CANNABINOID RECEPTOR MODULATORS
    2.
    发明申请

    公开(公告)号:US20220306586A1

    公开(公告)日:2022-09-29

    申请号:US17520952

    申请日:2021-11-08

    Abstract: The present invention relates to certain compounds of Formula Ia and pharmaceutical compositions thereof that modulate the activity of the cannabinoid CB2 receptor. The present invention further relates to certain compounds of Formula Ia and pharmaceutical compositions thereof that modulate the activities of both the CB1 receptor and the CB2 receptor. Compounds of the present invention and pharmaceutical compositions thereof are directed to methods useful in the treatment of: pain, for example bone and joint pain, muscle pain, dental pain, migraine and other headache pain, inflammatory pain, neuropathic pain, pain that occurs as an adverse effect of therapeutics and pain associated with osteoarthritis; hyperalgesia; allodynia; inflammatory hyperalgesia; neuropathic hyperalgesia; acute nociception; osteoporosis; multiple sclerosis-associated spasticity; autoimmune disorders; allergic reactions; CNS inflammation; atherosclerosis; undesired immune cell activity and inflammation; age-related macular degeneration; cough; leukemia; lymphoma; CNS tumors; prostate cancer; Alzheimer's disease; stroke-induced damage; dementia; amyotrophic lateral sclerosis, and Parkinson's disease.

    SUBSTITUTED TRICYCLIC ACID DERIVATIVES AS S1P1 RECEPTOR AGONISTS USEFUL IN THE TREATMENT OF AUTOIMMUNE AND INFLAMMATORY DISORDERS
    8.
    发明申请
    SUBSTITUTED TRICYCLIC ACID DERIVATIVES AS S1P1 RECEPTOR AGONISTS USEFUL IN THE TREATMENT OF AUTOIMMUNE AND INFLAMMATORY DISORDERS 审中-公开
    作为S1P1受体激动剂治疗自身免疫性疾病和炎症性疾病有用的替代三聚酸衍生物

    公开(公告)号:US20150336966A1

    公开(公告)日:2015-11-26

    申请号:US14817954

    申请日:2015-08-04

    CPC classification number: C07D487/04 C07D471/04

    Abstract: The present invention relates to certain substituted tricyclic acid derivatives of Formula (I) and pharmaceutically acceptable salts thereof, which exhibit useful pharmacological properties, for example, as agonists of the S1P1 receptor. Also provided by the present invention are pharmaceutical compositions containing compounds of the invention, and methods of using the compounds and compositions of the invention in the treatment of S1P1-associated disorders, for example, psoriasis, rheumatoid arthritis, Crohn's disease, transplant rejection, multiple sclerosis, systemic lupus erythematosus, ulcerative colitis, type I diabetes, acne, myocardial ischemia-reperfusion injury, hypertensive nephropathy, glomerulosclerosis, gastritis, polymyositis, thyroiditis, vitiligo, hepatitis, biliary cirrhosis, microbial infections and associated diseases, viral infections and associated diseases, diseases and disorders mediated by lymphocytes, auto immune diseases, inflammatory diseases, and cancer.

    Abstract translation: 本发明涉及某些取代的式(I)的三环酸衍生物及其药学上可接受的盐,其表现出有用的药理学性质,例如作为S1P1受体的激动剂。 本发明还提供了含有本发明化合物的药物组合物,以及使用本发明化合物和组合物治疗S1P1相关病症的方法,例如牛皮癣,类风湿性关节炎,克罗恩病,移植排斥反应,多发性 硬化症,系统性红斑狼疮,溃疡性结肠炎,I型糖尿病,痤疮,心肌缺血再灌注损伤,高血压肾病,肾小球硬化,胃炎,多发性肌炎,甲状腺炎,白癜风,肝炎,胆汁性肝硬化,微生物感染和相关疾病,病毒感染和相关疾病 ,由淋巴细胞介导的疾病和病症,自身免疫疾病,炎性疾病和癌症。

Patent Agency Ranking