Maria A. Cichy-Knight

Modulation of Receptor and Receptor Subtype Affinities Using Diastereomeric and Enantiomeric Monosaccharide Scaffolds as a Means to Structural and Biological Diversity. A New Route to Ether Synthesis

Ralph Hirschmann, John Hynes, Maria A. Cichy-Knight et al. · Journal of Medicinal Chemistry · 1998 · 108 citations · Full text

N-(3-Cyano-4,5,6,7-tetrahydro-1-benzothien-2-yl)amides as potent, selective, inhibitors of JNK2 and JNK3

Richard Angell, Francis Atkinson, Murray J. B. Brown et al. · Bioorganic & Medicinal Chemistry Letters · 2006 · 90 citations · Full text

Medicinal Chemistry, Medicine, Rational Drug Design +4

Synthesis of Potent Cyclic Hexapeptide NK-1 Antagonists. Use of a Minilibrary in Transforming a Peptidal Somatostatin Receptor Ligand into an NK-1 Receptor Ligand via a Polyvalent Peptidomimetic

Ralph Hirschmann, Wenqing Yao, Margaret A. Cascieri et al. · Journal of Medicinal Chemistry · 1996 · 60 citations · Full text

Discovery of potent, selective sulfonylfuran urea endothelial lipase inhibitors

Krista Goodman, Michael J. Bury, Mui Cheung et al. · Bioorganic & Medicinal Chemistry Letters · 2008 · 52 citations · Full text

Pharmaceutical Science, Medicine, Drug Development +3

Amino acid anthranilamide derivatives as a new class of glycogen phosphorylase inhibitors

Karen A. Evans, Yue H. Li, Frank T. Coppo et al. · Bioorganic & Medicinal Chemistry Letters · 2008 · 11 citations · Full text

Medicinal Chemistry, Bioorganic Chemistry, Biochemistry +13