Abstract: A method of synthesizing commercial quantities of the pentapeptide L-aspartyl-L-seryl-L-aspartyl-L-prolyl-L-arginine, and salts or solvates thereof, e.g., the hydrochloride or acetate salt or water solvate, compounds useful in pharmaceutical compositions for the treatment of allergic conditions, is disclosed, as are novel intermediate compounds produced in the course of the synthesis.
Type:
Grant
Filed:
December 21, 1988
Date of Patent:
May 18, 1993
Assignee:
Immunetech Pharmaceuticals, Inc.
Inventors:
John C. Tolle, Wenying Z. Gifford, Kenneth W. Funk
Abstract: Methods and compositions for the treatment of inflammatory bowel diseases, chemically-induced irritation and inflammation, and other irritative or inflammatory conditions utilizing the peptide sequences Asp-Ser-Asp-Pro-Arg, Asp-Ser-Asn-Pro-Arg, or derivatives or salts thereof are disclosed.
Abstract: Methods and compositions for the treatment of non-IgE-mediated inflammatory disease conditions utilizing the peptide Asp-Ser-Asp-Pro-Arg, or derivative thereof are disclosed.
Abstract: Anti-inflammatory peptides of the formula A-B-C-D-E, useful in treating allergies, autoimmune diseases, and other disorders, and methods for using them are described.
Abstract: A method of modulating immune responses in mammals by blocking immune complex binding to immunoglobulin Fc receptors is described, comprising administering a peptide comprising a portion selected from the amino acid sequence-Pro-Asp-Ala-Arg-His-Ser-Thr-Thr-Gln-Pro-Arg-Specific uses in reducing immune complex mediated inflammation or tissue destruction and in reducing the human allergic response are disclosed.
Abstract: A method of modulating immune complex mediated immune responses in mammals is described, comprising administering a peptide comprising the amino acid sequence-Thr-Ile-Ser-Lys-Ala-Lys-Gly-Gln-Pro-Arg-Specific uses in reducing immune complex mediated inflammation or tissue destruction and in modulating the proliferation or function of mononuclear cells are disclosed.
Abstract: Peptides and peptide compositions are disclosed which act as competitive antagonists for the C5a receptor and thus block inflammatory and immunomodulatory activity mediated by endogenous C5a.
Abstract: A peptide having the amino acid sequence Asp-Ser-Glu-Pro-Arg and capable of blocking immune complex binding to immunoglobulin Fc receptors is disclosed.