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Publications by Takuya Hayakawa
Syntheses of 2-Deoxy-2,3-Didehydro-N-Acetylneuraminic Acid Analogues Modified by ^|^#945;-Acylaminoamido Groups at the C-4 Position Using Isocyanide-Based Four-Component Coupling and Biological Evaluation as Inhibitors of Human Parainfluenza Virus Type 1
Chemical and Pharmaceutical Bulletin
Medicine
Drug Discovery
Chemistry
Related publications
Isocyanide-Based Four-Component Synthesis of Benzo[a]pyrano[2,3-C]phenazines
Synthesis
Organic Chemistry
Catalysis
Catalysis by a New Sialidase, Deaminoneuraminic Acid Residue-Cleaving Enzyme (KDNase Sm), Initially Forms a Less Stable Α-Anomer of 3-Deoxy-D-Glycero-D-Galacto-Nonulosonic Acid and Is Strongly Inhibited by the Transition State Analogue, 2-Deoxy-2,3-Didehydro-D-Glycero-D-Galacto-2-Nonulopyranosonic Acid, but Not by 2-Deoxy-2,3-Didehydro-N-Acetylneuraminic Acid
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Targeting Human Parainfluenza Virus Type-1 Haemagglutinin-Neuraminidase With Mechanism-Based Inhibitors
Viruses
Virology
Infectious Diseases
Stereoselective Synthesis and Biological Evaluations of Novel 3′-Deoxy-4′-Azaribonucleosides as Inhibitors of Hepatitis C Virus RNA Replication
Journal of Medicinal Chemistry
Drug Discovery
Molecular Medicine
N, N-Bisbenzylidenebenzene-1, 4-Diamines and N, N-Bisbenzylidenenaphthalene-1, 4-Diamines as Sirtuin Type 2 (SIRT2) Inhibitors
Biological Evaluation of 2,3-Dioxoindolin-N-Phenylacetamide Derivatives as Potent CDC25B and PTP1B Phosphatase Inhibitors
Brazilian Journal of Pharmaceutical Sciences
Toxicology
Pharmaceutics
Pharmacology
Synthesis of Sialic Acid Derivatives Having Inhibitory Activities Against Human Parainfluenza Virus Type 1
Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry
Organic Chemistry
Synthesis and Biological Properties of 1.beta.-Methyl-Carbapenems With N-Methylpyrrolidinylthio Group at C-2 Position.
Journal of Antibiotics
Drug Discovery
Pharmacology
Design, Synthesis, Biological and Structural Evaluation of Functionalized Resveratrol Analogues as Inhibitors of Quinone Reductase 2
Bioorganic and Medicinal Chemistry
Organic Chemistry
Molecular Medicine
Molecular Biology
Biochemistry
Clinical Biochemistry
Pharmaceutical Science
Drug Discovery
