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=C2C=CC=C4)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

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 17:05:27 UTC 2023
Edited
by admin
on Fri Dec 15 17:05:27 UTC 2023
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  
Official 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 Fri Dec 15 17:05:28 UTC 2023 , Edited by admin on Fri Dec 15 17:05:28 UTC 2023
NCI_THESAURUS C66885
Created by admin on Fri Dec 15 17:05:28 UTC 2023 , Edited by admin on Fri Dec 15 17:05:28 UTC 2023
WHO-VATC QN02CX01
Created by admin on Fri Dec 15 17:05:28 UTC 2023 , Edited by admin on Fri Dec 15 17:05:28 UTC 2023
Code System Code Type Description
IUPHAR
93
Created by admin on Fri Dec 15 17:05:28 UTC 2023 , Edited by admin on Fri Dec 15 17:05:28 UTC 2023
PRIMARY
SMS_ID
100000092611
Created by admin on Fri Dec 15 17:05:28 UTC 2023 , Edited by admin on Fri Dec 15 17:05:28 UTC 2023
PRIMARY
DRUG BANK
DB06153
Created by admin on Fri Dec 15 17:05:28 UTC 2023 , Edited by admin on Fri Dec 15 17:05:28 UTC 2023
PRIMARY
CHEBI
50213
Created by admin on Fri Dec 15 17:05:28 UTC 2023 , Edited by admin on Fri Dec 15 17:05:28 UTC 2023
PRIMARY
MESH
D010918
Created by admin on Fri Dec 15 17:05:28 UTC 2023 , Edited by admin on Fri Dec 15 17:05:28 UTC 2023
PRIMARY
PUBCHEM
27400
Created by admin on Fri Dec 15 17:05:28 UTC 2023 , Edited by admin on Fri Dec 15 17:05:28 UTC 2023
PRIMARY
RXCUI
8373
Created by admin on Fri Dec 15 17:05:28 UTC 2023 , Edited by admin on Fri Dec 15 17:05:28 UTC 2023
PRIMARY RxNorm
NCI_THESAURUS
C87214
Created by admin on Fri Dec 15 17:05:28 UTC 2023 , Edited by admin on Fri Dec 15 17:05:28 UTC 2023
PRIMARY
DRUG CENTRAL
2220
Created by admin on Fri Dec 15 17:05:28 UTC 2023 , Edited by admin on Fri Dec 15 17:05:28 UTC 2023
PRIMARY
WIKIPEDIA
PIZOTIFEN
Created by admin on Fri Dec 15 17:05:28 UTC 2023 , Edited by admin on Fri Dec 15 17:05:28 UTC 2023
PRIMARY
EPA CompTox
DTXSID6023490
Created by admin on Fri Dec 15 17:05:28 UTC 2023 , Edited by admin on Fri Dec 15 17:05:28 UTC 2023
PRIMARY
CHEBI
50212
Created by admin on Fri Dec 15 17:05:28 UTC 2023 , Edited by admin on Fri Dec 15 17:05:28 UTC 2023
PRIMARY
CAS
15574-96-6
Created by admin on Fri Dec 15 17:05:28 UTC 2023 , Edited by admin on Fri Dec 15 17:05:28 UTC 2023
PRIMARY
ECHA (EC/EINECS)
239-632-9
Created by admin on Fri Dec 15 17:05:28 UTC 2023 , Edited by admin on Fri Dec 15 17:05:28 UTC 2023
PRIMARY
EVMPD
SUB09954MIG
Created by admin on Fri Dec 15 17:05:28 UTC 2023 , Edited by admin on Fri Dec 15 17:05:28 UTC 2023
PRIMARY
INN
2693
Created by admin on Fri Dec 15 17:05:28 UTC 2023 , Edited by admin on Fri Dec 15 17:05:28 UTC 2023
PRIMARY
MERCK INDEX
m8899
Created by admin on Fri Dec 15 17:05:28 UTC 2023 , Edited by admin on Fri Dec 15 17:05:28 UTC 2023
PRIMARY Merck Index
FDA UNII
0BY8440V3N
Created by admin on Fri Dec 15 17:05:28 UTC 2023 , Edited by admin on Fri Dec 15 17:05:28 UTC 2023
PRIMARY
ChEMBL
CHEMBL294951
Created by admin on Fri Dec 15 17:05:28 UTC 2023 , Edited by admin on Fri Dec 15 17:05:28 UTC 2023
PRIMARY
Related Record Type Details
TARGET -> INHIBITOR
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
TARGET -> INHIBITOR
Related Record Type Details
ACTIVE MOIETY