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Icos Corporation Patents
Assignee:
Icos Corporation
Address:
Bothell, WA
No. of patents:
143
Patents:


1 2 3


Patent Number Title Of Patent Date Issued
7608618 Urea or thiourea substituted 1,4-pyrazine compounds useful as anti-cancer agents and for inhibit October 27, 2009
Compounds of the formula ##STR00001## wherein: Y' is O or S, W' is ##STR00002## optionally substituted, Z' is selected from the group consisting of ##STR00003## wherein Q' is OR.sup.7 and R.sup.7 is C.sub.1-3alkyleneC.sub.3-8heterocycloalkyl useful in the treatment of diseases and
7560462 Compounds useful for inhibiting CHK1 July 14, 2009
Substituted urea compounds useful in the treatment of diseases and C.sub.1-3alkyleneOR.sup.3 conditions related to DNA damage or lesions in DNA replication are disclosed formula (I), wherein X.sup.1 is null, --O--, --S--, --CH.sub.2--, or --N(R.sup.1)--; X.sup.2 is --O--, . -.English
7179912 Materials and methods to potentiate cancer treatment February 20, 2007
Compounds that inhibit DNA-dependent protein kinase, compositions comprising the compounds, methods to inhibit the DNA-PK biological activity, methods to sensitize cells the agents that cause DNA lesions, and methods to potentiate cancer treatment are disclosed.
7176229 Cyclic AMP-specific phosphodiesterase inhibitors February 13, 2007
Novel pyrrolidine compounds that are potent and selective inhibitors of PDE4, as well as methods of making the same, are disclosed. Use of the compounds in the treatment of inflammatory diseases and other diseases involving elevated levels of cytokines, as well as central nervous system
7087634 Cyclic AMP-specific phosphodiesterase inhibitors August 8, 2006
Pyrazole compounds that are potent and selective inhibitors of PDE4, as well as methods of making the same, are disclosed. Use of the compounds in the treatment of inflammatory diseases and other diseases involving elevated levels of cytokines, as well as central nervous system (CNS)
7067506 Compounds useful for inhibiting Chk1 June 27, 2006
Aryl- and heteroaryl-substituted urea compounds useful in the treatment of diseases and conditions related to DNA damage or lesions in DNA replication are disclosed. Methods of making the compounds, and their use as therapeutic agents, for example, in treating cancer and other diseases
7018627 Macrophage derived chemokine (MDC), MDC analogs, MDC inhibitor substances, and uses thereof March 28, 2006
The present invention provides purified and isolated polynucleotide sequences encoding a novel macrophage-derived C--C chemokine designated "Macrophage Derived Chemokine" (MDC), and polypeptide fragments and analogs thereof. Also provided are materials and methods for the recombinant
6998416 Cyclic AMP-specific phosphodiesterase inhibitors February 14, 2006
Novel pyrrolidine compounds that are potent and selective inhibitors of PDE4, as well as methods of making the same, are disclosed. Use of the compounds in the treatment of inflammatory diseases and other diseases involving elevated levels of cytokines, as well as central nervous system
6989260 Human poly(ADP-ribose) polymerase 2 materials and methods January 24, 2006
The invention provides a novel human poly(ADP-ribose) polymerase (hPARP2) polypeptides, polynucleotides encoding the polypeptides, expression constructs comprising the polynucleotides, and host cells transformed with the expression constructs. Also provided are methods for producing
6949535 Inhibitors of human phosphatidyl-inositol 3-kinase delta September 27, 2005
Methods of inhibiting phosphatidylinositol 3-kinase delta isoform (PI3K.delta.) activity, and methods of treating diseases, such as disorders of immunity and inflammation, in which PI3K.delta. plays a role in leukocyte function are disclosed. Preferably, the methods employ active age
6924284 PARP inhibitors August 2, 2005
The present invention provides compounds comprising a bicyclic aryl moiety, such as 2H-phthalazin-1-one or derivatives thereof, compositions comprising the same, and methods for producing and using the same. In particular, the present invention provides compounds of the formula: ##ST
6864070 Phosphodiesterase 10 March 8, 2005
The present invention provides novel human PDE10 polypeptides, polynucleotides encoding the polypeptides, expression constructs comprising the polynucleotides, host cells transformed with the expression constructs; methods for producing PDE10 polypeptides; antisense polynucleotides;
6818743 I-CAM related protein November 16, 2004
