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EXTRACTION PROFILE OF FLAVAN-3-OLS FROM INTACT GRAPE SEEDS WITH AQUEOUS ETHANOL AND COMPARISON OF GRAPE SEED EXTRACTS FROM INTACT AND PULVERIZED SEEDS

Acta horticulturae, 2014 (1023), p.83-90

2014

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Matrix metalloproteinase activity is enhanced during corneal wound repair in high glucose condition

Current eye research, 2000, Vol.21 (2), p.608-615

2000

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Novel vasopressin V2 receptor-selective antagonists, pyrrolo[2,1- a]quinoxaline and pyrrolo[2,1- c][1,4]benzodiazepine derivatives

Bioorganic & medicinal chemistry, 1999-06, Vol.7 (6), p.1247-1254

1999

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Production and Application of New Monoclonal Antibodies Specific for a Fecal Helicobacter pylori Antigen

Clinical and Diagnostic Laboratory Immunology, 2002-01, Vol.9 (1), p.75-78

2002

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Catalase, a Specific Antigen in the Feces of Human Subjects Infected with Helicobacter pylori

Clinical and Diagnostic Laboratory Immunology, 2002-07, Vol.9 (4), p.784-788

2002

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The Effects of Several Vasopressin Receptor Antagonists on Normal Intraocular Pressure and the Intraocular Distribution of Vasopressin Receptor Subtypes

Biological and Pharmaceutical Bulletin, 2002, Vol.25(2), pp.251-255

2002

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Histopathological Study of Kidney Abnormalities in an Experimental SIADH Rat Model and Its Application to the Evaluation of the Pharmacologic Profile of VP-343, a Selective Vasopressin V2 Receptor Antagonist

Biological and Pharmaceutical Bulletin, 2001, Vol.24(8), pp.897-901

2001

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Affinity chromatography for purification of two urokinases from human urine

Journal of chromatography. B, Biomedical sciences and applications, 2000-05, Vol.742 (1), p.71-78

2000

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Pharmacological Profile of VP-343, a Novel Selective Vasopressin V2 Receptor Antagonist, in Rats

Biological and Pharmaceutical Bulletin, 2000/02/01, Vol.23(2), pp.182-189

2000

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The Therapeutic Efficacy of VP-343, a Selective Vasopressin V2 Receptor Antagonist, in the Experimental SIADH Rat Model

Biological and Pharmaceutical Bulletin, 2000/11/01, Vol.23(11), pp.1323-1327

2000

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Structure of the novel α-glucosidase inhibitor 4-O-α-d-glucopyranosyl-N-methylmoranoline

Acta crystallographica. Section C, Crystal structure communications, 1987-09, Vol.43 (9), p.1809-1811

1987

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Lipid Nano-Sphere(LNS), a protein-free analogue of lipoproteins, as a novel drug carrier for parenteral administration. IV

Journal of controlled release, 1994, Vol.28 (1), p.352-353

1994

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Effect of dissolved oxygen and pH on moranoline (1-deoxynojirimycin) fermentation by Streptomyces lavendulae

Journal of fermentation and bioengineering, 1995, Vol.79 (4), p.391-394

1995

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Manufacturing High Purity Maltose and Maltotetraose from Starch by a Novel and Efficient Procedure Named "Reducing End Modification Method"

Bioscience, biotechnology, and biochemistry, 1997, Vol.61 (11), p.1931-1933

1997

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Enzymatic synthesis of 4-O-β-D-galactopyranosyl-moranoline and 3-O-β-D-galactopyranosyl-moranoline by using β-galactosidase from Bacillus circulans

Bioscience, biotechnology, and biochemistry, 1996-04, Vol.60 (4), p.694-696

1996

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Enzymatic Synthesis of High Purity Maltotetraose Using Moranoline(1-Deoxynojirimycin)

Bioscience, biotechnology, and biochemistry, 1993, Vol.57 (3), p.499-501

1993

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An Efficient Synthesis of Sulfo Lewis X Analog Containing 1-Deoxynojirimycin

Journal of carbohydrate chemistry, 1998-05, Vol.17 (4-5), p.729-738

1998

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OF4949, NEW INHIBITORS OF AMINOPEPTIDASE B: II. ELUCIDATION OF STRUCTURE

The Journal of Antibiotics, 1986, Vol.39(12), pp.1685-1696

1986

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Enzymatic Synthesis of 4-O-α-d-Glucopyranosyl-moranoline

Agricultural and biological chemistry, 1985-01, Vol.49 (7), p.2159-2165

Ezure, Yohji

1985

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Synthesis and α-Glucosidase-Inhibiting Activity of a New α-Glucosidase Inhibitor, 4-O-α-D-Glucopyranosylmoranoline and Its N-Substituted Derivatives

Chemical and Pharmaceutical Bulletin, 1989/01/25, Vol.37(1), pp.106-109

1989

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A novel and efficient method for enzymatic synthesis of high purity maltose using moranoline (1-deoxynojirimycin)

