Potent, Selective, and Orally Efficacious Antagonists of Melanin-Concentrating Hormone Receptor 1
Tavares, F. X.* et al. J. Med. Chem. 2006, 49, 7095.
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6-(4-Chlorophenyl)-3-substituted-thieno[3,2-d]pyrimidin-4 (3H)-one-Based Melanin-Concentrating Hormone
Receptor 1 Antagonist
Tavares, F. X.* et al. J. Med. Chem. 2006, 49, 7108.
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N-Phenyl-4-pyrazolo[1,5-b]pyridazin-3-ylpyrimidin-2-amines as Potent and Selective Inhibitors of Glycogen Synthase Kinase 3 with Good Cellular Efficacy
Tavares, F. X.* et al. J. Med. Chem. 2004, 47, 4716.
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Editorial
Tavares, F. X.* Curr. Top. Med. Chem. 2005, 5, 1587
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Design of cathepsin K inhibitors for osteoporosis
Tavares, F. X.* et al. Curr. Top. Med Chem. 2005, 5, 1639.
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Ketoheterocycle-based inhibitors of cathepsin K: A novel entry into the synthesis of peptidic ketoheterocycles
Tavares, F. X.* et al. Bioorg. Med. Chem. Lett. 2005, 15, 3891.
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Ketoamide-Based Inhibitors of Cysteine Protease, Cathepsin K: P3 Modifications
Tavares, F. X.* et al. J. Med. Chem. 2004, 47, 5057.
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Potent and Selective Ketoamide-Based Inhibitors of Cysteine Protease, Cathepsin K
Tavares, F. X.* et al. J. Med. Chem. 2004, 47, 5049.
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Design of Potent, Selective, and Orally Bioavailable Inhibitors of Cysteine Protease Cathepsin K
Tavares, F. X.* et al. J. Med. Chem. 2004, 47, 588.
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Enantioselective synthesis of a taxane C-ring component using the Schultz asymmetric Birch reduction methodology
Magnus, P.;* Tavares, F.; Westwood, N. Tetrahedron Lett. 1997, 38, 1341.
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Total Synthesis of Streptogramin Antibiotics. (-)-Madumycin II
Tavares, F.; Lawson, J. P.; Meyers, A. I.*. J. Am. Chem. Soc. 1996, 118, 3303.
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Total synthesis of the streptogramin antibiotic, (-)-Madumycin II
Tavares, F.* Lawson, J. P.; Meyers, A. I. 211th ACS National Meeting, New Orleans, LA, March 24-28, 1996, ORGN-171.