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A Benzyne Insertion Approach to Hetisine-Type Diterpenoid Alkaloids: Synthesis of Cossonidine (Davisine)

Journal of the American Chemical Society, 2018-07, Vol.140 (26), p.8105-8109

2018

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Protic-Solvent-Mediated Cycloisomerization of Quinoline and Isoquinoline Propargylic Alcohols: Syntheses of (±)-3-Demethoxyerythratidinone and (±)-Cocculidine

Angewandte Chemie International Edition, 2013-10, Vol.52 (42), p.11129-11133

International ed. in English, 2013

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Synthesis and structure-activity relationship of 4-alkoxy-thieno[2,3-b]pyridine derivatives as potent alkaline phosphatase enhancers for osteoporosis treatment

Bioorganic & medicinal chemistry letters, 2019-07, Vol.29 (14), p.1769-1773

2019

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Simultaneous Inhibition of PGE2 and PGI2 Signals Is Necessary to Suppress Hyperalgesia in Rat Inflammatory Pain Models

Mediators of inflammation, 2016, Vol.2016 (2016), p.1-10

2016

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A novel selective prostaglandin E2 synthesis inhibitor relieves pyrexia and arthritis in Guinea pigs inflammatory models

Journal of pharmacological sciences, 2016-02, Vol.130 (2), p.128-135

2016

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A Novel Selective Prostaglandin E2 Synthesis Inhibitor Relieves Pyrexia and Chronic Inflammation in Rats

Inflammation, 2016-04, Vol.39 (2), p.907-915

2016

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Total Synthesis of Pleofugin A, a Potent Inositol Phosphorylceramide Synthase Inhibitor

Organic letters, 2018-08, Vol.20 (15), p.4637-4640

2018

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Correction to Total Synthesis of Pleofugin A, a Potent Inositol Phosphorylceramide Synthase Inhibitor

Organic letters, 2018-10, Vol.20 (20), p.6610-6610

2018

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Total synthesis and NMR conformational study of signal peptidase II inhibitors, globomycin and SF-1902 A5

Tetrahedron, 2003-03, Vol.59 (10), p.1685-1697

2003

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Discovery of DS79182026: A potent orally active hepcidin production inhibitor

Bioorganic & medicinal chemistry letters, 2017-08, Vol.27 (16), p.3716-3722

2017

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Discovery of DS28120313 as a potent orally active hepcidin production inhibitor: Design and optimization of novel 4,6-disubstituted indazole derivatives

Bioorganic & medicinal chemistry letters, 2017-12, Vol.27 (23), p.5252-5257

2017

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Crystal Structure and Total Synthesis of Globomycin: Establishment of Relative and Absolute Configurations

Journal of the American Chemical Society, 2000-10, Vol.122 (41), p.10214-10215

2000

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Alutacenoic Acids A and B, Rare Naturally Occurring Cyclopropenone Derivatives Isolated from Fungi: Potent Non-Peptide Factor XIIIa Inhibitors

Journal of the American Chemical Society, 2000-03, Vol.122 (8), p.1842-1843

2000

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Potent Prostaglandin A1 Analogs That Suppress Tumor Cell Growth through Induction of p21 and Reduction of Cyclin E

The Journal of biological chemistry, 1998-07, Vol.273 (29), p.18522-18527

1998

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Protic Solvent Mediated Cycloisomerization of Quinoline and Isoquinoline Propargylic Carbinols: Syntheses of (±)-3-Demethoxyerythratidinone and (±)-Cocculidine

Angewandte Chemie International Edition, 2013-09, Vol.52 (42), p.11129-11133

2013

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Simultaneous Inhibition of [PGE.sub.2] and [PGI.sub.2] Signals Is Necessary to Suppress Hyperalgesia in Rat Inflammatory Pain Models

Mediators of inflammation, 2016-01

2016

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Simultaneous Inhibition of PGE 2 and PGI 2 Signals Is Necessary to Suppress Hyperalgesia in Rat Inflammatory Pain Models

Mediators of inflammation, 2016, Vol.2016, p.1-10

2016

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Synthetic Study on Globomycins toward the Development of New Antibiotics

Journal of Synthetic Organic Chemistry, Japan, 2005/01/01, Vol.63(1), pp.51-62

2005

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A Novel Selective Prostaglandin E sub(2) Synthesis Inhibitor Relieves Pyrexia and Chronic Inflammation in Rats

Inflammation, 2016-04, Vol.39 (2), p.907-915

2016

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A Novel Selective Prostaglandin E^sub 2^ Synthesis Inhibitor Relieves Pyrexia and Chronic Inflammation in Rats

