Anti hepatitis C virus antibody and uses thereof |
| OF THE PRESENT INVENTION Accordingly, the technical problem of the invention is to provide means ... |
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Chemical and/or biological decontamination system |
| OF THE INVENTION The present invention provides a composition that is effective in the ... |
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Immunostimulant bacterial membrane fractions in cancer treatment |
| The invention claimed is: 1. A method of stimulating an immune response and/or inducing an ... |
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Cloning and characterization of a human adenylyl cyclase |
| One aspect of the invention is an isolated and purified human type VI adenylyl cyclase (hAC6) ... |
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Tumor antigen based on products of the tumor suppressor gene WT1 |
| What is claimed is: 1. An isolated polypeptide which consists of at most 12 contiguous amino acid ... |
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Methods of inhibiting GPR-9-6 function |
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Method for cloning of a rare, specifically mutated cell |
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Vaccine against Gram-negative bacterial infections |
| OF THE PREFERRED EMBODIMENTS According to the present invention, a non-covalent, polyvalent ... |
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Inhibitor of stem cell proliferation and uses thereof |
| The present invention relates to polypeptides which are inhibitors of stem cell proliferation ("INPR... |
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Polypeptide and protein derivatives and process for their preparation
| Details |
Inventors: Offord, Robin Ewart; Rose, Keith;
Assignee: Amylin Pharmaceuticals, Inc. (San Diego, CA)
Primary Examiner: Weber; Jon
Assistant Examiner: Mohamed; Abdel A.
Attorney, Agent or Firm: Edell, Shapiro & Finnan, LLC
Protein and polypeptid derivatives and their salts are claimed characterized in that a protein or polypeptide is conjugated via an intermediate grouping containing at least one radical of the formula --C(R).dbd.N-- (or --N.dbd.C(R)--) or --CH(R)--NH-- (or --NH--CH(R)--), wherein R is hydrogen or a hydrocarbon residue which may be substituted, with the same or a different protein or polypeptide, with a reporter group or a cytotoxic agent as well as a process for their preparation and the novel intermediates therefor. |
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DETAILED DESCRIPTION What we claim is: 1. A method of producing a composition containing modified protein or polypeptide molecules, or salts thereof, wherein said modified protein or polypeptide molecules of said composition consist essentially of a compound selected from A-X-Z-X'--B wherein A is a residue of a protein or polypeptide having a carboxy and amino terminus and is connected to X-Z-X'--B exclusively at said carboxy or amino terminus; B is a polymeric compound; X and X' independently from each other are bivalent organic radicals or independently from each other are present or absent; Z is a bivalent radical selected from the group consisting of: --C(R). dbd. N--, --N. dbd. C(R)--, --CH(R)--NH--, --NH--CH(R)--, --C(R). dbd. N--Y--NC(R)--, --N. dbd. C(R)--Y--C(R)N--, --CH(R)--NH--Y--NH--CH(R)-- and --NH--CH(R)--Y--CH(R)--NH--, --C(R). dbd. N--O--, --O--N. dbd. C(R)--, --CH(R)--NH--O--, --O--NH--CH(R)--, --C(R). dbd. N--O--Y--O--N. dbd. C(R)--, --O--N. dbd. C(R)--Y--C(R). dbd. N--O--, --CH(R)--NH--O--Y--O--NH--CH(R)-- and --O--NH--CH(R)--Y--CH(R)--NH--O--; where R is hydrogen or an aliphatic, cycloaliphatic, aromatic or araliphatic hydrocarbon group; and Y is a bivalent organic group, wherein said method comprises condensing a compound of the formula: A-X--R. sup. 1 wherein R. sup. 1 is a --CO--R group, an acetalized formyl group, or an amino or protected amino group, and A,R, and X are as defined above, with a compound of formula: R. sup. 2--X'--B or a compound of formula: R. sup. 2--Y--R. sup. 2 where R. sup. 2 is amino when R. sup. 1 is --CO--R or acetalized formyl and R2 is --CO--R or acetalized formyl when R. sup. 1 is amino, and X', Y, R and B are as defined above, to form a Schiff base, hydrazone, oxime or azomethine compound, and optionally, reducing the --C(R). dbd. N-- or --N. dbd. C(R) formed by the condensation to CH(R)--NH-- or NH--CH(R)--, respectively, and optionally forming a salt. 2. The method of producing a composition of claim 1, wherein said residue A is a carboxy terminal residue. 3. The method of producing a composition of claim 1, wherein said residue A is an amino terminal residue
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