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

Details

Stereochemistry RACEMIC
Molecular Formula C14H23BrNO3.I
Molecular Weight 460.146
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FUBROGONIUM IODIDE

SMILES

[I-].CC[N+](C)(CC)CCC(C)OC(=O)C1=CC=C(Br)O1

InChI

InChIKey=KROWHJNUJMVHNU-UHFFFAOYSA-M
InChI=1S/C14H23BrNO3.HI/c1-5-16(4,6-2)10-9-11(3)18-14(17)12-7-8-13(15)19-12;/h7-8,11H,5-6,9-10H2,1-4H3;1H/q+1;/p-1

HIDE SMILES / InChI

Molecular Formula HI
Molecular Weight 127.9124
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C14H23BrNO3
Molecular Weight 333.241
Charge 1
Count
Stereochemistry MIXED
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Fubromegan, a ganglionic blocking agent as an iodide salt, FUBROGONIUM IODIDE was used in Russia in patients with peptic ulcer and in the symptomatic therapy of patients with pneumoconioses. The antispasmodic effect of fubromegan was due to the effect on m- and n-cholinergic structures of smooth muscles and ganglia.

Approval Year

PubMed

PubMed

TitleDatePubMed
[Roentgenological studies on the effect of fubromegan in dyskinesias of the biliary tract].
1961
[Quateleron and Fubromegan in the treatment of peptic ulcer].
1961 Dec
[Effect of fubromegan on the motor-evacuation activity of the stomach (roentgenological studies)].
1961 Nov
[Use of a new domestic preparation fubromegan in the treatment of peptic ulcer].
1961 Nov
[COMPARATIVE EVALUATION OF THE EFFECT OF CHOLINOLYTIC DRUGS (HEXONIUM, FUBROMEGAN AND QUATALERON) ON THE DEVELOPMENT OF EXPERIMENTAL ULCER].
1963 Nov-Dec
Patents

Sample Use Guides

the initial dosage: 30 mg with increasing up to 60-100 мmg. 2-3 times/day during 2-3 weeks
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:08:14 GMT 2023
Edited
by admin
on Fri Dec 15 16:08:14 GMT 2023
Record UNII
4791MN0PVE
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FUBROGONIUM IODIDE
INN  
INN  
Official Name English
fubrogonium iodide [INN]
Common Name English
DIETHYL (3-HYDROXYBUTYL)METHYLAMMONIUM IODIDE 5-BROMO-2-FUROATE
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C29696
Created by admin on Fri Dec 15 16:08:14 GMT 2023 , Edited by admin on Fri Dec 15 16:08:14 GMT 2023
NCI_THESAURUS C66886
Created by admin on Fri Dec 15 16:08:14 GMT 2023 , Edited by admin on Fri Dec 15 16:08:14 GMT 2023
Code System Code Type Description
EVMPD
SUB07824MIG
Created by admin on Fri Dec 15 16:08:14 GMT 2023 , Edited by admin on Fri Dec 15 16:08:14 GMT 2023
PRIMARY
INN
2433
Created by admin on Fri Dec 15 16:08:14 GMT 2023 , Edited by admin on Fri Dec 15 16:08:14 GMT 2023
PRIMARY
MESH
C007788
Created by admin on Fri Dec 15 16:08:14 GMT 2023 , Edited by admin on Fri Dec 15 16:08:14 GMT 2023
PRIMARY
PUBCHEM
71529
Created by admin on Fri Dec 15 16:08:14 GMT 2023 , Edited by admin on Fri Dec 15 16:08:14 GMT 2023
PRIMARY
ChEMBL
CHEMBL2110930
Created by admin on Fri Dec 15 16:08:14 GMT 2023 , Edited by admin on Fri Dec 15 16:08:14 GMT 2023
PRIMARY
CAS
3690-58-2
Created by admin on Fri Dec 15 16:08:14 GMT 2023 , Edited by admin on Fri Dec 15 16:08:14 GMT 2023
PRIMARY
EPA CompTox
DTXSID90958102
Created by admin on Fri Dec 15 16:08:14 GMT 2023 , Edited by admin on Fri Dec 15 16:08:14 GMT 2023
PRIMARY
FDA UNII
4791MN0PVE
Created by admin on Fri Dec 15 16:08:14 GMT 2023 , Edited by admin on Fri Dec 15 16:08:14 GMT 2023
PRIMARY
SMS_ID
100000080671
Created by admin on Fri Dec 15 16:08:14 GMT 2023 , Edited by admin on Fri Dec 15 16:08:14 GMT 2023
PRIMARY
NCI_THESAURUS
C65776
Created by admin on Fri Dec 15 16:08:14 GMT 2023 , Edited by admin on Fri Dec 15 16:08:14 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
PARENT -> SALT/SOLVATE
ENANTIOMER -> RACEMATE