55 results on '"Jeong, Lak Shin"'
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2. Stereochemical influence of 4ʹ-methyl substitutions on truncated 4ʹ-thioadenosine derivatives: Impact on A3 adenosine receptor binding and antagonism
3. Identification of 6′-β-fluoro-homoaristeromycin as a potent inhibitor of chikungunya virus replication
4. Design, synthesis and anticancer activity of fluorocyclopentenyl-purines and – pyrimidines
5. 2,3,4-Trihydroxybenzyl-hydrazide analogues as novel potent coxsackievirus B3 3C protease inhibitors
6. Design, synthesis, and anticancer activity of C8-substituted-4′-thionucleosides as potential HSP90 inhibitors
7. Discovery of 2-aminoquinolone acid derivatives as potent inhibitors of SARS-CoV-2
8. Synthesis of oligonucleotides containing 5′-homo-4′-selenouridine derivative and its increased resistance against nuclease
9. Structure–activity relationships of 2′-modified-4′-selenoarabinofuranosyl-pyrimidines as anticancer agents
10. The Selective A3AR Antagonist LJ-1888 Ameliorates UUO-Induced Tubulointerstitial Fibrosis
11. Stereoselective synthesis and anti-HCV activity of conformationally restricted 2′- C-substituted carbanucleosides
12. Suppression of inflammation response by a novel A 3 adenosine receptor agonist thio-Cl-IB-MECA through inhibition of Akt and NF-κB signaling
13. A3 Adenosine Receptor Agonist Reduces Brain Ischemic Injury and Inhibits Inflammatory Cell Migration in Rats
14. Design, synthesis, and binding of homologated truncated 4′-thioadenosine derivatives at the human A 3 adenosine receptors
15. Synthesis and anti-hepatitis C virus (HCV) activity of 3′-C-substituted-methyl pyrimidine and purine nucleosides
16. Nucleoside-derived antagonists to A 3 adenosine receptors lower mouse intraocular pressure and act across species
17. Efficient and practical synthesis of l-hamamelose
18. Design and synthesis of N6-substituted-4′-thioadenosine-5′-uronamides as potent and selective human A 3 adenosine receptor agonists
19. Structure–activity relationships of truncated adenosine derivatives as highly potent and selective human A 3 adenosine receptor antagonists
20. Design and synthesis of novel 2′,3′-dideoxy-4′-selenonucleosides as potential antiviral agents
21. Selective A 3 adenosine receptor antagonists derived from nucleosides containing a bicyclo[3.1.0]hexane ring system
22. Inhibition of cell proliferation through cell cycle arrest and apoptosis by thio-Cl-IB-MECA, a novel A 3 adenosine receptor agonist, in human lung cancer cells
23. Design, synthesis, and biological evaluation of novel iso- d-2′,3′-dideoxy-3′-fluorothianucleoside derivatives
24. Docking studies of agonists and antagonists suggest an activation pathway of the A 3 adenosine receptor
25. Design, synthesis, and biological activity of N6-substituted-4′-thioadenosines at the human A 3 adenosine receptor
26. Asymmetric synthesis of homo-apioneplanocin A from d-ribose
27. Synthesis of d- and l-apio nucleoside analogues with 2′-hydroxyl group as potential anti-HIV agents
28. Synthesis and biological evaluation of novel thioapio dideoxynucleosides
29. Synthesis of novel (2 R,4 R)- and (2 S,4 S)- iso dideoxynucleosides with exocyclic methylene as potential antiviral agents
30. Improved and alternative synthesis of d- and l-cyclopentenone derivatives, the versatile intermediates for the synthesis of carbocyclic nucleosides
31. Study of the stability of carbocations by chlorosulfonyl isocyanate reaction with ethers
32. Design, synthesis and anticancer activity of novel dihydrobenzofuro[4,5- b][1,8]naphthyridin-6-one derivatives
33. Synthesis and structure–activity relationship studies of tyrosine-based antagonists at the human P2X 7 receptor
34. Structure–activity relationships of 2-chloro- N6-substituted-4′-thioadenosine-5′- N, N-dialkyluronamides as human A 3 adenosine receptor antagonists
35. 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
36. Synthesis of 2- C-hydroxymethylribofuranosylpurines as potent anti-hepatitis C virus (HCV) agents
37. Conversion of A 3 adenosine receptor agonists into selective antagonists by modification of the 5′-ribofuran-uronamide moiety
38. A highly efficient synthesis of unnatural l-sugars from d-ribose
39. Synthesis of fluorinated cyclopentenyladenine as potent inhibitor of S-adenosylhomocysteine hydrolase
40. Synthesis of 5′-substituted fluoro-neplanocin A analogues: importance of a hydrogen bonding donor at 5′-position for the inhibitory activity of S-adenosylhomocysteine hydrolase
41. Design and synthesis of 3′-ureidoadenosine-5′-uronamides: effects of the 3′-ureido group on binding to the A 3 adenosine receptor
42. Synthesis and biological evaluation of thymine nucleosides fused with 3′,4′-tetrahydrofuran ring
43. Design, synthesis and binding affinity of 3′-fluoro analogues of Cl-IB-MECA as adenosine A 3 receptor ligands
44. Synthesis and Biological Evaluation of Novel d-2′-Azido-2′,3′-dideoxyarabinofuranosyl-4′-thiopyrimidines and purines
45. A short and efficient synthetic approach to hydroxy ( E)-stilbenoids via solid-phase cross metathesis
46. Stereoselective synthesis of amino-substituted apio dideoxynucleosides through a distant neighboring group effect
47. Design, Synthesis, and Anti-HCV Activity of 2′-Modified-4′-selenonucleosides
48. Synthesis and antiviral activity of novel d- and l-2′-azido-2′,3′-dideoxyribofuranosyl-4′-thiopyrimidines and purines
49. Corrigendum to “Synthesis and structure–activity relationship studies of tyrosine-based antagonists at the human P2X 7 receptor” [Bioorg. Med. Chem. Lett. 18 (2008) 571–575]
50. Corrigendum to ‘Design, Synthesis and Binding Affinity of 3′-Fluoro Analogues of C1-IB-MECA as Adenosine A 3 Receptor Ligands’[Bioorg. Med. Chem. Lett. 13 (2003) 817] †
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