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(1aR,5aR)-2-(4-fluoro-pyridin-2-yl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalene-4-carboxylic acid | 1268883-41-5

中文名称
——
中文别名
——
英文名称
(1aR,5aR)-2-(4-fluoro-pyridin-2-yl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalene-4-carboxylic acid
英文别名
(2R,4R)-9-(4-fluoropyridin-2-yl)-8,9-diazatricyclo[4.3.0.02,4]nona-1(6),7-diene-7-carboxylic acid
(1aR,5aR)-2-(4-fluoro-pyridin-2-yl)-1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalene-4-carboxylic acid化学式
CAS
1268883-41-5
化学式
C13H10FN3O2
mdl
——
分子量
259.24
InChiKey
BWDKOEHVYVSFLZ-HTRCEHHLSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    1.6
  • 重原子数:
    19
  • 可旋转键数:
    2
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.31
  • 拓扑面积:
    68
  • 氢给体数:
    1
  • 氢受体数:
    5

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • Cannabinoid receptor modulators
    申请人:Jones Robert M.
    公开号:US08778950B2
    公开(公告)日:2014-07-15
    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.
    本发明涉及化合物Ia的某些化合物及其制药组合物,该化合物调节大麻素CB2受体的活性。本发明还涉及化合物Ia的某些化合物及其制药组合物,该化合物调节CB1受体和CB2受体的活性。本发明的化合物及其制药组合物适用于治疗以下疾病的方法:疼痛,例如骨骼和关节疼痛,肌肉疼痛,牙痛,偏头痛和其他头痛,炎症性疼痛,神经痛,作为治疗副作用发生的疼痛和与骨关节炎有关的疼痛;高痛觉性;触痛;炎症性高痛觉性;神经病性高痛觉性;急性伤害感受;骨质疏松症;多发性硬化相关痉挛;自身免疫性疾病;过敏反应;中枢神经系统炎症;动脉硬化;不良的免疫细胞活性和炎症;年龄相关的黄斑变性;咳嗽;白血病;淋巴瘤;中枢神经系统肿瘤;前列腺癌;阿尔茨海默病;中风引起的损伤;痴呆症;肌萎缩性侧索硬化症和帕森病。
  • Compounds and Methods for Treatment of Visceral Pain
    申请人:Arena Pharmaceuticals, Inc.
    公开号:US20200078358A1
    公开(公告)日:2020-03-12
    The present invention relates to certain compounds of Formula Ia and pharmaceutical compositions thereof and their use in methods for the alleviation and/or treatment of visceral pain, for example abdominal pain; pelvic pain; male pelvic pain; pain from an internal organ; bladder pain; painful bladder syndrome; post-surgical abdominal pain (e.g., GI resection, hysterectomy, oophorectomy, C-section, and the like); or pain arising from or related to: pancreatitis (e.g., chronic pancreatitis), prostatitis (e.g., chronic prostatitis), inflammatory bowel disease (e.g., Crohn's disease), endometriosis, interstitial cystitis, prostatitis (e.g., chronic prostatitis), epididymitis (e.g., chronic epididymitis), or post-surgical abdominal lesions. In some embodiments, the visceral pain is consequent to inflammatory bowel disease, for example Crohn's disease.
  • US8778950B2
    申请人:——
    公开号:US8778950B2
    公开(公告)日:2014-07-15
  • US9492447B2
    申请人:——
    公开号:US9492447B2
    公开(公告)日:2016-11-15
  • US9597340B2
    申请人:——
    公开号:US9597340B2
    公开(公告)日:2017-03-21
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