DNA sequences encoding a novel human intercellular adhesion molecule polypeptide (designated "ICAM-R") and variants thereof are disclosed along with methods and materials for production of the same by recombinant procedures. Antibodies substances specific for ICAM-R and variants thereof
6815532 ATR-2 cell cycle checkpoint November 9, 2004
Polynucleotides encoding novel Atr-2 cell cycle checkpoint polypeptides are disclosed, along with expression constructs comprising the polynucleotides, host cells transformed with the expression constructs, methods to make the Atr-2 polypeptides using the host cells, Atr-2 polypeptid
6797811 Antibodies to chemokine receptor 88C September 28, 2004
The present invention provides polynucleotides that encode the chemokine receptors 88-2B or 88C and materials and methods for the recombinant production of these two chemokine receptors. Also provided are assays utilizing the polynucleotides which facilitate the identification of lig
6790947 Polynucleotides encoding macrophage derived chemokine September 14, 2004
The present invention provides purified and isolated polynucleotide sequences encoding a novel human macrophage-derived C--C chemokine designated MDC. Also provided are materials and methods for the recombinant production of the chemokine, and purified and isolated chemokine protein.
6787542 Aryl phenylheterocyclyl sulfide derivatives and their use as cell adhesion-inhibiting anti-infla September 7, 2004
The present invention relates to novel heterocyclyl-containing diaryl sulfide compounds that are useful for treating inflammatory and immune diseases, to pharmaceutical compositions comprising these compounds, and to methods of inhibiting inflammation or suppressing immune response in a
6784179 Tetracyclic derivatives, process of preparation and use August 31, 2004
A compound of formula (I) ##STR1##and salts and solvates thereof, in which: R.sup.0 represents hydrogen, halogen or C.sub.1-6 alkyl; R.sup.1 represents hydrogen, C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.2-6 alkynyl, halo C.sub.1-6 alkyl, C.sub.3-8 cycloalkyl, C.sub.3-8 cycloalkylC
6737513 Macrophage derived chemokine (MDC) and chemokine analogs and assay to identify modulators of MDC May 18, 2004
The present invention provides purified and isolated polynucleotide sequences encoding a novel human macrophage-derived C-C chemokine designated Macrophage Derived Chemokine (MDC), and polypeptide analogs thereof Also provided are materials and methods for the recombinant production
6737059 Methods of inhibiting inflammatory processes and alleviating symptoms associated with multiple s May 18, 2004
Disclosed are methods for the alleviation of symptoms associated with inflammatory disease states, and more particularly to the inhibition of inflammatory disease processes associated with the multiple sclerosis disease, by adminstering to a patient a phamaceutically effective amount
6734003 Phosphodiesterase 10 May 11, 2004
The present invention provides novel human PDE10 polypeptides, polynucleotides encoding the polypeptides, expression constructs comprising the polynucleotides, host cells transformed with the expression constructs; methods for producing PDE10 polypeptides; antisense polynucleotides;
6716871 Cyclic AMP-specific phosphodie sterase inhibitors April 6, 2004
Novel pyrrolidine compounds that are potent and selective inhibitors of PDE4, as well as methods of making the same, are disclosed. Use of the compounds in the treatment of inflammatory diseases and other diseases involving elevated levels of cytokines, as well as central nervous system
6680336 Cyclic AMP-specific phosphodiesterase inhibitors January 20, 2004
Novel compounds that are potent and selective inhibitors of PDE4, as well as methods of making the same, are disclosed. Use of the compounds in the treatment of inflammatory diseases and other diseases involving elevated levels of cytokines, as well as central nervous system (CNS) disord
6667300 Inhibitors of human phosphatidylinositol 3-kinase delta December 23, 2003
Methods of inhibiting phosphatidylinositol 3-kinase delta isoform (PI3K.delta.) activity, and methods of treating diseases, such as disorders of immunity and inflammation, in which PI3K.delta. plays a role in leukocyte function are disclosed. Preferably, the methods employ active age
6620915 Monoclonal antibodies specific for integrin .alpha.-d subunit September 16, 2003
The present invention relates to monoclonal antibodies immunospecific for .alpha..sub.d integrin, and antibodies that compete with said antibodies for .alpha..sub.d binding.
