-18-16-9-4-6-12-20(16)24-21(17)18/h3-6,8-12H,7,13-14H2,1-2H3

HIDE SMILES / InChI
Oxetorone is an antimigraine drug used for the disease-modifying treatment of migraines and marketed in several European countries. It works by non-selective inhibition of serotonin receptors and antihistamine agent. The therapeutic effects of oxetorone are primarily linked to antiserotonergic and also antihistamine and anti-adrenergic properties. Antidopaminergic properties are also suspected because hyperprolactinemia and extrapyramidal reactions have been observed. Adverse effects are: hypertonia, drowsiness at the start of treatment, diarrhoea and lymphocytic colitis. Acute intoxications by oxetorone, although uncommon, are potentially severe poisonings.

Approval Year

Patents

Sample Use Guides

1 to 2 tablets (60 to 120 mg) a day
Route of Administration: Oral
Name Type Language
OXETORONE
INN   MI   WHO-DD  
INN  
Official Name English
Oxetorone [WHO-DD]
Common Name English
OXETORONE [MI]
Common Name English
N,N-DIMETHYLBENZOFURO(3,2-C)(1)BENZOXEPIN-D6(12H),G-PROPYLAMINE
Common Name English
oxetorone [INN]
Common Name English
1-PROPANAMINE, 3-BENZOFURO(3,2-C)(1)BENZOXEPIN-6(12H)-YLIDENE-N,N-DIMETHYL-
Common Name English
Classification Tree Code System Code
WHO-ATC N02CX06
Created by admin on Fri Dec 15 17:31:25 GMT 2023 , Edited by admin on Fri Dec 15 17:31:25 GMT 2023
WHO-VATC QN02CX06
Created by admin on Fri Dec 15 17:31:25 GMT 2023 , Edited by admin on Fri Dec 15 17:31:25 GMT 2023
NCI_THESAURUS C66885
Created by admin on Fri Dec 15 17:31:25 GMT 2023 , Edited by admin on Fri Dec 15 17:31:25 GMT 2023
Code System Code Type Description
CAS
26020-55-3
Created by admin on Fri Dec 15 17:31:25 GMT 2023 , Edited by admin on Fri Dec 15 17:31:25 GMT 2023
PRIMARY
RXCUI
32633
Created by admin on Fri Dec 15 17:31:25 GMT 2023 , Edited by admin on Fri Dec 15 17:31:25 GMT 2023
PRIMARY RxNorm
SMS_ID
100000083058
Created by admin on Fri Dec 15 17:31:25 GMT 2023 , Edited by admin on Fri Dec 15 17:31:25 GMT 2023
PRIMARY
ECHA (EC/EINECS)
247-411-3
Created by admin on Fri Dec 15 17:31:25 GMT 2023 , Edited by admin on Fri Dec 15 17:31:25 GMT 2023
PRIMARY
DRUG BANK
DB13463
Created by admin on Fri Dec 15 17:31:25 GMT 2023 , Edited by admin on Fri Dec 15 17:31:25 GMT 2023
PRIMARY
EVMPD
SUB09518MIG
Created by admin on Fri Dec 15 17:31:25 GMT 2023 , Edited by admin on Fri Dec 15 17:31:25 GMT 2023
PRIMARY
INN
2840
Created by admin on Fri Dec 15 17:31:25 GMT 2023 , Edited by admin on Fri Dec 15 17:31:25 GMT 2023
PRIMARY
MESH
C011962
Created by admin on Fri Dec 15 17:31:25 GMT 2023 , Edited by admin on Fri Dec 15 17:31:25 GMT 2023
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DRUG CENTRAL
2019
Created by admin on Fri Dec 15 17:31:25 GMT 2023 , Edited by admin on Fri Dec 15 17:31:25 GMT 2023
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WIKIPEDIA
OXETORONE
Created by admin on Fri Dec 15 17:31:25 GMT 2023 , Edited by admin on Fri Dec 15 17:31:25 GMT 2023
PRIMARY
ChEMBL
CHEMBL2111020
Created by admin on Fri Dec 15 17:31:25 GMT 2023 , Edited by admin on Fri Dec 15 17:31:25 GMT 2023
PRIMARY
MERCK INDEX
m8303
Created by admin on Fri Dec 15 17:31:25 GMT 2023 , Edited by admin on Fri Dec 15 17:31:25 GMT 2023
PRIMARY Merck Index
NCI_THESAURUS
C84037
Created by admin on Fri Dec 15 17:31:25 GMT 2023 , Edited by admin on Fri Dec 15 17:31:25 GMT 2023
PRIMARY
EPA CompTox
DTXSID50865262
Created by admin on Fri Dec 15 17:31:25 GMT 2023 , Edited by admin on Fri Dec 15 17:31:25 GMT 2023
PRIMARY
FDA UNII
T3XOS33TIQ
Created by admin on Fri Dec 15 17:31:25 GMT 2023 , Edited by admin on Fri Dec 15 17:31:25 GMT 2023
PRIMARY
PUBCHEM
36846
Created by admin on Fri Dec 15 17:31:25 GMT 2023 , Edited by admin on Fri Dec 15 17:31:25 GMT 2023
PRIMARY