Mao‐Chin Liu

Triapine (3-aminopyridine-2-carboxaldehyde- thiosemicarbazone): A potent inhibitor of ribonucleotide reductase activity with broad spectrum antitumor activity

Rick A. Finch, Mao‐Chin Liu, Susan P. Grill et al. · Biochemical Pharmacology · 2000 · 367 citations

Life Sciences, Medicinal Chemistry, Pharmacology +8

Synthesis and Biological Evaluation of 2',3'-Dideoxy-L-pyrimidine Nucleosides as Potential Antiviral Agents against Human Immunodeficiency Virus (HIV) and Hepatitis B Virus (HBV)

Tai‐Shun Lin, Mei‐Zhen Luo, Mao‐Chin Liu et al. · Journal of Medicinal Chemistry · 1994 · 156 citations

Pharmacy, Medicinal Chemistry, Pharmacology +16

Design and Synthesis of 2‘,3‘-Dideoxy- 2‘,3‘-didehydro-β-<scp>l</scp>-cytidine (β-<scp>l</scp>-d4C) and 2‘,3‘-Dideoxy-2‘,3‘-didehydro-β-<scp>l</scp>-5- fluorocytidine (β-<scp>l</scp>-Fd4C), Two Exceptionally Potent Inhibitors of Human Hepatitis B Virus (HBV) and Potent Inhibitors of Human Immunodeficiency Virus (HIV) in Vitro

Tai‐Shun Lin, Mei‐Zhen Luo, Mao‐Chin Liu et al. · Journal of Medicinal Chemistry · 1996 · 117 citations

Medicine, Medicinal Chemistry, Pharmacology +8

Inhibitors of ribonucleotide reductase

Joseph G. Cory, Ann H. Cory, Germana Rappa et al. · Biochemical Pharmacology · 1994 · 109 citations

Life Sciences, Biochemistry, Molecular Biology +5

Antiviral activity of 2′,3′-dideoxy-β-L-5-fluorocytidine (β-L-FddC) and 2′,3′-dideoxy-β-L-cytidine (β-L-ddC) against hepatitis B virus and human immunodeficiency virus type 1 in vitro

Tai‐Shun Lin, Mei‐Zhen Luo, Mao‐Chin Liu et al. · Biochemical Pharmacology · 1994 · 93 citations

Medicine, Infectious Diseases, Medicinal Chemistry +7