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Determining the absolute configuration of vanitaracin A, an anti-hepatitis B virus agent

Journal of antibiotics, 2022-02, Vol.75 (2), p.92-97

2022

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Low doses of the mycotoxin citrinin protect cortical neurons against glutamate-induced excitotoxicity

The Journal of Toxicological Sciences, 2016/04/01, Vol.41(2), pp.311-319

2016

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Design, Synthesis, and Biological Evaluation of EdAP, a 4'-Ethynyl-2'-Deoxyadenosine 5'-Monophosphate Analog, as a Potent Influenza a Inhibitor

Molecules (Basel, Switzerland), 2019-07, Vol.24 (14), p.2603

2019

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Identification and characterization of the direct interaction between methotrexate (MTX) and high-mobility group box 1 (HMGB1) protein

PloS one, 2013-05, Vol.8 (5), p.e63073

2013

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Identification of proteins that bind to the neuroprotective agent neoechinulin A

Bioscience, biotechnology, and biochemistry, 2018-03, Vol.82 (3), p.442-448

2018

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High-Power Abiotic Direct Glucose Fuel Cell Using a Gold–Platinum Bimetallic Anode Catalyst

ACS omega, 2018-12, Vol.3 (12), p.18323-18333

2018

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Synthesis of nucleotide analogues, EFdA, EdA and EdAP, and the effect of EdAP on hepatitis B virus replication

Bioscience, biotechnology, and biochemistry, 2020-02, Vol.84 (2), p.217-227

2020

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MA026, an anti-hepatitis C virus compound, opens tight junctions of the epithelial cell membrane

Journal of antibiotics, 2017-05, Vol.70 (5), p.691-694

2017

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Anti-cancer targeting telomerase inhibitors: β-rubromycin and oleic acid

Mini reviews in medicinal chemistry, 2012-10, Vol.12 (11), p.1135

2012

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Anticancer agent α-sulfoquinovosyl-acylpropanediol enhances the radiosensitivity of human malignant mesothelioma in nude mouse models

Journal of radiation research, 2022-01, Vol.63 (1), p.19-29

2022

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The natural sulfoglycolipid derivative SQAP improves the therapeutic efficacy of tissue factor-targeted radioimmunotherapy in the stroma-rich pancreatic cancer model BxPC-3

Translational oncology, 2022-01, Vol.15 (1), p.101285-101285, Article 101285

2022

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Cyclosporin A associated helicase-like protein facilitates the association of hepatitis C virus RNA polymerase with its cellular cyclophilin B

PloS one, 2011-04, Vol.6 (4), p.e18285

2011

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Enhancement of Cellulose Degradation by Cattle Saliva

PloS one, 2015-09, Vol.10 (9), p.e0138902-e0138902

2015

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Anti‐angiogenesis effect of 3′‐sulfoquinovosyl‐1′‐monoacylglycerol via upregulation of thrombospondin 1

Cancer science, 2012-08, Vol.103 (8), p.1546-1552

2012

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A Eukaryotic Molecular Target Candidate of Roxithromycin: Fungal Differentiation as a Sensitive Drug Target Analysis System

Bioscience, biotechnology, and biochemistry, 2013-07, Vol.77 (7), p.1539-1547

2013

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In Memoriam Professor Kyohei Yamashita

Regulation of Plant Growth & Development, 2019, Vol.54(1), pp.87-89

Sugawara, Fumio

2019

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3-O-methylfunicone, a selective inhibitor of mammalian Y-family DNA polymerases from an Australian sea salt fungal strain

Marine drugs, 2009-11, Vol.7 (4), p.624-639

2009

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Novel terpenoids, trichoderonic acids A and B isolated from Trichoderma virens, are selective inhibitors of family X DNA polymerases

Bioscience, biotechnology, and biochemistry, 2010, Vol.74 (4), p.793-801

2010

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A screening of a library of T7 phage-displayed peptide identifies E2F-4 as an etoposide-binding protein

Molecules (Basel, Switzerland), 2011-05, Vol.16 (5), p.4278-4294

2011

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Neoechinulin A Imparts Resistance to Acute Nitrosative Stress in PC12 Cells: A Potential Link of an Elevated Cellular Reserve Capacity for Pyridine Nucleotide Redox Turnover with Cytoprotection

Biological and Pharmaceutical Bulletin, 2012/07/01, Vol.35(7), pp.1105-1117

2012

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Neoechinulin A Protects PC12 Cells against MPP -induced Cytotoxicity

Journal of antibiotics, 2008-05, Vol.61 (5), p.330-333

2008

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Synthesis and Biological Activities of Neoechinulin A Derivatives: New Aspects of Structure–Activity Relationships for Neoechinulin A

Chemical and Pharmaceutical Bulletin, 2008/12/01, Vol.56(12), pp.1738-1743

2008

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Downregulation of Tie2 gene by a novel antitumor sulfolipid, 3′‐sulfoquinovosyl‐1′‐monoacylglycerol, targeting angiogenesis

Cancer science, 2008-05, Vol.99 (5), p.1063-1070

2008

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Structure-activity Relationships of Neoechinulin A Analogues with Cytoprotection against Peroxynitrite-induced PC12 Cell Death

Journal of antibiotics, 2007-10, Vol.60 (10), p.614-621

2007

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The aryl hydrocarbon receptor–cytochrome P450 1A1 pathway controls lipid accumulation and enhances the permissiveness for hepatitis C virus assembly

The Journal of biological chemistry, 2018-12, Vol.293 (51), p.19559-19571

2018

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Determining the absolute configuration of vanitaracin A, an anti-hepatitis B virus agent

Low doses of the mycotoxin citrinin protect cortical neurons against glutamate-induced excitotoxicity

Design, Synthesis, and Biological Evaluation of EdAP, a 4'-Ethynyl-2'-Deoxyadenosine 5'-Monophosphate Analog, as a Potent Influenza a Inhibitor

Identification and characterization of the direct interaction between methotrexate (MTX) and high-mobility group box 1 (HMGB1) protein

Identification of proteins that bind to the neuroprotective agent neoechinulin A

High-Power Abiotic Direct Glucose Fuel Cell Using a Gold–Platinum Bimetallic Anode Catalyst

Synthesis of nucleotide analogues, EFdA, EdA and EdAP, and the effect of EdAP on hepatitis B virus replication

MA026, an anti-hepatitis C virus compound, opens tight junctions of the epithelial cell membrane

Anti-cancer targeting telomerase inhibitors: β-rubromycin and oleic acid

Anticancer agent α-sulfoquinovosyl-acylpropanediol enhances the radiosensitivity of human malignant mesothelioma in nude mouse models

The natural sulfoglycolipid derivative SQAP improves the therapeutic efficacy of tissue factor-targeted radioimmunotherapy in the stroma-rich pancreatic cancer model BxPC-3

Cyclosporin A associated helicase-like protein facilitates the association of hepatitis C virus RNA polymerase with its cellular cyclophilin B

Enhancement of Cellulose Degradation by Cattle Saliva

Anti‐angiogenesis effect of 3′‐sulfoquinovosyl‐1′‐monoacylglycerol via upregulation of thrombospondin 1

A Eukaryotic Molecular Target Candidate of Roxithromycin: Fungal Differentiation as a Sensitive Drug Target Analysis System

In Memoriam Professor Kyohei Yamashita

3-O-methylfunicone, a selective inhibitor of mammalian Y-family DNA polymerases from an Australian sea salt fungal strain

Novel terpenoids, trichoderonic acids A and B isolated from Trichoderma virens, are selective inhibitors of family X DNA polymerases

A screening of a library of T7 phage-displayed peptide identifies E2F-4 as an etoposide-binding protein

Neoechinulin A Imparts Resistance to Acute Nitrosative Stress in PC12 Cells: A Potential Link of an Elevated Cellular Reserve Capacity for Pyridine Nucleotide Redox Turnover with Cytoprotection

Neoechinulin A Protects PC12 Cells against MPP -induced Cytotoxicity

Synthesis and Biological Activities of Neoechinulin A Derivatives: New Aspects of Structure–Activity Relationships for Neoechinulin A

Downregulation of Tie2 gene by a novel antitumor sulfolipid, 3′‐sulfoquinovosyl‐1′‐monoacylglycerol, targeting angiogenesis

Structure-activity Relationships of Neoechinulin A Analogues with Cytoprotection against Peroxynitrite-induced PC12 Cell Death

The aryl hydrocarbon receptor–cytochrome P450 1A1 pathway controls lipid accumulation and enhances the permissiveness for hepatitis C virus assembly

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