Jinha Yu
Affiliations: | 2016-2018 | Chemical Kinomics Research Center | KIST (Korea Institute of Science and Technology) |
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Parents
Sign in to add mentorKenneth A. Jacobson | post-doc | 2016-2018 | KIST (Korea Institute of Science and Technology) |
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Publications
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Kim G, Jarhad DB, Lee G, et al. (2024) Structural Modification and Biological Evaluation of 2,8-Disubstituted Adenine and Its Nucleosides as A Adenosine Receptor Antagonists: Exploring the Roles of Ribose at Adenosine Receptors. Journal of Medicinal Chemistry |
Kim G, Hou X, Byun WS, et al. (2024) Correction to "Structure-Activity Relationship of Truncated 2,8-Disubstituted-Adenosine Derivatives as Dual A/A Adenosine Receptor Antagonists and Their Cancer Immunotherapeutic Activity". Journal of Medicinal Chemistry |
Kim G, Hou X, Byun WS, et al. (2023) Structure-Activity Relationship of Truncated 2,8-Disubstituted-Adenosine Derivatives as Dual A/A Adenosine Receptor Antagonists and Their Cancer Immunotherapeutic Activity. Journal of Medicinal Chemistry |
Son Y, Kim J, Kim Y, et al. (2022) Discovery of dioxo-benzo[b]thiophene derivatives as potent YAP-TEAD interaction inhibitors for treating breast cancer. Bioorganic Chemistry. 131: 106274 |
Shiriaeva A, Park D, Kim G, et al. (2022) GPCR Agonist-to-Antagonist Conversion: Enabling the Design of Nucleoside Functional Switches for the A Adenosine Receptor. Journal of Medicinal Chemistry |
Park S, Ahn Y, Kim Y, et al. (2022) Design, Synthesis and Biological Evaluation of 1,3,5-Triazine Derivatives Targeting hA and hA Adenosine Receptor. Molecules (Basel, Switzerland). 27 |
Abel B, Murakami M, Tosh DK, et al. (2022) Interaction of A adenosine receptor ligands with the human multidrug transporter ABCG2. European Journal of Medicinal Chemistry. 231: 114103 |
Choi H, Jacobson KA, Yu J, et al. (2021) Design and Synthesis of 2,6-Disubstituted-4'-Selenoadenosine-5'-,-Dimethyluronamide Derivatives as Human A Adenosine Receptor Antagonists. Pharmaceuticals (Basel, Switzerland). 14 |
An S, Kim G, Kim HJ, et al. (2020) Discovery and Structure-Activity Relationships of Novel Template, Truncated 1'-Homologated Adenosine Derivatives as Pure Dual PPARγ/δ Modulators. Journal of Medicinal Chemistry |
Jung YH, Yu J, Wen Z, et al. (2020) Exploration of Alternative Scaffolds for P2Y Receptor Antagonists Containing a Biaryl Core. Journal of Medicinal Chemistry |