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Suzanne M. Mandala

Merck & Co.

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synthesis.to enhanced inhibition of cell wall water-soluble, semisynthetic pneumocandin, is Increased antifungal activity of L-733,560, a

2013
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Magnetic resonance imaging assisted detection of hypoxia induced right ventricular hypertrophy in mice

2008 The FASEB Journal
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Essential role of sphingosine 1–phosphate receptor 2 in pathological angiogenesis of the mouse retina

2007 Journal of Clinical Investigation
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SAR studies of 3-arylpropionic acids as potent and selective agonists of sphingosine-1-phosphate receptor-1 (S1P1) with enhanced pharmacokinetic properties.

2007 Bioorganic & Medicinal Chemistry Letters
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2,5-Disubstituted pyrrolidine carboxylates as potent, orally active sphingosine-1-phosphate (S1P) receptor agonists

2006 Bioorganic & Medicinal Chemistry Letters
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Identification of Leu276 of the S1P1 Receptor and Phe263 of the S1P3 Receptor in Interaction with Receptor Specific Agonists by Molecular Modeling, Site-Directed Mutagenesis, and Affinity Studies

2006 Molecular Pharmacology
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Discovery of 3-arylpropionic acids as potent agonists of sphingosine-1-phosphate receptor-1 (S1P1) with high selectivity against all other known S1P receptor subtypes.

2006 Bioorganic & Medicinal Chemistry Letters
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2-Aryl(pyrrolidin-4-yl)acetic acids are potent agonists of sphingosine-1-phosphate (S1P) receptors

2006 Bioorganic & Medicinal Chemistry Letters
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Discovery of Potent 3,5-Diphenyl-1,2,4-oxadiazole Sphingosine-1-phosphate-1 (S1P1) Receptor Agonists with Exceptional Selectivity against S1P2 and S1P3

2005 Journal of Medicinal Chemistry
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Sphingosine-1-Phosphate Agonists Increase Macrophage Homing, Lymphocyte Contacts, and Endothelial Junctional Complex Formation in Murine Lymph Nodes

2005 Journal of Immunology
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Citations (82)