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Synthesis and Characterization of Orally Active Nonpeptide Vasopressin V2 Receptor Antagonists

Chemical and Pharmaceutical Bulletin, 1999/04/15, Vol.47(4), pp.501-510

1999

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WA8242A1, A2 and B, Novel Secretary Phospholipase A2 Inhibitors Produced by Streptomyces violaeeusniger. III. Structure Elucidation and Total Synthesis of WA8242B

Journal of antibiotics, 1998, Vol.51 (7), p.655-664

1998

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SYNTHESIS OF OPTICALLY ACTIVE β-METHYLTRYPTOPHANS FROM AZIRIDINE-2-CARBOXYLATES

Chemical and Pharmaceutical Bulletin, 1990/02/25, Vol.38(2), pp.564-566

1990

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Total synthesis of FK-156 isolated from a Streptomyces as an immunostimulating peptide: application of a novel copper chelate amino protection

Journal of the American Chemical Society, 1981-11, Vol.103 (23), p.7026-7028

1981

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Studies on Phosphonic Acid Antibiotics. IV. Synthesis and Antibacterial Activity of Analogs of 3-(N-Acetyl-N-hydroxyamino)-propylphosphonic Acid (FR-900098)

Chemical and Pharmaceutical Bulletin, 1982/01/25, Vol.30(1), pp.111-118

1982

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DIKETOPIPERAZINE DERIVATIVES, A NEW SERIES OF PLATELET-ACTIVATING FACTOR INHIBITORS

Chemical and Pharmaceutical Bulletin, 1987/08/25, Vol.35(8), pp.3527-3530

1987

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Synthesis of Nocardicins from Penicillins

Chemical and Pharmaceutical Bulletin, 1987/08/25, Vol.35(8), pp.3464-3466

1987

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Total synthesis of urogastrone (human epidermal growth factor, h-EGF). Part 1. Synthesis of the fully protected urogastrone

Journal of the Chemical Society, Perkin Transactions 1, 1989 (12), p.2187

1989

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WF-10129, A NOVEL ANGIOTENSIN CONVERTING ENZYME INHIBITOR PRODUCED BY A FUNGUS, DORATOMYCES PUTREDINIS

The Journal of Antibiotics, 1987/04/25, Vol.40(4), pp.468-475

1987

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Reaction of serine proteases with substituted isocoumarins: discovery of 3,4-dichloroisocoumarin, a new general mechanism based serine protease inhibitor

Biochemistry (Easton), 1985-04, Vol.24 (8), p.1831-1841

1985

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Studies on phosphonic acid antibiotics. III. Structure and synthesis of 3-(N-acetyl-N-hydroxyamino)propylphosphonic acid (FR-900098) and 3-(N-acetyl-N-hydroxyamino)-2(R)-hydroxypropylphosphonic acid (FR-33289)

Chemical & pharmaceutical bulletin, 1981, Vol.29 (3), p.646-650

1981

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STUDIES ON A NEW IMMUNOACTIVE PEPTIDE, FK-156: IV. SYNTHESIS OF FK-156 AND ITS GEOMETRIC ISOMER

The Journal of Antibiotics, 1982, Vol.35(10), pp.1300-1311

1982

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Studies on Structure-Activity Relationships of FK-156, an Immunostimulating Peptide, and Related Compounds. II. Synthesis of N2-(γ-D-Glutamyl)-2 (L), 2' (D)-diaminopimelic Acid as the Minimal Essential Structure of FK-156

Chemical and Pharmaceutical Bulletin, 1984/08/25, Vol.32(8), pp.2932-2941

1984

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WA8242A1, A2 and B, Novel Secretary Phospholipase A2 Inhibitors Produced by Streptomyces violaceusniger: III. Structure Elucidation and Total Synthesis of WA8242B

The Journal of Antibiotics, 1998/07/25, Vol.51(7), pp.655-664

1998

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Photocyclization of N-Chloroacetyl-3-methoxyphenethylamine and N-Chloroacetyl-3, 5-dimethoxyphenethylamine

Chemical and Pharmaceutical Bulletin, 1972/06/25, Vol.20(6), pp.1164-1169

1972

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4-Azabicyclo [5, 2, 2] undeca-8, 10-dien-3-ones. Photochemical Formations and Novel Rearrangements

Chemical and Pharmaceutical Bulletin, 1972/05/25, Vol.20(5), pp.998-1005

1972

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PAF inhibitory activity of diketopiperazines: Structure‐activity relationships

Lipids, 1991-12, Vol.26 (12Part1), p.1175-1178

1991

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Studies on phosphonic acid antibiotics. I. Structure and synthesis of 3-(n-acetyl-n-hydroxyamino)propylphosphonic acid (FR-900098) and its n-formyl analogue (FR-31564)

Tetrahedron letters, 1980, Vol.21 (1), p.95-98

1980

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Diketopiperazines as a new class of platelet-activating factor inhibitors

Journal of medicinal chemistry, 1987-10, Vol.30 (10), p.1706-1709

1987

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Inhibition of human leukocyte elastase, cathepsin G, chymotrypsin A alpha, and porcine pancreatic elastase with substituted isobenzofuranones and benzopyrandiones

Biochemistry (Easton), 1985-04, Vol.24 (8), p.1841-1848

1985

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Total synthesis of urogastrone (human epidermal growth factor, h-EGF). Part 2. Synthesis of urogastrone having the structure proposed for the natural compound

