摘要:
This invention relates to substituted heteroanilide compounds which are modulators, agonists or antagonists, of the CCR5 receptor. In addition, this invention relates to the treatment and prevention of disease states mediated by CCR5.
摘要:
This invention relates to substituted anilides which are modulators, agonists or antagonists, of the CCR5 receptor. In addition, this invention relates to the treatment and prevention of disease states mediated by CCR5.
摘要:
This invention relates to novel compounds of Formula (I), and compositions thereof, useful in the treatment of disease states mediated by the chemokine, Interleukin-8 (IL-8).
摘要:
The invention provides herpes virus OBP-NT polypeptides and polynucleotides encoding OBP-NT polypeptides and methods for producing such polypeptides by recombinant techniques. Also provided are methods for utilizing OBP-NT polypeptides to screen for antiviral compounds.
摘要:
The present invention provides amino-indanone inhibitors of transcription factor NF-λB and pharmaceutically acceptable salts, hydrates and solvates thereof, pharmaceutical compositions of such compounds, and methods for treating diseases in which activation of NF-λB is implicated. More specifically, the present invention provides methods of treatment of a variety of diseases associated with NF-λB activation including inflammatory disorders; particularly rheumatoid arthritis, inflammatory bowel disease, and asthma; dermatosis, including psoriasis and acute dermatosis; autoimmune diseases; tissue and organ rejection; Alzheimer's disease; stroke; atherosclerosis; restenosis; cancer, including Hodgkins disease; and certain viral infections, including AIDS; osteoarthritis; osteoporosis; and Ataxia Telangiestasia by administering to a patient in need thereof a compound of the present invention.
摘要:
The present invention provides pharmaceutical compositions of salicylanilide inhibitors of transcription factor NF-λB, and methods for treating diseases in which activation of NF-λB is implicated. More specifically, the present invention provides methods of treatment of a variety of diseases associated with NF-λB activation including inflammatory disorders; particularly rheumatoid arthritis, inflammatory bowel disease, and asthma; dermatosis, including psoriasis and atopic dermatitis; autoimmune diseases; tissue and organ rejection; Alzheimer's disease; stroke; atherosclerosis; restenosis; cancer, including Hodgkin's disease; certain viral infections, including AIDS; osteoarthritis; osteoporosis; and Ataxia Telangiestasia by administering to a patient in need thereof a compound of the present invention.
摘要:
The present invention is related to novel 2-alkyl substituted imidazole compounds of Formula (I) useful for the treatment of CSBP kinase mediated diseases.