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

Details

Stereochemistry ACHIRAL
Molecular Formula C20H27N2O
Molecular Weight 311.4412
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 1

SHOW SMILES / InChI
Structure of AMBUTONIUM

SMILES

CC[N+](C)(C)CCC(C(N)=O)(C1=CC=CC=C1)C2=CC=CC=C2

InChI

InChIKey=KFZMXOLSYABOSE-UHFFFAOYSA-O
InChI=1S/C20H26N2O/c1-4-22(2,3)16-15-20(19(21)23,17-11-7-5-8-12-17)18-13-9-6-10-14-18/h5-14H,4,15-16H2,1-3H3,(H-,21,23)/p+1

HIDE SMILES / InChI

Description

Ambutonium is anticholinergic agent. It is a muscarinic antagonist. Ambutonium was used for the treatment of ulcerous disease and gastrointestinal disease in general.

Approval Year

1958
128
Sourcing

Sourcing

Vendor/AggregatorIDURL
ABI Chem
AC1L1QNE
AbovChem LLC
HY-U00067
Alfa Chemistry
115-51-5
BOC Sciences
115-51-5
ChemTik
CTK0H7392
Hangzhou Yuhao Chemical Technology
RT3341
MuseChem
M054755
NCI Plated 2007
9549
Toronto Research Chemicals
A576000
ZINC
ZINC000001700052
http://zinc15.docking.org/substances/ZINC000001700052
eMolecules
31591982
mcule
MCULE-3153796205
mcule
MCULE-8152223078
PubMed

PubMed

TitleDatePubMed
The effect of ambutonium bromide, a new anticholinergic agent in ulcer therapy.
1960 Jun
Patents

Patents

US3553324A
2
Name Type Language
AMBUTONIUM
WHO-DD  
Common Name English
AMBUTONIUM CATION
Common Name English
AMBUTONIUM ION
Common Name English
(3-CARBAMOYL-3,3-DIPHENYLPROPYL)ETHYLDIMETHYLAMMONIUM
Systematic Name English
Ambutonium [WHO-DD]
Common Name English
Classification Tree Code System Code
WHO-ATC A03CA07
Created by admin on Fri Dec 15 16:02:59 GMT 2023 , Edited by admin on Fri Dec 15 16:02:59 GMT 2023
NCI_THESAURUS C29704
Created by admin on Fri Dec 15 16:02:59 GMT 2023 , Edited by admin on Fri Dec 15 16:02:59 GMT 2023
WHO-VATC QA03CA07
Created by admin on Fri Dec 15 16:02:59 GMT 2023 , Edited by admin on Fri Dec 15 16:02:59 GMT 2023
Code System Code Type Description
NCI_THESAURUS
C79895
Created by admin on Fri Dec 15 16:02:59 GMT 2023 , Edited by admin on Fri Dec 15 16:02:59 GMT 2023
PRIMARY
FDA UNII
4O677EQ77U
Created by admin on Fri Dec 15 16:02:59 GMT 2023 , Edited by admin on Fri Dec 15 16:02:59 GMT 2023
PRIMARY
PUBCHEM
8277
Created by admin on Fri Dec 15 16:02:59 GMT 2023 , Edited by admin on Fri Dec 15 16:02:59 GMT 2023
PRIMARY
CAS
14007-49-9
Created by admin on Fri Dec 15 16:02:59 GMT 2023 , Edited by admin on Fri Dec 15 16:02:59 GMT 2023
PRIMARY
DRUG CENTRAL
149
Created by admin on Fri Dec 15 16:02:59 GMT 2023 , Edited by admin on Fri Dec 15 16:02:59 GMT 2023
PRIMARY
SMS_ID
300000033980
Created by admin on Fri Dec 15 16:02:59 GMT 2023 , Edited by admin on Fri Dec 15 16:02:59 GMT 2023
PRIMARY
EPA CompTox
DTXSID40871594
Created by admin on Fri Dec 15 16:02:59 GMT 2023 , Edited by admin on Fri Dec 15 16:02:59 GMT 2023
PRIMARY
ACTIVE MOIETY
Structure of AMBUTONIUM
SALT/SOLVATE (PARENT)
Structure of AMBUTONIUM BROMIDE
NIH
NCATS
PRIVACY ACT
ACCESSIBILITY
DISCLAIMER
HHS VULNERABILITY DISCLOSURE
For language access assistance, contact the NCATS Public Information Officer
National Center for Advancing Translational Sciences (NCATS),
6701 Democracy Boulevard, Bethesda MD 20892-4874 • 301-594-8966