Abstract: The invention provides compounds of Formula I:
These compounds may be in the form of pharmaceutical salts or compositions, and racemic mixtures or pure enantiomers thereof. The compounds of Formula I are useful in pharmaceuticals in which &agr;7 is known to be involved.
Type:
Grant
Filed:
August 17, 2001
Date of Patent:
July 29, 2003
Assignee:
Pharmacia & Upjohn Company
Inventors:
Jason K. Myers, Bruce N. Rogers, Vincent E. Groppi, Jr., David W. Piotrowski, Alice L. Bodnar, Eric Jon Jacobsen, Jeffrey W. Corbett
Abstract: According to the invention there is provided a sterile, pyrogen-free, ready-to-use solution of an anthracycline glycoside, especially doxorubicin, which consists essentially of a physiologically acceptable salt of an anthracycline glycoside dissolved in a physiologically acceptable solvent therefor, which has not been reconstituted from a lyophilizate and which has a pH of from 2.5 to 6.5. The solution of the invention is particularly advantageous for the administration by injection of the anthracycline glycoside drugs, e.g. doxorubicin, in the treatment of both human and animal tumors.
Type:
Grant
Filed:
August 30, 2001
Date of Patent:
July 22, 2003
Assignee:
Pharmacia & Upjohn Company
Inventors:
Gaetano Gatti, Diego Oldani, Giuseppe Bottoni, Carlo Confalonieri, Luciano Gambini, Roberto De Ponti
Abstract: The present invention relates to small molecules according to the formula [I]:
which are potent inhibitors of &agr;4&bgr;1 mediated adhesion to either VCAM or CS-1 and which can be used for treating or preventing &agr;4&bgr;1 adhesion mediated conditions in a mammal such as a human.
Type:
Grant
Filed:
July 12, 2002
Date of Patent:
July 22, 2003
Assignees:
Tanabe Seiyaku Co., Ltd., Pharmacia & Upjohn Company
Inventors:
Thomas J. Lobl, Bradley R. Teegarden, Alexander Polinsky, Gilbert M. Rishton, Masafumi Yamagishi, Steven Tanis, Jed F. Fisher, Edward W. Thomas, Robert A. Chrusciel
Abstract: There are provided the combined use of 4-demethoxy-3′-deamino-3′-aziridinyl-4′-methansulfonyl daunorubicin or 4-demethoxy-N,N-bis(2-chloroethyl)-4′-methansulfonyl daunorubicin and an anti-neoplastic anti-mitotic compound and/or a platinum derivative in the treatment of tumors, as well as in the prevention or treatment of metastasis or in the treatment of tumors by inhibition of angiogenesis.
Abstract: The invention provides methods for diagnosing and treating amyloid-related conditions and compounds useful for the same. The invention provides for detecting, imaging, monitoring, diagnosing, and treating conditions characterized by the binding or aggregation of amyloid fibrils. More particularly, the invention relates to using quinolinehydrazone compounds for diagnosing and treating amyloidotic conditions and also as an antioxidant.
Type:
Grant
Filed:
September 22, 2000
Date of Patent:
July 8, 2003
Assignee:
Pharmacia & Upjohn Company
Inventors:
Thomas J. Raub, Geri A. Sawada, Steven P. Tanis, Gregory J. Fici, Allen Edwin Buhl, Donald Bainbridge Carter, Tiziano Bandiera, Jacqueline Lansen, Cesare Pellerano, Luisa Savini
Abstract: Among other things, assays and methods of diagnosis and treatment of disease (e.g., Alzheimer's disease) based on the surprising observation of an interaction between amyloid &bgr; or its aggregates with the sodium channel are provided. In particular, methods to identify compounds that modulate this interaction are provided, as well as methods of diagnosis and treatment that are based on this interaction.
Type:
Grant
Filed:
December 21, 2000
Date of Patent:
July 8, 2003
Assignee:
Pharmacia & Upjohn Company
Inventors:
Kai S. Lee, Xiao-Dong Sun, Bruce M. Taylor, Dennis E. Epps, Allen E. Buhl
Abstract: A method of preventing or treating migraine headaches is disclosed comprising administering to a person in need thereof a pharmacologically effective amount of specific substituted phenylazacycloalkanes. These compounds can treat or prevent symptoms associated with migraine headaches and yet avoid undesirable side affects associated with conventional migraine treatment compositions. Additionally, other agents used to treat migraine headaches can be used in combination therewith.
Abstract: This invention discloses a commercially advantageous process for extraction and purification of protein from microorganisms. The initial steps of the process are useful for purifying many insoluble proteins while later steps are designed to renature denatured somatotropins produced by transformed microorganisms. The process is especially useful for purifying recombinantly-produced bovine somatotropin.
Abstract: The invention provides compounds of Formula (I):
wherein R1-R4, p and q have any of the values described in the specification, as well as pharmaceutical salts thereof, and pharmaceutical compositions containing such compounds or salts. The compounds and salts are 5-HT ligands and are useful for treating diseases, disorders, and/or conditions in a mammal wherein activity of a 5-HT receptor is implicated. The compounds and salts are particularly useful for treating diseases of the central nervous system.
