The present invention relates to (hetero)arylalkylamino-pyrazolopyridazine derivatives having dual pharmacological activity towards both the α2δ subunit, in particular the α2δ 1 subunit, of the voltage-gated calcium channel and the Noradrenaline transporter (NET), to processes of preparation of such compounds, to pharmaceutical compositions comprising them, and to their use in therapy, in particular for the treatment of pain.
本发明涉及具有对电压门控
钙通道的α2δ亚基,特别是α2δ 1亚基,和
去甲肾上腺素转运蛋白(NET)具有双重药理活性的(杂)芳基烷基
氨基
吡唑吡啶嘧啶衍
生物,涉及制备这类化合物的方法,包括它们的药物组合物,以及它们在治疗中的应用,特别是用于疼痛治疗。