Tryptase inhibitors

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Heterocyclic carbon compounds containing a hetero ring...

Reexamination Certificate

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C514S540000, C514S595000, C514S619000, C514S621000, C514S636000, C514S654000, C544S386000, C544S400000, C544S403000, C560S025000, C560S034000, C560S035000, C560S041000, C560S158000, C560S163000, C560S168000, C564S156000

Reexamination Certificate

active

06960588

ABSTRACT:
Compounds of formula (I)in which M, B1, B2, B3, B4, B5, B6, A1, A2, A3, A4, A5, A6, K1 and K2 have the meanings as indicated in the description, are novel effective tryptase inhibitors.

REFERENCES:
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patent: 96/09297 (1996-03-01), None
patent: 98/04537 (1998-02-01), None
patent: 99/12918 (1999-03-01), None
patent: 99/24395 (1999-05-01), None
patent: 99/24407 (1999-05-01), None
patent: 99/40083 (1999-08-01), None
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Burgess, “Mast Cell Tryptase as a Target for Drug Design” Drug News Perspectives, vol. 13(3), pp. 147-157 (Apr. 2000).
Wright et al, “Inhibition of Allergen-Induced Pulmonary Responses by the Selective Tryptase Inhibitor 1,5-bis-{4-[(3-Carbamidoyl-benzenesulfonylamino)-methyl]-phenoxy}-pentane (AMG-126737)” Biochemical Pharmacology, vol. 58, pp. 1989-1996 (1999).
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Rice, K.D., et al., “Inhibitors of Tryptase for the Treatment of Mast Cell-Mediated Diseases”,Current Pharmaceutical Design, V. 4, No. 5, pp. 381-396, (1998).
Krishna, et al., “Inhibition of mast cell tryptase by inhaled APC 366 attenuates allergen-induced late-phase airway obstruction in asthma”,J. Allergy Clin. Immunol., Jun., 2001, pp. 1039-1045.
Rice, et al., “Dibasic Inhibitors of human mast cell tryptase. Part 2: Structure-Activity Relationships and Requirements for Potent Activity”, Bioorganic & Medicinal Chemistry Letters 10, pp. 2361-2366 (2000).

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