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Details

Stereochemistry RACEMIC
Molecular Formula C23H26N2O2.ClH
Molecular Weight 398.926
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BENZETIMIDE HYDROCHLORIDE

SMILES

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

InChI

InChIKey=XSOOSXRNMDUWEM-UHFFFAOYSA-N
InChI=1S/C23H26N2O2.ClH/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);1H

HIDE SMILES / InChI

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C23H26N2O2
Molecular Weight 362.4647
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

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
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
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:35:44 GMT 2023
Edited
by admin
on Fri Dec 15 17:35:44 GMT 2023
Record UNII
V6ERX20PHB
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BENZETIMIDE HYDROCHLORIDE
MI   USAN  
USAN  
Official Name English
JANSSEN-R-492
Code English
BENZETIMIDE HCL
Common Name English
MCN-JR-4929-11
Code English
JANSSEN R 492
Code English
(3,4'-BIPIPERIDINE)-2,6-DIONE, 3-PHENYL-1'-(PHENYLMETHYL)-, MONOHYDROCHLORIDE
Common Name English
DIOXATRINE
Brand Name English
2-(1-Benzyl-4-piperidyl)-2-phenylglutarimide monohydrochloride
Systematic Name English
BENZETIMIDE HYDROCHLORIDE [USAN]
Common Name English
BENZETIMIDE HYDROCHLORIDE [MI]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29704
Created by admin on Fri Dec 15 17:35:44 GMT 2023 , Edited by admin on Fri Dec 15 17:35:44 GMT 2023
Code System Code Type Description
SMS_ID
300000029154
Created by admin on Fri Dec 15 17:35:44 GMT 2023 , Edited by admin on Fri Dec 15 17:35:44 GMT 2023
PRIMARY
ChEMBL
CHEMBL10272
Created by admin on Fri Dec 15 17:35:44 GMT 2023 , Edited by admin on Fri Dec 15 17:35:44 GMT 2023
PRIMARY
CAS
5633-14-7
Created by admin on Fri Dec 15 17:35:44 GMT 2023 , Edited by admin on Fri Dec 15 17:35:44 GMT 2023
PRIMARY
EPA CompTox
DTXSID101036320
Created by admin on Fri Dec 15 17:35:44 GMT 2023 , Edited by admin on Fri Dec 15 17:35:44 GMT 2023
PRIMARY
PUBCHEM
21846
Created by admin on Fri Dec 15 17:35:44 GMT 2023 , Edited by admin on Fri Dec 15 17:35:44 GMT 2023
PRIMARY
ECHA (EC/EINECS)
227-072-8
Created by admin on Fri Dec 15 17:35:44 GMT 2023 , Edited by admin on Fri Dec 15 17:35:44 GMT 2023
PRIMARY
MERCK INDEX
m2347
Created by admin on Fri Dec 15 17:35:44 GMT 2023 , Edited by admin on Fri Dec 15 17:35:44 GMT 2023
PRIMARY Merck Index
NCI_THESAURUS
C78062
Created by admin on Fri Dec 15 17:35:44 GMT 2023 , Edited by admin on Fri Dec 15 17:35:44 GMT 2023
PRIMARY
FDA UNII
V6ERX20PHB
Created by admin on Fri Dec 15 17:35:44 GMT 2023 , Edited by admin on Fri Dec 15 17:35:44 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY