362 results on '"Kim, Hea Ok"'
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2. Stereoselective synthesis and anti-HCV activity of conformationally restricted 2′- C-substituted carbanucleosides
3. Design, synthesis, and binding of homologated truncated 4′-thioadenosine derivatives at the human A 3 adenosine receptors
4. Synthesis and anti-hepatitis C virus (HCV) activity of 3′-C-substituted-methyl pyrimidine and purine nucleosides
5. Design and synthesis of N6-substituted-4′-thioadenosine-5′-uronamides as potent and selective human A 3 adenosine receptor agonists
6. Structure–activity relationships of truncated adenosine derivatives as highly potent and selective human A 3 adenosine receptor antagonists
7. Design and synthesis of novel 2′,3′-dideoxy-4′-selenonucleosides as potential antiviral agents
8. Synthesis of novel apio carbocyclic nucleoside analogues as selective A3 adenosine receptor agonists
9. Synthesis of 2-alkyl-substituted-N6-methyladenine derivatives as potential adenosine receptor ligand
10. Synthesis and antiviral activity of fluoro-substituted apio dideoxynucleosides
11. Design, synthesis, and biological activity of N6-substituted-4′-thioadenosines at the human A 3 adenosine receptor
12. Asymmetric synthesis of homo-apioneplanocin A from d-ribose
13. Synthesis of cyclopropyl-fused carbocyclic nucleosides via the regioselective opening of cyclic sulfites
14. Synthesis and antiviral activity of 2′-fluorohexopyranosyl nucleosides
15. Synthesis of d- and l-apio nucleoside analogues with 2′-hydroxyl group as potential anti-HIV agents
16. Structural determinants of efficacy at A3 adenosine receptors: modification of the ribose moiety
17. Design, Synthesis, and Anti-RNA Virus Activity of 6′-Fluorinated-Aristeromycin Analogues
18. Synthesis and biological evaluation of novel thioapio dideoxynucleosides
19. Synthesis of novel (2 R,4 R)- and (2 S,4 S)- iso dideoxynucleosides with exocyclic methylene as potential antiviral agents
20. Improved and alternative synthesis of d- and l-cyclopentenone derivatives, the versatile intermediates for the synthesis of carbocyclic nucleosides
21. Characterization of porous collagen/hyaluronic acid scaffold modified by 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide cross-linking
22. Design, Synthesis, and Anti-RNA Virus Activity of 6′-Fluorinated-Aristeromycin Analogues.
23. Structure-Activity Relationships of Truncated D- and L-4′-Thioadenosine Derivatives as Species-Independent A3 Adenosine Receptor Antagonists1
24. Syntheses and Biological Activity of Neplanocin and Analogues
25. Synthesis and Anti-Renal Fibrosis Activity of Conformationally Locked Truncated 2-Hexynyl-N6-Substituted-(N)-Methanocarba-nucleosides as A3 Adenosine Receptor Antagonists and Partial Agonists
26. Structure–activity relationships of 2-chloro- N6-substituted-4′-thioadenosine-5′- N, N-dialkyluronamides as human A 3 adenosine receptor antagonists
27. Preparative Synthesis of the Key Intermediate, (4R,5R)-3-Benzyloxymethyl-4,5-isopropylidenedioxycyclopent-2-enone for Carbocyclic Nucleosides
28. Fluorocyclopentenyl-cytosine with Broad Spectrum and Potent Antitumor Activity
29. Structure–Activity Relationships of Truncated C2- or C8-Substituted Adenosine Derivatives as Dual Acting A2A and A3 Adenosine Receptor Ligands
30. Correction to Stereoselective Synthesis of MLN4924, an Inhibitor of NEDD8-Activating Enzyme
31. Stereoselective Synthesis of MLN4924, an Inhibitor of NEDD8-Activating Enzyme
32. X-ray Crystal Structure and Binding Mode Analysis of Human S-Adenosylhomocysteine Hydrolase Complexed with Novel Mechanism-Based Inhibitors, Haloneplanocin A Analogues
33. Design, synthesis, and binding of homologated truncated 4′-thioadenosine derivatives at the human A3 adenosine receptors
34. Discovery of A New Human A2A Adenosine Receptor Agonist, Truncated 2-Hexynyl-4′-thioadenosine
35. ChemInform Abstract: Synthesis of Cyclopropyl-Fused Carbocyclic Nucleosides via the Regioselective Opening of Cyclic Sulfites.
36. ChemInform Abstract: Synthesis and Antiviral Activity of D- and L-2′-Azido-2′,3′-dideoxy-4′-thiopyrimidine and Purine Nucleosides
37. ChemInform Abstract: Synthesis of Novel (2R,4R)- and (2S,4S)-iso Dideoxynucleosides with Exocyclic Methylene as Potential Antiviral Agents.
38. ChemInform Abstract: Synthesis and Biological Evaluation of Novel Thioapio Dideoxynucleosides.
39. ChemInform Abstract: Synthesis and Biological Evaluation of Novel D-2′-Azido-2′,3′-dideoxyarabinofuranosyl-4′-thiopyrimidines and Purines.
40. A New DNA Building Block, 4′-Selenothymidine: Synthesis and Modification to 4′-Seleno-AZT as a Potential Anti-HIV Agent
41. Design, synthesis, and molecular modeling studies of 5′-deoxy-5′-ureidoadenosine: 5′-ureido group as multiple hydrogen bonding donor in the active site of S-adenosylhomocysteine hydrolase
42. Design and synthesis of N6-substituted-4′-thioadenosine-5′-uronamides as potent and selective human A3 adenosine receptor agonists
43. ChemInform Abstract: Syntheses and Biological Activity of Neplanocin and Analogues
44. Discovery of a New Template for Anticancer Agents: 2′-deoxy-2′-fluoro-4′-selenoarabinofuranosyl-cytosine (2′-F-4′-Seleno-ara-C)
45. Structure–activity relationships of truncated adenosine derivatives as highly potent and selective human A3 adenosine receptor antagonists
46. Structure−Activity Relationships of Truncatedd- andl-4′-Thioadenosine Derivatives as Species-Independent A3Adenosine Receptor Antagonists(1)
47. ChemInform Abstract: Synthesis of 3′‐(Ureido)adenosine Derivatives and Their High Binding Affinity at the Mutant A3 Adenosine Receptor
48. Synthesis of 3′-Acetamidoadenosine Derivatives as Potential A3Adenosine Receptor Agonists
49. ChemInform Abstract: Synthesis and anti-HCV Activity of 2′-β-Hydroxymethylated Nucleosides
50. ChemInform Abstract: Stereoselective Synthesis of 1′-Functionalized-4′-thionucleosides
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