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Steven P. Seitz

Wilmington University

19

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605

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Increased Antiviral Activity of Cyclic Urea HIV Protease Inhibitors by Modifying the P1/P1′ Substituents.

2010 ChemInform
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Synthesis and biological activities of potential metabolites of the non-nucleoside reverse transcriptase inhibitor Efavirenz

2001 Bioorganic & Medicinal Chemistry Letters
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Quinazolines as cyclin dependent kinase inhibitors.

2001 Bioorganic & Medicinal Chemistry Letters
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Synthesis and evaluation of analogs of Efavirenz (SUSTIVATM) as HIV-1 reverse transcriptase inhibitors

1999 Bioorganic & Medicinal Chemistry Letters
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Increased antiviral activity of cyclic urea HIV protease inhibitors by modifying the P1/P1' substituents.

1999 Bioorganic & Medicinal Chemistry Letters
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Design and selection of DMP 850 and DMP 851: the next generation of cyclic urea HIV protease inhibitors

1998 Chemistry & Biology
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The synthesis of symmetrical and unsymmetrical P1/P1' cyclic ureas as HIV protease inhibitors.

1998 Bioorganic & Medicinal Chemistry Letters
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Functionalized aliphatic P2/P2' analogs of HIV-1 protease inhibitor DMP323

1997 Bioorganic & Medicinal Chemistry Letters
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The synthesis and antitumor evaluation of unsymmetrical bis-imides

1997 Bioorganic & Medicinal Chemistry Letters
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Functionalized aliphatic P2/P2' analogs of HIV-1 protease inhibitor DMP323

1997 Bioorganic & Medicinal Chemistry Letters
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Citations (3)