The present invention relates to fused dihydroindazole derivatives having pharmacological activity towards the α2δ subunit, in particular the α2δ subunit, of the voltage-gated calcium channel. It also relates to compounds having dual pharmacological activity towards both the α2δ subunit, in particular the α2δ subunit, of the voltage-gated calcium channel and the δ1 receptor. The present invention also relates 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α2δ亚基,特别是电压门控
钙通道的α2δ亚基具有药理活性的融合二氢
吲唑衍
生物。它还涉及具有对电压门控
钙通道的α2δ亚基,特别是α2δ亚基,以及δ1受体双重药理活性的化合物。本发明还涉及制备这类化合物的方法,包括它们的药物组合物,以及它们在疗法中的使用,特别是用于疼痛治疗。