Bioscience, biotechnology, and biochemistry, 1992, Vol.56 (9), p.1406-1409

1992

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Effects of Moranoline, 4-O-α-D-Glucopyranosylmoranoline and Their N-Substituted Derivatives on Thermostability of Cyclodextrin Glycosyltransferase, Glucoamylase, and β-Amylase

Bioscience, biotechnology, and biochemistry, 1993, Vol.57 (8), p.1294-1298

1993

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OF4949, NEW INHIBITORS OF AMINOPEPTIDASE B: I. TAXONOMY, FERMENTATION, ISOLATION AND CHARACTERIZATION

The Journal of Antibiotics, 1986, Vol.39(12), pp.1674-1684

1986

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Effects of moranoline, 4-ortho-alpha-D-glucopyranosylmoranoline and their N-substituted derivatives on thermostability of cyclodextrin glycosyltransferase [from Bacillus stearothermophilus], glucoamylase, and beta-amylase

Bioscience, biotechnology, and biochemistry, 1993-08, Vol.57 (8)

1993

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Natural Convective Flow between Heated Vertical Parallel Plates

JOURNAL OF CHEMICAL ENGINEERING OF JAPAN, 1989, Vol.22(6), pp.649-654

1989

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EXTRACTION PROFILE OF FLAVAN-3-OLS FROM INTACT GRAPE SEEDS WITH AQUEOUS ETHANOL AND COMPARISON OF GRAPE SEED EXTRACTS FROM INTACT AND PULVERIZED SEEDS

Matrix metalloproteinase activity is enhanced during corneal wound repair in high glucose condition

Novel vasopressin V2 receptor-selective antagonists, pyrrolo[2,1- a]quinoxaline and pyrrolo[2,1- c][1,4]benzodiazepine derivatives

Production and Application of New Monoclonal Antibodies Specific for a Fecal Helicobacter pylori Antigen

Catalase, a Specific Antigen in the Feces of Human Subjects Infected with Helicobacter pylori

The Effects of Several Vasopressin Receptor Antagonists on Normal Intraocular Pressure and the Intraocular Distribution of Vasopressin Receptor Subtypes

Histopathological Study of Kidney Abnormalities in an Experimental SIADH Rat Model and Its Application to the Evaluation of the Pharmacologic Profile of VP-343, a Selective Vasopressin V2 Receptor Antagonist

Affinity chromatography for purification of two urokinases from human urine

Pharmacological Profile of VP-343, a Novel Selective Vasopressin V2 Receptor Antagonist, in Rats

The Therapeutic Efficacy of VP-343, a Selective Vasopressin V2 Receptor Antagonist, in the Experimental SIADH Rat Model

Structure of the novel α-glucosidase inhibitor 4-O-α-d-glucopyranosyl-N-methylmoranoline

Lipid Nano-Sphere(LNS), a protein-free analogue of lipoproteins, as a novel drug carrier for parenteral administration. IV

Effect of dissolved oxygen and pH on moranoline (1-deoxynojirimycin) fermentation by Streptomyces lavendulae

Manufacturing High Purity Maltose and Maltotetraose from Starch by a Novel and Efficient Procedure Named "Reducing End Modification Method"

Enzymatic synthesis of 4-O-β-D-galactopyranosyl-moranoline and 3-O-β-D-galactopyranosyl-moranoline by using β-galactosidase from Bacillus circulans

Enzymatic Synthesis of High Purity Maltotetraose Using Moranoline(1-Deoxynojirimycin)

An Efficient Synthesis of Sulfo Lewis X Analog Containing 1-Deoxynojirimycin

OF4949, NEW INHIBITORS OF AMINOPEPTIDASE B: II. ELUCIDATION OF STRUCTURE

Enzymatic Synthesis of 4-O-α-d-Glucopyranosyl-moranoline

Synthesis and α-Glucosidase-Inhibiting Activity of a New α-Glucosidase Inhibitor, 4-O-α-D-Glucopyranosylmoranoline and Its N-Substituted Derivatives

A novel and efficient method for enzymatic synthesis of high purity maltose using moranoline (1-deoxynojirimycin)

Effects of Moranoline, 4-O-α-D-Glucopyranosylmoranoline and Their N-Substituted Derivatives on Thermostability of Cyclodextrin Glycosyltransferase, Glucoamylase, and β-Amylase

OF4949, NEW INHIBITORS OF AMINOPEPTIDASE B: I. TAXONOMY, FERMENTATION, ISOLATION AND CHARACTERIZATION

Effects of moranoline, 4-ortho-alpha-D-glucopyranosylmoranoline and their N-substituted derivatives on thermostability of cyclodextrin glycosyltransferase [from Bacillus stearothermophilus], glucoamylase, and beta-amylase

Natural Convective Flow between Heated Vertical Parallel Plates

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