Journal of the Chemical Society, Perkin Transactions 1, 1989 (12), p.2199

1989

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New mechanism based serine protease inhibitors: inhibition of human leukocyte elastase, porcine pancreatic elastase, human leukocyte cathepsin G, and chymotrypsin by 3-chloroisocoumarin and 3,3-dichlorophthalide

Journal of the American Chemical Society, 1983-10, Vol.105 (21), p.6518-6520

1983

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N2-(.gamma.-D-glutamyl)-meso-2-(L),2'(D)-diaminopimelic acid as the minimal prerequisite structure of FK-156: its acyl derivatives with potent immunostimulating activity

Journal of medicinal chemistry, 1982-04, Vol.25 (4), p.335-337

1982

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Inhibition of human leukocyte elastase, cathepsin G, chymotrypsin A.alpha., and porcine pancreatic elastase with substituted isobenzofuranones and benzopyrandiones

Biochemistry (Easton), 1985-04, Vol.24 (8), p.1841-1848

1985

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Studies on phosphonic acid antibiotics. II. Synthesis of 3-(n-acetyl-n-hydroxyamino)-2(r)-hydroxypropylphosphonic acid (FR-33289) and 3-(n-formyl-n-hydroxyamino)-1- [formula omitted]-propenylphosphonic acid (FR-32863)

Tetrahedron letters, 1980, Vol.21 (1), p.99-102

1980

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Synthesis and Characterization of Orally Active Nonpeptide Vasopressin V2 Receptor Antagonists

WA8242A1, A2 and B, Novel Secretary Phospholipase A2 Inhibitors Produced by Streptomyces violaeeusniger. III. Structure Elucidation and Total Synthesis of WA8242B

SYNTHESIS OF OPTICALLY ACTIVE β-METHYLTRYPTOPHANS FROM AZIRIDINE-2-CARBOXYLATES

Total synthesis of FK-156 isolated from a Streptomyces as an immunostimulating peptide: application of a novel copper chelate amino protection

Studies on Phosphonic Acid Antibiotics. IV. Synthesis and Antibacterial Activity of Analogs of 3-(N-Acetyl-N-hydroxyamino)-propylphosphonic Acid (FR-900098)

DIKETOPIPERAZINE DERIVATIVES, A NEW SERIES OF PLATELET-ACTIVATING FACTOR INHIBITORS

Synthesis of Nocardicins from Penicillins

Total synthesis of urogastrone (human epidermal growth factor, h-EGF). Part 1. Synthesis of the fully protected urogastrone

WF-10129, A NOVEL ANGIOTENSIN CONVERTING ENZYME INHIBITOR PRODUCED BY A FUNGUS, DORATOMYCES PUTREDINIS

Reaction of serine proteases with substituted isocoumarins: discovery of 3,4-dichloroisocoumarin, a new general mechanism based serine protease inhibitor

Studies on phosphonic acid antibiotics. III. Structure and synthesis of 3-(N-acetyl-N-hydroxyamino)propylphosphonic acid (FR-900098) and 3-(N-acetyl-N-hydroxyamino)-2(R)-hydroxypropylphosphonic acid (FR-33289)

STUDIES ON A NEW IMMUNOACTIVE PEPTIDE, FK-156: IV. SYNTHESIS OF FK-156 AND ITS GEOMETRIC ISOMER

Studies on Structure-Activity Relationships of FK-156, an Immunostimulating Peptide, and Related Compounds. II. Synthesis of N2-(γ-D-Glutamyl)-2 (L), 2' (D)-diaminopimelic Acid as the Minimal Essential Structure of FK-156

WA8242A1, A2 and B, Novel Secretary Phospholipase A2 Inhibitors Produced by Streptomyces violaceusniger: III. Structure Elucidation and Total Synthesis of WA8242B

Photocyclization of N-Chloroacetyl-3-methoxyphenethylamine and N-Chloroacetyl-3, 5-dimethoxyphenethylamine

4-Azabicyclo [5, 2, 2] undeca-8, 10-dien-3-ones. Photochemical Formations and Novel Rearrangements

PAF inhibitory activity of diketopiperazines: Structure‐activity relationships

Studies on phosphonic acid antibiotics. I. Structure and synthesis of 3-(n-acetyl-n-hydroxyamino)propylphosphonic acid (FR-900098) and its n-formyl analogue (FR-31564)

Diketopiperazines as a new class of platelet-activating factor inhibitors

Inhibition of human leukocyte elastase, cathepsin G, chymotrypsin A alpha, and porcine pancreatic elastase with substituted isobenzofuranones and benzopyrandiones

Total synthesis of urogastrone (human epidermal growth factor, h-EGF). Part 2. Synthesis of urogastrone having the structure proposed for the natural compound

New mechanism based serine protease inhibitors: inhibition of human leukocyte elastase, porcine pancreatic elastase, human leukocyte cathepsin G, and chymotrypsin by 3-chloroisocoumarin and 3,3-dichlorophthalide

N2-(.gamma.-D-glutamyl)-meso-2-(L),2'(D)-diaminopimelic acid as the minimal prerequisite structure of FK-156: its acyl derivatives with potent immunostimulating activity

Inhibition of human leukocyte elastase, cathepsin G, chymotrypsin A.alpha., and porcine pancreatic elastase with substituted isobenzofuranones and benzopyrandiones

Studies on phosphonic acid antibiotics. II. Synthesis of 3-(n-acetyl-n-hydroxyamino)-2(r)-hydroxypropylphosphonic acid (FR-33289) and 3-(n-formyl-n-hydroxyamino)-1- [formula omitted]-propenylphosphonic acid (FR-32863)

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