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C-[1-(2-甲氧基-乙基)-吡咯烷-3-基]-甲胺 | 910443-61-7

中文名称
C-[1-(2-甲氧基-乙基)-吡咯烷-3-基]-甲胺
中文别名
——
英文名称
1-[1-(2-Methoxyethyl)pyrrolidin-3-yl]methanamine
英文别名
[1-(2-methoxyethyl)pyrrolidin-3-yl]methanamine
C-[1-(2-甲氧基-乙基)-吡咯烷-3-基]-甲胺化学式
CAS
910443-61-7
化学式
C8H18N2O
mdl
MFCD08059731
分子量
158.24
InChiKey
SVWDIDWSZJLAMB-UHFFFAOYSA-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

物化性质

  • 沸点:
    215.3±10.0 °C(Predicted)
  • 密度:
    0.959±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    -0.4
  • 重原子数:
    11
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    38.5
  • 氢给体数:
    1
  • 氢受体数:
    3

安全信息

  • 危险等级:
    IRRITANT
  • 危险品标志:
    Xi
  • 海关编码:
    2933990090

文献信息

  • CANNABINOID RECEPTOR MODULATORS
    申请人:Jones Robert M.
    公开号:US20120214766A1
    公开(公告)日:2012-08-23
    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.
    本发明涉及公式Ia的某些化合物及其制药组合物,其调节大麻素CB2受体的活性。本发明还涉及公式Ia的某些化合物及其制药组合物,其调节CB1受体和CB2受体的活性。本发明的化合物和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,炎性疼痛,神经痛,由治疗副作用引起的疼痛和与骨关节炎相关的疼痛;过敏症;炎性过敏症;神经病性过敏症;急性疼痛感受;骨质疏松症;多发性硬化症相关痉挛;自身免疫疾病;过敏反应;中枢神经系统炎症;动脉粥样硬化;不良的免疫细胞活动和炎症;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。
  • Cannabinoid receptor modulators
    申请人:Arena Pharmaceuticals, Inc.
    公开号:US11214548B2
    公开(公告)日:2022-01-04
    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.
    本发明涉及某些调节大麻素 CB2 受体活性的式 Ia 化合物及其药物组合物。本发明还涉及某些能调节 CB1 受体和 CB2 受体活性的式 Ia 化合物及其药物组合物。本发明的化合物及其药物组合物用于治疗以下疾病的方法:疼痛,例如骨痛和关节痛、肌肉痛、牙痛、偏头痛和其他头痛、炎症性疼痛、神经性疼痛、作为治疗药物的不良反应出现的疼痛以及与骨关节炎相关的疼痛;痛觉减退;异动症;炎症性痛觉减退;神经性痛觉减退;急性痛觉;骨质疏松症;多发性硬化症相关的痉挛、自身免疫性疾病、过敏反应、中枢神经系统炎症、动脉粥样硬化、不想要的免疫细胞活性和炎症、老年性黄斑变性、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、肌萎缩性脊髓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
  • US9944606B2
    申请人:——
    公开号:US9944606B2
    公开(公告)日:2018-04-17
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