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filingDate 2013-02-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2016-03-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2014136463-A
titleOfInvention Cycloalkane derivative
abstract 1. The compound represented by formula (I) or a pharmacologically acceptable salt thereof: [Formula 1], wherein Ar and Ar each independently represent a heteroaryl group or an aryl group, R, R and R each independently represent a hydrogen atom, a halogen atom, A C1-C6 alkyl group, a halogenated C1-C6 alkyl group, a hydroxy C1-C6 alkyl group, a C1-C6 alkoxy C1-C6 alkyl group, a C3-C7 cycloalkyl group or a cyano group, R and R, each independently represent a hydrogen atom, halogen atom, C1-C6 alkyl group, halogenated C1-C6 alkyl th group, hydroxyl group, hydroxy C1-C6 alkyl group, C1-C6 alkoxy C1-C6 alkyl group, C3-C7 cycloalkyl group or C1-C6 alkoxy group, and n is an integer of 1 to 3, also heteroaryl the group or aryl group optionally contains one or two substituents independently selected from a halogen atom, a C1-C6 alkyl group, a halogenated C1-C6 alkyl group, a hydroxyl group, a hydroxy C1-C6 alkyl group, a C1-C6 alkoxy C1-C6 alkyl group, C3 -C7 cycloalkyl group, carboxy group, cyano group , amino groups, C1-C3 alkylamino groups and di-C1-C3 alkylamino groups, and when a heteroaryl group or an aryl group contains two such groups, these two groups are the same or different from each other. 2. The compound or its pharmacologically acceptable salt according to claim 1, wherein, in the formula (I), Ar and Ar each independently represent a heteroaryl group, R, R and R each independently represent a hydrogen atom, a halogen atom, a C1-C6 alkyl group , a halogenated C1-C6 alkyl group or a C3-C7 cycloalkyl group, R and R each independently represent a hydrogen atom, a halogen atom, a C1-C6 alkyl group or a halogenated C1-C6 alkyl group
priorityDate 2012-02-09-04:00^^<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: 54.