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Publications by Reiko Nishino

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

English

Two-Dimensional XPS Analysis of Rosin Distribution in Paper Sheets Tub-Sized With Dispersed Rosin Size.

Manufacturing Engineering

Plastics

Chemical Engineering

2001

English

Related publications

Isocyanide-Based Four-Component Synthesis of Benzo[a]pyrano[2,3-C]phenazines

English

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

English

Targeting Human Parainfluenza Virus Type-1 Haemagglutinin-Neuraminidase With Mechanism-Based Inhibitors

English

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

2009

English

N, N-Bisbenzylidenebenzene-1, 4-Diamines and N, N-Bisbenzylidenenaphthalene-1, 4-Diamines as Sirtuin Type 2 (SIRT2) Inhibitors

English

Biological Evaluation of 2,3-Dioxoindolin-N-Phenylacetamide Derivatives as Potent CDC25B and PTP1B Phosphatase Inhibitors

Brazilian Journal of Pharmaceutical Sciences

English

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

2008

English

Synthesis and Biological Properties of 1.beta.-Methyl-Carbapenems With N-Methylpyrrolidinylthio Group at C-2 Position.

Journal of Antibiotics

Drug Discovery

Pharmacology

1992

English

Design, Synthesis, Biological and Structural Evaluation of Functionalized Resveratrol Analogues as Inhibitors of Quinone Reductase 2

Bioorganic and Medicinal Chemistry

Clinical Biochemistry

Pharmaceutical Science

Drug Discovery

2013

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Reiko Nishino

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

Two-Dimensional XPS Analysis of Rosin Distribution in Paper Sheets Tub-Sized With Dispersed Rosin Size.

Related publications

Isocyanide-Based Four-Component Synthesis of Benzo[a]pyrano[2,3-C]phenazines

Targeting Human Parainfluenza Virus Type-1 Haemagglutinin-Neuraminidase With Mechanism-Based Inhibitors

Stereoselective Synthesis and Biological Evaluations of Novel 3′-Deoxy-4′-Azaribonucleosides as Inhibitors of Hepatitis C Virus RNA Replication

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

Synthesis of Sialic Acid Derivatives Having Inhibitory Activities Against Human Parainfluenza Virus Type 1

Synthesis and Biological Properties of 1.beta.-Methyl-Carbapenems With N-Methylpyrrolidinylthio Group at C-2 Position.

Design, Synthesis, Biological and Structural Evaluation of Functionalized Resveratrol Analogues as Inhibitors of Quinone Reductase 2