SUBSTITUTED 3-AMINO-1-OXO OR THIOXO-1,2,5,6,7,8-HEXAHYDRO-2,7-NAPHTHYRIDINE-4-CARBONITRILES ARE SELECTIVE ALPHA 2B ANTAGONISTS
    6.
    发明申请
    SUBSTITUTED 3-AMINO-1-OXO OR THIOXO-1,2,5,6,7,8-HEXAHYDRO-2,7-NAPHTHYRIDINE-4-CARBONITRILES ARE SELECTIVE ALPHA 2B ANTAGONISTS 审中-公开
    取代的3-氨基-1-氧代或硫代-1,2,5,6,7,8-十六氢-2,7-萘啶-4-羰基酮是选择性ALPHA 2B拮抗剂

    公开(公告)号:US20100076194A1

    公开(公告)日:2010-03-25

    申请号:US12554316

    申请日:2009-09-04

    IPC分类号: C07D471/04

    CPC分类号: C07D471/04

    摘要: The present invention provides compounds which are subtype selective antagonists of the alpha 2B adrenergic receptor and have no or weak antagonist activity at the other alpha adrenergic receptors. These compounds are useful as tool compounds and, in particular, as tool compounds for developing compounds useful in treating diseases that include but are not limited to chronic pain, visceral pain, corneal pain, neuropathic pain, glaucoma, ischemic neuropathies and other neurodegenerative diseases and conditions. These compounds are also useful as compounds for treating myocardial infarction and preventing acute coronary events. The compounds of this invention are 3-amino-1-thioxo or oxo-1,2,5,6,7,8-hexahydro-2,7-naphthyridine-4-carbonitriles or substituted derivatives thereof.

    摘要翻译: 本发明提供作为α2B肾上腺素能受体的亚型选择性拮抗剂并且在其它α肾上腺素能受体上没有或弱拮抗剂活性的化合物。 这些化合物可用作工具化合物,特别是用作开发用于治疗疾病的化合物的工具化合物,所述化合物包括但不限于慢性疼痛,内脏痛,角膜痛,神经性疼痛,青光眼,缺血性神经病和其它神经变性疾病,以及 条件。 这些化合物也可用作治疗心肌梗死和预防急性冠状动脉事件的化合物。 本发明的化合物是3-氨基-1-硫代或氧代-1,2,5,6,7,8-六氢-2,7-萘啶-4-腈或其取代的衍生物。