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

Details

Stereochemistry ACHIRAL
Molecular Formula C12H21N
Molecular Weight 179.3018
Optical Activity NONE
Defined Stereocenters 0 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MEMANTINE

SMILES

CC12CC3CC(C)(C1)CC(N)(C3)C2

InChI

InChIKey=BUGYDGFZZOZRHP-UHFFFAOYSA-N
InChI=1S/C12H21N/c1-10-3-9-4-11(2,6-10)8-12(13,5-9)7-10/h9H,3-8,13H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C12H21N
Molecular Weight 179.3018
Charge 0
Count
Stereochemistry MIXED
Additional Stereochemistry No
Defined Stereocenters 0 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:59:40 UTC 2023
Edited
by admin
on Fri Dec 15 15:59:40 UTC 2023
Record UNII
W8O17SJF3T
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MEMANTINE
HSDB   INN   MI   VANDF   WHO-DD  
INN  
Official Name English
3,5-DIMETHYL-1-ADAMANTANAMINE
Systematic Name English
D-145
Code English
MEMANTINE [VANDF]
Common Name English
MEMANTINE [MI]
Common Name English
TRICYCLO(3.3.1.1(SUP 3,7))DECAN-1-AMINE, 3,5-DIMETHYL-
Common Name English
1-AMINO-3,5-DIMETHYLADAMANTANE
Systematic Name English
NEMDATINE
Brand Name English
Memantine [WHO-DD]
Common Name English
NSC-757843
Code English
memantine [INN]
Common Name English
DRG-0267
Code English
3,5-DIMETHYLTRICYCLO(3.3.1.1(SUP 3,7))DECAN-1-AMINE
Systematic Name English
MEMANTINE [HSDB]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C1509
Created by admin on Fri Dec 15 15:59:40 UTC 2023 , Edited by admin on Fri Dec 15 15:59:40 UTC 2023
NDF-RT N0000020015
Created by admin on Fri Dec 15 15:59:40 UTC 2023 , Edited by admin on Fri Dec 15 15:59:40 UTC 2023
NCI_THESAURUS C38149
Created by admin on Fri Dec 15 15:59:40 UTC 2023 , Edited by admin on Fri Dec 15 15:59:40 UTC 2023
WHO-ATC N06DX01
Created by admin on Fri Dec 15 15:59:40 UTC 2023 , Edited by admin on Fri Dec 15 15:59:40 UTC 2023
WHO-ATC N06DA52
Created by admin on Fri Dec 15 15:59:40 UTC 2023 , Edited by admin on Fri Dec 15 15:59:40 UTC 2023
WHO-VATC QN06DA52
Created by admin on Fri Dec 15 15:59:40 UTC 2023 , Edited by admin on Fri Dec 15 15:59:40 UTC 2023
NDF-RT N0000175745
Created by admin on Fri Dec 15 15:59:40 UTC 2023 , Edited by admin on Fri Dec 15 15:59:40 UTC 2023
WHO-VATC QN06DX01
Created by admin on Fri Dec 15 15:59:40 UTC 2023 , Edited by admin on Fri Dec 15 15:59:40 UTC 2023
LIVERTOX NBK547981
Created by admin on Fri Dec 15 15:59:40 UTC 2023 , Edited by admin on Fri Dec 15 15:59:40 UTC 2023
WHO-ATC N06DA53
Created by admin on Fri Dec 15 15:59:40 UTC 2023 , Edited by admin on Fri Dec 15 15:59:40 UTC 2023
NDF-RT N0000020015
Created by admin on Fri Dec 15 15:59:40 UTC 2023 , Edited by admin on Fri Dec 15 15:59:40 UTC 2023
EMA ASSESSMENT REPORTS NEMDATINE (AUTHORIZED: ALZHEIMER DISEASE)
Created by admin on Fri Dec 15 15:59:40 UTC 2023 , Edited by admin on Fri Dec 15 15:59:40 UTC 2023
Code System Code Type Description
FDA UNII
W8O17SJF3T
Created by admin on Fri Dec 15 15:59:40 UTC 2023 , Edited by admin on Fri Dec 15 15:59:40 UTC 2023
PRIMARY
SMS_ID
100000085447
Created by admin on Fri Dec 15 15:59:40 UTC 2023 , Edited by admin on Fri Dec 15 15:59:40 UTC 2023
PRIMARY
RXCUI
6719
Created by admin on Fri Dec 15 15:59:40 UTC 2023 , Edited by admin on Fri Dec 15 15:59:40 UTC 2023
PRIMARY RxNorm
INN
3952
Created by admin on Fri Dec 15 15:59:40 UTC 2023 , Edited by admin on Fri Dec 15 15:59:40 UTC 2023
PRIMARY
CAS
19982-08-2
Created by admin on Fri Dec 15 15:59:40 UTC 2023 , Edited by admin on Fri Dec 15 15:59:40 UTC 2023
PRIMARY
EPA CompTox
DTXSID5045174
Created by admin on Fri Dec 15 15:59:40 UTC 2023 , Edited by admin on Fri Dec 15 15:59:40 UTC 2023
PRIMARY
HSDB
7327
Created by admin on Fri Dec 15 15:59:40 UTC 2023 , Edited by admin on Fri Dec 15 15:59:40 UTC 2023
PRIMARY
IUPHAR
4253
Created by admin on Fri Dec 15 15:59:40 UTC 2023 , Edited by admin on Fri Dec 15 15:59:40 UTC 2023
PRIMARY
NCI_THESAURUS
C73269
Created by admin on Fri Dec 15 15:59:40 UTC 2023 , Edited by admin on Fri Dec 15 15:59:40 UTC 2023
PRIMARY
CLINICAL_TRIALS.GOV
NCT03527472
Created by admin on Fri Dec 15 15:59:40 UTC 2023 , Edited by admin on Fri Dec 15 15:59:40 UTC 2023
PRIMARY Memantine for the Treatment of Cognitive Impairment in Systemic Lupus Erythematosus (ClearMEMory)
PUBCHEM
4054
Created by admin on Fri Dec 15 15:59:40 UTC 2023 , Edited by admin on Fri Dec 15 15:59:40 UTC 2023
PRIMARY
DRUG CENTRAL
1679
Created by admin on Fri Dec 15 15:59:40 UTC 2023 , Edited by admin on Fri Dec 15 15:59:40 UTC 2023
PRIMARY
NSC
757843
Created by admin on Fri Dec 15 15:59:40 UTC 2023 , Edited by admin on Fri Dec 15 15:59:40 UTC 2023
PRIMARY
EVMPD
SUB08731MIG
Created by admin on Fri Dec 15 15:59:40 UTC 2023 , Edited by admin on Fri Dec 15 15:59:40 UTC 2023
PRIMARY
DAILYMED
W8O17SJF3T
Created by admin on Fri Dec 15 15:59:40 UTC 2023 , Edited by admin on Fri Dec 15 15:59:40 UTC 2023
PRIMARY
DRUG BANK
DB01043
Created by admin on Fri Dec 15 15:59:40 UTC 2023 , Edited by admin on Fri Dec 15 15:59:40 UTC 2023
PRIMARY
WIKIPEDIA
MEMANTINE
Created by admin on Fri Dec 15 15:59:40 UTC 2023 , Edited by admin on Fri Dec 15 15:59:40 UTC 2023
PRIMARY
MERCK INDEX
m7167
Created by admin on Fri Dec 15 15:59:40 UTC 2023 , Edited by admin on Fri Dec 15 15:59:40 UTC 2023
PRIMARY Merck Index
MESH
D008559
Created by admin on Fri Dec 15 15:59:40 UTC 2023 , Edited by admin on Fri Dec 15 15:59:40 UTC 2023
PRIMARY
ChEMBL
CHEMBL807
Created by admin on Fri Dec 15 15:59:40 UTC 2023 , Edited by admin on Fri Dec 15 15:59:40 UTC 2023
PRIMARY
CHEBI
64312
Created by admin on Fri Dec 15 15:59:40 UTC 2023 , Edited by admin on Fri Dec 15 15:59:40 UTC 2023
PRIMARY
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TRANSPORTER -> INHIBITOR
TRANSPORTER -> SUBSTRATE
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ALZHEIMERS DISEASE DRUG ANTAGONIZING NMDA RECEPTOR, ANTAGONISM OF .ALPHA.7 NACHR IS A SIDE PATHWAY.
BINDER->LIGAND
BINDING
EXCRETED UNCHANGED
AMOUNT EXCRETED
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TRANSPORTER -> INHIBITOR
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TRANSPORTER -> INHIBITOR
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ACTIVE MOIETY
Name Property Type Amount Referenced Substance Defining Parameters References
Tmax PHARMACOKINETIC ORAL ADMINISTRATION

Biological Half-life PHARMACOKINETIC Elimination
PHARMACOKINETIC
Volume of Distribution PHARMACOKINETIC