Substituted heterocyclic compounds and methods of use

C - Chemistry – Metallurgy – 07 – D

Patent

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Details

C07D 403/04 (2006.01) A61K 31/505 (2006.01)

Patent

CA 2542995

The present invention relates to hydroxybenzimidazole pyrimidines or pyridines or pharmaceutically-acceptable salts thereof. Also included is a method of treatment of inflammation, inhibition of T cell activation and proliferation, arthritis, rheumatoid arthritis, psoriatic arthritis, osteoarthritis, organ transplant, acute transplant or heterograft or homograft rejection, transplantation tolerance induction, ischemic or reperfusion injury, myocardial infarction, stroke, multiple sclerosis, inflammatory bowel disease, including ulcerative colitis, Crohn's disease, lupus, contact hypersensitivity, delayed-type hypersensitivity, and gluten-sensitive enteropathy, type 1 diabetes, psoriasis, contact dermatitis, Hashimoto's thyroiditis, Sjogren's syndrome, autoimmune hyperthyroidism, Addison's disease, autoimmune polyglandular disease, autoimmune alopecia, pernicious anemia, vitiligo, autoimmune hypopituatarism, Guillain-Barre syndrome, glomerulonephritis, serum sickness, uticaria, allergic diseases, asthma, hayfever, allergic rhinitis, scleracielma, mycosis fungoides, dermatomyositis, alopecia areata, chronic actinic dermatitis, eczema, Behcet's disease, Pustulosis palmoplanteris, Pyoderma gangrenum, Sezary's syndrome, atopic dermatitis, systemic schlerosis, morphea, atopic dermatitis, colon carcinoma or thymoma in a mammal comprising administering a therapeutically-effective amount a compound as described above.

La présente invention porte sur des hydroxybenzimidazole pyrimidines ou des pyridines ou des sels de celles-ci acceptables d'un point de vue pharmaceutique. L'invention porte également sur une méthode de traitement de l'inflammation, sur l'inhibition de l'activation et de la prolifération des lymphocytes T, l'arthrite, l'arthrite rhumatoïde, l'arthrite psoriatique, l'ostéoarthrite, la transplantation d'organe, la transplantation d'urgence ou le rejet d'hétérogreffe ou d'homogreffe, l'induction de la tolérance de la transplantation, les lésions ischémiques ou la reperfusion, l'infarctus du myocarde, l'accident vasculaire cérébral, la sclérose en plaques, la maladie intestinale inflammatoire telle que la colite ulcérative, la maladie de Crohn, le lupus, l'hypersensibilité de contact, l'hypersensibilité retardée et l'entéropathie sensible au gluten, le diabète de type 1, le psoriasis, la dermatite de contact, la thyroïdite d'Hashimoto, le syndrome de Sjogren, l'hyperthyroïdie auto-immune, la maladie d'Addison, la maladie polyglandulaire auto-immune, l'alopécie auto-immune, l'anémie pernicieuse, le vitiligo, l'hypopituatarisme auto-immun, le syndrome de Guillain-Barre, la glomérulonéphrite, la maladie sérique, l'urticaire, les maladies allergiques, l'asthme, le rhume des foins, la rhinite allergique, sclérodermie, la mycose fongoïde, la dermatomyosite, la pelade, la dermatite actinique chronique, l'eczéma, la maladie de Behcet, la pustulose palmo-plantaire, l'idiophagédénisme, le syndrome de Sezary, la dermatite atopique, la sclérose systémique, le cancer du côlon ou thymome chez un mammifère. Le procédé de cette invention consiste à administrer une quantité efficace d'un point de vue thérapeutique d'un des composés précités.

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