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Details

Stereochemistry ACHIRAL
Molecular Formula C16H28N2O2
Molecular Weight 280.4057
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TROMANTADINE

SMILES

CN(C)CCOCC(=O)NC12CC3CC(CC(C3)C1)C2

InChI

InChIKey=UXQDWARBDDDTKG-UHFFFAOYSA-N
InChI=1S/C16H28N2O2/c1-18(2)3-4-20-11-15(19)17-16-8-12-5-13(9-16)7-14(6-12)10-16/h12-14H,3-11H2,1-2H3,(H,17,19)

HIDE SMILES / InChI

Molecular Formula C16H28N2O2
Molecular Weight 280.4057
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Tromantadine HCl under brand name Virumerz is used to treat the herpes simplex virus by inhibiting the cellular process such as glycoprotein processing, which occurs after the synthesis of the fusion protein but before its expression on the cell surface.

Approval Year

PubMed

PubMed

TitleDatePubMed
Tromantadine: inhibitor of early and late events in herpes simplex virus replication.
1982 Dec
Separation methods for tricyclic antiviral drugs.
2001 Nov 25
Dimethyl sulfoxide blocks herpes simplex virus-1 productive infection in vitro acting at different stages with positive cooperativity. Application of micro-array analysis.
2002 May 24
Nona-arginine facilitates delivery of quantum dots into cells via multiple pathways.
2010
The susceptibility of magpies to a highly pathogenic avian influenza virus subtype H5N1.
2010 Jun

Sample Use Guides

Unknown
Route of Administration: Topical
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:35:49 UTC 2023
Edited
by admin
on Fri Dec 15 15:35:49 UTC 2023
Record UNII
H191JFG8WA
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TROMANTADINE
II   INN   MI   WHO-DD  
INN  
Official Name English
tromantadine [INN]
Common Name English
Tromantadine [WHO-DD]
Common Name English
TROMANTADINE [MI]
Common Name English
TROMANTADINE [II]
Common Name English
N-1-ADAMANTYL-2-(2-(DIMETHYLAMINO)ETHOXY)ACETAMIDE
Systematic Name English
Classification Tree Code System Code
WHO-VATC QJ05AC03
Created by admin on Fri Dec 15 15:35:49 UTC 2023 , Edited by admin on Fri Dec 15 15:35:49 UTC 2023
WHO-ATC D06BB02
Created by admin on Fri Dec 15 15:35:49 UTC 2023 , Edited by admin on Fri Dec 15 15:35:49 UTC 2023
WHO-ATC J05AC03
Created by admin on Fri Dec 15 15:35:49 UTC 2023 , Edited by admin on Fri Dec 15 15:35:49 UTC 2023
NCI_THESAURUS C281
Created by admin on Fri Dec 15 15:35:49 UTC 2023 , Edited by admin on Fri Dec 15 15:35:49 UTC 2023
WHO-VATC QD06BB02
Created by admin on Fri Dec 15 15:35:49 UTC 2023 , Edited by admin on Fri Dec 15 15:35:49 UTC 2023
Code System Code Type Description
DRUG CENTRAL
3634
Created by admin on Fri Dec 15 15:35:49 UTC 2023 , Edited by admin on Fri Dec 15 15:35:49 UTC 2023
PRIMARY
SMS_ID
100000076957
Created by admin on Fri Dec 15 15:35:49 UTC 2023 , Edited by admin on Fri Dec 15 15:35:49 UTC 2023
PRIMARY
PUBCHEM
64377
Created by admin on Fri Dec 15 15:35:49 UTC 2023 , Edited by admin on Fri Dec 15 15:35:49 UTC 2023
PRIMARY
WIKIPEDIA
TROMANTADINE
Created by admin on Fri Dec 15 15:35:49 UTC 2023 , Edited by admin on Fri Dec 15 15:35:49 UTC 2023
PRIMARY
NCI_THESAURUS
C81608
Created by admin on Fri Dec 15 15:35:49 UTC 2023 , Edited by admin on Fri Dec 15 15:35:49 UTC 2023
PRIMARY
FDA UNII
H191JFG8WA
Created by admin on Fri Dec 15 15:35:49 UTC 2023 , Edited by admin on Fri Dec 15 15:35:49 UTC 2023
PRIMARY
MESH
C004279
Created by admin on Fri Dec 15 15:35:49 UTC 2023 , Edited by admin on Fri Dec 15 15:35:49 UTC 2023
PRIMARY
EVMPD
SUB11335MIG
Created by admin on Fri Dec 15 15:35:49 UTC 2023 , Edited by admin on Fri Dec 15 15:35:49 UTC 2023
PRIMARY
ECHA (EC/EINECS)
258-770-0
Created by admin on Fri Dec 15 15:35:49 UTC 2023 , Edited by admin on Fri Dec 15 15:35:49 UTC 2023
PRIMARY
ChEMBL
CHEMBL1742451
Created by admin on Fri Dec 15 15:35:49 UTC 2023 , Edited by admin on Fri Dec 15 15:35:49 UTC 2023
PRIMARY
MERCK INDEX
m11220
Created by admin on Fri Dec 15 15:35:49 UTC 2023 , Edited by admin on Fri Dec 15 15:35:49 UTC 2023
PRIMARY Merck Index
INN
3234
Created by admin on Fri Dec 15 15:35:49 UTC 2023 , Edited by admin on Fri Dec 15 15:35:49 UTC 2023
PRIMARY
RXCUI
38868
Created by admin on Fri Dec 15 15:35:49 UTC 2023 , Edited by admin on Fri Dec 15 15:35:49 UTC 2023
PRIMARY RxNorm
EPA CompTox
DTXSID00202062
Created by admin on Fri Dec 15 15:35:49 UTC 2023 , Edited by admin on Fri Dec 15 15:35:49 UTC 2023
PRIMARY
CAS
53783-83-8
Created by admin on Fri Dec 15 15:35:49 UTC 2023 , Edited by admin on Fri Dec 15 15:35:49 UTC 2023
PRIMARY
DRUG BANK
DB13288
Created by admin on Fri Dec 15 15:35:49 UTC 2023 , Edited by admin on Fri Dec 15 15:35:49 UTC 2023
PRIMARY
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