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Peter V. Simpson

Researcher at Curtin University

Publications -  43
Citations -  1020

Peter V. Simpson is an academic researcher from Curtin University. The author has contributed to research in topics: Carbene & Palladium. The author has an hindex of 18, co-authored 41 publications receiving 808 citations. Previous affiliations of Peter V. Simpson include University of Würzburg & Australian National University.

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Metal-based antitumor compounds: beyond cisplatin.

TL;DR: The use of metal-based small molecules in chemotherapy is reviewed, focusing on recent studies, and how new nonplatinum-based agents are prompting scientists to increase drug specificity to overcome chemoresistance in cancer cells is discussed.
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Antibacterial and Antiparasitic Activity of Manganese(I) Tricarbonyl Complexes with Ketoconazole, Miconazole, and Clotrimazole Ligands

TL;DR: Five manganese(I) tricarbonyl complexes of the general formula [Mn(CO)3(bpyR,R)(azole)]PF6 with R = H, COOCH3, and azole were synthesized and fully charaterized, including X-ray structure analysis for the ctz compound.
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Palladium, rhodium and platinum complexes of ortho-xylyl-linked bis-N-heterocyclic carbenes: Synthesis, structure and catalytic activity

TL;DR: In this article, the Pt-bis N-heterocyclic carbene (NHC) complexes with an ortho-xylyl group were described and structurally and spectroscopically characterised.
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Synthesis, Cellular Uptake and Biological Activity Against Pathogenic Microorganisms and Cancer Cells of Rhodium and Iridium N‐Heterocyclic Carbene Complexes Bearing Charged Substituents

TL;DR: Four new N-heterocyclic carbene rhodium and iridium complexes decorated with anionic or cationic pendant groups to increase their water solubility and biological activity have been synthesised and characterised and cellular uptake studies clearly confirmed that the cationIC phosphonium groups facilitated uptake, which was linked with higher biological activity.
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Defining the Anti-Cancer Activity of Tricarbonyl Rhenium complexes: Induction of G2/M cell cycle arrest and Blockade of Aurora-A Kinase Phosphorylation

TL;DR: An in-depth biological study revealed the origin of the anticancer properties of the rhenium tricarbonyl fragment and found that the ruthenium complexes induce cell cycle arrest at the G2/M phase by inhibiting the phosphorylation of Aurora-A kinase.