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Details

Stereochemistry MIXED
Molecular Formula C18H22NO3S
Molecular Weight 332.437
Optical Activity UNSPECIFIED
Defined Stereocenters 0 / 3
E/Z Centers 0
Charge 1

SHOW SMILES / InChI
Structure of HETERONIUM

SMILES

C[N+]1(C)CCC(C1)OC(=O)C(O)(C2=CC=CS2)C3=CC=CC=C3

InChI

InChIKey=IGWCFPFGZULDHY-UHFFFAOYSA-N
InChI=1S/C18H22NO3S/c1-19(2)11-10-15(13-19)22-17(20)18(21,16-9-6-12-23-16)14-7-4-3-5-8-14/h3-9,12,15,21H,10-11,13H2,1-2H3/q+1

HIDE SMILES / InChI

Molecular Formula C18H21NO3S
Molecular Weight 331.429
Charge 0
Count
Stereochemistry MIXED
Additional Stereochemistry No
Defined Stereocenters 0 / 3
E/Z Centers 0
Optical Activity UNSPECIFIED

Heteronium is an anticholinergic agent. As a bromide salt, it was investigated in the clinic for the treatment of peptic ulcer and other gastrointestinal disorders.

Approval Year

PubMed

PubMed

TitleDatePubMed
Evaluation of the antisecretory effect of a new anticholinergic agent--heteronium bromide.
1969-05
A double-blind study of heteronium bromide and amobarbital in the management of gastrointestinal conditions associated with anxiety.
1968-10
Substance Class Chemical
Created
by admin
on Mon Mar 31 20:36:59 GMT 2025
Edited
by admin
on Mon Mar 31 20:36:59 GMT 2025
Record UNII
2FN14CSE90
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
.ALPHA.+.BETA.-(±)-(1-METHYL-3-PYRROLIDINYL) .ALPHA.-PHENYL-.ALPHA.-(2-THIENYL)GLYCOLATE
Preferred Name English
HETERONIUM
Common Name English
PYRROLIDINIUM, 3-((2-HYDROXY-2-PHENYL-2-(2-THIENYL)ACETYL)OXY)-1,1-DIMETHYL-
Systematic Name English
HETERONIUM ION
Common Name English
(±)-3-HYDROXY-1,1-DIMETHYLPYRROLIDINIUM .ALPHA.-PHENYL-2-THIOPHENEGLYCOLATE
Systematic Name English
HETERONIUM CATION
Common Name English
PYRROLIDINIUM, 3-((HYDROXYPHENYL-2-THIENYLACETYL)OXY)-1,1-DIMETHYL-
Systematic Name English
Code System Code Type Description
CAS
21379-80-6
Created by admin on Mon Mar 31 20:36:59 GMT 2025 , Edited by admin on Mon Mar 31 20:36:59 GMT 2025
PRIMARY
MESH
C014023
Created by admin on Mon Mar 31 20:36:59 GMT 2025 , Edited by admin on Mon Mar 31 20:36:59 GMT 2025
PRIMARY
FDA UNII
2FN14CSE90
Created by admin on Mon Mar 31 20:36:59 GMT 2025 , Edited by admin on Mon Mar 31 20:36:59 GMT 2025
PRIMARY
PUBCHEM
13965
Created by admin on Mon Mar 31 20:36:59 GMT 2025 , Edited by admin on Mon Mar 31 20:36:59 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY