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About:
Synthesis and pharmacological evaluation of (2-oxaadamant-1-yl)amines
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An Entity of Type :
schema:ScholarlyArticle
, within Data Space :
wasabi.inria.fr
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document(s)
Type:
Academic Article
research paper
schema:ScholarlyArticle
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
title
Synthesis and pharmacological evaluation of (2-oxaadamant-1-yl)amines
Creator
De Clercq, Erik
Naesens, Lieve
Vázquez, Santiago
López-Querol, Marta
Camps, Pelayo
Mallol, Jordi
Montaner, Silvia
Profire, Lenuta
Duque, María
Kelly, John
Sureda, Francesc
Radhika Prathalingam, S
source
Elsevier; Medline; PMC
abstract
The synthesis of several (2-oxaadamant-1-yl)amines is reported. They were evaluated as NMDA receptor antagonists and several of them were more active than amantadine, but none was more potent than memantine. None of the tested compounds displayed antiviral activity. Two of the derivatives showed a significant level of trypanocidal activity.
has issue date
2009-04-01
(
xsd:dateTime
)
bibo:doi
10.1016/j.bmc.2009.02.007
bibo:pmid
19251424
has license
green-oa
sha1sum (hex)
6f3c265edcc79d8926bde1a4ae95c6106206c154
schema:url
https://doi.org/10.1016/j.bmc.2009.02.007
resource representing a document's title
Synthesis and pharmacological evaluation of (2-oxaadamant-1-yl)amines
has PubMed Central identifier
PMC3217223
has PubMed identifier
19251424
schema:publication
Bioorganic & Medicinal Chemistry
resource representing a document's body
covid:6f3c265edcc79d8926bde1a4ae95c6106206c154#body_text
is
schema:about
of
named entity '282'
named entity 'amantadine'
named entity 'antagonists'
named entity 'DISPLAYED'
named entity 'SIGNIFICANT'
named entity 'SYNTHESIS'
named entity '282'
named entity 'EVALUATION'
named entity 'PHARMACOLOGICAL'
named entity 'SYNTHESIS'
named entity 'TESTED'
named entity 'AMANTADINE'
named entity 'ANTIVIRAL ACTIVITY'
named entity 'BUT'
named entity 'EVALUATED'
named entity 'ACTIVE'
named entity 'TRYPANOCIDAL ACTIVITY'
named entity 'MEMANTINE'
named entity 'NMDA RECEPTOR ANTAGONISTS'
named entity 'LEVEL'
named entity 'REPORTED'
covid:arg/6f3c265edcc79d8926bde1a4ae95c6106206c154
named entity 'NMDA receptor'
named entity 'None'
named entity 'pharmacological'
named entity '37 °C'
named entity 'T. brucei'
named entity 'EtOH'
named entity 'NMDA receptor antagonism'
named entity 'EtOH'
named entity 'HCl'
named entity 'UV light'
named entity 'influenza A virus'
named entity 'parent compound'
named entity 'MeOH'
named entity 'NMDA receptor antagonist'
named entity 'species complex'
named entity '7.92'
named entity 'formaldehyde'
named entity 'benzyl group'
named entity 'Column chromatography'
named entity 'CH 2'
named entity 'substituent'
named entity 'GraphPad Prism'
named entity 'HMBC'
named entity 'chromatography'
named entity 'HCl'
named entity 'RNA viruses'
named entity '2-propanol'
named entity 'gas chromatograph'
named entity 'EtOAc'
named entity 'amine'
named entity 'amine'
named entity 'NMDA'
named entity 'Amine'
named entity 'amantadine'
named entity 'parasites'
named entity 'potency'
named entity 'HCl'
named entity 'hemocytometer'
named entity '75.4'
named entity 'CH 2'
named entity 'vacuo'
named entity 'antiviral activity'
named entity 'HCl'
named entity 'mmol'
named entity 'amines'
named entity 'silica gel'
named entity 'mmol'
named entity 'Phenyl'
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