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

Details

Stereochemistry ACHIRAL
Molecular Formula C25H46NO2.Br
Molecular Weight 472.542
Optical Activity NONE
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of AMANTANIUM BROMIDE

SMILES

[Br-].CCCCCCCCCC[N+](C)(C)CCOC(=O)C12CC3CC(CC(C3)C1)C2

InChI

InChIKey=VSKHGXKMGTVPPY-UHFFFAOYSA-M
InChI=1S/C25H46NO2.BrH/c1-4-5-6-7-8-9-10-11-12-26(2,3)13-14-28-24(27)25-18-21-15-22(19-25)17-23(16-21)20-25;/h21-23H,4-20H2,1-3H3;1H/q+1;/p-1

HIDE SMILES / InChI

Molecular Formula BrH
Molecular Weight 80.912
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C25H46NO2
Molecular Weight 392.6382
Charge 1
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity NONE

Amantanium is a quaternary ammonium antibacterial/antifungal agent. It was developed by Italian company Rotta Research in the 1980s, and marketed under tradename Amantol for the topical therapy of mucous and cutaneous infections.

Approval Year

Substance Class Chemical
Created
by admin
on Wed Apr 02 06:53:40 GMT 2025
Edited
by admin
on Wed Apr 02 06:53:40 GMT 2025
Record UNII
K0435HZQ57
Record Status Validated (UNII)
Record Version
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Name Type Language
AMANTANIUM BROMIDE
INN   MART.   MI  
INN  
Official Name English
AMANTOL
Preferred Name English
AMANTANIUM BROMIDE [MI]
Common Name English
DECYL(2-HYDROXYETHYL)DIMETHYLAMMONIUM BROMIDE 1-ADAMANTANECARBOXYLATE
Systematic Name English
1-DECANAMINIUM, N,N-DIMETHYL-N-(2-((TRICYCLO(3.3.1.13,7)DEC-1-YLCARBONYL)OXY)ETHYL)-, BROMIDE (1:1)
Systematic Name English
amantanium bromide [INN]
Common Name English
AMANTANIUM BROMIDE [MART.]
Common Name English
1-DECANAMINIUM, N,N-DIMETHYL-N-(2-((TRICYCLO(3.3.1.13,7)DEC-1-YLCARBONYL)OXY)ETHYL)-, BROMIDE
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C29698
Created by admin on Wed Apr 02 06:53:40 GMT 2025 , Edited by admin on Wed Apr 02 06:53:40 GMT 2025
Code System Code Type Description
EPA CompTox
DTXSID40973729
Created by admin on Wed Apr 02 06:53:40 GMT 2025 , Edited by admin on Wed Apr 02 06:53:40 GMT 2025
PRIMARY
PUBCHEM
168906
Created by admin on Wed Apr 02 06:53:40 GMT 2025 , Edited by admin on Wed Apr 02 06:53:40 GMT 2025
PRIMARY
CAS
58158-77-3
Created by admin on Wed Apr 02 06:53:40 GMT 2025 , Edited by admin on Wed Apr 02 06:53:40 GMT 2025
PRIMARY
EVMPD
SUB05390MIG
Created by admin on Wed Apr 02 06:53:40 GMT 2025 , Edited by admin on Wed Apr 02 06:53:40 GMT 2025
PRIMARY
MERCK INDEX
m28
Created by admin on Wed Apr 02 06:53:40 GMT 2025 , Edited by admin on Wed Apr 02 06:53:40 GMT 2025
PRIMARY Merck Index
SMS_ID
100000087664
Created by admin on Wed Apr 02 06:53:40 GMT 2025 , Edited by admin on Wed Apr 02 06:53:40 GMT 2025
PRIMARY
FDA UNII
K0435HZQ57
Created by admin on Wed Apr 02 06:53:40 GMT 2025 , Edited by admin on Wed Apr 02 06:53:40 GMT 2025
PRIMARY
NCI_THESAURUS
C73151
Created by admin on Wed Apr 02 06:53:40 GMT 2025 , Edited by admin on Wed Apr 02 06:53:40 GMT 2025
PRIMARY
ChEMBL
CHEMBL2110921
Created by admin on Wed Apr 02 06:53:40 GMT 2025 , Edited by admin on Wed Apr 02 06:53:40 GMT 2025
PRIMARY
INN
4342
Created by admin on Wed Apr 02 06:53:40 GMT 2025 , Edited by admin on Wed Apr 02 06:53:40 GMT 2025
PRIMARY
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ACTIVE MOIETY