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Cloning, functional expression, and characterization of the human prostaglandin E2 receptor EP2 subtype

The Journal of biological chemistry, 1994-04, Vol.269 (16), p.11873-11877

1994

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Cloning and expression of a cDNA for the human prostanoid FP receptor

The Journal of biological chemistry, 1994-01, Vol.269 (4), p.2632-2636

1994

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Cloning and expression of a cDNA for the human prostanoid IP receptor

The Journal of biological chemistry, 1994-04, Vol.269 (16), p.12173-12178

1994

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Structure-activity relationship of biaryl acylsulfonamide analogues on the human EP3 prostanoid receptor

Bioorganic & medicinal chemistry letters, 2002-09, Vol.12 (18), p.2583-2586

2002

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Expression of Prostaglandin D synthase and the Prostaglandin D 2 receptors DP and CRTH2 in human nasal mucosa

Journal of allergy and clinical immunology, 2004, Vol.113 (2), p.S29-S29

2004

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Discovery of MK-0476, a potent and orally active leukotriene D4 receptor antagonist devoid of peroxisomal enxyme induction

Bioorganic & medicinal chemistry letters, 1995-02, Vol.5 (3), p.283-288

1995

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Microsomal glutathione S-transferase is the predominant leukotriene C4 binding site in cellular membranes

The Journal of biological chemistry, 1994-04, Vol.269 (17), p.12816-12823

1994

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Photoaffinity labeling of the leukotriene D4 receptor in guinea pig lung

The Journal of biological chemistry, 1993-03, Vol.268 (9), p.6487-6495

1993

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Structure–Activity Relationship of Biaryl Acylsulfonamide Analogues on the Human EP 3 Prostanoid Receptor

Bioorganic & medicinal chemistry letters, 2002, Vol.12 (18), p.2583-2586

2002

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A series of non-quinoline cysLT1 receptor antagonists : Sar study on pyridyl analogs of singulair

Bioorganic & medicinal chemistry letters, 1998-03, Vol.8 (5), p.453-458

1998

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Evolution of a series of non-quinoline leukotriene D4 receptor antagonist; synthesis and sar of benzothiazoles and thiazoles substituted benzyl alcohols as potent LTD4 antagonists

Bioorganic & medicinal chemistry letters, 1995-08, Vol.5 (15), p.1615-1620

1995

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Chromogranin A can act as a reversible processing enzyme inhibitor: Evidence from the inhibition of the IRCM-serine protease 1 cleavage of pro-enkephalin and ACTH at pairs of basic amino acids

FEBS letters, 1987-01, Vol.211 (2), p.144-150

1987

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A series of non-quinoline cysLT 1 receptor antagonists: Sar study on pyridyl analogs of singulair

Bioorganic & medicinal chemistry letters, 1998, Vol.8 (5), p.453-458

1998

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A new series of potent LTD 4 antagonists in the styrylquinoline class

Bioorganic & medicinal chemistry letters, 1993, Vol.3 (6), p.1125-1130

1993

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A new series of potent LTD4 antagonists in the styrylquinoline class

Bioorganic & medicinal chemistry letters, 1993-06, Vol.3 (6), p.1125-1130

1993

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Discovery of L-740,515, a potent thienopyridine cysLT1 receptor (LTD4 receptor) antagonist

Bioorganic & medicinal chemistry letters, 1995-11, Vol.5 (21), p.2551-2556

1995

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The discovery of L-699,392, a novel potent and orally active leukotriene D4 receptor antagonist

Bioorganic & medicinal chemistry letters, 1994-02, Vol.4 (3), p.463-468

1994

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The discovery of a new structural class of potent orally active leukotriene D4 antagonists

Bioorganic & medicinal chemistry letters, 1992-09, Vol.2 (9), p.1141-1146

1992

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Evolution of a series of non-quinoline leukotriene D 4 receptor antagonist; synthesis and sar of benzothiazoles and thiazoles substituted benzyl alcohols as potent LTD 4 antagonists