6608065 Use of cGMP phosphodiesterase inhibitors in methods to treat female sexual dysfunction August 19, 2003
The use of (6R, 12aR)-2,3,6,7,12,12a-hexahydro-2-methyl-6-(3,4-methylenedioxyphenyl)-pyraz ino[2',1':6,1]pyrido[3,4-b]indole -1,4-dione, (3S, 6R, 12aR)-2,3,6,7,12,12a-hexahydro-2,3-dimethyl-6-(3,4-methylenedioxyphenyl)py razino[2', 1':6,1]pyrido[3,4-b]indole-1,4-dione, and physiologica
6599727 Human poly (ADP-ribose) polymerase 2 materials and methods July 29, 2003
The invention provides a novel human poly(ADP-ribose) polymerase (hPARP2) polypeptides, polynucleotides encoding the polypeptides, expression constructs comprising the polynucleotides, and host cells transformed with the expression constructs. Also provided are methods for producing the
6569890 Cyclic AMP-specific phosphodiesterase inhibitors May 27, 2003
Pyrrole compounds that are potent and selective inhibitors of PDE4, as well as methods of making the same, are disclosed. Use of the compounds in the treatment of inflammatory diseases and other diseases involving elevated levels of cytokines, as well as central nervous system (CNS) diso
6569885 Cyclic AMP-specific phosphodiesterase inhibitors May 27, 2003
Pyrazole compounds that are potent and selective inhibitors of PDE4, as well as methods of making the same, are disclosed. Use of the compounds in the treatment of inflammatory diseases and other diseases involving elevated levels of cytokines, as well as central nervous system (CNS)
6566087 Phosphodiesterase 8A May 20, 2003
The present invention provides novel human PDE8 polypeptides, polynucleotides encoding the polypeptides, expression constructs comprising the polynucleotides, host cells transformed with the expression constructs; methods for producing PDE8 polypeptides; antisense polynucleotides; an
6521619 Aryl phenylcyclopropyl sulfide derivatives and their use as cell adhesion inhibiting anti-inflam February 18, 2003
The present invention relates to novel cyclopropane-containing diaryl sulfide compounds that are useful for treating inflammatory and immune diseases, to pharmaceutical compositions comprising these compounds, and to methods of inhibiting inflammation or suppressing immune response in a
6518277 Inhibitors of human phosphatidylinositol 3-kinase delta February 11, 2003
Methods of inhibiting phosphatidylinositol 3-kinase delta isoform (PI3K.delta.) activity, and methods of treating diseases, such as disorders of immunity and inflammation, in which PI3K.delta. plays a role in leukocyte function are disclosed. Preferably, the methods employ active age
6500856 Cyclic AMP-specific phosphodiesterase inhibitors December 31, 2002
Novel compounds that are potent and selective inhibitors of PDE4, as well as methods of making the same, are disclosed. Use of the compounds in the treatment of inflammatory diseases and other diseases involving elevated levels of cytokines, as well as central nervous system (CNS) disord
6498015 Methods of identifying agents that modulate the binding between MDC and an MDC receptor December 24, 2002
The present invention provides purified and isolated polynucleotide sequences encoding a novel human macrophage-derived C-C chemokine designated Macrophage Derived Chemokine (MDC), and polypeptide analogs thereof. Also provided are materials and methods for the recombinant production
6486186 Thiazole compounds as cyclic AMP-specific phosphodiesterase inhibitors and method of using the s November 26, 2002
Novel compounds that are potent and selective inhibitors of PDE4, as well as methods of making the same, are disclosed. Use of the compounds in the treatment of inflammatory diseases and other diseases involving elevated levels of cytokines, as well as central nervous system (CNS) disord
6479256 Lectomedin materials and methods November 12, 2002
Disclosed are novel seven transmembrane receptor polypeptides having characteristic extracellular structure including lectin-binding, olfactomedin-like and mucin-like domains.
