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Details

Stereochemistry RACEMIC
Molecular Formula C23H26N2O2
Molecular Weight 362.4647
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BENZETIMIDE

SMILES

O=C1CCC(C2CCN(CC3=CC=CC=C3)CC2)(C(=O)N1)C4=CC=CC=C4

InChI

InChIKey=LQQIVYSCPWCSSD-UHFFFAOYSA-N
InChI=1S/C23H26N2O2/c26-21-11-14-23(22(27)24-21,19-9-5-2-6-10-19)20-12-15-25(16-13-20)17-18-7-3-1-4-8-18/h1-10,20H,11-17H2,(H,24,26,27)

HIDE SMILES / InChI
Benzetimide, a muscarinic acetylcholine receptor antagonist that was investigated as an antiparkinson-agent and was studied in the treatment of diarrheas of cattle and calves. Benzetimide is an enantiomer of dexetimide that has been used to treat neuroleptic-induced Parkinsonism.

Approval Year

PubMed

PubMed

TitleDatePubMed
The allosteric interaction of otenzepad (AF-DX 116) at muscarinic M2 receptors in guinea pig atria.
2001 Mar 30
Labelling of the solvent DMSO as side reaction of methylations with n.c.a. [11C]CH3I.
2001 Sep
Variable effects of previously untested muscarinic receptor antagonists on experimental myopia.
2003 Mar
Sequential 123I-iododexetimide scans in temporal lobe epilepsy: comparison with neuroimaging scans (MR imaging and 18F-FDG PET imaging).
2005 Feb
Defects in muscarinic receptor-coupled signal transduction in isolated parotid gland cells after in vivo irradiation: evidence for a non-DNA target of radiation.
2005 Feb 14
Reduced posterior cingulate binding of I-123 iodo-dexetimide to muscarinic receptors in mild Alzheimer's disease.
2005 May
Synthesis and structure-activity relationship of benzetimide derivatives as human CXCR3 antagonists.
2008 Nov 1
Name Type Language
BENZETIMIDE
INN   MI  
INN  
Official Name English
SPASMENTAL
Brand Name English
BENZETIMIDE [MI]
Common Name English
2-(1-BENZYL-4-PIPERIDYL)-2-PHENYLGLUTARIMIDE
Systematic Name English
(3,4'-BIPIPERIDINE)-2,6-DIONE, 3-PHENYL-1'-(PHENYLMETHYL)-
Systematic Name English
benzetimide [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29704
Created by admin on Fri Dec 15 16:08:39 GMT 2023 , Edited by admin on Fri Dec 15 16:08:39 GMT 2023
WHO-VATC QA03AB90
Created by admin on Fri Dec 15 16:08:39 GMT 2023 , Edited by admin on Fri Dec 15 16:08:39 GMT 2023
Code System Code Type Description
PUBCHEM
21847
Created by admin on Fri Dec 15 16:08:39 GMT 2023 , Edited by admin on Fri Dec 15 16:08:39 GMT 2023
PRIMARY
EVMPD
SUB05747MIG
Created by admin on Fri Dec 15 16:08:39 GMT 2023 , Edited by admin on Fri Dec 15 16:08:39 GMT 2023
PRIMARY
ChEMBL
CHEMBL10272
Created by admin on Fri Dec 15 16:08:39 GMT 2023 , Edited by admin on Fri Dec 15 16:08:39 GMT 2023
PRIMARY
INN
1708
Created by admin on Fri Dec 15 16:08:39 GMT 2023 , Edited by admin on Fri Dec 15 16:08:39 GMT 2023
PRIMARY
EPA CompTox
DTXSID2046173
Created by admin on Fri Dec 15 16:08:39 GMT 2023 , Edited by admin on Fri Dec 15 16:08:39 GMT 2023
PRIMARY
CAS
14051-33-3
Created by admin on Fri Dec 15 16:08:39 GMT 2023 , Edited by admin on Fri Dec 15 16:08:39 GMT 2023
PRIMARY
NCI_THESAURUS
C73007
Created by admin on Fri Dec 15 16:08:39 GMT 2023 , Edited by admin on Fri Dec 15 16:08:39 GMT 2023
PRIMARY
MERCK INDEX
m2347
Created by admin on Fri Dec 15 16:08:39 GMT 2023 , Edited by admin on Fri Dec 15 16:08:39 GMT 2023
PRIMARY Merck Index
FDA UNII
B987T0L5FX
Created by admin on Fri Dec 15 16:08:39 GMT 2023 , Edited by admin on Fri Dec 15 16:08:39 GMT 2023
PRIMARY
SMS_ID
100000086383
Created by admin on Fri Dec 15 16:08:39 GMT 2023 , Edited by admin on Fri Dec 15 16:08:39 GMT 2023
PRIMARY
CAS
119391-55-8
Created by admin on Fri Dec 15 16:08:39 GMT 2023 , Edited by admin on Fri Dec 15 16:08:39 GMT 2023
SUPERSEDED