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Ge Zhang

Bristol-Myers Squibb

22

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514

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Structure-based design of inhibitors of coagulation factor XIa with novel P1 moieties

2015 Bioorganic & Medicinal Chemistry Letters
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Phenylimidazoles as Potent and Selective Inhibitors of Coagulation Factor XIa with in Vivo Antithrombotic Activity

2014 Journal of Medicinal Chemistry
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Tetrahydroquinoline derivatives as potent and selective factor XIa inhibitors.

2014 Journal of Medicinal Chemistry
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Synthesis and SAR of potent and selective tetrahydropyrazinoisoquinolinone 5-HT2C receptor agonists

2013 Bioorganic & Medicinal Chemistry Letters
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Synthesis and SAR of 2,3,3a,4-tetrahydro-1H-pyrrolo[3,4-c]isoquinolin-5(9bH)-ones as 5-HT2C receptor agonists.

2013 Bioorganic & Medicinal Chemistry Letters
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Identification of potent 11mer Glucagon-Like Peptide-1 Receptor agonist peptides with novel C-terminal amino acids: Homohomophenylalanine analogs

2010 Peptides
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Exploration of structure–activity relationships at the two C-terminal residues of potent 11mer Glucagon-Like Peptide-1 receptor agonist peptides via parallel synthesis

2010 Peptides
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Tricyclic dihydroquinazolinones as novel 5-HT2C selective and orally efficacious anti-obesity agents.

2010 Bioorganic & Medicinal Chemistry Letters
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8-(4-Methoxyphenyl)pyrazolo[1,5-a]-1,3,5-triazines: Selective and Centrally Active Corticotropin-Releasing Factor Receptor-1 (CRF1) Antagonists

2009 Journal of Medicinal Chemistry
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Synthesis and structure-activity relationships of 8-(pyrid-3-yl)pyrazolo[1,5-a]-1,3,5-triazines: potent, orally bioavailable corticotropin releasing factor receptor-1 (CRF1) antagonists.

2009 Journal of Medicinal Chemistry
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Citations (51)