Peggy P. Huang

Titanium Tetraisopropoxide Catalyzed Synthesis of Base‐Sensitive Cyanoguanidine Analogs

P. Huang, H. Bai, J. Lynch, 2005 .

Longer wavelength fluorescence resonance energy transfer depsipeptide substrates for hepatitis C virus NS3 protease.

P. Richardson, U. Warrior, J. Randolph, 2007, Analytical biochemistry.

Synthesis, antiviral activity, and conformational studies of a P3 aza-peptide analog of a potent macrocyclic tripeptide HCV protease inhibitor.

D. Kempf, J. Randolph, W. Kati, 2008, Bioorganic & medicinal chemistry letters.

Mutations Conferring Resistance to a Potent Hepatitis C Virus Serine Protease Inhibitor In Vitro

A. Molla, H. Mo, T. Pilot‐Matias, 2004, Antimicrobial Agents and Chemotherapy.

Synthesis, antiviral activity, and pharmacokinetic evaluation of P3 pyridylmethyl analogs of oximinoarylsulfonyl HIV-1 protease inhibitors.

A. Molla, D. Kempf, H. Mo, 2006, Bioorganic & Medicinal Chemistry.

Synthesis and evaluation of inhibitors of cytochrome P450 3A (CYP3A) for pharmacokinetic enhancement of drugs.

D. Kempf, J. Randolph, K. Marsh, 2009, Bioorganic & medicinal chemistry letters.

Structure-activity studies related to ABT-594, a potent nonopioid analgesic agent: effect of pyridine and azetidine ring substitutions on nicotinic acetylcholine receptor binding affinity and analgesic activity in mice.

D. Donnelly-roberts, S. Arneric, J. Sullivan, 1998, Bioorganic & medicinal chemistry letters.

Synthesis and antiviral activity of P1' arylsulfonamide azacyclic urea HIV protease inhibitors.

V. Stoll, S. Vasavanonda, D. Kempf, 2004, Bioorganic & medicinal chemistry letters.