Author

Alison I. Muir

Observed name: Alison Muir

Observed institutions: Research Triangle Park Foundation, GlaxoSmithKline (United Kingdom), Harlow College

OpenAlex ID: A5110030604

The Orphan G Protein-coupled Receptors GPR41 and GPR43 Are Activated by Propionate and Other Short Chain Carboxylic Acids

2003 · Andrew J. Brown, Susan M. Goldsworthy, et al. · Journal of Biological Chemistry · 2,494

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The Orphan G Protein-coupled Receptor GPR40 Is Activated by Medium and Long Chain Fatty Acids

2003 · Celia P. Briscoe, Mohammad Tadayyon, et al. · Journal of Biological Chemistry · 1,128

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AXOR12, a Novel Human G Protein-coupled Receptor, Activated by the Peptide KiSS-1

2001 · Alison I. Muir, Larissa Chamberlain, et al. · Journal of Biological Chemistry · 931

Melanin-concentrating hormone is the cognate ligand for the orphan G-protein-coupled receptor SLC-1

1999 · Jon Chambers, Robert S. Ames, et al. · Nature · 494

Identification, Molecular Cloning, Expression, and Characterization of a Cysteinyl Leukotriene Receptor

1999 · Henry M. Sarau, Robert S. Ames, et al. · Molecular Pharmacology · 342

Molecular Cloning and Functional Characterization of MCH2, a Novel Human MCH Receptor

2001 · Jeffrey Hill, Malcolm Duckworth, et al. · Journal of Biological Chemistry · 227

Neuromedin U Is a Potent Agonist at the Orphan G Protein-coupled Receptor FM3

2000 · Philip G. Szekeres, Alison I. Muir, et al. · Journal of Biological Chemistry · 179

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Orphan G‐protein‐coupled receptors: the next generation of drug targets?

1998 · Shelagh Wilson, Derk J. Bergsma, et al. · British Journal of Pharmacology · 124

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Prokineticin-2, motilin, ghrelin and metoclopramide: Prokinetic utility in mouse stomach and colon

2005 · Anna K. Bassil, Narinder B. Dass, et al. · European Journal of Pharmacology · 62

Discovery of N-(3-Fluorophenyl)-1-[(4-([(3S)-3-methyl-1-piperazinyl]methyl)phenyl)acetyl]-4-piperidinamine (GSK962040), the First Small Molecule Motilin Receptor Agonist Clinical Candidate

2009 · Susan M. Westaway, Samantha L. Brown, et al. · Journal of Medicinal Chemistry · 28

Discovery of potent and stable conformationally constrained analogues of the MCH R1 antagonist SB-568849

2006 · David R. Witty, John Bateson, et al. · Bioorganic & Medicinal Chemistry Letters · 22

Potent achiral agonists of the ghrelin (growth hormone secretagogue) receptor. Part I: Lead identification

2007 · Tom D. Heightman, Jackie S. Scott, et al. · Bioorganic & Medicinal Chemistry Letters · 17

The Discovery of a Selective, Small Molecule Agonist for the Mas-Related Gene X1 Receptor

2009 · Berthold Wroblowski, Mark J. Wigglesworth, et al. · Journal of Medicinal Chemistry · 15

Identification of small molecule agonists of the motilin receptor

2008 · Tom D. Heightman, Elizabeth Conway, et al. · Bioorganic & Medicinal Chemistry Letters · 15

Potent achiral agonists of the growth hormone secretagogue (ghrelin) receptor. Part 2: Lead optimisation

2008 · Jason Witherington, Lee Abberley, et al. · Bioorganic & Medicinal Chemistry Letters · 15

SAR of biphenyl carboxamide ligands of the human melanin-concentrating hormone receptor 1 (MCH R1): Discovery of antagonist SB-568849

2006 · David R. Witty, John H. Bateson, et al. · Bioorganic & Medicinal Chemistry Letters · 13

The discovery and optimisation of benzazepine sulfonamide and sulfones as potent agonists of the motilin receptor

2009 · James M. Bailey, Jackie S. Scott, et al. · Bioorganic & Medicinal Chemistry Letters · 6

Aryl sulphonyl amides as potent agonists of the growth hormone secretagogue (ghrelin) receptor

2008 · Jason Witherington, Lee Abberley, et al. · Bioorganic & Medicinal Chemistry Letters · 4

Screening Orphan Receptors for Native Ligands

2019 · Shelagh Wilson, J. Randall Slemmon, et al. · CRC Press eBooks · 1

Works count: 19

Citation count: 6,117

H-index: 15

I10-index: 16