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Evidence for calmodulin inter-domain compaction in solution induced by W-7 binding

FEBS letters, 1999-01, Vol.442 (2), p.173-177

1999

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Novel Potassium Channel Activators. III. Synthesis and Pharmacological Evaluation of 3, 4-Dihydro-2H-1, 4-benzoxazine Derivatives : Modification at the 2 Position

Chemical and Pharmaceutical Bulletin, 2000/03/01, Vol.48(3), pp.428-432

2000

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Novel potassium channel activators. II. Synthesis and pharmacological evaluation of 3,4-dihydro-2H-1,4-benzoxazine derivatives : Modification of the aromatic part

Chemical & pharmaceutical bulletin, 1999, Vol.47 (7), p.971-979

1999

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Reversed phase HPLC of Met58 oxidized rhIL-11 : Oxidation enhanced by plastic tubes

Journal of pharmaceutical and biomedical analysis, 2000-12, Vol.24 (2), p.317-324

2000

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Selective Muscarinic Antagonists. II. Synthesis and Antimuscarinic Properties of Biphenylylcarbamate Derivatives

Chemical and Pharmaceutical Bulletin, 1998/08/15, Vol.46(8), pp.1286-1294

1998

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Selective Muscarinic Antagonists. I. Synthesis and Antimuscarinic Properties of 4-Piperidyl Benzhydrylcarbamate Derivatives

Chemical and Pharmaceutical Bulletin, 1998/08/15, Vol.46(8), pp.1274-1285

1998

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Synthesis and Biological Evaluation of 1, 2, 3, 4-Tetrahydroisoquinoline Derivatives as Potent and Selective M2 Muscarinic Receptor Antagonists

Chemical and Pharmaceutical Bulletin, 1999/05/15, Vol.47(5), pp.672-677

1999

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Spiro-Substituted Piperidines as Neurokinin Receptor Antagonists. I. Design and Synthesis of (.+-.)-N-(2-(3,4-Dichlorophenyl)-4-(spiro(isobenzofuran-1(3H),4'-piperidin)-1'-yl)butyl)-N-methylbenzamide, YM-35375, as a New Lead Compound for Novel Neurokinin Receptor Antagonists

Chemical & pharmaceutical bulletin, 1998, Vol.46 (2), p.351-354

1998

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Spiro-Substituted Piperidines as Neurokinin Receptor Antagonists. II. Syntheses and NK2 Receptor-Antagonistic Activities of N-(2-Aryl-4-(spiro-substituted piperidin-1'-yl)butyl)carboxamides

Chemical & pharmaceutical bulletin, 1998, Vol.46 (2), p.242-254

1998

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Peptide Based Interleukin-1.BETA. Converting Enzyme(ICE) Inhibitors: Synthesis, Structure Activity Relationships and Crystallographic Study of the ICE-inhibitor Complex

Chemical & pharmaceutical bulletin, 1999, Vol.47 (1), p.11-21

1999

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Novel potassium channel openers. Part 4: Transformation of the 1,4-benzoxazine skeleton into 1,4-benzothiazine, 1,2,3,4-tetrahydroquinoline, 1,2,3,4-tetrahydroquinoxaline, indoline, and 1,5-benzoxazepine

Bioorganic & medicinal chemistry, 2000-02, Vol.8 (2), p.393-404

2000

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Spiro-Substituted Piperidines as Neurokinin Receptor Antagonists. III. Synthesis of (.+-.)-N-12-(3,4-Dichlorophenyl)-4-(spiro-substituted piperidin-1-yl)butyll-N-methylbenzamides and Evaluation of NK1-NK2 Dual Antagonistic Activities

Chemical & pharmaceutical bulletin, 1998, Vol.46 (10), p.1538-1544

1998

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A CONVENIENT METHOD FOR THE PREPARATION OF CARBODIIMIDES USING 2-CHLOROPYRIDINIUM SALT

Chemistry letters, 1977-05, Vol.6 (5), p.575-576

1977

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STUDIES ON β-LACTAM ANTIBIOTICS: II. SYNTHESIS AND ANTIBACTERIAL ACTIVITY OF CEPHALOSPORINS WITH SUBSTITUTED 1, 3-DITHIETANE DIRECTLY ATTACHED TO THE C-3 POSITION

