Publications by authors named "Dae Hong Shin"

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Inhibition of cell proliferation through cell cycle arrest and apoptosis by thio-Cl-IB-MECA, a novel A3 adenosine receptor agonist, in human lung cancer cells.
Sun-Jack Kim, Hye-Young Min, Hwa-Jin Chung, Eun-Jung Park, Ji-Young Hong, Dae-Hong Shin, Lak Shin Jeong

Cancer Lett· June 2008

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Chiral separation of beta-blockers after derivatization with a new chiral derivatization agent, GATC.
Mi Young Ko, Dae Hong Shin, Joung Weon Oh, Workaferhaw Shibru Asegahegn, Kyeong Ho Kim

Arch Pharm Res· November 2006

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S
Structure-activity relationships of uridine 5'-diphosphate analogues at the human P2Y6 receptor.
Pedro Besada, Dae Hong Shin, Stefano Costanzi, Hyojin Ko, Christophe Mathé

J Med Chem· September 2006

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Agonists and antagonists for P2 receptors.
Kenneth A Jacobson, Stefano Costanzi, Bhalchandra V Joshi, Pedro Besada, Dae Hong Shin

Novartis Found Symp· August 2006

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Design, synthesis, and biological activity of N6-substituted-4'-thioadenosines at the human A3 adenosine receptor.
Lak Shin Jeong, Hyuk Woo Lee, Hea Ok Kim, Ji Young Jung, Zhan-Guo Gao, Dae Hong Shin

Bioorg Med Chem· July 2006

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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, Kyung-A Hong, Hyun-Jun Kim, Dong-Hui Shin, Dae Hong Shin, Lak Shin Jeong

Mol Cancer Ther· March 2006

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Structure-activity relationships of 2-chloro-N6-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, Hea Ok Kim, Dae Hong Shin

J Med Chem· January 2006

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D
D-4'-thioadenosine derivatives as highly potent and selective agonists at the human A3 adenosine receptor.
Hyouk Woo Lee, Dae Hong Shin, Ji Young Jeong, Hea Ok Kim, Moon Woo Chun, Lak Shin Jeong

Nucleosides Nucleotides Nucleic Acids· December 2005

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Stereoselective synthesis of 3-hydroxymethyl-D-cyclopentenone, the versatile intermediate for the synthesis of carbocyclic nucleosides.
Won Jun Choi, Hyung Ryong Moon, Hea Ok Kim, Young Mi Ko, Hye Jin Kim, Dae Hong Shin, Lak Shin Jeong

Nucleosides Nucleotides Nucleic Acids· December 2005

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A novel adenosine analog, thio-Cl-IB-MECA, induces G0/G1 cell cycle arrest and apoptosis in human promyelocytic leukemia HL-60 cells.
Eun-Jin Lee, Hye-Young Min, Hwa-Jin Chung, Eun-Jung Park, Dae-Hong Shin, Lak Shin Jeong

Biochem Pharmacol· September 2005

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Recent advances in 4'-thionucleosides as potential antiviral and antitumor agents.
Prashantha Gunaga, Hyung Ryong Moon, Won Jun Choi, Dae Hong Shin, Jae Gyu Park, Lak Shin Jeong

Curr Med Chem· October 2004

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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, Byul Nae Yoo, Jeong A Lee, Dae Hong Shin, Lak Shin Jeong

J Org Chem· April 2004

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Structural determinants of efficacy at A3 adenosine receptors: modification of the ribose moiety.
Zhan-Guo Gao, Lak Shin Jeong, Hyung Ryong Moon, Hea Ok Kim, Won Jun Choi, Dae Hong Shin

Biochem Pharmacol· March 2004

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Synthesis and biological evaluation of halo-neplanocin A as novel mechanism-based inhibitors of S-adenosylhomocysteine hydrolase.
Lak Shin Jeong, Hyung Ryong Moon, Jae Gyu Park, Dae Hong Shin, Won Jun Choi

Nucleosides Nucleotides Nucleic Acids· December 2003

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N6-substituted D-4'-thioadenosine-5'-methyluronamides: potent and selective agonists at the human A3 adenosine receptor.
Lak Shin Jeong, Dong Zhe Jin, Hea Ok Kim, Dae Hong Shin, Hyung Ryong Moon

J Med Chem· August 2003

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