38 results on '"Choi, Nam Song"'
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2. Synthesis and anti-platelet activity of obovatol derivatives
3. Functional divergency oriented synthesis of azoninones as the key intermediates for bioactive indolizidine alkaloids analogs
4. CoMFA and coMSIA 3d qsar studies on pimarane cyclooxygenase-2 (COX-2) inhibitors
5. Isolation and Identification of Eukaryotic Initiation Factor 4A as a Molecular Target for the Marine Natural Product Pateamine A
6. RhoB induces apoptosis via direct interaction with TNFAIP1 in HeLa cells
7. Synthesis of 1,2,3-Triazole and Pyrazole Analogues as Bioisosteres of Biphenyl-Neolignans
8. Functional divergency oriented synthesis of azoninones as the key intermediates for bioactive indolizidine alkaloids analogs
9. Discovery of a Highly Specific and Potent Pan‐RAF Inhibitor
10. Synthesis of 1,2,3‐Triazole and Pyrazole Analogues as Bioisosteres of Biphenyl‐Neolignans.
11. Identification of chalcones as potent and selective PDE5A1 inhibitors
12. Discovery of a potent tubulin polymerization inhibitor: Synthesis and evaluation of water-soluble prodrugs of benzophenone analog
13. Inhibition of IRAK-4 activity for rescuing endotoxin LPS-induced septic mortality in mice by lonicerae flos extract
14. Abstract 941: Discovery of novel VEGFR2 and Raf-1 kinase inhibitorsuppressing MAPK signaling pathway in K-Ras mutant cancer cell-lines.
15. Quinazolines as potent and highly selective PDE5 inhibitors as potential therapeutics for male erectile dysfunction
16. Abstract 1803: Discovery of novel B-Raf kinase inhibitor with potent orally anticancer activity
17. Identification of CKD-516: A Potent Tubulin Polymerization Inhibitor with Marked Antitumor Activity against Murine and Human Solid Tumors
18. ChemInform Abstract: Practical and Versatile Syntheses of Angular Hydroxymethylated Decalones.
19. Discovery of potent, selective, and orally bioavailable PDE5 inhibitor: Methyl-4-(3-chloro-4-methoxybenzylamino)-8-(2-hydroxyethyl)-7-methoxyquinazolin-6-ylmethylcarbamate (CKD 533)
20. RhoB induces apoptosisviadirect interaction with TNFAIP1 in HeLa cells
21. ChemInform Abstract: Quinazolines as Potent and Highly Selective PDE5 Inhibitors as Potential Therapeutics for Male Erectile Dysfunction.
22. Synthesis of novel diaryl ethers and their evaluation as antimitotic agents
23. Inhibition of Eukaryotic Translation Initiation by the Natural Product Pateamine A
24. Inhibition of Eukaryotic Translation Initiation by the Marine Natural Product Pateamine A
25. Total synthesis and antiangiogenic activity of cyclopentane analogues of fumagillol
26. Angular Hydroxymethyl Directed Intramolecular Diels—Alder Approach for the Stereo- and Regioselective Synthesis of Pimaraditerpenes.
27. Syntheses and anti-MRSA activities of the C3 analogs of mansonone F, a potent anti-bacterial sesquiterpenoid: insights into its structural requirements for anti-MRSA activity
28. 5‐Demethoxyfumagillol, a Potent Angiogenesis Inhibitor Isolated from Aspergillus fumigatus.
29. Evidence for Separate Binding and Scaffolding Domains in the Immunosuppressive and Antitumor Marine Natural Product, Pateamine A: Design, Synthesis, and Activity Studies Leading to a Potent Simplified Derivative
30. ChemInform Abstract: Practical Synthesis of (S)‐7‐(2‐Isopropylamino)ethylcamptothecin Hydrochloride, Potent Topoisomerase I Inhibitor.
31. Practical synthesis of (S)-7-(2-isopropylamino)ethylcamptothecin hydrochloride, potent topoisomerase I inhibitor
32. Design and synthesis of highly potent fumagillin analogues from homology modeling for a human MetAP-2
33. Practical and versatile syntheses of angular hydroxymethylated decalones
34. Angular hydroxymethyl directed intramolecular Diels–Alder approach for the stereo- and regioselective synthesis of pimaraditerpenes
35. Construction of oxocane skeleton via unusually regioselective CC bond forming cyclization: Synthesis of (+) and (−)-lauthisan
36. ChemInform Abstract: Practical and Versatile Syntheses of Angular Hydroxymethylated Decalones.
37. Concise Synthesis of Broussonone A.
38. Isolation and identification of eukaryotic initiation factor 4A as a molecular target for the marine natural product Pateamine A.
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