The Journal of Antibiotics, 1991/04/25, Vol.44(4), pp.415-421

1991

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Adsorption of endotoxins on glass in the presence of cationic proteins

Journal of pharmaceutical and biomedical analysis, 2001-07, Vol.25 (5-6), p.1001-1007

2001

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Synthesis of New Water-soluble Dihydropyridine Vasodilators

Chemical and Pharmaceutical Bulletin, 1979/06/25, Vol.27(6), pp.1426-1440

1979

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A CONVENIENT METHOD FOR THE PREPARATION OF ISOTHIOCYANATES USING 2-CHLOROPYRIDINIUM SALT

Chemistry letters, 1977-05, Vol.6 (5), p.573-574

1977

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One-Pot Preparation of 1-Substituted Imidazole-2-thione from Isothiocyanate and Amino Acetal

Synthetic communications, 1997-10, Vol.27 (20), p.3565-3571

1997

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Peptide Based Interleukin-1β Converting Enzyme (ICE) Inhibitors : Synthesis, Structure Activity Relationships and Crystallographic Study of the ICE-inhibitor Complex

Chemical and Pharmaceutical Bulletin, 1999/01/15, Vol.47(1), pp.11-21

1999

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Spiro-Substituted Piperidines as Neurokinin Receptor Antagonists. I. Design and Synthesis of (±)-N-[2-(3, 4-Dichlorophenyl)-4-(spiro[isobenzofuran-1(3H), 4'-piperidin]-1'-yl)butyl]-N-methylbenzamide, YM-35375, as a New Lead Compound for Novel Neurokinin Receptor Antagonists

Chemical and Pharmaceutical Bulletin, 1998/02/15, Vol.46(2), pp.351-354

1998

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Reversed phase HPLC of Met 58 oxidized rhIL-11: oxidation enhanced by plastic tubes

Journal of pharmaceutical and biomedical analysis, 2000, Vol.24 (2), p.317-324

2000

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Elimination of Artifactual Bands from Polyacrylamide Gels

Analytical biochemistry, 2000-04, Vol.280 (1), p.188-189

2000

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Spiro-Substituted Piperidines as Neurokinin Receptor Antagonists. III. Synthesis of (±)-N-[2-(3, 4-Dichlorophenyl)-4-(spiro-substituted piperidin-1'-yl)butyl]-N-methylbenzamides and Evaluation of NK1-NK2 Dual Antagonistic Activities

Chemical and Pharmaceutical Bulletin, 1998/10/15, Vol.46(10), pp.1538-1544

1998

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Synthesis of Optically Active 2-(N-Benzyl-N-methylamino)ethyl Methyl 2, 6-Dimethyl-4-(m-nitrophenyl)-1, 4-dihydropyridine-3, 5-dicarboxylate (Nicardipine)

Chemical and Pharmaceutical Bulletin, 1980/09/25, Vol.28(9), pp.2809-2812

1980

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STUDIES ON β-LACTAM ANTIBIOTICS: I. SYNTHESIS AND IN VITRO ANTI-PSEUDOMONAL ACTIVITY OF 3-ISOTHIAZOLE-CEPHALOSPORIN DERIVATIVES

The Journal of Antibiotics, 1987/02/25, Vol.40(2), pp.173-181

1987

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Evidence for calmodulin inter-domain compaction in solution induced by W-7 binding

Novel Potassium Channel Activators. III. Synthesis and Pharmacological Evaluation of 3, 4-Dihydro-2H-1, 4-benzoxazine Derivatives : Modification at the 2 Position

Novel potassium channel activators. II. Synthesis and pharmacological evaluation of 3,4-dihydro-2H-1,4-benzoxazine derivatives : Modification of the aromatic part

Reversed phase HPLC of Met58 oxidized rhIL-11 : Oxidation enhanced by plastic tubes

Selective Muscarinic Antagonists. II. Synthesis and Antimuscarinic Properties of Biphenylylcarbamate Derivatives

