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

Details

Stereochemistry ACHIRAL
Molecular Formula C19H25NO3
Molecular Weight 315.4067
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DOPAMANTINE

SMILES

OC1=CC=C(CCNC(=O)C23CC4CC(CC(C4)C2)C3)C=C1O

InChI

InChIKey=ZWKFENYDXISLGK-UHFFFAOYSA-N
InChI=1S/C19H25NO3/c21-16-2-1-12(8-17(16)22)3-4-20-18(23)19-9-13-5-14(10-19)7-15(6-13)11-19/h1-2,8,13-15,21-22H,3-7,9-11H2,(H,20,23)

HIDE SMILES / InChI
Dopamantine is the adamantine derivative. It combined elements of both amantadine and dopamine in its structure, shares some pharmacological effects of amantadine. Dopamantine is the anti-Parkinson drug, which has passed clinical trials. Dopamantine showed a high activity against Plasmodium berghei parasites that cause malaria.

Approval Year

PubMed

PubMed

TitleDatePubMed
Use of the adamantane structure in medicinal chemistry.
2010
Name Type Language
DOPAMANTINE
INN   USAN  
USAN   INN  
Official Name English
N-ADAMANTANOYL DOPAMINE
INCI  
INCI  
Preferred Name English
N-(3,4-Dihydroxyphenethyl)-1-adamantanecarboxamide
Systematic Name English
SCH-15507
Code English
SCH 15507
Code English
NSC-172619
Code English
TRICYCLO(3,3,1,1(SUP 3,7)DECANE-1-CARBOXAMIDE, N-(2-(3,4-DIHYDROXYPHENYL)ETHYL)-
Common Name English
DOPAMANTINE [USAN]
Common Name English
dopamantine [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C38149
Created by admin on Wed Apr 02 08:28:50 GMT 2025 , Edited by admin on Wed Apr 02 08:28:50 GMT 2025
Code System Code Type Description
ChEMBL
CHEMBL2106204
Created by admin on Wed Apr 02 08:28:50 GMT 2025 , Edited by admin on Wed Apr 02 08:28:50 GMT 2025
PRIMARY
FDA UNII
7EZN745FXZ
Created by admin on Wed Apr 02 08:28:50 GMT 2025 , Edited by admin on Wed Apr 02 08:28:50 GMT 2025
PRIMARY
SMS_ID
100000080762
Created by admin on Wed Apr 02 08:28:50 GMT 2025 , Edited by admin on Wed Apr 02 08:28:50 GMT 2025
PRIMARY
EPA CompTox
DTXSID70192961
Created by admin on Wed Apr 02 08:28:50 GMT 2025 , Edited by admin on Wed Apr 02 08:28:50 GMT 2025
PRIMARY
EVMPD
SUB06364MIG
Created by admin on Wed Apr 02 08:28:50 GMT 2025 , Edited by admin on Wed Apr 02 08:28:50 GMT 2025
PRIMARY
NSC
172619
Created by admin on Wed Apr 02 08:28:50 GMT 2025 , Edited by admin on Wed Apr 02 08:28:50 GMT 2025
PRIMARY
PUBCHEM
38361
Created by admin on Wed Apr 02 08:28:50 GMT 2025 , Edited by admin on Wed Apr 02 08:28:50 GMT 2025
PRIMARY
ECHA (EC/EINECS)
254-697-3
Created by admin on Wed Apr 02 08:28:50 GMT 2025 , Edited by admin on Wed Apr 02 08:28:50 GMT 2025
PRIMARY
CAS
39907-68-1
Created by admin on Wed Apr 02 08:28:50 GMT 2025 , Edited by admin on Wed Apr 02 08:28:50 GMT 2025
PRIMARY
NCI_THESAURUS
C81561
Created by admin on Wed Apr 02 08:28:50 GMT 2025 , Edited by admin on Wed Apr 02 08:28:50 GMT 2025
PRIMARY
INN
3569
Created by admin on Wed Apr 02 08:28:50 GMT 2025 , Edited by admin on Wed Apr 02 08:28:50 GMT 2025
PRIMARY