The invention relates to the hetaryl-substituted guanidine compounds of general formula (I), enantiomeres, diastereomeres and/or tautomeres thereof, in addition to the pharmaceutically acceptable salts thereof and the prodrugs of the known compounds. The invention also relates to the use of said hetaryl-substituted guanidine compounds as binding partners for 5-HT5-receptors for treating and/or for the prophylaxis of illnesses which are modulated by a 5-HT5-receptor activity, in particular, for treating and/or for the prophylaxis of neurodegenerative and neuropsychiatric disorders, and signs, symptoms and dysfunctions associated with said disorders.
本发明涉及一般式(I)的杂环取代
鸟氨酸化合物,其对映异构体、顺反异构体和/或互变异构体,以及其药学上可接受的盐和已知化合物的前药。本发明还涉及将上述杂环取代
鸟氨酸化合物用作5-HT5受体的结合伴侣,用于治疗和/或预防由5-HT5受体活性调节的疾病,特别是用于治疗和/或预防神经退行性和神经精神障碍以及与该类障碍相关的症状和功能障碍。