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filingDate 2008-03-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7fad041d14e13bfed4cec1d27b9de420
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publicationDate 2013-09-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CY-1107903-T1
titleOfInvention ACYLAMINOTHIACEALE PRODUCTS AND THEIR USE AS BETA-AMYLOID INHIBITORS
abstract Compound corresponding to general formula (I): R 1 represents a C 1-6 alkyl substituted, a C 3-7 -cycloalkyl, a thiophene, a benzothiophene, a pyridinyl, a furanyl or a phenyl; the phenyl groups are; R2 and R2 'represent independently of one another a hydrogen atom, a halogen atom, a hydroxy, a C1-3 alkoxy, a C1-3 alkyl, a C3-7 cycloalkyl, a C-C (O) group -C1-6 alkyl, or R2 and R2 'form an oxo group; R3 represents a hydrogen atom or a C1-6 alkyl having a substituent from a hydroxy or C1-3 alkoxy; R4 and R5 represent, independently of one another a hydrogen atom, a substituted C1-7 alkyl, a C3-7 cycloalkyl, a phenyl, a naphthyl or one - C (X) R6; the C3-7 cycloalkyl and phenyl groups are substituted; provided that at least one group R4 or R5 represents a group - C (X) R6; X represents an oxygen atom or a sulfur atom; R6 represents a C1-6 alkoxy group, a hydroxy or a group - NR7R8; the C1-6 alkoxy group is substituted by a phenyl; R7 and R8 are substituted represent, independently of one another a hydrogen atom, a substituted C1-6 alkyl group, a C3-7 cycloalkyl, a C1-6 alkoxy or a phenyl; or R7 and R8 together with its atom the nitrogen bearing them form a cycle of aziridine, azetidine, pyrrolidine, piperidine or morpholine; the C3-7 cycloalkyl and phenyl groups are substituted; as a base, an addition salt to an acid, a hydrate or a solvent in a acid. Application to treatment.
priorityDate 2002-07-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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