Tristan Rawling
Affiliations: | University of Technology, Sydney (UTS) |
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Collaborators
Sign in to add collaborator| Subhodeep Sarker | collaborator | 2017-2019 | University of Technology, Sydney (UTS) |
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Publications
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| Gallagher CI, Frangos ZJ, Sheipouri D, et al. (2023) Novel Phenylene Lipids That Are Positive Allosteric Modulators of Glycine Receptors and Inhibitors of Glycine Transporter 2. Acs Chemical Neuroscience |
| York E, McNaughton DA, Roseblade A, et al. (2022) Structure-Activity Relationship and Mechanistic Studies of Bisaryl Urea Anticancer Agents Indicate Mitochondrial Uncoupling by a Fatty Acid-Activated Mechanism. Acs Chemical Biology |
| Roy R, Roseblade A, Rawling T. (2020) Expansion of the structure-activity relationship of branched chain fatty acids: effect of unsaturation and branching group size on anticancer activity. Chemistry and Physics of Lipids. 104952 |
| Gallagher CI, Sheipouri D, Shimmon S, et al. (2020) Identification of N-acyl amino acids that are positive allosteric modulators of glycine receptors. Biochemical Pharmacology. 114117 |
| Mostyn SN, Sarker S, Muthuraman P, et al. (2020) A photoswitchable ORG25543 congener enables optical control of glycine transporter 2. Acs Chemical Neuroscience |
| Rawling T, MacDermott-Opeskin H, Roseblade A, et al. (2020) Aryl urea substituted fatty acids: a new class of protonophoric mitochondrial uncoupler that utilises a synthetic anion transporter Chemical Science |
| Murray M, Roseblade A, Chen Y, et al. (2019) Carbon chain length modulates MDA-MB-231 breast cancer cell killing mechanisms by mitochondrially targeted aryl-urea fatty acids. Chemmedchem |
| Murray M, Gillani TB, Rawling T, et al. (2019) Inhibition of Hepatic CYP2D6 by the Active N-Oxide Metabolite of Sorafenib. The Aaps Journal. 21: 107 |
| Mostyn SN, Wilson KA, Schumann-Gillett A, et al. (2019) Identification of an allosteric binding site on the human glycine transporter, GlyT2, for bioactive lipid analgesics. Elife. 8 |
| Mostyn SN, Rawling T, Mohammadi S, et al. (2019) Development of an N-acyl amino acid that selectively inhibits the glycine transporter 2 to produce analgesia in a rat model of chronic pain. Journal of Medicinal Chemistry |