Platinum-based metal complexes as chloride transporters that trigger apoptosis.
- Publisher:
- ROYAL SOC CHEMISTRY
- Publication Type:
- Journal Article
- Citation:
- Chem Sci, 2024, 15, (29), pp. 11584-11593
- Issue Date:
- 2024-07-24
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Field | Value | Language |
---|---|---|
dc.contributor.author | Wang, P | |
dc.contributor.author | Fares, M | |
dc.contributor.author | Eladwy, RA | |
dc.contributor.author | Bhuyan, DJ | |
dc.contributor.author | Wu, X | |
dc.contributor.author | Lewis, W | |
dc.contributor.author | Loeb, SJ | |
dc.contributor.author | Macreadie, LK | |
dc.contributor.author | Gale, PA | |
dc.date.accessioned | 2024-08-21T03:40:11Z | |
dc.date.available | 2024-06-21 | |
dc.date.available | 2024-08-21T03:40:11Z | |
dc.date.issued | 2024-07-24 | |
dc.identifier.citation | Chem Sci, 2024, 15, (29), pp. 11584-11593 | |
dc.identifier.issn | 2041-6520 | |
dc.identifier.issn | 2041-6539 | |
dc.identifier.uri | http://hdl.handle.net/10453/180439 | |
dc.description.abstract | In this paper we demonstrate that Pt(ii) complexes can function as efficient transmembrane chloride transporters. A series of Pt(ii) metal complexes with urea-appended isoquinoline ligands were synthesised and operate via classical hydrogen bonding interactions rather than ligand exchange. A number of the complexes exhibited potent transmembrane chloride activity in vesicle studies, while also showing strong antiproliferative activity in cisplatin-resistant cell lines via induction of apoptosis and inhibition of intracellular ROS. | |
dc.format | Electronic-eCollection | |
dc.language | eng | |
dc.publisher | ROYAL SOC CHEMISTRY | |
dc.relation | http://purl.org/au-research/grants/arc/DP200100453 | |
dc.relation.ispartof | Chem Sci | |
dc.relation.isbasedon | 10.1039/d4sc02115k | |
dc.rights | info:eu-repo/semantics/openAccess | |
dc.subject | 03 Chemical Sciences | |
dc.subject.classification | 34 Chemical sciences | |
dc.title | Platinum-based metal complexes as chloride transporters that trigger apoptosis. | |
dc.type | Journal Article | |
utslib.citation.volume | 15 | |
utslib.location.activity | England | |
utslib.for | 03 Chemical Sciences | |
pubs.organisational-group | University of Technology Sydney | |
pubs.organisational-group | University of Technology Sydney/Faculty of Science | |
pubs.organisational-group | University of Technology Sydney/Strength - TKC - The Kidman Centre | |
pubs.organisational-group | University of Technology Sydney/All Manual Groups | |
pubs.organisational-group | University of Technology Sydney/All Manual Groups/The Kidman Centre (TKC) | |
utslib.copyright.status | open_access | * |
dc.rights.license | This work is licensed under a Creative Commons Attribution 4.0 International License (CC BY 4.0). To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/ | |
dc.date.updated | 2024-08-21T03:40:06Z | |
pubs.issue | 29 | |
pubs.publication-status | Published online | |
pubs.volume | 15 | |
utslib.citation.issue | 29 |
Abstract:
In this paper we demonstrate that Pt(ii) complexes can function as efficient transmembrane chloride transporters. A series of Pt(ii) metal complexes with urea-appended isoquinoline ligands were synthesised and operate via classical hydrogen bonding interactions rather than ligand exchange. A number of the complexes exhibited potent transmembrane chloride activity in vesicle studies, while also showing strong antiproliferative activity in cisplatin-resistant cell lines via induction of apoptosis and inhibition of intracellular ROS.
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