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ACS Medicinal Chemistry Letters|October 18, 2024
Structure-Activity Relationship of Truncated 4'-Selenonucleosides: A3 Adenosine Receptor Activity and Binding SelectivityMinjae Kim, Hongseok Choi, Akshata Nayak, et al.Nature|December 25, 2015
Processing and properties of magnesium containing a dense uniform dispersion of nanoparticlesLian-Yi Chen, Jia-Quan Xu, Hongseok Choi, et al.ACS Medicinal Chemistry Letters|July 21, 2022
Design, Synthesis, and Biological Activity of l-1'-Homologated Adenosine DerivativesMai Nguyen, Seungchan An, Yen Nguyen, et al.ACS Medicinal Chemistry Letters|December 17, 2025
Design, Synthesis, and Biological Evaluation of C2-(N-Substituted Amino) Truncated 4'-Thioadenosine Derivatives as A2AAR and A3AR Dual LigandsMisuk Joung, Hongseok Choi, Minjae Kim, et al.European Journal of Medicinal Chemistry|April 7, 2017
Design, synthesis, and structure-activity relationship study of halogen containing 2-benzylidene-1-indanone derivatives for inhibition of LPS-stimulated ROS production in RAW 264.7 macrophagesAarajana Shrestha, Hye Jin Oh, Mi Jin Kim, et al.ACS Medicinal Chemistry Letters|January 15, 2025
Synthesis and Biological Evaluation of 5'-Deoxy-adenosine Derivatives as A3 Adenosine Receptor LigandsMinjae Kim, Siddhi D Naik, Hongseok Choi, et al.Journal of Medicinal Chemistry|July 28, 2025
Regio- and Stereoselective Ribose Modification in Truncated 2,8-Disubstituted Adenosine Scaffold to Develop Highly Potent A2A Adenosine Receptor AntagonistsGibae Kim, Seung Woo Kim, Hongseok Choi, et al.ACS Medicinal Chemistry Letters|December 17, 2025
Discovery of a Novel Template, N3‑1'-Homologated 4'-Truncated Thiosugar-Substituted Xanthine as an A3AR Antagonist via Conversion of an A1AR AntagonistMisuk Joung, Minjae Kim, Hongseok Choi, et al.ACS Medicinal Chemistry Letters|November 19, 2025
Design, Synthesis, and Antiviral Activity of 8‑Aza Fluoroneplanocin Derivatives Targeting SAH Hydrolase and Viral RdRpJiyoon Song, Hongseok Choi, Minjae Kim, et al.Bioorganic Chemistry|November 2, 2025
Design and development of 5'-modified 7-substituted 4'-thionucleosides as potent Haspin inhibitors: Synthesis and biological evaluationYun A Yum, Sung Chul Jang, Seung Woo Kim, et al.Pageof 4