Abstract: Compounds of general formula (I) wherein R1, R2 and R3 are as defined in the specification, as well as salts, enantiomers thereof and pharmaceutical compositions including the compounds are prepared.
Type:
Grant
Filed:
November 5, 2003
Date of Patent:
August 7, 2007
Assignee:
AstraZeneca AB
Inventors:
William Brown, Andrew Griffin, Paul Jones, Daniel Pagé, Niklas Plobeck, Christopher Walpole
Abstract: The present invention relates to new compounds of formula (I), to pharmaceutical formulations containing the compounds, and to the use of the compounds in the prevention and/or treatment of mGluR5 receptor-mediated disorders.
Type:
Application
Filed:
February 15, 2005
Publication date:
August 2, 2007
Applicants:
AstraZeneca AB, NPS PHARMACEUTICALS, INC.
Inventors:
Louise Edwards, Methvin Isaac, Martin Johansson, Annika Kers, Johan Malmberg, Donald Mcleod, Alexander Minidis, Karin Staaf, Abdelmalik Slassi, Tomislav Stefanac, Thomas Stormann, David Wensbo, Tao Xin, Jalaj Arora
Abstract: The invention provides new triazolo[4,5-d]pyrimidine compounds, their use as medicaments, compositions containing them and processes for their preparation.
Type:
Grant
Filed:
September 21, 2005
Date of Patent:
July 31, 2007
Assignee:
AstraZeneca AB
Inventors:
David Hardern, Anthony Ingall, Brian Springthorpe, Paul Willis, Simon Guile
Abstract: The invention provides new forms of a chemical compound of formula (I). The invention relates to forms of a chemical compound (I), in particular to crystalline and amorphous forms, more particularly four crystalline forms and an amorphous form. The invention further relates to processes for the preparation of such forms, to pharmaceutical compositions comprising the compound in crystalline and/or amorphous form and to therapeutic use of such forms.
Type:
Application
Filed:
October 3, 2005
Publication date:
July 26, 2007
Applicant:
AstraZeneca AB
Inventors:
Martin Bohlin, Steve Cosgrove, Bo Lassen
Abstract: A radioactive compound having the formula: and pharmaceutically-acceptable salts thereof, wherein R1 and Ar are as defined in the specification, enantiomers, in vivo-hydrolysable precursors, pharmaceutical compositions and formulations containing them, methods of using them to treat diseases and conditions either alone or in combination with other therapeutically-active compounds or substances, processes and intermediates used to prepare them and uses of them for diagnostic and analytic purposes.
Type:
Application
Filed:
September 24, 2004
Publication date:
July 26, 2007
Applicant:
AstraZeneca AB
Inventors:
Peter Dorff, John Gordon, John Heys, Richard Keith, Dennis Mccarthy, Mark Smith, Eifion Phillips
Abstract: A method for determining the release of a peptide from a sustained release polylactide formulation which can be carried out in a shorter time than a real-time method by accelerating the release of the peptide from the formulation. It can be used to discriminate between batches of formulations for quality control purposes and to discriminate between formulations, for example, having different drug loadings.
Type:
Grant
Filed:
October 5, 2001
Date of Patent:
July 24, 2007
Assignee:
AstraZeneca AB
Inventors:
Brian Collingwood Clark, David Michael Cross, Paul Richard Gellert, Rodney Simon Kittlety
Abstract: The invention relates to a group of novel thieno-pyrrole compounds of Formula (I) wherein: R1, R2, R3, R4 and R5 are as defined in the specification, which are useful as gonadotrophin releasing hormone antagonists. The invention also relates to pharmaceutical formulations of said compounds, methods of treatment using said compounds and to processes for the preparation of said compounds.
Type:
Application
Filed:
February 17, 2005
Publication date:
July 19, 2007
Applicant:
ASTRAZENECA AB
Inventors:
Jean-Claude Arnould, Craig Harris, Paul Jones
Abstract: Compounds of formula (I) or pharmaceutically acceptable salts thereof: Formula (I) wherein R1, R2, RF1, RF2 and Z are as defined in the specification as well as salts and pharmaceutical compositions including the compounds are prepared.
Type:
Grant
Filed:
June 9, 2004
Date of Patent:
July 17, 2007
Assignee:
AstraZeneca AB
Inventors:
Daniel Pagé, Christopher Walpole, Hua Yang
Abstract: Compounds of formula (I): wherein L is CH or N; M is CH or N; provided that L and M are not both CH; compositions comprising them, processes for preparing them and their use in medical therapy (for example modulating CCR5 receptor activity in a warm blooded animal).
Abstract: Compounds of general formula: wherein n, R1, R2, R3, R4 and Ar are as defined in the specification, as well as salts, enantiomers thereof and pharmaceutical compositions including the compounds are prepared. They are useful in therapy, in particular in the management of pain.
Type:
Application
Filed:
February 2, 2005
Publication date:
July 12, 2007
Applicant:
ASTRAZENECA AB
Inventors:
Yun-Jin Hu, Miroslaw Tomaszewski, Christopher Walpole
Abstract: There is provided compounds of formula I wherein R1, Rx, Y, Ry, n and B have meanings given in the description which are useful as competitive inhibitors of trypsin-like proteases, such as thrombin, and in particular in the treatment of conditions where inhibition of thrombin is required (e.g. thrombosis) or as anticoagulants.
Abstract: The present invention relates to certain phenalkyloxy-phenyl derivatives of formula (I) and analogs, to a process for preparing such compounds, having the utility in clinical conditions associated with insulin resistance, to methods for their therapeutic use and to pharmaceutical compositions containing them.
Type:
Grant
Filed:
May 30, 2003
Date of Patent:
July 10, 2007
Assignee:
Astrazeneca AB
Inventors:
Jonas Fagerhad, Lanna Li, Lindstedt Alstermark Eva-Lotte
Abstract: Compounds of general formula:[Chemical formula should be inserted here. Please see paper copy] wherein R1, R2, and R3 are as defined in the specification, as well as salts, enantiomers thereof and pharmaceutical compositions including the compounds are prepared.
Abstract: The present invention provides a compound of a formula (I): wherein the variables are defined herein; to a process for preparing such a compound; and to the use of such a compound in the treatment of a chemokine (such as CCR3) or H1 mediated disease state.
Type:
Grant
Filed:
May 13, 2003
Date of Patent:
July 3, 2007
Assignee:
AstraZeneca AB
Inventors:
Aaron Rigby, Hitesh Sanganee, Brian Springthorpe, Louise Lawrence
Abstract: The present invention is directed to a novel neurotensin-like receptor expressed in the central nervous system of humans. The invention encompasses the receptor protein as well as nucleic acids encoding the protein. In addition, the invention is directed to methods and compositions which utilize the receptor.
Type:
Grant
Filed:
July 14, 2004
Date of Patent:
July 3, 2007
Assignee:
Astrazeneca Canada Inc.
Inventors:
Sultan Ahmad, Jack Cao, Dajan O'Donnell, Philippe Walker
Abstract: The invention provides a compound of formula (I): T is C(O) or S(O)2; W is CH2, (CH2)2, CH(CH3), CH(CH3)O or cyclopropyl; X is O, CH2, C(O), S, S(O), S(O)2 or NR3; m is 0 or 1; R1 is optionally substituted aryl or optionally substituted heterocyclyl; R2 is alkyl (optionally substituted by OH), cycloalkyl, optionally substituted aryl or optionally substituted heterocyclyl; that are modulators of chemokine (especially CCR3) activity and are especially useful for treating asthma and/or rhinitis.
Abstract: The present invention relates to compounds of formula (I): wherein Rv, R1, R2, Rx, Ry, R3, R4, R5, R6, Rz and v are as defined within; pharmaceutically acceptable salts, solvates, solvates or such salts and prodrugs thereof and their use as ileal bile acid transport (IBAT) inhibitors for the treatment of hyperlipidaemia. Processes for their manufacture and pharmaceutical compositions containing them are also described.
Type:
Grant
Filed:
April 23, 2003
Date of Patent:
July 3, 2007
Assignee:
AstraZeneca AB
Inventors:
Ingemar Starke, Mikael Ulf Johan Dahlstrom, Mats Peter Nordberg, Suzanne Alenfalk, Andreas Christer Wallberg, Stig Jonas Bostrom
Abstract: This invention relates to novel compounds having the structural diagram (I) and to their pharmaceutical compositions and to their methods of use. These novel compounds provide a treatment or prophylaxis of cancer.
Type:
Application
Filed:
March 10, 2004
Publication date:
June 28, 2007
Applicant:
AstraZeneca AB
Inventors:
Susan Ashwell, Jayachandran Ezhuthachan, Paul Lyne, Nicholas Newcombe, Martin Pass, Vibha Oza, Mei Su, Dorin Toader, Dingwei Yu, Yan Yu
Abstract: The present invention relates to certain novel guanidine or amidine acid derivatives and analogs, to a process for preparing such compounds, having the utility in clinical conditions associated with insulin resistance, to methods for their therapeutic use and to pharmaceutical compositions containing them.