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research article

Synthesis of diphenoxyadamantane alkylamines with pharmacological interest

Georgiadis, Markos-Orestis
•
Kourbeli, Violeta
•
Ioannidou, Vaya
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June 1, 2019
Bioorganic & Medicinal Chemistry Letters

In this work, the synthesis and the pharmacological evaluation of diphenoxyadamantane alkylamines Ia-f and IIa-f is described. The new diphenoxy-substituted adamantanes share structural features present in trypanocidal and antitubercular agents. 1-Methylpiperazine derivative Ia is the most potent against T. brucei compound, whilst its hexylamine congener IIf exhibits a significant antimycobacterial activity.

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Type
research article
DOI
10.1016/j.bmcl.2019.04.010
Web of Science ID

WOS:000465546100004

Author(s)
Georgiadis, Markos-Orestis
Kourbeli, Violeta
Ioannidou, Vaya
Karakitsios, Evangelos
Papanastasiou, Ioannis
Tsotinis, Andrew
Komiotis, Dimitri
Vocat, Anthony  
Cole, Stewart T.  
Taylor, Martin C.
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Date Issued

2019-06-01

Publisher

PERGAMON-ELSEVIER SCIENCE LTD

Published in
Bioorganic & Medicinal Chemistry Letters
Volume

29

Issue

11

Start page

1278

End page

1281

Subjects

Chemistry, Medicinal

•

Chemistry, Organic

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Pharmacology & Pharmacy

•

Chemistry

•

diphenoxyadamantane

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substituted piperazine

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aminoalkane side chain

•

trypanocidal activity

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antimycobacterial activity

•

solid pharmaceutical formulations

•

vitro controlled-release

•

adamantane aminoethers

•

resistance

•

epoxides

•

drugs

Editorial or Peer reviewed

REVIEWED

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EPFL

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UPCOL  
UPDANGELO  
Available on Infoscience
June 18, 2019
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/157927
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