Abstract: The present invention provides for a polypeptide aggregation screening assay for the purpose of detecting modulators of polypeptide aggregation, which can provide for new therapies in pathologic states associated with polypeptide aggregation, especially considered is Alzheimer's Disease.
Abstract: The present invention provides the enzyme and enzymatic procedures for cleaving the ? secretase cleavage site of the APP protein and associated nucleic acids, peptides, vectors, cells and cell isolates and assays. An enzyme that cleaves the ?-secretase site of APP also is provided. The invention further provides a modified APP protein and associated nucleic acids, peptides, vectors, cells, and cell isolates, and assays that are particularly useful for identifying candidate therapeutics for treatment or prevention of Alzheimer's disease.
Abstract: The treatment of addictive disorders, psychoactive substance use disorders, intoxication disorders, inhalation disorders, alcohol addiction, tobacco addiction, and nicotine addiction using a heterocyclic amine, a phenylazacycloalkane, a cabergoline, or an aromatic bicyclic amine active agent, or a pharmaceutically acceptable derivative or salt of any said active agent is described herein.
Type:
Grant
Filed:
August 14, 2001
Date of Patent:
January 11, 2005
Assignee:
Pharmacia & Upjohn
Inventors:
Richard W. Anderson, Sylvia S. McBrinn, David W. Robertson, Robert C. Marshall
Abstract: The present invention is a novel pharmaceutical agent, (5R)-5-(methylamino)-5,6-dihydro-4H-imidazo[4,5,1-ij]quinoline-2(1H)-thione 1
Type:
Application
Filed:
July 23, 2004
Publication date:
December 30, 2004
Applicant:
Pharmacia & Upjohn Company
Inventors:
Brad A. Acker, Richard Frederick Heier, Alan Q. Jin, Malcolm Wilson Moon
Abstract: The present invention provides the enzyme and enzymatic procedures for cleaving the &bgr; secretase cleavage site of the APP protein and associated nucleic acids, peptides, vectors, cells and cell isolates and assays.
Type:
Grant
Filed:
September 17, 2001
Date of Patent:
December 28, 2004
Assignee:
Pharmacia & Upjohn Company
Inventors:
Mark E. Gurney, Michael Jerome Bienkowski, Robert Leroy Heinrikson, Luis A. Parodi, Riqiang Yan
Abstract: The present invention provides a Drosophila melanogaster GPCR (DmGPCR) polypeptides and polynucleotides which identify and encode such a DmGPCR. In addition, the invention provides expression vectors, host cells and methods for its production. The invention also provides methods for the identification of homologs in other animals, and of DmGPCR agonists/antagonists, useful for the treatment of diseases in animals and for the control of insects that are injurious or harmful to plants or animals.
Type:
Grant
Filed:
October 20, 2000
Date of Patent:
December 28, 2004
Assignee:
Pharmacia & Upjohn Company
Inventors:
David E. Lowery, Valdin G. Smith, Teresa M. Kubiak, Martha J. Larsen
Abstract: The present invention relates to polymorphs of the 3-pyrrole substituted 2-indolinone compound 5-(5-fluoro-2-oxo-1,2-dihydro-indol-3-ylidenemethyl)-2,4-dimethyl-1H-pyrrole-3-carboxylic acid (2-pyrrolidin-1-yl-ethyl)-amide.
Type:
Application
Filed:
February 12, 2004
Publication date:
December 23, 2004
Applicant:
Pharmacis & Upjohn Company
Inventors:
Changquan Sun, Todd P. Foster, Fusen Han, Michael Hawley, Tom Thamann
Abstract: The present invention provides novel human caspase-12 polynucleotides and polypeptides; constructs and recombinant host cells incorporating the polynucleotides; the human caspase-12 polypeptides encoded by the polynucleotides; antibodies to the polypeptides; and methods of making and using all of the foregoing.
Type:
Grant
Filed:
May 8, 2001
Date of Patent:
December 21, 2004
Assignee:
Pharmacia & Upjohn Company
Inventors:
Rolf F. Kletzien, Ilene M. Reardon, Katherine L. Weiland
Abstract: Methods of synthesizing pharmacologically useful oxazolidinones are disclosed, and, in particular, a method of manufacturing a 5-(tert-butylcarbamoyl)-aminomethyl-oxazolidinone by condensing a carbamate with a tert-butylcarbamoyl protected derivative of glycidylamine or 3-amino-1-halopropanol.
Abstract: The present invention is directed to novel substrates for Hu-Asp. More particularly, the invention provides peptide substrates and fusion polypeptide substrates comprising a &bgr;-secretase cleavage site. Methods and compositions for making and using the peptides are disclosed.
Type:
Application
Filed:
March 16, 2004
Publication date:
December 16, 2004
Applicant:
Pharmacia & Upjohn Company, a Delaware corporation
Inventors:
Riqiang Yan, Alfredo G. Tomasselli, Mark E. Gurney, Thomas L. Emmons, Michael Jerome Bienkowski, Robert L. Heinrikson
Abstract: The present invention is directed to novel substrates for Hu-Asp. More particularly, the invention provides peptide substrates and fusion polypeptide substrates comprising a &bgr;-secretase cleavage site. Methods and compositions for making and using the peptides are disclosed.
