Dae Hong Shin

N⁶-Substituted D-4‘-Thioadenosine-5‘-methyluronamides:  Potent and Selective Agonists at the Human A₃Adenosine Receptor

Lak Shin Jeong, Dong Zhe Jin, Hea Ok Kim et al. · Journal of Medicinal Chemistry · 2003 · 86 citations · Full text

Preparative and Stereoselective Synthesis of the Versatile Intermediate for Carbocyclic Nucleosides:  Effects of the Bulky Protecting Groups to Enforce Facial Selectivity

Won Jun Choi, Hyung Ryong Moon, Hea Ok Kim et al. · The Journal of Organic Chemistry · 2004 · 82 citations

Structure−Activity Relationships of 2-Chloro-<i>N</i>⁶-substituted-4‘-thioadenosine-5‘-uronamides as Highly Potent and Selective Agonists at the Human A₃ Adenosine Receptor

Lak Shin Jeong, Hyuk Woo Lee, Kenneth A. Jacobson et al. · Journal of Medicinal Chemistry · 2005 · 70 citations · Full text

Structure−Activity Relationships of Uridine 5‘-Diphosphate Analogues at the Human P2Y₆Receptor

Pedro Besada, Dae Hong Shin, Stefano Costanzi et al. · Journal of Medicinal Chemistry · 2006 · 70 citations · Full text

The antitumor effect of LJ-529, a novel agonist to A3 adenosine receptor, in both estrogen receptor–positive and estrogen receptor–negative human breast cancers

Heekyoung Chung, Ji‐Youn Jung, Sung‐Dae Cho et al. · Molecular Cancer Therapeutics · 2006 · 47 citations