wherein R1 and R3 are, independently, -H, -CH3, -CO(C1-C6 alkyl), or -COAr, where Ar is optionally substituted phenyl;R3 is selected from the group consisting of pyrrolidine, piperidine, and hexamethyleneimino; ora pharmaceutically acceptable salt or solvate thereof, in the preparation of a pharmaceutical formulation for inhibiting detrimental side-effects of GnRH or a GnRH agonist in a mammal."/> Benzo(b)thiophene derivatives for inhibiting detrimental side-effects due to GnRH or GnRH agonist administration
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Benzo(b)thiophene derivatives for inhibiting detrimental side-effects due to GnRH or GnRH agonist administration

机译:苯并(b)噻吩衍生物用于抑制由于GnRH或GnRH激动剂给药引起的有害副作用

摘要

The use of a compound of formula I wherein R1 and R3 are, independently, -H, -CH3, -CO(C1-C6 alkyl), or -COAr, where Ar is optionally substituted phenyl;R3 is selected from the group consisting of pyrrolidine, piperidine, and hexamethyleneimino; ora pharmaceutically acceptable salt or solvate thereof, in the preparation of a pharmaceutical formulation for inhibiting detrimental side-effects of GnRH or a GnRH agonist in a mammal.
机译:式I化合物的用途 <图像文件=“ IMGA0001.GIF” he =“ 38” imgContent =“ chem” imgFormat =“ GIF” wi =“ 95” /> 其中R 1 < / Sup>和R 3 独立地是-H,-CH 3 ,-CO(C 1 -C 6 < / Sub>烷基)或-COAr,其中Ar是任选取代的苯基; R 3 选自吡咯烷,哌啶和六亚甲基亚氨基;或 其药学上可接受的盐或溶剂化物,用于制备抑制哺乳动物GnRH或GnRH激动剂的有害副作用的药物制剂。

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