Chung-Chi Lee

发表

Design, synthesis, and anti-HCV activity of thiourea compounds.

Y. Chao, T. Hsu, Iou-Jiun Kang, 2009, Bioorganic & medicinal chemistry letters.

Synthesis and antipicornavirus activity of (R)- and (S)-1-[5-(4'-chlorobiphenyl-4-yloxy)-3-methylpentyl]-3-pyridin-4-yl-imidazolidin-2-one.

S. Shih, Iou-Jiun Kang, Chung-Chi Lee, 2005, Bioorganic & medicinal chemistry letters.

Design, synthesis, and structure-activity relationships of pyrazolo[3,4-d]pyrimidines: a novel class of potent enterovirus inhibitors.

S. Shih, T. Hsu, Kak‐Shan Shia, 2004, Bioorganic & medicinal chemistry letters.

Synthesis, activity, and pharmacokinetic properties of a series of conformationally-restricted thiourea analogs as novel hepatitis C virus inhibitors.

A. Yueh, Y. Chao, T. Yeh, 2010, Bioorganic & medicinal chemistry.

Design and synthesis of indole, 2,3-dihydro-indole, and 3,4-dihydro-2H-quinoline-1-carbothioic acid amide derivatives as novel HCV inhibitors.

A. Yueh, Y. Chao, T. Hsu, 2009, Bioorganic & medicinal chemistry letters.

Design and efficient synthesis of novel arylthiourea derivatives as potent hepatitis C virus inhibitors.

A. Yueh, Y. Chao, T. Hsu, 2009, Bioorganic & medicinal chemistry letters.

A novel, potent, and orally bioavailable thiazole HCV NS5A inhibitor for the treatment of hepatitis C virus.

C. Chen, A. Yueh, Y. Chao, 2019, European journal of medicinal chemistry.

A Potent, Selective, and Orally Bioavailable HCV NS5A Inhibitor for Treatment of Hepatitis C Virus: (S)-1-((R)-2-(Cyclopropanecarboxamido)-2-phenylacetyl)-N-(4-phenylthiazol-2-yl)pyrrolidine-2-carboxamide.

A. Yueh, Y. Chao, Jen‐Shin Song, 2017, Journal of medicinal chemistry.

Design, synthesis, and antipicornavirus activity of 1-[5-(4-arylphenoxy)alkyl]-3-pyridin-4-ylimidazolidin-2-one derivatives.

Ying-Ting Lin, S. Shih, Chung-Chi Lee, 2005, Journal of medicinal chemistry.

Isatin-β-thiosemicarbazones as potent herpes simplex virus inhibitors.

A. Yueh, Y. Chao, S. Shih, 2011, Bioorganic & medicinal chemistry letters.

Heterocyclic Compounds. I. Reactions of o-Amino-carboxamide with b-Diketones: Synthesis of Imidazo[1,5-a]pyrimidine and Pyrazolo[1,5-a]pyrimidine Derivatives

J. Chern, Y. Liaw, Chung-Chi Lee, 1992 .

Design, synthesis, and structure-activity relationship of pyridyl imidazolidinones: a novel class of potent and selective human enterovirus 71 inhibitors.

Chia-Liang Tai, Yen-Chun Lee, Shin-Ru Shih, 2002, Journal of medicinal chemistry.

Synthesis and antienteroviral activity of a series of novel, oxime ether-containing pyridyl imidazolidinones.

Chia-Liang Tai, Yen-Chun Lee, Ying-Ting Lin, 2004, Bioorganic & medicinal chemistry letters.

Design, Synthesis, and Structure—Activity Relationships of Pyrazolo[3,4‐d]pyrimidines: A Novel Class of Potent Enterovirus Inhibitors.

S. Shih, T. Hsu, Kak‐Shan Shia, 2004 .

Mutation in Enterovirus 71 Capsid Protein VP1 Confers Resistance to the Inhibitory Effects of Pyridyl Imidazolidinone

Y. Chao, Guang-Wu Chen, S. Shih, 2004, Antimicrobial Agents and Chemotherapy.

Synthesis and in vitro cytotoxicity of 5-substituted 2-cyanoimino-4-imidazodinone and 2-cyanoimino-4-pyrimidinone derivatives.

Ying-Ting Lin, Chung-Ming Chang, Kak‐Shan Shia, 2004, Bioorganic & medicinal chemistry letters.

Arsenic trioxide-mediated growth inhibition in MC/CAR myeloma cells via cell cycle arrest in association with induction of cyclin-dependent kinase inhibitor, p21, and apoptosis.

Y. Y. Lee, Young Y. Lee, W. Park, 2000, Cancer research.