Bioorganic & medicinal chemistry letters, 1995, Vol.5 (15), p.1615-1620

1995

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The discovery of L-699,392, a novel potent and orally active leukotriene D 4 receptor antagonist

Bioorganic & medicinal chemistry letters, 1994-02, Vol.4 (3), p.463-468

1994

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Discovery of MK-0476, a potent and orally active leukotriene D 4 receptor antagonist devoid of peroxisomal enxyme induction

Bioorganic & medicinal chemistry letters, 1995, Vol.5 (3), p.283-288

1995

Volltextzugriff (PDF)

Discovery of L-740,515, a potent thienopyridine cysLT 1 receptor (LTD 4 receptor) antagonist

Bioorganic & medicinal chemistry letters, 1995, Vol.5 (21), p.2551-2556

1995

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Chromogranin A can act as a reversible processing enzyme inhibitor

FEBS letters, 1987-01, Vol.211 (2), p.144-150

1987

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Opioid peptide precursors in striatum

FEBS letters, 1980-12, Vol.122 (1), p.135-137

1980

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Partial purification and characterisation of a 31 kDalton putative enkephalin precursor from guinea pig striatum

Neuropeptides (Edinburgh), 1985-02, Vol.5 (4), p.505-508

1985

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Cloning, functional expression, and characterization of the human prostaglandin E2 receptor EP2 subtype

Cloning and expression of a cDNA for the human prostanoid FP receptor

Cloning and expression of a cDNA for the human prostanoid IP receptor

Structure-activity relationship of biaryl acylsulfonamide analogues on the human EP3 prostanoid receptor

Expression of Prostaglandin D synthase and the Prostaglandin D 2 receptors DP and CRTH2 in human nasal mucosa

Discovery of MK-0476, a potent and orally active leukotriene D4 receptor antagonist devoid of peroxisomal enxyme induction

Microsomal glutathione S-transferase is the predominant leukotriene C4 binding site in cellular membranes

Photoaffinity labeling of the leukotriene D4 receptor in guinea pig lung

Structure–Activity Relationship of Biaryl Acylsulfonamide Analogues on the Human EP 3 Prostanoid Receptor

A series of non-quinoline cysLT1 receptor antagonists : Sar study on pyridyl analogs of singulair

Evolution of a series of non-quinoline leukotriene D4 receptor antagonist; synthesis and sar of benzothiazoles and thiazoles substituted benzyl alcohols as potent LTD4 antagonists

Chromogranin A can act as a reversible processing enzyme inhibitor: Evidence from the inhibition of the IRCM-serine protease 1 cleavage of pro-enkephalin and ACTH at pairs of basic amino acids

A series of non-quinoline cysLT 1 receptor antagonists: Sar study on pyridyl analogs of singulair

A new series of potent LTD 4 antagonists in the styrylquinoline class

A new series of potent LTD4 antagonists in the styrylquinoline class

Discovery of L-740,515, a potent thienopyridine cysLT1 receptor (LTD4 receptor) antagonist

The discovery of L-699,392, a novel potent and orally active leukotriene D4 receptor antagonist

The discovery of a new structural class of potent orally active leukotriene D4 antagonists

Evolution of a series of non-quinoline leukotriene D 4 receptor antagonist; synthesis and sar of benzothiazoles and thiazoles substituted benzyl alcohols as potent LTD 4 antagonists

The discovery of L-699,392, a novel potent and orally active leukotriene D 4 receptor antagonist

Discovery of MK-0476, a potent and orally active leukotriene D 4 receptor antagonist devoid of peroxisomal enxyme induction

Discovery of L-740,515, a potent thienopyridine cysLT 1 receptor (LTD 4 receptor) antagonist

Chromogranin A can act as a reversible processing enzyme inhibitor

Opioid peptide precursors in striatum

Partial purification and characterisation of a 31 kDalton putative enkephalin precursor from guinea pig striatum

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