| 摘要 |
<p>The invention concerns compounds of general formula (I) : wherein Z 1 , Z 2 , Z 3 , and Z 4 represent, independently of one another, a nitrogen atom or a C(R 6 ) group, at least one of which corresponds to a nitrogen atom and at least one of which corresponds to a C(R 6 ) group, n is equal to 0, 1, 2 or 3, Y represents an optionally substituted aryl or heteroaryl, and Z represents a cyclic amine bound by the nitrogen atom of formula , in the base or acid addition salt state, and in the hydrate or solvate state. The invention also concerns a preparation method and a therapeutic application.</p> |
