| abstract |
In the present invention there is described the use of the 2-phenyl-3-aroylbenzothiophene derivative of the general formula I, in which Re1 and Re3 represent independently on each other a hydrogen atom, methyl or the group of the general formula a) or b), Ar represents phenyl or a phenyl group being substituted once or twice with an alkyl group containing 1 to 6 carbon atoms, an alkoxy group containing 1 to 4 carbon atoms, a hydroxy group, a nitro group, a chlorine atom, a fluorine atom or a trichloro- or trifluoromethyl group, Re2 is selected from a group comprising a pyrrolidino group a piperidino group, or pharmaceutically acceptable salt or solvate thereof for preparing a pharmaceutical preparation intended for preparing a medicament for inhibition of uterus fibrosis. |