Type:
Application
Filed:
March 16, 2004
Publication date:
December 16, 2004
Applicant:
Pharmacia & Upjohn Company, a Delaware corporation
Inventors:
Riqiang Yan, Alfredo G. Tomasselli, Mark E. Gurney, Thomas L. Emmons, Michael Jerome Bienkowski, Robert L. Heinrikson
Abstract: The present invention is directed to novel substrates for Hu-Asp. More particularly, the invention provides peptide substrates and fusion polypeptide substrates comprising a &bgr;-secretase cleavage site. Methods and compositions for making and using the peptides are disclosed.
Type:
Application
Filed:
March 16, 2004
Publication date:
December 16, 2004
Applicant:
Pharmacia & Upjohn Company, a Delaware corporation
Inventors:
Riqiang Yan, Alfredo G. Tomasselli, Mark E. Gurney, Thomas L. Emmons, Michael Jerome Bienkowski, Robert L. Heinrikson
Abstract: The present invention provides a compound of formula as described herein, which are useful as antiviral agents, in particular, as agents against viruses of the herpes family.
Type:
Grant
Filed:
August 27, 2003
Date of Patent:
December 14, 2004
Assignee:
Pharmacia & Upjohn
Inventors:
Mark E. Schnute, Fred L. Ciske, Michael J. Genin, Joseph Walter Strohbach, Suvit Thaisrivongs
Abstract: The present invention provides certain thiadiazinone derivatives of oxazolidinones of the following formula I:
or pharmaceutically acceptable salts thereof that are antibacterial agents, pharmaceutical compositions containing them, methods for their use, and methods for preparing these compounds.
Type:
Grant
Filed:
February 4, 2003
Date of Patent:
December 7, 2004
Assignee:
Pharmacia & Upjohn Company
Inventors:
Gary W. Leuhr, Mikhail F. Gordeev, Dinesh V. Patel
Abstract: The invention provides compounds of Formula I:
wherein W0 is a bicyclic moiety and is
These compounds may be in the form of pharmaceutical salts or compositions, may be in pure enantiomeric form or racemic mixtures, and are useful to treat diseases or conditions in which &agr;7 is known to be involved.
Type:
Grant
Filed:
June 6, 2002
Date of Patent:
December 7, 2004
Assignee:
Pharmacia & Upjohn Company
Inventors:
Daniel Patrick Walker, Donn G. Wishka, David W. Piotrowski, Vincent E. Groppi, Jr.
Abstract: The present invention provides the enzyme and enzymatic procedures for cleaving the &bgr; secretase cleavage site of the APP protein and associated nucleic acids, peptides, vectors, cells and cell isolates and assays. The invention further provides a modified APP protein and associated nucleic acids, peptides, vectors, cells, and cell isolates, and assays that are particularly useful for identifying candidate therapeutics for treatment or prevention of Alzheimer's disease.
Type:
Grant
Filed:
February 27, 2001
Date of Patent:
December 7, 2004
Assignee:
Pharmacia & Upjohn Company
Inventors:
Mark E. Gurney, Michael J. Bienkowski, Robert L. Heinrikson, Luis A. Parodi, Riqiang Yan
Abstract: The present invention is a novel process for the transformation of 17&agr;-hydroxy-6&agr;-methylpregn-4-ene-3,20-dione 17-acetate (I)
to 11&bgr;,17&agr;,21-trihydroxy-6&agr;-methylpregna-1,4-diene-3,20-dione 21-acetate (VI)
Type:
Grant
Filed:
June 14, 2002
Date of Patent:
December 7, 2004
Assignee:
Pharmacia and Upjohn Company
Inventors:
Bruce Allen Pearlman, Michael J. White, Ivan G. Gilbert
Abstract: The present invention is directed to novel substrates for Hu-Asp. More particularly, the invention provides peptide substrates and fusion polypeptide substrates comprising a &bgr;-secretase cleavage site. Methods and compositions for making and using the peptides are disclosed.
Type:
Application
Filed:
March 16, 2004
Publication date:
December 2, 2004
Applicant:
Pharmacia & Upjohn Company, a Delaware corporation
Inventors:
Riqiang Yan, Alfredo G. Tomasselli, Mark E. Gurney, Thomas L. Emmons, Michael Jerome Bienkowski, Robert L. Heinrikson
Abstract: The present invention provides the enzyme and enzymatic procedures for cleaving the &bgr; secretase cleavage site of the APP protein and associated nucleic acids, peptides, vectors, cells and cell isolates and assays. The invention further provides a modified APP protein and associated nucleic acids, peptides, vectors, cells, and cell isolates, and assays that are particularly useful for identifying candidate therapeutics for treatment or prevention of Alzheimer's disease.
Type:
Grant
Filed:
April 12, 2000
Date of Patent:
November 30, 2004
Assignee:
Pharmacia & Upjohn Company
Inventors:
Mark E. Gurney, Michael J. Bienkowski, Robert L. Heinrikson, Luis A. Parodi, Riqiang Yan