Selective Muscarinic Antagonists. I. Synthesis and Antimuscarinic Properties of 4-Piperidyl Benzhydrylcarbamate Derivatives

Synthesis and Biological Evaluation of 1, 2, 3, 4-Tetrahydroisoquinoline Derivatives as Potent and Selective M2 Muscarinic Receptor Antagonists

Spiro-Substituted Piperidines as Neurokinin Receptor Antagonists. I. Design and Synthesis of (.+-.)-N-(2-(3,4-Dichlorophenyl)-4-(spiro(isobenzofuran-1(3H),4'-piperidin)-1'-yl)butyl)-N-methylbenzamide, YM-35375, as a New Lead Compound for Novel Neurokinin Receptor Antagonists

Spiro-Substituted Piperidines as Neurokinin Receptor Antagonists. II. Syntheses and NK2 Receptor-Antagonistic Activities of N-(2-Aryl-4-(spiro-substituted piperidin-1'-yl)butyl)carboxamides

Peptide Based Interleukin-1.BETA. Converting Enzyme(ICE) Inhibitors: Synthesis, Structure Activity Relationships and Crystallographic Study of the ICE-inhibitor Complex

Novel potassium channel openers. Part 4: Transformation of the 1,4-benzoxazine skeleton into 1,4-benzothiazine, 1,2,3,4-tetrahydroquinoline, 1,2,3,4-tetrahydroquinoxaline, indoline, and 1,5-benzoxazepine

Spiro-Substituted Piperidines as Neurokinin Receptor Antagonists. III. Synthesis of (.+-.)-N-12-(3,4-Dichlorophenyl)-4-(spiro-substituted piperidin-1-yl)butyll-N-methylbenzamides and Evaluation of NK1-NK2 Dual Antagonistic Activities

A CONVENIENT METHOD FOR THE PREPARATION OF CARBODIIMIDES USING 2-CHLOROPYRIDINIUM SALT

STUDIES ON β-LACTAM ANTIBIOTICS: II. SYNTHESIS AND ANTIBACTERIAL ACTIVITY OF CEPHALOSPORINS WITH SUBSTITUTED 1, 3-DITHIETANE DIRECTLY ATTACHED TO THE C-3 POSITION

Adsorption of endotoxins on glass in the presence of cationic proteins

Synthesis of New Water-soluble Dihydropyridine Vasodilators

A CONVENIENT METHOD FOR THE PREPARATION OF ISOTHIOCYANATES USING 2-CHLOROPYRIDINIUM SALT

One-Pot Preparation of 1-Substituted Imidazole-2-thione from Isothiocyanate and Amino Acetal

Peptide Based Interleukin-1β Converting Enzyme (ICE) Inhibitors : Synthesis, Structure Activity Relationships and Crystallographic Study of the ICE-inhibitor Complex

Spiro-Substituted Piperidines as Neurokinin Receptor Antagonists. I. Design and Synthesis of (±)-N-[2-(3, 4-Dichlorophenyl)-4-(spiro[isobenzofuran-1(3H), 4'-piperidin]-1'-yl)butyl]-N-methylbenzamide, YM-35375, as a New Lead Compound for Novel Neurokinin Receptor Antagonists

Reversed phase HPLC of Met 58 oxidized rhIL-11: oxidation enhanced by plastic tubes

Elimination of Artifactual Bands from Polyacrylamide Gels

Spiro-Substituted Piperidines as Neurokinin Receptor Antagonists. III. Synthesis of (±)-N-[2-(3, 4-Dichlorophenyl)-4-(spiro-substituted piperidin-1'-yl)butyl]-N-methylbenzamides and Evaluation of NK1-NK2 Dual Antagonistic Activities

Synthesis of Optically Active 2-(N-Benzyl-N-methylamino)ethyl Methyl 2, 6-Dimethyl-4-(m-nitrophenyl)-1, 4-dihydropyridine-3, 5-dicarboxylate (Nicardipine)

STUDIES ON β-LACTAM ANTIBIOTICS: I. SYNTHESIS AND IN VITRO ANTI-PSEUDOMONAL ACTIVITY OF 3-ISOTHIAZOLE-CEPHALOSPORIN DERIVATIVES

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