dc.creator | Georgiadis M.-O., Kourbeli V., Ioannidou V., Karakitsios E., Papanastasiou I., Tsotinis A., Komiotis D., Vocat A., Cole S.T., Taylor M.C., Kelly J.M. | en |
dc.date.accessioned | 2023-01-31T07:40:40Z | |
dc.date.available | 2023-01-31T07:40:40Z | |
dc.date.issued | 2019 | |
dc.identifier | 10.1016/j.bmcl.2019.04.010 | |
dc.identifier.issn | 0960894X | |
dc.identifier.uri | http://hdl.handle.net/11615/72127 | |
dc.description.abstract | 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. © 2019 Elsevier Ltd | en |
dc.language.iso | en | en |
dc.source | Bioorganic and Medicinal Chemistry Letters | en |
dc.source.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85064075312&doi=10.1016%2fj.bmcl.2019.04.010&partnerID=40&md5=9f1236d5ebe5adbbcaea6624b76c94c1 | |
dc.subject | aliphatic amine | en |
dc.subject | antitrypanosomal agent | en |
dc.subject | diphenoxyadamantane alkylamine | en |
dc.subject | tuberculostatic agent | en |
dc.subject | unclassified drug | en |
dc.subject | adamantane | en |
dc.subject | amine | en |
dc.subject | antitrypanosomal agent | en |
dc.subject | tuberculostatic agent | en |
dc.subject | antibacterial activity | en |
dc.subject | Article | en |
dc.subject | bacterial growth | en |
dc.subject | controlled study | en |
dc.subject | drug structure | en |
dc.subject | drug synthesis | en |
dc.subject | growth inhibition | en |
dc.subject | Mycobacterium tuberculosis | en |
dc.subject | nonhuman | en |
dc.subject | trypanocidal activity | en |
dc.subject | Trypanosoma brucei | en |
dc.subject | chemical structure | en |
dc.subject | chemistry | en |
dc.subject | dose response | en |
dc.subject | drug effect | en |
dc.subject | drug sensitivity | en |
dc.subject | structure activity relation | en |
dc.subject | synthesis | en |
dc.subject | Trypanosoma brucei brucei | en |
dc.subject | Adamantane | en |
dc.subject | Amines | en |
dc.subject | Antitubercular Agents | en |
dc.subject | Dose-Response Relationship, Drug | en |
dc.subject | Molecular Structure | en |
dc.subject | Mycobacterium tuberculosis | en |
dc.subject | Parasitic Sensitivity Tests | en |
dc.subject | Structure-Activity Relationship | en |
dc.subject | Trypanocidal Agents | en |
dc.subject | Trypanosoma brucei brucei | en |
dc.subject | Elsevier Ltd | en |
dc.title | Synthesis of diphenoxyadamantane alkylamines with pharmacological interest | en |
dc.type | journalArticle | en |