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dc.contributor.authorDane, Chianna
dc.contributor.authorCumbers, Grace A.
dc.contributor.authorAllen, Beau
dc.contributor.authorMontgomery, Andrew P.
dc.contributor.authorDanon, Jonathan J.
dc.contributor.authorKassiou, Michael
dc.date.accessioned2024-08-30T05:40:21Z
dc.date.available2024-08-30T05:40:21Z
dc.date.issued2024en_AU
dc.identifier.urihttps://hdl.handle.net/2123/33036
dc.description.abstractThe unique structural and physicochemical properties of adamantane and its derivatives have attracted considerable attention in the field of medicinal chemistry. Substituting phenyl rings for adamantane or its derivatives has provided a promising strategy to introduce lipophilicity and escape the ‘flat land’ of modern drug discovery. Additionally, the unique three-dimensional structure of adamantane facilitates the precise positioning of substituents allowing for a more effective exploration of drug targets. Evidently, we have seen an increased use of adamantane in pharmaceutically relevant molecules. The following Account highlights our group’s research in five drug discovery programs over the past 15 years showcasing the use of adamantane and its analogues in these studies.en_AU
dc.language.isoenen_AU
dc.publisherCSIRO Publishingen_AU
dc.relation.ispartofAustralian Journal of Chemistryen_AU
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivatives 4.0en_AU
dc.subjectadamantaneen_AU
dc.subjectcannabinoid receptorsen_AU
dc.subjectCNSen_AU
dc.subjectmedicinal chemistryen_AU
dc.subjectNMDA receptoren_AU
dc.subjectP2X7 receptoren_AU
dc.subjectsigma-2 receptoren_AU
dc.subjectstructure–activity relationshipsen_AU
dc.subjecttau aggregationen_AU
dc.titleUnlocking therapeutic potential: the role of adamantane in drug discoveryen_AU
dc.typeArticleen_AU
dc.identifier.doi10.1071/CH24075
dc.type.pubtypePublisher's versionen_AU
dc.rights.other© 2024 The Author(s) (or their employer(s)). Published by CSIRO Publishing. This is an open access article distributed under the Creative Commons AttributionNonCommercial-NoDerivatives 4.0 International License (CC BY-NC-ND)en_AU
dc.relation.otherThe work presented herein was supported by the Australian Research Council and the National Health and Medical Research Council.
usyd.facultySeS faculties schools::Faculty of Science::School of Chemistryen_AU
usyd.citation.volume77en_AU
usyd.citation.issue8en_AU
usyd.citation.spage1en_AU
usyd.citation.epage16en_AU
workflow.metadata.onlyNoen_AU


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