Abstract: The invention relates to new heterocyclic compounds of general formula (I), and their salts with a base or an acid: The invention also relates to a process for the preparation of these compounds as well as their use as medicaments, in particular as anti-bacterial agents.
Type:
Grant
Filed:
June 7, 2007
Date of Patent:
April 3, 2012
Assignee:
AstraZeneca
Inventors:
Joseph Aszodi, Maxime Lampilas, Branislav Musicki, David Alan Rowlands, Pascal Colette
Abstract: Polymorphs of N,N-diethyl-4-(3-fluorophenyl-piperidin-4-ylidene-methyl)-benzamide hydrochloride salt, methods of making these polymorphs and uses thereof are described.
Type:
Grant
Filed:
October 5, 2005
Date of Patent:
April 3, 2012
Assignee:
AstraZeneca AB
Inventors:
Simon Nicholas Black, Steve Cook, Louis Joseph Diorazio, James Hulsizer, Gary Moore, Kathryn Quigley
Abstract: The invention relates to substituted phenylacetic acids as useful pharmaceutical compounds for treating respiratory disorders, pharmaceutical compositions containing them, and processes for their preparation.
Type:
Grant
Filed:
October 5, 2006
Date of Patent:
April 3, 2012
Assignee:
AstraZeneca AB
Inventors:
Timothy Jon Luker, Rukhsana Tasneem Mohammed, Stephen Thom, Anil Patel
Abstract: The present invention relates to a new compound of formula (I) wherein R1 is hydrogen or fluoro; R2 and R3 are independently selected from hydrogen or methyl; or a pharmaceutically acceptable salt thereof, pharmaceutical formulations containing said compound, to the use of said active compound in therapy, to the use for the treatment of conditions associated with glycogen synthase kinase-3 related disorders, such as Alzheimer's disease, as well as for the method of treatment of said disorders, comprising administering to a mammal, including human in need of such treatment, a therapeutically effective amount of said compound.
Type:
Application
Filed:
April 14, 2010
Publication date:
March 29, 2012
Applicant:
ASTRAZENECA AB
Inventors:
Jeremy Nicholas Burrows, Per I. Arvidsson, Erica Tjerneld, Ulrika Yngve
Abstract: The present invention relates to new compounds of formula (I) and to pharmaceutical composition containing said compounds and to the use of said compounds in therapy. The present invention further relates to processes for the preparation of said compounds and to new intermediates useful in the preparation thereof.
Type:
Grant
Filed:
April 22, 2008
Date of Patent:
March 27, 2012
Assignee:
AstraZeneca AB
Inventors:
Yevgeni Besidski, Inger Kers, Martin Nylöf, Lars Sandberg, Karin Skogholm
Abstract: A compound of Formula (I): is useful in the treatment or prevention of a disease or medical condition mediated through glucokinase (GLK or GK), leading to a decreased glucose threshold for insulin secretion.
Type:
Grant
Filed:
August 4, 2009
Date of Patent:
March 27, 2012
Assignee:
Astrazeneca AB
Inventors:
Stuart Norman Lile Bennett, Roger John Butlin, Leonie Campbell, Robert Darren Morse Davies, Graeme Richard Robb, Rolf Peter Walker, Michael James Waring, Helen Claire Pointon, Mikael Dan Brink, Jonas Rickard Fägerhag, Ulrik Jurva, Volker Schnecke, Anette Marie Svensson Henriksson, Christer Ralf Westerlund, Peter Gustaf Bonn
Abstract: The invention relates to a formulation comprising formoterol and budesonide for use in the treatment of respiratory diseases. The composition further contains HFA 227, PVP and PEG, preferably PVP K25 and PEG 1000.
Abstract: The invention provides certain thiazolopyrimidine compounds of formula (I) or a pharmaceutically acceptable salt or solvate thereof, processes and intermediates used in their preparation, pharmaceutical compositions containing them and their use in therapy.
Type:
Grant
Filed:
April 29, 2009
Date of Patent:
March 27, 2012
Assignee:
AstraZeneca AB
Inventors:
Paul Andrew Willis, Roger Bonnert, Simon Fraser Hunt, Iain Alistair Stewart Walters
Abstract: Compounds of formula (I): The present invention relates to novel indazolyl ester or amide derivatives, to pharmaceutical compositions comprising such derivatives, to processes for preparing such novel derivatives and to the use of such derivatives as medicaments.
Inventors:
Markus Berger, Jan Dahmén, Karl Edman, Anders Eriksson, Balint Gabos, Thomas Hansson, Martin Hemmerling, Krister Henriksson, Svetlana Ivanova, Matti Lepistö, Darren McKerrecher, Magnus Munck af Rosenschöld, Stinabritt Nilsson, Hartmut Rehwinkel, Camilla Taflin
Abstract: The invention provides methods for treating a patient having type 2 diabetes who has failed on previous regimens of one or more oral and/or injectable anti-diabetic agents, which include the step of administering a therapeutically effective amount of an SGLT2 inhibitor alone or in combination with another anti-diabetic agent and/or other therapeutic agent to such patient. A pharmaceutical composition containing dapagliflozin or dapagliflozin-S-propylene glycol solvate and one or more diabetic agents and/or other therapeutic agents for use in the methods of the invention is also provided.
Type:
Application
Filed:
May 26, 2010
Publication date:
March 22, 2012
Applicants:
ASTRAZENECA UK LIMITED, BRISTOL-MYERS SQUIBB COMPANY
Inventors:
Paul Strumph, Stephanie Moran, James List
Abstract: A compound of formula (I) or a pharmaceutically acceptable salt thereof, processes for their preparation, pharmaceutical compositions containing them and their use in therapy, for example in the treatment of proliferative disease such as cancer and particularly in disease mediated by an mTOR kinase and/or one or more PI3K enzyme.
Abstract: The present invention provides 8-oxoadenine derivatives, processes for their preparation, pharmaceutical compositions containing them and their use in therapy. The 8-oxoadenine derivatives act as modulators of Toll-like Receptor (TLR) 7 and thus may be used in the treatment of asthma, hepatitis, allergic diseases, viral and bacterial infection as well as cancer.
Type:
Grant
Filed:
July 3, 2007
Date of Patent:
March 20, 2012
Assignees:
AstraZeneca AB, Dainippon Sumitomo Pharma Co Ltd.
Inventors:
Anthony Cook, Tom McInally, Stephen Thom, Hiroki Wada
Abstract: The present invention relates to pyrazinone derivatives of formula (I): wherein R1, R2, R3, R4, R5, R6 and R7 are as herein defined; processes for their preparation, pharmaceutical compositions containing them and their use in therapy.
Type:
Application
Filed:
June 26, 2008
Publication date:
March 15, 2012
Applicant:
AstraZeneca AB
Inventors:
Stephen BROUGH, Richard Evans, Timothy Jon Luker, Piotr Raubo
Abstract: Formula (I) wherein R1 is a (2-4C)alkyl and is substituted by two or more fluorine groups and R2 is methyl or ethyl, or a pharmaceutically acceptable salt thereof; processes for their preparation, pharmaceutical compositions containing them and their use in the treatment of diseases or medical conditions mediated by metalloproteinase enzymes.
Abstract: This invention relates to novel compounds having the formula (I); and to their pharmaceutical compositions and to their methods of use. These novel compounds provide a treatment for cancer.
Type:
Grant
Filed:
February 15, 2006
Date of Patent:
March 6, 2012
Assignee:
AstraZeneca AB
Inventors:
Michelle Lamb, Tao Wang, Dingwei Yu, Peter Mohr, Bin Wang
Abstract: Compounds of general formula: 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, depression and anxiety.
Type:
Grant
Filed:
December 22, 2009
Date of Patent:
March 6, 2012
Assignee:
AstraZeneca AB
Inventors:
William Brown, Andrew Griffin, Thomas Hudzik, Carla Maciag, Gennady Smagin, Christopher Walpole
Abstract: A compound of the formula (I): wherein: A and B together represent an optionally substituted, fused aromatic ring; X and Y are selected from CH and CH, CF and CH, CH and CF and N and CH respectively; RC is selected from H, C1-4 alkyl; and R1 is selected from C1-7 alkyl, C3-20 heterocyclyl and C5-20 aryl, which groups are optionally substituted; or RC and R1 together with the carbon and oxygen atoms to which they are attached form a spiro-C5-7 oxygen-containing heterocyclic group, which is optionally substituted or fused to a C5-7 aromatic ring.
Type:
Grant
Filed:
January 22, 2009
Date of Patent:
March 6, 2012
Assignee:
AstraZeneca AB
Inventors:
Keith Allan Menear, Muhammad Hashim Javaid, Sylvie Gomez, Marc Geoffrey Hummersone, Carlos Fenandez Lence, Niall Morrison Barr Martin, David Alan Rudge, Craig Anthony Roberts, Kevin Blades
Abstract: There is provided a compound of formula (I): or a pharmaceutically acceptable salt thereof. There are also provided processes for the manufacture of a compound of Formula 1, and the use of a compound of Formula 1 as a medicament and in the treatment of cancer.
Type:
Grant
Filed:
April 30, 2010
Date of Patent:
March 6, 2012
Assignee:
AstraZeneca AB
Inventors:
Kevin Michael Foote, Maria-Elena Theoclitou, Andrew Peter Thomas, David Buttar
Abstract: The disclosure relates to an inhaler, comprising an outlet and a plurality of sealed compartments containing medicament. An opening mechanism is provided to open the compartment presently aligned with the outlet. An indexing mechanism sequentially aligns the compartments with the outlet. A latch is provided for latching the opening mechanism in an energized position. The latch cannot latch the opening mechanism before the indexing mechanism has aligned the next compartment with the outlet. The disclosure also relates to a method of priming an inhaler and a method of dispensing a medicament from an inhaler.
Type:
Application
Filed:
October 7, 2009
Publication date:
March 1, 2012
Applicant:
ASTRAZENECA AB
Inventors:
John Briant, Patrick Campbell, Charles Cooke, Christopher Groombridge, Daniel James John, John Trevor Penhallurick, Nicholas Smartt, Nicholas Harrison, William Bakewell
Abstract: The present invention relates to compounds of Formula V(A): that demonstrate antibacterial activity, processes for their preparation, pharmaceutical compositions containing them as the active ingredient, to their use as medicaments and to their use in the manufacture of medicaments for use in the treatment of bacterial infections in warm-blooded animals such as humans. In particular this invention relates to compounds of Formula V(A) useful for the treatment of bacterial infections in warm-blooded animals such as humans, more particularly to the use of these compounds in the manufacture of medicaments for use in the treatment of bacterial infections in warm-blooded animals such as humans.
Type:
Grant
Filed:
December 9, 2010
Date of Patent:
February 28, 2012
Assignee:
AstraZeneca AB
Inventors:
Gloria Breault, Charles Joseph Eyermann, Bolin Geng, Marshall Morningstar, Folkert Reck