6462047 Carboline derivatives as cGMP phosphodiesterase inhibitors October 8, 2002
Compounds of general structural formula (I) wherein A represents a 5- or 6-membered heteroaryl group containing at least one heteroatom selected from the group consisting of oxygen, nitrogen, and sulfur, and use of the compounds, and salts and solvates thereof, as therapeutic agents, are
6458787 Cyclic AMP-specific phosphodiesterase inhibitors October 1, 2002
Novel pyrrolidine compounds that are potent and selective inhibitors of PDE4, as well as methods of making the same, are disclosed. Use of the compounds in the treatment of inflammatory diseases and other diseases involving elevated levels of cytokines, as well as central nervous system
6455562 Cyclic AMP-specific phosphodiesterase inhibitors September 24, 2002
Novel compounds that are potent and selective inhibitors of PDE4, as well as methods of making the same, are disclosed. Use of the compounds in the treatment of inflammatory diseases and other diseases involving elevated levels of cytokines, as well as central nervous system (CNS) disord
6444671 Cyclic AMP-specific phosphodiesterase inhibitors September 3, 2002
Novel compounds that are potent and selective inhibitors of PDE4, as well as methods of making the same, are disclosed. Use of the compounds in the treatment of inflammatory diseases and other diseases involving elevated levels of cytokines, as well as central nervous system (CNS) disord
6432404 Methods of inhibiting locomotor damage following spinal cord injury with .alpha. D-specific anti August 13, 2002
Methods to treat spinal cord injury using .alpha..sub.d monoclonal antibodies are disclosed.
6423710 Cyclic AMP-specific phosphodiesterase inhibitors July 23, 2002
Novel pyrrolidine compounds that are potent and selective inhibitors of PDE4, as well as methods of making the same, are disclosed. Use of the compounds in the treatment of inflammatory diseases and other diseases involving elevated levels of cytokines, as well as central nervous system
6399571 Chitinase chitin-binding fragments June 4, 2002
The present invention provides chitin-binding fragments of human chitinase, fragment analogs, purified and isolated polynucleotide sequences encoding such fragments and analogs, and materials and methods for the recombinant production of human chitinase fragment products which are expect
6376489 Cyclic AMP-specific phosphodiesterase inhibitors April 23, 2002
Novel compounds that are potent and selective inhibitors of PDE4, as well as methods of making the same, are disclosed. Use of the compounds in the treatment of inflammatory disease and other diseases involving elevated levels of cytokines, as well as central nervous system (CNS) disorde
6372777 Cyclic AMP-specific phosphodiesterase inhibitors April 16, 2002
Pyrrole compounds that are potent and selective inhibitors of PDE4, as well as methods of making the same, are disclosed. Use of the compounds in the treatment of inflammatory diseases and other diseases involving elevated levels of cytokines, as well as central nervous system (CNS) diso
6372212 Chitinase materials and methods April 16, 2002
The present invention provides purified and isolated polynucleotide sequences encoding human chitinase. Also provided are materials and methods for the recombinant production of human chitinase products which are expected to be useful as products for treating fungal infections or for
6369059 Tetracyclic derivatives, process of preparation and use April 9, 2002
A compound of formula (I) ##STR1##and salts and solvates thereof, in which:R.sup.0 represents hydrogen, halogen or C.sub.1-6 alkyl;R.sup.1 represents hydrogen, C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.2-6 alkynyl, haloC.sub.1-6 alkyl, C.sub.3-8 cycloalkyl, C.sub.3-8 cycloalkylC.sub.1-3
6362213 Cyclic AMP-specific phosphodiesterase inhibitors March 26, 2002
Novel compounds that are potent and selective inhibitors of PDE4, as well as methods of making the same, are disclosed. Use of the compounds in the treatment of inflammatory diseases and other diseases involving elevated levels of cytokines, as well as central nervous system (CNS) disord
6350603 Phosphodiesterase 10 February 26, 2002
The present invention provides novel human PDE10 polypeptides, polynucleotides encoding the polypeptides, expression constructs comprising the polynucleotides, host cells transformed with the expression constructs; methods for producing PDE10 polypeptides; antisense polynucleotides;
6348602 Cyclic AMP-specific phosphodiesterase inhibitors February 19, 2002
Novel compounds that are potent and selective inhibitors of PIDE4, as well as methods of making the same, are disclosed. Use of the compounds in the treatment of inflammatory diseases and other diseases involving elevated levels of cytokines, as well as central nervous system (CNS) disor
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