Type:
Grant
Filed:
September 20, 2001
Date of Patent:
July 1, 2003
Assignee:
Pharmacia & Upjohn Company
Inventors:
Kristine E. Frank, Brad A. Acker, Michael D. Ennis, Jed F. Fisher, Jian-min Fu, Eric Jon Jacobsen, William W. McWhorter, Jr., Jeanette K. Morris, Donald Joseph Rogier
Abstract: The present invention provides pharmaceutically active compounds useful for the treatment of diseases or disorders of the central nervous system.
Type:
Grant
Filed:
October 2, 2001
Date of Patent:
July 1, 2003
Assignee:
Pharmacia & Upjohn Company
Inventors:
Eric Jon Jacobsen, Stephen J. King, Kalpana M. Merchant
Abstract: The present invention is an improved prosess to prepare (5R)-(methylamino)-5,6-dihydro-4H-imidazo[4,5,1-ij]quinolin-2(1H)-one the compound of formula (VII)
Abstract: This patent application describes the treatment of Addictive disorders, Psychoactive Substance Use disorders, Intoxication disorders, Inhalation disorders, Alcohol addiction, Tobacco addiction and or Nicotine addiction; and Attention Deficit Hyperactivity Disorder (ADHD); comprising administering a therapeutically effective, nontoxic dose of Reboxetine and derivatives and or pharmaceutically acceptable salts thereof to a patient.
Type:
Grant
Filed:
August 13, 2001
Date of Patent:
July 1, 2003
Assignee:
Pharmacia & Upjohn Company
Inventors:
Fred Hassan, John Michael McCall, Duncan Paul Taylor, Philip F. Von Voigtlander, Erik Ho Fong Wong
Abstract: Disclosed are compounds of Formula (I):
wherein R1-R4, p and q have any of the values described in the specification, as well as pharmaceutical salts thereof, and pharmaceutical compositions containing such compounds or salts. The compounds and salts are 5-HT ligands and are useful for treating diseases, disorders, and/or conditions in a mammal wherein activity of a 5-HT receptor is implicated. The compounds and salts are particularly useful for treating diseases of the central nervous system.
Type:
Grant
Filed:
September 20, 2001
Date of Patent:
June 24, 2003
Assignee:
Pharmacia & Upjohn Company
Inventors:
Kristine E. Frank, Brad A. Acker, Michael D. Ennis, Jed F. Fisher, Jian-min Fu, William W. McWhorter, Jr., Jeanette K. Morris, Donald Joseph Rogier, Eric Jon Jacobsen
Abstract: The present invention provides a method for identifying a test compound that binds to a target species. The method includes: incubating at least one test mixture under isothermal denaturing conditions, each test mixture comprising at least one test compound, and at least one target species, wherein the isothermal denaturing conditions are effective to cause at least a portion of the target species to denature to a measurable extent; detecting a denaturation signal of each target species in the presence of the at least one test compound by a change in the diffusion properties of the target molecule using fluorescence correlation spectroscopy; and comparing the denaturation signal of each target species in the presence of at least one test compound with a denaturation signal of the same target species in the absence of the at least one test compound under the same isothermal denaturing conditions.
Type:
Grant
Filed:
December 9, 1999
Date of Patent:
June 24, 2003
Assignee:
Pharmacia & Upjohn Company
Inventors:
Dennis E. Epps, Paul K. Tomich, Ferenc J. Kezdy, Charles K. Marschke
Abstract: The present invention provides pharmaceutically active compounds useful for the treatment of diseases or disorders of the central nervous system.
Abstract: The present invention is a process, including intermediates, to produce (2S)-2-dipropylamino)-6-ethoxy-2,3-dihydro-1H-indene-5-carboxamide
which is a useful pharmaceutical agent.
Type:
Grant
Filed:
June 6, 2002
Date of Patent:
June 10, 2003
Assignee:
Pharmacia & Upjohn Company
Inventors:
Jiong Jack Chen, Arthur Glenn Romero, Styrbjorn Bystrom
Abstract: The present invention relates to an administration schedule comprising the intravenous administration of a &agr;-halogen-acryloyl distamycin derivative of formula (I)
wherein R is a bromine or chlorine atom; or a pharmaceutically acceptable salt thereof. The above administration allows the treatment of a variety of tumors in mammals.
Type:
Grant
Filed:
October 2, 2000
Date of Patent:
June 10, 2003
Assignees:
Pharmacia Italia S.p.A., Pharmacia & Upjohn Company
Inventors:
Camilla Fowst, Franzanne Vreeland, Maria Cristina Rosa Geroni
Abstract: The present invention relates to pyrrole substituted 2-indolinone compounds and their pharmaceutically acceptable salts which modulate the activity of protein kinases and therefore are expected to be useful in the prevention and treatment of protein kinase related cellular disorders such as cancer.
Type:
Grant
Filed:
February 15, 2001
Date of Patent:
June 3, 2003
Assignees:
Sugen, Inc., Pharmacia & Upjohn Co.
Inventors:
Peng Cho Tang, Todd A. Miller, Xiaoyuan Li, Li Sun, Chung Chen Wei, Shahrzad Shirazian, Congxin Liang, Tomas Vojkovsky, Asaad S. Nematalla, Michael Hawley