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Details

Stereochemistry ACHIRAL
Molecular Formula C15H33N2O2
Molecular Weight 273.4347
Optical Activity NONE
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 1

SHOW SMILES / InChI
Structure of DIBUTOLINE

SMILES

CCCCN(CCCC)C(=O)OCC[N+](C)(C)CC

InChI

InChIKey=SDEXVKFYBBHUKN-UHFFFAOYSA-N
InChI=1S/C15H33N2O2/c1-6-9-11-16(12-10-7-2)15(18)19-14-13-17(4,5)8-3/h6-14H2,1-5H3/q+1

HIDE SMILES / InChI

Molecular Formula C15H33N2O2
Molecular Weight 273.4347
Charge 1
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity NONE

DIBUTOLINE, an antispasmodic drug, produces paresis of smooth muscles innervated by the parasympathetic nervous system. Its effect on the smooth muscles, therefore, simulates that of paralysis of the oculomotor nerve, that is, paresis of the sphincter of the iris and the ciliary muscles. DIBUTOLINE has no effect on the ocular muscles innervated by the sympathetic nervous system.

Approval Year

PubMed

PubMed

TitleDatePubMed
Further clinical observations on the use of dibutoline, a new antispasmodic drug.
1948-08
Clinical evaluation of dibutoline in diseases of the gastro-intestinal tract.
1948-02-15
Report of a preliminary clinical trial of dibutoline, a new antispasmotic drug.
1947-02
Substance Class Chemical
Created
by admin
on Mon Mar 31 17:45:10 GMT 2025
Edited
by admin
on Mon Mar 31 17:45:10 GMT 2025
Record UNII
1B3Q705AQH
Record Status Validated (UNII)
Record Version
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Name Type Language
DIBUTOLINE
Common Name English
DIBUTOLINE CATION
Preferred Name English
DIBUTOLINE ION
Common Name English
ETHANAMINIUM, 2-(((DIBUTYLAMINO)CARBONYL)OXY)-N-ETHYL-N,N-DIMETHYL-
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID90176369
Created by admin on Mon Mar 31 17:45:11 GMT 2025 , Edited by admin on Mon Mar 31 17:45:11 GMT 2025
PRIMARY
PUBCHEM
10764
Created by admin on Mon Mar 31 17:45:11 GMT 2025 , Edited by admin on Mon Mar 31 17:45:11 GMT 2025
PRIMARY
CAS
21962-82-3
Created by admin on Mon Mar 31 17:45:11 GMT 2025 , Edited by admin on Mon Mar 31 17:45:11 GMT 2025
PRIMARY
FDA UNII
1B3Q705AQH
Created by admin on Mon Mar 31 17:45:11 GMT 2025 , Edited by admin on Mon Mar 31 17:45:11 GMT 2025
PRIMARY