Hea O. Kim

2-Substitution of N6-Benzyladenosine-5'-uronamides Enhances Selectivity for A3 Adenosine Receptors

Hea O. Kim, Xiao-duo Ji, Suhaib M. Siddiqi et al. · Journal of Medicinal Chemistry · 1994 · 204 citations · Full text

Medicine, Medicinal Chemistry, Pharmacology +8

Synthesis of enantiomerically pure (2'R,5'S)-(-)-1-(2-hydroxymethyloxathiolan-5-yl)cytosine as a potent antiviral agent against hepatitis B virus (HBV) and human immunodeficiency virus (HIV)

Joseph Warren Beach, Lak Shin Jeong, Antônio J. Alves et al. · The Journal of Organic Chemistry · 1992 · 192 citations

Medicine, Medicinal Chemistry, Pharmacology +6

Induction of Apoptosis in HL-60 Human Promyelocytic Leukemia Cells by Adenosine A3Receptor Agonists

Yutaka Kohno, Yoshitatsu Sei, M. Koshiba et al. · Biochemical and Biophysical Research Communications · 1996 · 174 citations · Full text

Life Sciences, Oncology, Pharmacology +14

Activation of Hippocampal Adenosine A₃Receptors Produces a Desensitization of A₁Receptor-Mediated Responses in Rat Hippocampus

Thomas V. Dunwiddie, Lihong Diao, Hea O. Kim et al. · Journal of Neuroscience · 1997 · 173 citations · Full text

Life Sciences, Neuroscience, Pharmacology +16

Asymmetric synthesis and biological evaluation of .beta.-L-(2R,5S)- and .alpha.-L-(2R,5R)-1,3-oxathiolane-pyrimidine and -purine nucleosides as potential anti-HIV agents

Lak Shin Jeong, Raymond F. Schinazi, Joseph Warren Beach et al. · Journal of Medicinal Chemistry · 1993 · 130 citations

Pharmacy, Medicinal Chemistry, Pharmacology +17