| 摘要 |
An aryl-substituted alicyclic compound of the formula (I): wherein U is 1,4,5,6-tetrahydropyrimidin-2-yl, etc., A is phenylene, etc., B is piperidine-1,4-diyl, etc., Z is -CONH-, etc., R<3 >is hydrogen, etc., R<5 >is hydrogen, aryl, etc., R<6 >is a mono-substituted amino (e,g., benzyloxycarbonylamino), R<7 >is hydrogen, etc., and a process for preparation thereof, and a pharmaceutical composition containing the same. The compound of the present invention has a high selectivity for alphavbeta3 integrin, and exhibits a potent inhibitory activity thereto, and hence, it is useful as a preventive or/and a therapeutic agent for a disease in which alphavbeta3 integrin is involved.
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