http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AR-059064-A1

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publicationDate 2008-03-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber AR-059064-A1
titleOfInvention TIAZOL COMPOUNDS, PHARMACEUTICAL COMPOSITIONS THAT CONTAIN THEM AND USES IN THE TREATMENT OF DISEASES MEDIATED BY PROTEIN KINASE B (PKB), SUCH AS CANCER.
abstract Claim 1: A compound of the formula (1) wherein: A is as shown in the formula (2) or aryl; Y is -N (R5) R6 or -OR6; X is O, S, or -N (R7); R1 is R8, -CHR11-N (H) -R8, -CHR11-O-R8, C2-6 alkynyl, C2-6 hydroxyalkynyl or -C ::: N; R2 is aryl or heteroaryl; R3 is -H, C1-6 alkyl, which may be interrupted by one or more heteroatoms, - (CR9R10) t (aryl), - (CR9R 10) t (heteroaryl), - (CR9R10) t (cycloalkyl) or - ( CR9R10) t (heterocyclyl); R4 is C1-6 alkyl, which may be interrupted by one or more heteroatoms, - (CR9R10) t (aryl), - (CR9R 10) t (heteroaryl), - (CR9R10) t (cycloalkyl) or - (CR9R10) t (heterocyclyl); or R3 and R4, together with the carbon atom to which both are bonded, join to form a C3-10 carbocyclic or heterocyclic ring system, or R4 and R7 join to form a C3-10 heterocyclic ring; R5 is -H, C1-8 alkyl, -C (O) (CR9R10) t) N (R7) 2, -C (O) (CR9R10) t -C (O) 2 (CR9R10) t, - (CR9R10) t (aryl), - (CR9R10) t (heteroaryl), - (CR9R10) t (cycloalkyl) or - (CR9R10) t (heterocyclyl), or R4 and R5 join to form a C3-10 heterocyclic ring; R6 and R7 are independently selected from -H, C1-8 alkyl, - (C1-6 alkyl) aryl, or -C (O) (C1-6 alkyl), or R6 and R7, together with the atoms to which they are linked, join to form a 5- to 6-membered heterocyclic ring, or R5 and R6, together with the nitrogen atom to which they are linked, join to form a 5- to 6-membered heterocyclic or heteroaryl ring; R8 is -H, C1-6 alkyl, - (C1-6 alkyl) aryl, aryl or heteroaryl; and R9, R10 and R11 are independently selected from -H, C1-6 alkyl or aryl; where n is an integer from 1 to 6; m is an integer from 0 to 2; and each t is, independently, an integer from 0 to 3; wherein each of the aforementioned alkyl, aryl, heteroaryl, cycloalkyl and heterocyclyl fractions, and heterocyclic and carbocyclic rings are optionally and independently substituted by 1 to 3 substituents which are selected from: amino, aryl, heteroaryl, cycloalkyl or heterocyclyl optionally substituted by 1 to 5 substituents selected from C1-6 alkoxy, C1-6 alkyl optionally substituted by halo, aryl, halo, hydroxyl, heteroaryl, C1-6 hydroxyalkyl, or -NHS (O) 2- (C1-6 alkyl); C 1-6 alkyl, C 2-6 haloalkyl, C 1-6 hydroxyalkyl, C 1-6 alkoxy, C 1-6 alkyl, amino, C 2-6 alkenyl or C 2-6 alkynyl, where each of which may be interrupted by one or more heteroatoms, cyano, halo, hydroxyl, nitro, or -O-aryl; or a pharmaceutically acceptable salt, hydrate or stereoisomer thereof.
priorityDate 2006-01-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 45.