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Catalytic asymmetric epoxidation and kinetic resolution: modified procedures including in situ derivatization

Journal of the American Chemical Society, 1987-09, Vol.109 (19), p.5765-5780

1987

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Selective adenosine A3 receptor stimulation reduces ischemic myocardial injury in the rabbit heart

Cardiovascular research, 1997-02, Vol.33 (2), p.410-415

1997

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Evidence for a role for both the adenosine A1 and A3 receptors in protection of isolated human atrial muscle against simulated ischaemia

Cardiovascular research, 1997-10, Vol.36 (1), p.52-59

1997

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The discovery of CP-96,021 and CP-96,486, balanced, combined, potent and orally active leukotriene D 4 (LTD 4)/platelet activating factor (PAF) receptor antagonists

Bioorganic & medicinal chemistry letters, 1995-07, Vol.5 (13), p.1377-1382

1995

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Biarylcarboxylic Acids and -amides: Inhibition of Phosphodiesterase Type IV versus [3H]Rolipram Binding Activity and Their Relationship to Emetic Behavior in the Ferret

Journal of medicinal chemistry, 1996-01, Vol.39 (1), p.120-125

1996

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Synthesis and pharmacological profile of two novel heterocyclic chromanols, CP-80,798 and CP-85,958, as potent LTD4 receptor antagonists

Bioorganic & medicinal chemistry letters, 1995-07, Vol.5 (13), p.1365-1370

1995

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Specific expression and temperature-dependent expression of the acid protease-encoding gene ( pepA) in Aspergillus oryzae in solid-state culture (Rice-Koji)

Journal of bioscience and bioengineering, 2002, Vol.93 (6), p.563-567

2002

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High-molecular components of cancer viewed from blood group stances of ABO type

Gann, 1953-09, Vol.44 (2-3), p.82

MASAMUNE, H

1953

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Synthesis and in vitro profile of a novel series of catechol benzimidazoles. The discovery of potent, selective phosphodiesterase type IV inhibitors with greatly attenuated affinity for the [ 3H]rolipram binding site

Bioorganic & medicinal chemistry letters, 1995-09, Vol.5 (17), p.1969-1972

1995

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Selective activation of adenosine A3 receptors with n6-(3-chlorobenzyl)-5'-N-methylcarboxamidoadenosine (CB-MECA) provides cardioprotection via KATP channel activation

Cardiovascular research, 1998-10, Vol.40 (1), p.138-145

1998

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A MICROMETHOD FOR THE DETERMINATION OF BLOOD PEROXIDASE

Journal of biochemistry (Tokyo), 1932-01, Vol.14 (3), p.475-479

1932

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Differences of high-molecular components of gastric cancer from those of gastric mucosa. I

Gann, 1957-12, Vol.48 (4), p.629

1957

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The discovery of CP-96,021 and CP-96,486, balanced, combined, potent and orally active leukotriene D4 (LTD4)/platelet activating factor (PAF) receptor antagonists

Bioorganic & medicinal chemistry letters, 1995-07, Vol.5 (13), p.1377-1382

1995

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p-Nitrobenzoate esters of epoxy alcohols: convenient synthons for water-soluble epoxy alcohols

Journal of organic chemistry, 1987-02, Vol.52 (4), p.667-671

1987

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A Hypothesis on the Spacial Configuration of Group A and Group B Substances

The Tohoku Journal of Experimental Medicine, 1953/10/25, Vol.58(3-4), pp.234-234

1953

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Synthesis and in vitro profile of 7-substituted quinoline chromanols as novel, non-acidic LTB 4 antagonists

Bioorganic & medicinal chemistry letters, 1995, Vol.5 (8), p.887-892

1995

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Effect of overexpression of LAS17 on stress tolerance and the stability of extrachromosomal DNA in Saccharomyces cerevisiae

Journal of bioscience and bioengineering, 2001, Vol.91 (1), p.33-39

2001

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Mucosin and Mucoitin, Preliminary Note

The Tohoku Journal of Experimental Medicine, 1952/02/25, Vol.55(2-3), pp.166-166

1952

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BIOCHEMICAL STUDIES ON CARBOHYDRATES

Journal of biochemistry (Tokyo), 1934-03, Vol.19 (2), p.353-375

MASAMUNE, H.

