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GPR103 Antagonists Demonstrating Anorexigenic Activity in Vivo: Design and Development of Pyrrolo[2,3‑c]pyridines That Mimic the C‑Terminal Arg-Phe Motif of QRFP26

Journal of medicinal chemistry, 2014-07, Vol.57 (14), p.5935-5948

2014

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Structure‐Based Drug Design of Mineralocorticoid Receptor Antagonists to Explore Oxosteroid Receptor Selectivity

ChemMedChem, 2017-01, Vol.12 (1), p.50-65

2017

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Correction to GPR103 Antagonists Demonstrating Anorexigenic Activity in Vivo: Design and Development of Pyrrolo[2,3‑c]pyridines That Mimic the C‑Terminal Arg-Phe Motif of QRFP26

Journal of medicinal chemistry, 2015-05, Vol.58 (9), p.4086-4086

2015

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Synthesis of a New Class of Druglike Angiotensin II C-Terminal Mimics with Affinity for the AT2 Receptor

Journal of medicinal chemistry, 2007-04, Vol.50 (7), p.1711-1715

2007

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Discovery of a series of 2-(pyridinyl)pyrimidines as potent antagonists of GPR40

MedChemComm, 2015-01, Vol.6 (6), p.1024-1029

2015

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Rapid Palladium-Catalyzed Synthesis of Esters from Aryl Halides Utilizing Mo(CO)6 as a Solid Carbon Monoxide Source

Journal of combinatorial chemistry, 2003-07, Vol.5 (4), p.350-352

2003

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Angiotensin II Pseudopeptides Containing 1,3,5-Trisubstituted Benzene Scaffolds with High AT2 Receptor Affinity

Journal of medicinal chemistry, 2005-10, Vol.48 (21), p.6620-6631

2005

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Synthesis of a New Class of Druglike Angiotensin II C-Terminal Mimics with Affinity for the AT 2 Receptor

Journal of medicinal chemistry, 2007-04, Vol.50 (7), p.1711-1715

2007

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Short pseudopeptides containing turn scaffolds with high AT2 receptor affinity

Bioorganic & medicinal chemistry, 2006-09, Vol.14 (17), p.5963-5972

2006

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Synthesis and Biological activity of kappa opioid receptor agonists. Part 2: Preparation of 3-aryl-2-pyridone analogues generated by solution- and solid-phase parallel synthesis methods

Bioorganic & medicinal chemistry letters, 2003-03, Vol.13 (6), p.1141-1145

2003

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Short pseudopeptides containing turn scaffolds with high AT(2) receptor affinity

Bioorganic & medicinal chemistry, 2006-09, Vol.14 (17), p.5963

2006

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Design and synthesis of novel at2 receptor ligands: from peptides to drug-like molecules

Georgsson, Jennie

2006

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Angiotensin II Pseudopeptides Containing 1,3,5-Trisubstituted Benzene Scaffolds with High AT 2 Receptor Affinity

Journal of medicinal chemistry, 2005-10, Vol.48 (21), p.6620-6631

2005

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Short pseudopeptides containing turn scaffolds with high AT 2 receptor affinity

Bioorganic & medicinal chemistry, 2006, Vol.14 (17), p.5963-5972

2006

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3-Aryl pyridone derivatives. Potent and selective kappa opioid receptor agonists

Bioorganic & medicinal chemistry letters, 2002-01, Vol.12 (2), p.197-200

2002

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Rapid palladium-catalyzed synthesis of esters from aryl halides utilizing Mo(CO)(6) as a solid carbon monoxide source

Journal of combinatorial chemistry, 2003-07, Vol.5 (4), p.350-352

2003

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Rapid Palladium-Catalyzed Synthesis of Esters from Aryl Halides Utilizing Mo(CO)6 as a Solid Carbon Monoxide Source

ChemInform, 2003-11, Vol.34 (45), p.no-no

2003

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Synthesis and Biological Activity of ϰ Opioid Receptor Agonists. Part 2. Preparation of 3-Aryl-2-pyridone Analogues Generated by Solution- and Solid-Phase Parallel Synthesis Methods

ChemInform, 2003-07, Vol.34 (28), p.no-no

2003

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GPR103 Antagonists Demonstrating Anorexigenic Activity in Vivo: Design and Development of Pyrrolo[2,3‑c]pyridines That Mimic the C‑Terminal Arg-Phe Motif of QRFP26

Structure‐Based Drug Design of Mineralocorticoid Receptor Antagonists to Explore Oxosteroid Receptor Selectivity

Correction to GPR103 Antagonists Demonstrating Anorexigenic Activity in Vivo: Design and Development of Pyrrolo[2,3‑c]pyridines That Mimic the C‑Terminal Arg-Phe Motif of QRFP26

Synthesis of a New Class of Druglike Angiotensin II C-Terminal Mimics with Affinity for the AT2 Receptor

Discovery of a series of 2-(pyridinyl)pyrimidines as potent antagonists of GPR40

Rapid Palladium-Catalyzed Synthesis of Esters from Aryl Halides Utilizing Mo(CO)6 as a Solid Carbon Monoxide Source

Angiotensin II Pseudopeptides Containing 1,3,5-Trisubstituted Benzene Scaffolds with High AT2 Receptor Affinity

Synthesis of a New Class of Druglike Angiotensin II C-Terminal Mimics with Affinity for the AT 2 Receptor

Short pseudopeptides containing turn scaffolds with high AT2 receptor affinity

Synthesis and Biological activity of kappa opioid receptor agonists. Part 2: Preparation of 3-aryl-2-pyridone analogues generated by solution- and solid-phase parallel synthesis methods

Short pseudopeptides containing turn scaffolds with high AT(2) receptor affinity

Design and synthesis of novel at2 receptor ligands: from peptides to drug-like molecules

Angiotensin II Pseudopeptides Containing 1,3,5-Trisubstituted Benzene Scaffolds with High AT 2 Receptor Affinity

Short pseudopeptides containing turn scaffolds with high AT 2 receptor affinity

3-Aryl pyridone derivatives. Potent and selective kappa opioid receptor agonists

Rapid palladium-catalyzed synthesis of esters from aryl halides utilizing Mo(CO)(6) as a solid carbon monoxide source

Rapid Palladium-Catalyzed Synthesis of Esters from Aryl Halides Utilizing Mo(CO)6 as a Solid Carbon Monoxide Source

Synthesis and Biological Activity of ϰ Opioid Receptor Agonists. Part 2. Preparation of 3-Aryl-2-pyridone Analogues Generated by Solution- and Solid-Phase Parallel Synthesis Methods

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