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Marina Taliani

Merck & Co.

11

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511

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Studies of metabolism and disposition of potent human immunodeficiency virus (HIV) integrase inhibitors using 19F-NMR spectroscopy

2007 Xenobiotica
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Discovery and Synthesis of HIV Integrase Inhibitors: Development of Potent and Orally Bioavailable N-Methyl Pyrimidones

2007 Journal of Medicinal Chemistry
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HCV NS5b RNA-dependent RNA polymerase inhibitors: From α, γ-diketoacids to 4,5-dihydroxypyrimidine- or 3-methyl-5-hydroxypyrimidinonecarboxylic acids. Design and synthesis

2004 Journal of Medicinal Chemistry
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DEVELOPMENT AND VALIDATION OF A HIGH-THROUGHPUT RADIOMETRIC CYP2C9 INHIBITION ASSAY USING TRITIATED DICLOFENAC

2004 Drug Metabolism and Disposition
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A New Method for Chemoselective Conjugation of Unprotected Peptides to Dauno- and Doxorubicin

2001 Bioorganic & Medicinal Chemistry Letters
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A New Method for Chemoselective Conjugation of Unprotected Peptides to Dauno‐ and Doxorubicin.

2001 ChemInform
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Potent peptide inhibitors of human hepatitis C virus NS3 protease are obtained by optimizing the cleavage products.

1998 Biochemistry
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An improved solid-phase synthesis of resonance energy transfer fluorescent peptides and depsipeptides employing the EDANS/DABCYL donor-acceptor pair

1997 Letters in Peptide Science
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A Continuous Assay of Hepatitis C Virus Protease Based on Resonance Energy Transfer Depsipeptide Substrates

1996 Analytical Biochemistry
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Synthetic Depsipeptide Substrates for the Assay of Human Hepatitis C Virus Protease

1996 Analytical Biochemistry
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Citations (30)