1934

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Synthesis and in vitro profile of 7-substituted quinoline chromanols as novel, non-acidic LTB4 antagonists

Bioorganic & medicinal chemistry letters, 1995-04, Vol.5 (8), p.887-892

1995

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Synthesis and pharmacological profile of two novel heterocyclic chromanols, CP-80,798 and CP-85,958, as potent LTD 4 receptor antagonists

Bioorganic & medicinal chemistry letters, 1995, Vol.5 (13), p.1365-1370

1995

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Biochemical studies on carbohydrates. CCXXIV. Oligosaccharides separated after acetolysis of the group mucopolysaccharide from pig stomach mucus. 4. Gastro-trisaccharide

Tohoku journal of experimental medicine, 1958-12, Vol.69 (1), p.59-63

1958

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Biochemical studies on carbohydrates. CCXXV. Oligosaccharides separated after acetolysis of the group mucopolysaccharide from pig stomach mucus. 5. On gastro-N-trisaccharide (a supplement of the first report)

Tohoku journal of experimental medicine, 1958-12, Vol.69 (1), p.65-67

1958

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Studies of high-molecular placental components in connection with pregnancy toxemia. VI. Pentose-nucleic acid

Tohoku journal of experimental medicine, 1957-08, Vol.66 (2), p.145-152

1957

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Studies of high-molecular placental components in connection with pregnancy toxemia. V. On placental itinsulfuric acids

Tohoku journal of experimental medicine, 1957-06, Vol.66 (1), p.61-72

1957

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Catalytic asymmetric epoxidation and kinetic resolution: modified procedures including in situ derivatization

Selective adenosine A3 receptor stimulation reduces ischemic myocardial injury in the rabbit heart

Evidence for a role for both the adenosine A1 and A3 receptors in protection of isolated human atrial muscle against simulated ischaemia

The discovery of CP-96,021 and CP-96,486, balanced, combined, potent and orally active leukotriene D 4 (LTD 4)/platelet activating factor (PAF) receptor antagonists

Biarylcarboxylic Acids and -amides: Inhibition of Phosphodiesterase Type IV versus [3H]Rolipram Binding Activity and Their Relationship to Emetic Behavior in the Ferret

Synthesis and pharmacological profile of two novel heterocyclic chromanols, CP-80,798 and CP-85,958, as potent LTD4 receptor antagonists

Specific expression and temperature-dependent expression of the acid protease-encoding gene ( pepA) in Aspergillus oryzae in solid-state culture (Rice-Koji)

High-molecular components of cancer viewed from blood group stances of ABO type

Synthesis and in vitro profile of a novel series of catechol benzimidazoles. The discovery of potent, selective phosphodiesterase type IV inhibitors with greatly attenuated affinity for the [ 3H]rolipram binding site

Selective activation of adenosine A3 receptors with n6-(3-chlorobenzyl)-5'-N-methylcarboxamidoadenosine (CB-MECA) provides cardioprotection via KATP channel activation

A MICROMETHOD FOR THE DETERMINATION OF BLOOD PEROXIDASE

Differences of high-molecular components of gastric cancer from those of gastric mucosa. I

The discovery of CP-96,021 and CP-96,486, balanced, combined, potent and orally active leukotriene D4 (LTD4)/platelet activating factor (PAF) receptor antagonists

p-Nitrobenzoate esters of epoxy alcohols: convenient synthons for water-soluble epoxy alcohols

A Hypothesis on the Spacial Configuration of Group A and Group B Substances

Synthesis and in vitro profile of 7-substituted quinoline chromanols as novel, non-acidic LTB 4 antagonists

Effect of overexpression of LAS17 on stress tolerance and the stability of extrachromosomal DNA in Saccharomyces cerevisiae

Mucosin and Mucoitin, Preliminary Note

BIOCHEMICAL STUDIES ON CARBOHYDRATES

Synthesis and in vitro profile of 7-substituted quinoline chromanols as novel, non-acidic LTB4 antagonists

Synthesis and pharmacological profile of two novel heterocyclic chromanols, CP-80,798 and CP-85,958, as potent LTD 4 receptor antagonists

Biochemical studies on carbohydrates. CCXXIV. Oligosaccharides separated after acetolysis of the group mucopolysaccharide from pig stomach mucus. 4. Gastro-trisaccharide

Biochemical studies on carbohydrates. CCXXV. Oligosaccharides separated after acetolysis of the group mucopolysaccharide from pig stomach mucus. 5. On gastro-N-trisaccharide (a supplement of the first report)

Studies of high-molecular placental components in connection with pregnancy toxemia. VI. Pentose-nucleic acid

Studies of high-molecular placental components in connection with pregnancy toxemia. V. On placental itinsulfuric acids

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