Abstract: The invention relates to stabilized solutions with F VIII coagulation activity, to a process for the preparation thereof and to the use thereof.
Abstract: Methods of making unnatural amino acids are provided which unnatural amino acids can be incorporated into peptides which either inhibit or promote the secretion of gonadotropins by the pituitary gland and inhibit the release of steroids by the gonads. These unnatural amino acids are useful in the synthesis of peptides and have the formula (a): ##STR1## where W is (CH.sub.2).sub.n or ##STR2## n is an integer from 1 to 6; j=1, 2 or 3, and preferably, Y is N--CN, X is NH and R.sub.2 is alkyl, modified alkyl, alkenyl, alkynyl, aryl or methyl pyridyl. Disclosed are peptides that are analogs of the decapeptide GnRH wherein there is at least one residue of an unnatural amino acid in the 3-, 5-, 6- and/or 8-positions.
Type:
Grant
Filed:
August 11, 1994
Date of Patent:
October 15, 1996
Assignee:
The Salk Institute for Biological Studies
Inventors:
Carl A. Hoeger, Jean E. F. Rivier, John S. Porter
Abstract: The invention relates to peptide compounds of formula (I):R.sub.1 --A--Gly--Asp--Trp--R.sub.2 (I)in which R.sub.1, R.sub.2 and A are as defined in the description, and anti-aggregation medicaments containing the same.
Type:
Grant
Filed:
August 11, 1994
Date of Patent:
October 15, 1996
Assignee:
Adir et Compagnie
Inventors:
Jean-Luc Fauchere, Angela D. Morris, Christophe Thurieau, Tony Verbeuren, Serge Simonet
Abstract: The present invention relates to a method to determine the concentration of an unknown substance in a colorimetric reaction using a fluorometric reader. The change in color can be monitored by observing the change of fluorescence of a known amount of a suitable fluorophore in the reaction chamber. Under appropriate conditions the absorption spectrum of the chromophore overlaps with the emission spectrum of the fluorophore thereby allowing the change in fluorescence to be proportional to the intensity of color in the reaction and thus, proportional to the quantity of the substance of interest. Specifically, 8-methoxypyrene tri-sulfonic acid is used as the fluorophore.
Type:
Grant
Filed:
December 27, 1995
Date of Patent:
October 15, 1996
Assignee:
Dade International Inc.
Inventors:
Shoshana Bascomb, Frank J. Swenson, Ted Sand
Abstract: The present invention provides anti-obesity proteins, which when administered to a patient regulate fat tissue. Accordingly, such agents allow patients to overcome their obesity handicap and live normal lives with much reduced risk for type II diabetes, cardiovascular disease and cancer.
Type:
Grant
Filed:
January 31, 1995
Date of Patent:
October 8, 1996
Assignee:
Eli Lilly and Company
Inventors:
Richard D. DiMarchi, David B. Flora, William F. Heath, Jr., James A. Hoffmann, James E. Shields, David L. Smiley
Abstract: The present invention provides anti-obesity proteins, which when administered to a patient regulate fat tissue. Accordingly, such agents allow patients to overcome their obesity handicap and live normal lives with much reduced risk for type II diabetes, cardiovascular disease and cancer.
Type:
Grant
Filed:
January 31, 1995
Date of Patent:
October 8, 1996
Assignee:
Eli Lilly and Company
Inventors:
Richard D. DiMarchi, David B. Flora, William F. Heath, Jr., James A. Hoffmann, James E. Shields, David L. Smiley
Abstract: The present invention provides anti-obesity proteins, which when administered to a patient regulate fat tissue. Accordingly, such agents allow patients to overcome their obesity handicap and live normal lives with much reduced risk for type II diabetes, cardiovascular disease and cancer.
Type:
Grant
Filed:
January 31, 1995
Date of Patent:
October 8, 1996
Assignee:
Eli Lilly and Company
Inventors:
Richard D. DiMarchi, David B. Flora, William F. Heath, Jr., James A. Hoffmann, James E. Shields, David L. Smiley
Abstract: There are disclosed a process for detecting and determining an oxidized lipid in a specimen, which is capable of readily and accurately determining a specimen as containing an oxidized lipid, and a process for forming a water-soluble oxidized lipid having a hydroperoxide group which has specific influence on a living body. A specimen is detected and determined to contain an oxidized lipid by adding a lanthanide shift reagent to a specimen, followed by spectroscopic analysis thereof. An oxidized lipid is formed by adding superoxide dismutase (SOD) and CuSO.sub.4 to (1) an emulsion prepared by dissolving linoleic acid or arachidonic acid in deuterated methyl alcohol and adding the solution to a deuterated phosphate buffer under stirring, or to (2) a low density lipoprotein solution sufficiently dialyzed against an undeuterated phosphate buffer; followed by irradiation with long-wave ultraviolet light.
Abstract: The present invention is directed to a method for screening samples for the identification of agents exhibiting potential fungicidal and insecticidal activity for a wide variety of agricultural, medical and pharmaceutical uses. The method utilizes cells that comprise a plasmid-born CTS gene of Saccharomyces cerevisiae, which allows for over expression of chitinase.