Inflammation, 2016-04, Vol.39 (2), p.907

2016

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Structure-activity relationships of globomycin analogues as antibiotics

Bioorganic & medicinal chemistry, 2004-01, Vol.12 (2), p.337-361

2004

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Δ7-Prostaglandin C1: A primary metabolite of antitumor Δ7-prostaglandin A1 in the sera

Tetrahedron, 1997-12, Vol.53 (50), p.17009-17014

1997

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Protic-Solvent-Mediated Cycloisomerization of Quinoline and Isoquinoline Propargylic Alcohols: Syntheses of (±)-3-Demethoxyerythratidinone and (±)-Cocculidine

Angewandte Chemie, 2013-10, Vol.125 (42), p.11335-11339

2013

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Total synthesis and NMR conformational study of signal peptidase II inhibitors, globomycin and SF-1902 A 5

Tetrahedron, 2003, Vol.59 (10), p.1685-1697

2003

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Synthesis and antimicrobial activity of novel globomycin analogues

Bioorganic & medicinal chemistry letters, 2003-07, Vol.13 (14), p.2315-2318

2003

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A Benzyne Insertion Approach to Hetisine-Type Diterpenoid Alkaloids: Synthesis of Cossonidine (Davisine)

Protic-Solvent-Mediated Cycloisomerization of Quinoline and Isoquinoline Propargylic Alcohols: Syntheses of (±)-3-Demethoxyerythratidinone and (±)-Cocculidine

Synthesis and structure-activity relationship of 4-alkoxy-thieno[2,3-b]pyridine derivatives as potent alkaline phosphatase enhancers for osteoporosis treatment

Simultaneous Inhibition of PGE2 and PGI2 Signals Is Necessary to Suppress Hyperalgesia in Rat Inflammatory Pain Models

A novel selective prostaglandin E2 synthesis inhibitor relieves pyrexia and arthritis in Guinea pigs inflammatory models

A Novel Selective Prostaglandin E2 Synthesis Inhibitor Relieves Pyrexia and Chronic Inflammation in Rats

Total Synthesis of Pleofugin A, a Potent Inositol Phosphorylceramide Synthase Inhibitor

Correction to Total Synthesis of Pleofugin A, a Potent Inositol Phosphorylceramide Synthase Inhibitor

Total synthesis and NMR conformational study of signal peptidase II inhibitors, globomycin and SF-1902 A5

Discovery of DS79182026: A potent orally active hepcidin production inhibitor

Discovery of DS28120313 as a potent orally active hepcidin production inhibitor: Design and optimization of novel 4,6-disubstituted indazole derivatives

Crystal Structure and Total Synthesis of Globomycin: Establishment of Relative and Absolute Configurations

Alutacenoic Acids A and B, Rare Naturally Occurring Cyclopropenone Derivatives Isolated from Fungi: Potent Non-Peptide Factor XIIIa Inhibitors

Potent Prostaglandin A1 Analogs That Suppress Tumor Cell Growth through Induction of p21 and Reduction of Cyclin E

Protic Solvent Mediated Cycloisomerization of Quinoline and Isoquinoline Propargylic Carbinols: Syntheses of (±)-3-Demethoxyerythratidinone and (±)-Cocculidine

Simultaneous Inhibition of [PGE.sub.2] and [PGI.sub.2] Signals Is Necessary to Suppress Hyperalgesia in Rat Inflammatory Pain Models

Simultaneous Inhibition of PGE 2 and PGI 2 Signals Is Necessary to Suppress Hyperalgesia in Rat Inflammatory Pain Models

Synthetic Study on Globomycins toward the Development of New Antibiotics

A Novel Selective Prostaglandin E sub(2) Synthesis Inhibitor Relieves Pyrexia and Chronic Inflammation in Rats

A Novel Selective Prostaglandin E^sub 2^ Synthesis Inhibitor Relieves Pyrexia and Chronic Inflammation in Rats

Structure-activity relationships of globomycin analogues as antibiotics

Δ7-Prostaglandin C1: A primary metabolite of antitumor Δ7-prostaglandin A1 in the sera

Protic-Solvent-Mediated Cycloisomerization of Quinoline and Isoquinoline Propargylic Alcohols: Syntheses of (±)-3-Demethoxyerythratidinone and (±)-Cocculidine

Total synthesis and NMR conformational study of signal peptidase II inhibitors, globomycin and SF-1902 A 5

Synthesis and antimicrobial activity of novel globomycin analogues

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