Compounds for Treating Protein-Kinase Mediated Disorders

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United States of America Patent

APP PUB NO 20080275029A1
SERIAL NO

11718943

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ATTORNEY / AGENT: (SPONSORED)

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Abstract

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The invention provides a compound of the formula (I) or a salt, solvate, tautomer or N-oxide thereof for use in the treatment or prophylaxis of a disease state or condition mediated by protein kinase A and/or protein kinase B; wherein the ring Q is a benzene ring; J.sup.2-J.sup.1 is N.dbd.CR.sup.7 or R.sup.1aN--CO; G is OH or NR.sup.5R.sup.6; E is CONR.sup.7, NR.sup.7CO, C(R.sup.8).dbd.C(R.sup.8) or (X).sub.m(CR.sup.8R.sup.8a).sub.n where X is O, S or NR.sup.7; provided that when J.sup.2-J.sup.1 is R.sup.1aN--CO, E is other than NR.sup.7CO; m and n are each 0 or 1, where m+n=1 or 2; A is a bond and R.sup.4 and R.sup.4a are absent or A is a saturated optionally substituted C.sub.1-7 hydrocarbon linker group having a maximum chain length of 5 atoms extending between E and G, one carbon atom in the linker group A being optionally replaced by O or N; R.sup.1, R.sup.1a, R.sup.2, and R.sup.3 are each H; halogen; C.sub.1-6 hydrocarbyl optionally substituted by halogen, OH or C.sub.1-2 alkoxy; CN; CONHR.sup.8; NH.sub.2; NHCOR.sup.10 or NHCONHR.sup.10; R.sup.4 is H or C.sub.1-4 alkyl; R.sup.4a is H, C.sub.1-4 alkyl or a group R.sup.9; R.sup.5 and R.sup.6 are each selected from H, R.sup.9 and C.sub.1-4 hydrocarbyl optionally substituted by halogen, C.sub.1-2 alkoxy or R.sup.9; or NR.sup.5R.sup.6 forms a saturated 4-7 membered monocyclic heterocyclic group; R.sup.7 is H or C.sub.1-4 alkyl; R.sup.8 and R.sup.8a each H or saturated C.sub.1-4 hydrocarbyl optionally substituted by fluorine; R.sup.9 is a monocyclic or bicyclic carbocyclic or heterocyclic group containing up to 3 ring heteroatoms selected from N, O and S; or R.sup.4, R.sup.4a and A together form a saturated monocyclic 4-7 membered heterocycle; or NR.sup.5R.sup.6, R.sup.4 and A form a saturated 4-7 membered monocyclic heterocycle; or R.sup.4, together with R.sup.7 or R.sup.8 and A and E form a 4-7 membered saturated monocyclic heterocycle; or NR.sup.5R.sup.6 and R.sup.7 or R.sup.8 together with A and E form a 4-7 membered saturated monocyclic heterocycle; and R.sup.10 is optionally substituted phenyl or benzyl.

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Patent Owner(s)

Patent OwnerAddress
CANCER RESEARCH TECHNOLOGY LIMITEDANGEL BUILDING 407 ST JOHN STREET LONDON EC1V4AD
ASTEX THERAPEUTICS LIMITEDCAMBRIDGE CAMBRIDGESHIRE CB4 0QA
THE INSTITUTE OF CANCER RESEARCH ROYAL CANCER HOSPITAL123 OLD BROMPTON ROAD LONDON SW7 3RP

International Classification(s)

Inventor(s)

Inventor Name Address # of filed Patents Total Citations
Berdini, Valerio Cambridge, GB 63 1305
Boyle, Robert George Cambridge, GB 36 393
Caldwell, John Sutton, GB 76 1581
Collins, Ian Redhill, GB 93 1712
Saxty, Gordon Cambridge, GB 55 1129
Sore, Hannah Fiona Cambridge, GB 11 102
Verdonk, Marinus Leendert Burwell, GB 13 119
Walker, David Winter Cambridge, GB 25 158
Woodhead, Steven John Cambridge, GB 32 655
Wyatt, Paul Graham Perth, GB 40 681

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