Abstract: A method for the healing of wounds caused by corneal injury, which includes administering to a mammalian patient in need thereof an effective wound healing amount of lactoferrin, lactoperoxidase or a combination of lactoferrin and lactoperoxidase as active ingredients, either alone or in admixture with at least one excipient.
Type:
Grant
Filed:
April 21, 1995
Date of Patent:
October 1, 1996
Assignee:
Santen Pharmaceutical Co., Ltd.
Inventors:
Shiro Mita, Mitsushi Hikida, Michel F. Degre
Abstract: A molecule having a peptide sequence of 80 or fewer amino acid residues containing the amino acid sequence of an anticouplone of any of the G proteins, which molecule is useful for inhibiting activation of the G protein by its G-coupled receptor.
Abstract: The present invention provides anti-obesity proteins, which when administered to a patient regulate fat tissue. Accordingly, such agents allow patients to overcome their obesity handicap and live normal lives with much reduced risk for type II diabetes, cardiovascular disease and cancer.
Type:
Grant
Filed:
February 6, 1995
Date of Patent:
September 24, 1996
Assignee:
Eli Lilly and Company
Inventors:
Margret B. Basinski, Richard D. DiMarchi, William F. Heath, Jr., Brigitte E. Schoner
Abstract: The invention concerns pharmaceutical compositions for use in the treatment of gastric disorders associated with Helicobacter pylori comprising a bacteriocin antimicrobial agent optionally coadministered with a release-delaying substance.
Abstract: A test strip for determining blood glucose levels comprising a reagent which incorporates a dye color. Whole blood reacts with the reagent of the test strip resulting in a color change on the reagent portion of the strip which is controlled by the dye color, indicating the blood glucose level by visual comparison with a color chart, or by the use a photometer. The use of a copolymer in the reagent which provides complete coalescence and a resulting smooth surface particle structure provides accurate readings of the reacted test strip by the photometer.
Abstract: The present invention provides anti-obesity proteins, which when administered to a patient regulate fat tissue. Accordingly, such agents allow patients to overcome their obesity handicap and live normal lives with much reduced risk for type II diabetes, cardiovascular disease and cancer.
Type:
Grant
Filed:
February 6, 1995
Date of Patent:
September 10, 1996
Assignee:
Eli Lilly and Company
Inventors:
Margret B. Basinski, Richard D. DiMarchi, William F. Heath, Jr., Brigitte E. Schoner
Abstract: The present invention provides anti-obesity proteins, which when administered to a patient regulate fat tissue. Accordingly, such agents allow patients to overcome their obesity handicap and live normal lives with much reduced risk for type II diabetes, cardiovascular disease and cancer.
Type:
Grant
Filed:
February 6, 1995
Date of Patent:
September 3, 1996
Assignee:
Eli Lilly and Company
Inventors:
Margret B. Basinski, Richard D. DiMarchi, William F. Heath, Jr., Brigitte E. Schoner
Abstract: The present invention provides anti-obesity proteins, which when administered to a patient regulate fat tissue. Accordingly, such agents allow patients to overcome their obesity handicap and live normal lives with much reduced risk for type II diabetes, cardiovascular disease and cancer.
Type:
Grant
Filed:
January 31, 1995
Date of Patent:
September 3, 1996
Assignee:
Eli Lilly and Company
Inventors:
Richard D. DiMarchi, David B. Flora, William F. Heath, Jr., James A. Hoffmann, James E. Shields, David L. Smiley
Abstract: A pharmaceutical formulation comprising a growth hormone and Lys-Gly-Asp-Ser (SEQ ID No: 1) as additive or buffering substance shows a very high stability against deamidation, oxidation and cleavage of peptide bonds. The stability of the product allows for the storing and shipment thereof in a lyophilized state or in the form of a dissolved or re-dissolved formulation at ambient temperature.
Type:
Grant
Filed:
June 5, 1995
Date of Patent:
September 3, 1996
Assignee:
Novo Nordisk A/S
Inventors:
Thorkild Christensen, Per Balschmidt, Hans S.o slashed.rensen, Ole Olsen, Lars Thim
Abstract: The present invention provides anti-obesity proteins, which when administered to a patient regulate fat tissue. Accordingly, such agents allow patients to overcome their obesity handicap and live normal lives with much reduced risk for type II diabetes, cardiovascular disease and cancer.
Type:
Grant
Filed:
February 6, 1995
Date of Patent:
September 3, 1996
Assignee:
Eli Lilly and Company
Inventors:
Margret B. Basinski, Richard D. DiMarchi, William F. Heath, Jr., Brigitte E. Schoner
Abstract: Disclosed herein is a combination of an antiviral nucleoside analog and a ribonucleotide reductase inhibiting peptide derivative. The combination is useful for combatting herpes infections.
Type:
Grant
Filed:
June 6, 1994
Date of Patent:
September 3, 1996
Assignee:
Bio-Mega Boehringer Ingelheim Research Inc.