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Details

Stereochemistry RACEMIC
Molecular Formula C23H34N3O3
Molecular Weight 400.5344
Optical Activity ( + / - )
Defined Stereocenters 3 / 3
E/Z Centers 0
Charge 1

SHOW SMILES / InChI
Structure of BEPERIDIUM

SMILES

CC[N@+]1(C)CC[C@@H](CC1)OC(=O)[C@H](N2CCCCCC2)C3=NOC4=CC=CC=C34

InChI

InChIKey=CNTJFDRCJSXDAU-WTSFKKHRSA-N
InChI=1S/C23H34N3O3/c1-3-26(2)16-12-18(13-17-26)28-23(27)22(25-14-8-4-5-9-15-25)21-19-10-6-7-11-20(19)29-24-21/h6-7,10-11,18,22H,3-5,8-9,12-17H2,1-2H3/q+1/t18-,22-,26+/m1/s1

HIDE SMILES / InChI

Molecular Formula C23H34N3O3
Molecular Weight 400.5344
Charge 1
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 3 / 3
E/Z Centers 0
Optical Activity UNSPECIFIED

Beperidium (also known as SX-810 ) is a competitive antagonist against acetylcholine. Experiments on animal have shown that this compound exhibited spasmolytic and antiulcerative activities without exerting systemic antimuscarinic side effects.

Approval Year

PubMed

PubMed

TitleDatePubMed
Pharmacological properties of the novel antimuscarinic agent 4-[2-(1,2-benzisoxazol-3-yl)-2-(hexahydro-1H-azepin-1-yl)a cetoxy]-1-et hyl-1- methylpiperidinium iodide.
1986 Jun
Patents

Patents

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:32:58 GMT 2023
Edited
by admin
on Fri Dec 15 15:32:58 GMT 2023
Record UNII
OT9SNF3EEF
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BEPERIDIUM
Common Name English
BEPERIDIUM CATION
Common Name English
BEPERIDIUM ION
Common Name English
PIPERIDINIUM, 4-((2-(1,2-BENZISOXAZOL-3-YL)-2-(HEXAHYDRO-1H-AZEPIN-1-YL)ACETYL)OXY)-1-ETHYL-1-METHYL-
Systematic Name English
Code System Code Type Description
CAS
86434-70-0
Created by admin on Fri Dec 15 15:32:58 GMT 2023 , Edited by admin on Fri Dec 15 15:32:58 GMT 2023
PRIMARY
PUBCHEM
91617581
Created by admin on Fri Dec 15 15:32:58 GMT 2023 , Edited by admin on Fri Dec 15 15:32:58 GMT 2023
PRIMARY
FDA UNII
OT9SNF3EEF
Created by admin on Fri Dec 15 15:32:58 GMT 2023 , Edited by admin on Fri Dec 15 15:32:58 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY