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Development of Naturally Inspired Peptide and Protein Chemistry

Chemical and Pharmaceutical Bulletin, 2022/11/01, Vol.70(11), pp.748-764

Otaka, Akira

2022

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Advances in Preparation of Peptide and Protein Thioesters Aiming to Use in Medicinal Sciences

Chemical and Pharmaceutical Bulletin, 2022/05/01, Vol.70(5), pp.316-323

2022

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Copper-Mediated Deprotection of Thiazolidine and Selenazolidine Derivatives Applied to Native Chemical Ligation

Journal of organic chemistry, 2020-02, Vol.85 (3), p.1425-1433

2020

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Development of a Turn-On Fluorescent Traceable Linker Employing N-Sulfanylethylcoumarinyl Amide for the Enrichment and Visualization of Target Proteins

Chemical and Pharmaceutical Bulletin, 2020/03/01, Vol.68(3), pp.216-219

2020

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Peptide probes containing a non‐hydrolyzable phosphotyrosine‐mimetic residue for enrichment of protein tyrosine phosphatases

Proteomics (Weinheim), 2022-02, Vol.22 (4), p.e2100144-n/a

2022

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A Photo-Activatable Peptide Mimicking Functions of Apolipoprotein A-I

Biological and Pharmaceutical Bulletin, 2019/06/01, Vol.42(6), pp.1019-1024

2019

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CXCL14 is a natural inhibitor of the CXCL12–CXCR4 signaling axis

FEBS letters, 2013-06, Vol.587 (12), p.1731-1735

2013

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Identification of Functional Domains of CXCL14 Involved in High-Affinity Binding and Intracellular Transport of CpG DNA

The Journal of immunology (1950), 2021-07, Vol.207 (2), p.459-469

2021

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Dual Kinetically Controlled Native Chemical Ligation Using a Combination of Sulfanylproline and Sulfanylethylanilide Peptide

Organic letters, 2011-10, Vol.13 (20), p.5588-5591

2011

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Chemical Synthetic Platform for Chlorpromazine Oligomers That Were Reported as Photo-degradation Products of Chlorpromazine

Chemical and Pharmaceutical Bulletin, 2017/12/01, Vol.65(12), pp.1161-1166

2017

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Examination of native chemical ligation using peptidyl prolyl thioesters

Chemical communications (Cambridge, England), 2014-01, Vol.50 (1), p.58-60

2014

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Safe Removal of the Allyl Protecting Groups of Allyl Esters using a Recyclable, Low-Leaching and Ligand-Free Palladium Nanoparticle Catalyst

Advanced synthesis & catalysis, 2015-06, Vol.357 (9), p.2119-2124

2015

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Sequence-Independent Traceless Method for Preparation of Peptide/Protein Thioesters Using CPaseY-Mediated Hydrazinolysis

Chemical and Pharmaceutical Bulletin, 2020/12/01, Vol.68(12), pp.1226-1232

2020

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One-Pot/Sequential Native Chemical Ligation Using N-Sulfanylethylanilide Peptide

Chemical record, 2012-10, Vol.12 (5), p.479-490

2012

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Heparin promotes fibril formation by the N‐terminal fragment of amyloidogenic apolipoprotein A‐I

FEBS letters, 2016-10, Vol.590 (20), p.3492-3500

2016

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Formation of stable nanodiscs by bihelical apolipoprotein A-I mimetic peptide

Journal of peptide science, 2016-02, Vol.22 (2), p.116-122

2016

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Dimeric peptides of the C-terminal region of CXCL14 function as CXCL12 inhibitors

FEBS letters, 2013-11, Vol.587 (23), p.3770-3775

2013

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Chemical Synthetic Platform for Chlorpromazine Oligomers That Were Reported as Photo-degradation Products of Chlorpromazine

Chemical and Pharmaceutical Bulletin, 2017-12, Vol.65 (12), p.1161-1166

2017

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Foreword

Biological & pharmaceutical bulletin, 2020-03, Vol.43 (3), p.361-361

Otaka, Akira

2020

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Foreword

Biological and Pharmaceutical Bulletin, 2020/03/01, Vol.43(3), pp.361-361

Otaka, Akira

2020

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Current Topics Drug Discovery : Recent Progress and the Future Foreword

Biological and Pharmaceutical Bulletin, 2020-03, Vol.43 (3), p.361-361

Akira Otaka

2020

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Foreword

Biological & pharmaceutical bulletin, 2020-01, Vol.43 (3), p.361

Otaka, Akira

2020

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T140 analogs as CXCR4 antagonists identified as anti-metastatic agents in the treatment of breast cancer

FEBS letters, 2003-08, Vol.550 (1), p.79-83

2003

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Synthesis of lactam-bridged cyclic peptides using sequential olefin metathesis and diimide reduction reactions

Tetrahedron, 2015-06, Vol.71 (24), p.4183-4191

2015

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The extreme N-terminal region of human apolipoprotein A-I has a strong propensity to form amyloid fibrils

FEBS letters, 2014-01, Vol.588 (3), p.389-394

2014

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Development of Naturally Inspired Peptide and Protein Chemistry

Advances in Preparation of Peptide and Protein Thioesters Aiming to Use in Medicinal Sciences

Copper-Mediated Deprotection of Thiazolidine and Selenazolidine Derivatives Applied to Native Chemical Ligation

Development of a Turn-On Fluorescent Traceable Linker Employing N-Sulfanylethylcoumarinyl Amide for the Enrichment and Visualization of Target Proteins

Peptide probes containing a non‐hydrolyzable phosphotyrosine‐mimetic residue for enrichment of protein tyrosine phosphatases

A Photo-Activatable Peptide Mimicking Functions of Apolipoprotein A-I

CXCL14 is a natural inhibitor of the CXCL12–CXCR4 signaling axis

Identification of Functional Domains of CXCL14 Involved in High-Affinity Binding and Intracellular Transport of CpG DNA

Dual Kinetically Controlled Native Chemical Ligation Using a Combination of Sulfanylproline and Sulfanylethylanilide Peptide

Chemical Synthetic Platform for Chlorpromazine Oligomers That Were Reported as Photo-degradation Products of Chlorpromazine

Examination of native chemical ligation using peptidyl prolyl thioesters

Safe Removal of the Allyl Protecting Groups of Allyl Esters using a Recyclable, Low-Leaching and Ligand-Free Palladium Nanoparticle Catalyst

Sequence-Independent Traceless Method for Preparation of Peptide/Protein Thioesters Using CPaseY-Mediated Hydrazinolysis

One-Pot/Sequential Native Chemical Ligation Using N-Sulfanylethylanilide Peptide

Heparin promotes fibril formation by the N‐terminal fragment of amyloidogenic apolipoprotein A‐I

Formation of stable nanodiscs by bihelical apolipoprotein A-I mimetic peptide

Dimeric peptides of the C-terminal region of CXCL14 function as CXCL12 inhibitors

Chemical Synthetic Platform for Chlorpromazine Oligomers That Were Reported as Photo-degradation Products of Chlorpromazine

Foreword

Foreword

Current Topics Drug Discovery : Recent Progress and the Future Foreword

Foreword

T140 analogs as CXCR4 antagonists identified as anti-metastatic agents in the treatment of breast cancer

Synthesis of lactam-bridged cyclic peptides using sequential olefin metathesis and diimide reduction reactions

The extreme N-terminal region of human apolipoprotein A-I has a strong propensity to form amyloid fibrils

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