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Kim Winborn

GlaxoSmithKline

13

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666

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

2009 Bioorganic & Medicinal Chemistry Letters
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Identification of small molecule agonists of the motilin receptor

2008 Bioorganic & Medicinal Chemistry Letters
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Potent achiral agonists of the ghrelin (growth hormone secretagogue) receptor. Part I: Lead identification

2007 Bioorganic & Medicinal Chemistry Letters
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SAR of biphenyl carboxamide ligands of the human melanin-concentrating hormone receptor 1 (MCH R1): Discovery of antagonist SB-568849

2006 Bioorganic & Medicinal Chemistry Letters
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Discovery of potent and stable conformationally constrained analogues of the MCH R1 antagonist SB-568849

2006 Bioorganic & Medicinal Chemistry Letters
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WITHDRAWN: Bicyclic heteroarylpiperazines as selective brain penetrant 5-HT6 receptor antagonists

2005 Bioorganic & Medicinal Chemistry
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Bicyclic heteroarylpiperazines as selective brain penetrant 5-HT6 receptor antagonists.

2005 Bioorganic & Medicinal Chemistry Letters
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Design and synthesis of trans-3-(2-(4-((3-(3-(5-methyl-1,2,4-oxadiazolyl))-phenyl)carboxamido)cyclohexyl )ethyl)-7-methylsulfonyl-2,3,4,5-tetrahydro-1H-3-benzazepine (SB-414796): A potent and selective dopamine D3 receptor antagonist

2003 Journal of Medicinal Chemistry
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Pharmacological and immunohistochemical characterization of the APJ receptor and its endogenous ligand apelin

2003 Journal of Neurochemistry
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Citations (348)