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

Details

Stereochemistry RACEMIC
Molecular Formula C27H31ClN2O
Molecular Weight 435.001
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CHLORBENZOXAMINE

SMILES

CC1=C(CN2CCN(CCOC(C3=CC=CC=C3)C4=CC=CC=C4Cl)CC2)C=CC=C1

InChI

InChIKey=VEVSKUJZSMGTMM-UHFFFAOYSA-N
InChI=1S/C27H31ClN2O/c1-22-9-5-6-12-24(22)21-30-17-15-29(16-18-30)19-20-31-27(23-10-3-2-4-11-23)25-13-7-8-14-26(25)28/h2-14,27H,15-21H2,1H3

HIDE SMILES / InChI

Molecular Formula C27H31ClN2O
Molecular Weight 435.001
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Chlorbenzoxamine is an antimuscarinic agent used for the treatment of peptic ulcer disease and other functional gastrointestinal disorders. Chlorbenzoxamine, a structural analog of hydroxyzine, produces a unique antagonism of gastric ulceration induced in rats and dogs by various procedures. This effect is not accompanied by a significant gastric secretory depression or a reduction in gastric acid concentration. Chlorbenzoxamine does not show anticholinergic or antihistaminic activity in vitro but does produce a nonspecific depression of isolated smooth muscle. The antiulcer effect of chlorbenzoxamine in rats is abolished by hypophysectomy suggesting a central or endocrine mechanism of action.

Approval Year

PubMed

PubMed

TitleDatePubMed
Development of a list of potentially inappropriate drugs for the korean elderly using the delphi method.
2010 Dec
Substance Class Chemical
Created
by admin
on Sat Dec 16 15:52:37 GMT 2023
Edited
by admin
on Sat Dec 16 15:52:37 GMT 2023
Record UNII
N52918SLYN
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CHLORBENZOXAMINE
INN   MI   WHO-DD  
INN  
Official Name English
Chlorbenzoxamine [WHO-DD]
Common Name English
CHLORBENZOXAMINE [MI]
Common Name English
chlorbenzoxamine [INN]
Common Name English
1-(2-(O-CHLORO-.ALPHA.-PHENYLBENZYLOXY)ETHYL)-4-O-METHYLBENZYLPIPERAZINE
Common Name English
Classification Tree Code System Code
WHO-VATC QA03AX03
Created by admin on Sat Dec 16 15:52:38 GMT 2023 , Edited by admin on Sat Dec 16 15:52:38 GMT 2023
NCI_THESAURUS C29704
Created by admin on Sat Dec 16 15:52:38 GMT 2023 , Edited by admin on Sat Dec 16 15:52:38 GMT 2023
WHO-ATC A03AX03
Created by admin on Sat Dec 16 15:52:38 GMT 2023 , Edited by admin on Sat Dec 16 15:52:38 GMT 2023
Code System Code Type Description
WIKIPEDIA
Chlorbenzoxamine
Created by admin on Sat Dec 16 15:52:38 GMT 2023 , Edited by admin on Sat Dec 16 15:52:38 GMT 2023
PRIMARY
DRUG CENTRAL
3090
Created by admin on Sat Dec 16 15:52:38 GMT 2023 , Edited by admin on Sat Dec 16 15:52:38 GMT 2023
PRIMARY
FDA UNII
N52918SLYN
Created by admin on Sat Dec 16 15:52:38 GMT 2023 , Edited by admin on Sat Dec 16 15:52:38 GMT 2023
PRIMARY
EPA CompTox
DTXSID80862108
Created by admin on Sat Dec 16 15:52:38 GMT 2023 , Edited by admin on Sat Dec 16 15:52:38 GMT 2023
PRIMARY
NCI_THESAURUS
C79940
Created by admin on Sat Dec 16 15:52:38 GMT 2023 , Edited by admin on Sat Dec 16 15:52:38 GMT 2023
PRIMARY
MERCK INDEX
m3351
Created by admin on Sat Dec 16 15:52:38 GMT 2023 , Edited by admin on Sat Dec 16 15:52:38 GMT 2023
PRIMARY Merck Index
ECHA (EC/EINECS)
208-323-0
Created by admin on Sat Dec 16 15:52:38 GMT 2023 , Edited by admin on Sat Dec 16 15:52:38 GMT 2023
PRIMARY
ChEMBL
CHEMBL2110781
Created by admin on Sat Dec 16 15:52:38 GMT 2023 , Edited by admin on Sat Dec 16 15:52:38 GMT 2023
PRIMARY
PUBCHEM
71636
Created by admin on Sat Dec 16 15:52:38 GMT 2023 , Edited by admin on Sat Dec 16 15:52:38 GMT 2023
PRIMARY
DRUG BANK
DB13788
Created by admin on Sat Dec 16 15:52:38 GMT 2023 , Edited by admin on Sat Dec 16 15:52:38 GMT 2023
PRIMARY
INN
806
Created by admin on Sat Dec 16 15:52:38 GMT 2023 , Edited by admin on Sat Dec 16 15:52:38 GMT 2023
PRIMARY
CAS
522-18-9
Created by admin on Sat Dec 16 15:52:38 GMT 2023 , Edited by admin on Sat Dec 16 15:52:38 GMT 2023
PRIMARY
SMS_ID
100000081559
Created by admin on Sat Dec 16 15:52:38 GMT 2023 , Edited by admin on Sat Dec 16 15:52:38 GMT 2023
PRIMARY
EVMPD
SUB06176MIG
Created by admin on Sat Dec 16 15:52:38 GMT 2023 , Edited by admin on Sat Dec 16 15:52:38 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY