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AstraZeneca AB Patents
Assignee:
AstraZeneca AB
Address:
Sodertalje, SE
No. of patents:
725
Patents:


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Patent Number Title Of Patent Date Issued
D582240 Blister pack device December 9, 2008
D578302 Container device October 14, 2008
D570171 Blister pack device June 3, 2008
D565838 Container device April 8, 2008
D561901 Device for communicating with a voice-disabled person February 12, 2008
D546198 Device for holding a blister pack July 10, 2007
D529605 Inhalation device October 3, 2006
D515203 Inhalation device February 14, 2006
D493519 Inhaler July 27, 2004
D483861 Injection device with pull off strip December 16, 2003
D480474 Inhaler October 7, 2003
D473298 Inhaler refill April 15, 2003
D461408 Device holder for a package August 13, 2002
D458366 Ampoule June 4, 2002
D455953 Blister pack April 23, 2002
D455345 Blister pack April 9, 2002
D455344 Blister pack April 9, 2002
D455212 Femoral fixture for a hip joint prosthesis April 2, 2002
D454781 Blister pack March 26, 2002
D454637 Connector March 19, 2002
D452735 Tie of an attachment for the trailing end of a urethral drainage tube January 1, 2002
D450382 Catheter November 13, 2001
D449882 Inhaler October 30, 2001
D449226 Container for medicinal dosage forms October 16, 2001
D448076 Inhaler September 18, 2001
D447560 Ampoule set September 4, 2001
D444225 Inhaler June 26, 2001
D443930 Rectal insertion device June 19, 2001
D443692 Abutment for temporary dental prosthesis June 12, 2001
7618993 Compounds November 17, 2009
The present invention relates to new compounds ##STR00001## or salts, solvates or solvated salts thereof, processes for their preparation and to new intermediates used in the preparation thereof, pharmaceutical compositions containing said compounds and to the use of said compounds
7615642 Therapeutic compounds November 10, 2009
Compounds of formula I or pharmaceutically acceptable salts thereof: ##STR00001## wherein R.sup.1, R.sup.2, R.sup.3 and R.sup.4 are as defined in the specification as well as salts and pharmaceutical compositions including the compounds are prepared. They are useful in therapy, in p
7615555 Piperidine derivatives as modulators of chemokine receptor CCR5 November 10, 2009
Compounds of formula (I): compositions comprising them, processes for preparing them and their use in medical therapy (for example modulating CCR5 receptor activity in a warm blooded animal). ##STR00001##
7615045 Hydrophilic urinary catheter having a water-containing sachet November 10, 2009
A wetting apparatus (110) for wetting a hydrophilic urinary catheter (103) comprises a wetting receptacle (101) which defines a wetting fluid receiving area (102) for receiving the hydrophilic urinary catheter and a hydrophilic urinary catheter wetting fluid container (106) having a
7612179 antibodies binding to a C-terminal fragment of apoliopoprotein E November 3, 2009
A human antibody fragment, which antibody or fragment: (i) binds to a polypeptide having the amino acid sequence shown in SEQ ID NO: 1 of the C-terminal domain of Apolipoprotein E (ApoE-CTD) or the amino acid sequence of a part thereof; and (ii) binds to human plaques.
7612077 Crystalline forms of the anti-cancer compound ZD1839 November 3, 2009
The invention concerns certain crystalline solvates and hydrates of the compound of the Formula (I) which is known inter alia by way of the code number ZD1839. In particular, the invention concerns a first solvate that occurs in the presence of methanol which is designated as Form 2 ZD18
7608628 Alkylsulphonamide quinolines October 27, 2009
Compounds of Formula II ##STR00001## wherein R.sup.1, A, R.sup.2, R.sup.3, R.sup.4, R.sup.5, R.sup.8, n, m and q are as described in the specification, pharmaceutically-acceptable salts, methods of making, pharmaceutical compositions containing and methods for using the same.
7598377 Inhibition of phosphoinositide 3-kinase .beta. October 6, 2009
The present invention relates to selective inhibitors of phosphoinositide (PI) 3-kinase .beta., use of the selective inhibitors in anti-thrombotic therapy, and a method for screening compounds useful for the new anti-thrombotic therapy by detecting selective inhibitory activity of PI
7595321 Compounds having selective inhibiting effect at GSK3 September 29, 2009
The present invention relates to new compounds of formula (I) wherein Z is N; Y is CONR.sup.5, NR.sup.5CO, SO.sub.2NR.sup.5, NR.sup.5SO.sub.2, CH.sub.2NR.sup.5, NR.sup.5, NR.sup.5CONR.sup.5, CH.sub.2CO, CO, O or CH.sub.2O; X is CH or N; P is phenyl or a 5 or 6 membered heteroaromatic
7595319 Compounds having selective inhibiting effect at GSK3 September 29, 2009
Selective phenyl substituted aminopyrazine inhibitors of GSK3 useful for the prevention and/or treatment of cognitive disorders.
7587988 Inhaler device counter September 15, 2009
Inhaler counter (20) comprising a counter housing (390), a rocker arm (200) with a pawl (210), the rocker arm being pivotally supported by the housing and arranged to perform a rocker movement in response to a linear actuation motion, a return spring (220) for resetting the rocker arm, a
7585881 Additional heteropolycyclic compounds and their use as metabotropic glutamate receptor antagonis September 8, 2009
The present invention relates to new compounds of formula I, ##STR00001## to pharmaceutical formulations containing the compounds, and to the use of the compounds in the prevention and/or treatment of mGluR5 receptor-mediated disorders.
7585867 Substituted thiazolo[4,5-d]pyrimidin-2(3H)-one September 8, 2009
A compound of formula (I) and pharmaceutically acceptable salts or solvates thereof for use in therapy. ##STR00001##
7585853 Compounds having selective inhibiting effect at GSK3 September 8, 2009
The present invention relates to new compounds of formula (I) wherein: Z is N and X is CH or N; Y is CONR.sup.5; P is phenyl or a 5 or 6 membered heteroaromatic ring containing one or more heteroatoms selected from N, O or S; Q is phenyl or a 5 or 6 membered aromatic heterocyclic ring
7582629 Derivatives of isothiazol-3(2H)-one 1,1-dioxides as liver X receptor modulators September 1, 2009
The present invention relates to certain novel compounds of the formula (I) to processes for preparing such compounds, to their the utility in modulation of nuclear hormone receptors Liver X Receptor (LXR) .alpha. (NR1H3) and/or .beta. (NR1H2) and in treating and/or preventing clinical
7579349 4-(pyrazol-3-ylamino) pyrimidine derivatives for use in the treatment of cancer August 25, 2009
A compound of Formula (I); wherein the substituents are as defined in the text for use in modulating insulin-like growth factor 1 receptor activity in a warm blooded animal such as man. ##STR00001##
7579344 Pyrimidine derivatives possessing cell-cycle inhibitors activity August 25, 2009
Compounds of the formula (I), and pharmaceutically acceptable salts and in vivo hydrolysable esters thereof are described. Also described are processes for their preparation and their use as medicaments, particularly medicaments for producing a cell cycle inhibitory (anti cell prolif
7576095 Therapeutic agents August 18, 2009
The present invention relates to 4,5-dihydropyrrolo[3,2-c]pyridin-4-one compounds of formula IA and processes for preparing such compounds, their use in the treatment of obesity, psychiatric and neurological disorders, to methods for their therapeutic use and to pharmaceutical compositio
7576093 Method of treatment of bone-related disorders or conditions August 18, 2009
The present invention relates to a new use of a compound of the formula (I) ##STR00001## wherein R.sub.1 is NH.sub.2, piperazin-1-yl, 4-methylpiperazin-1-yl,4-methyl-1,4-diazepan-1-yl or 4-ethylpiperazin-1-yl; R.sub.2 is hydrogen, fluoro, CH.sub.3, CH.sub.2CH.sub.3, OCH.sub.3, CF.su
7576077 Fused heterocyclic compounds and their use as metabotropic glutamate receptor antagonists August 18, 2009
The present invention is directed to compounds of formula I: ##STR00001## wherein X.sup.1, X.sup.2, X.sup.3, X.sup.4, X.sup.5, X.sup.6, X.sup.7, X.sup.8, X.sup.9, X.sup.10, R.sup.1, R.sup.2, R.sup.3, R.sup.4, and n are as defined for formula I in the description. The invention also relat
7572826 Thiophene-carboxamide derivatives and their use as inhibitors of the enzyme IKK-2 August 11, 2009
The invention relates to thiophene carboxamides of formula (I), wherein A, R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5 and X are as defined in the specification, processes and intermediates used in their preparation, pharmaceutical compositions containing them and their use in therapy.
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