Lak Shin Jeong
Affiliations: | Seoul National University, Seoul, South Korea |
Google:
"Lak Jeong"Mean distance: (not calculated yet)
Collaborators
Sign in to add collaborator| Kenneth A. Jacobson | collaborator | 2003- | Seoul National University |
BETA: Related publications
See more...
Publications
|
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
| 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 |
| 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 |
| Nguyen M, An S, Nguyen Y, et al. (2022) Design, Synthesis, and Biological Activity of l-1'-Homologated Adenosine Derivatives. Acs Medicinal Chemistry Letters. 13: 1131-1136 |
| Lee Y, Hou X, Lee JH, et al. (2021) Subtle Chemical Changes Cross the Boundary between Agonist and Antagonist: New A Adenosine Receptor Homology Models and Structural Network Analysis Can Predict This Boundary. Journal of Medicinal Chemistry |
| 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 |
| Shin YS, Jarhad DB, Jang MH, et al. (2019) Identification of 6'-β-fluoro-homoaristeromycin as a potent inhibitor of chikungunya virus replication. European Journal of Medicinal Chemistry. 187: 111956 |
| An S, Yu J, Choi H, et al. (2019) Selenium bioisosteric replacement of adenosine derivatives promoting adiponectin secretion increases the binding affinity to peroxisome proliferator-activated receptor δ. Bioorganic & Medicinal Chemistry. 115226 |