45 results on '"Yakushiji, Fumika"'
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2. Concise Synthesis of 11-Noriridoids via Pauson–Khand Reaction
3. Synthesis and biological evaluation of echinomycin analogues as potential colon cancer agent
4. Solid-Phase Synthesis of Nannocystin Ax and Its Analogues
5. Click strategy using disodium salts of amino acids improves the water solubility of plinabulin and KPU-300
6. Beneficial effects of a new neuroprotective compound in neuronal cells and MPTP-administered mouse model of Parkinson's disease.
7. Synthetic modifications of histones and their functional evaluation
8. Development of Novel Biologically Active Compounds Based on Synthetic Organic Chemistry
9. Solid-phase synthesis of fluorescent analogues of Park’s nucleotide, lipid I and lipid II
10. Structure, solubility, and permeability relationships in a diverse middle molecule library
11. Synthetic Modifications of Histones and Their Functional Evaluation.
12. Development of cyclic peptide derivatives from the N-terminal region of LANA for targeting the nucleosome acidic patch
13. Recent Advances in Iridoid Chemistry: Biosynthesis and Chemical Synthesis
14. Elucidating the Structural Requirement of Uridylpeptide Antibiotics for Antibacterial Activity
15. Total Synthesis of Acaulide and Acaulone A
16. Total Synthesis of Echinomycin and Its Analogues
17. Diversity-oriented Symposium: Diversity Experiences through Study Abroad
18. Synthesis and biological evaluation of a MraY selective analogue of tunicamycins
19. Study of the structure-activity relationship of polymyxin analogues
20. Polycomb Repressive Complex 2: Modulator Development for Functional Regulation of a Multiprotein Complex by Using Structural Information
21. Recent Advances in Iridoid Chemistry: Biosynthesis and Chemical Synthesis.
22. Synthesis and biological evaluation of a MraY selective analogue of tunicamycins.
23. Total Synthesis of Plusbacin A3 and Its Dideoxy Derivative Using a Solvent-Dependent Diastereodivergent Joullié–Ugi Three-Component Reaction
24. Total Synthesis of Tunicamycin V
25. Total Synthesis and Antibacterial Investigation of Plusbacin A3
26. One-pot Selective Synthesis of 2,3-Dihydro-4H-Furo[3,2-c]coumarins by Palladium-Catalyzed Silver-Assisted Propargylation/Intramolecular 5-exo-dig Cyclization
27. HIV-1 susceptibility of transgenic rat-derived primary macrophage/T cells and a T cell line that express human receptors, CyclinT1 and CRM1 genes
28. Novel Hybrid Compound of a Plinabulin Prodrug with an IgG Binding Peptide for Generating a Tumor Selective Noncovalent-Type Antibody–Drug Conjugate
29. Identification of a degrading enzyme in human serum that hydrolyzes a C‐terminal core sequence of neuromedin U
30. Effect of N-Terminal Acylation on the Activity of Myostatin Inhibitory Peptides
31. Total Synthesis of Plusbacin A3 and Its Dideoxy Derivative Using a Solvent-Dependent Diastereodivergent Joullié–Ugi Three-Component Reaction.
32. Development of the Thiol-Selective Solid-Supported Oligoarginine-Conjugating Reagent KSH-2
33. Structure–Activity Relationship Studies of 3-epi-Deoxynegamycin Derivatives as Potent Readthrough Drug Candidates
34. Discovery of Potent Hexapeptide Agonists to Human Neuromedin U Receptor 1 and Identification of Their Serum Metabolites
35. Identification of the Minimum Peptide from Mouse Myostatin Prodomain for Human Myostatin Inhibition
36. 3-Nitro-2-pyridinesulfenyl-mediated solid-phase disulfide ligation in the synthesis of disulfide bond-containing cyclic peptides
37. ChemInform Abstract: Palladium‐Catalyzed C3‐Selective Mono‐Arylation of 4‐Hydroxycoumarin.
38. Identification of the MinimumPeptide from Mouse MyostatinProdomain for Human Myostatin Inhibition.
39. Discovery of Natural Products Possessing Selective Eukaryotic Readthrough Activity: 3- epi-Deoxynegamycin and Its Leucine Adduct.
40. Discovery of Selective HexapeptideAgonists to HumanNeuromedin U Receptors Types 1 and 2.
41. Total Synthesis of Plusbacin A 3 and Its Dideoxy Derivative Using a Solvent-Dependent Diastereodivergent Joullié-Ugi Three-Component Reaction.
42. Total Synthesis of Tunicamycin V.
43. Solid-Phase Modular Synthesis of Park Nucleotide and Lipids I and II Analogues.
44. Identification of a degrading enzyme in human serum that hydrolyzes a C-terminal core sequence of neuromedin U.
45. Discovery of selective hexapeptide agonists to human neuromedin U receptors types 1 and 2.
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