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(1S)-1,3,3-trimethylbicyclo[2.2.1]heptan-2-amine

中文名称
——
中文别名
——
英文名称
(1S)-1,3,3-trimethylbicyclo[2.2.1]heptan-2-amine
英文别名
——
(1S)-1,3,3-trimethylbicyclo[2.2.1]heptan-2-amine化学式
CAS
——
化学式
C10H19N
mdl
——
分子量
153.26
InChiKey
CBYXIIFIKSBHEY-KTOWXAHTSA-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):
    2.3
  • 重原子数:
    11
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    26
  • 氢给体数:
    1
  • 氢受体数:
    1

文献信息

  • 4,5-Dihydro-(1H)-pyrazole derivatives as cannabinoid CB1 receptor modulators
    申请人:Lange H.M. Josephus
    公开号:US20070142362A1
    公开(公告)日:2007-06-21
    This invention is directed to 4,5-dihydro-(1H)-pyrazole(pyrazoline) derivatives as cannabinoid CB 1 receptor modulators, to pharmaceutical compositions containing these compounds, to methods for the preparation of these compounds, methods for preparing novel intermediates useful for their synthesis, and methods for preparing compositions. The invention also relates to the uses of such compounds and compositions, particularly their use in administering them to patients to achieve a therapeutic effect in disorders in which CB 1 receptors are involved, or that can be treated via manipulation of those receptors. The compounds have the general formula (I) wherein the symbols have the meanings given in the specification.
    这项发明涉及作为大麻素CB1受体调节剂的4,5-二氢-(1H)-吡唑烯(吡唑啉)衍生物,含有这些化合物的药物组合物,制备这些化合物的方法,用于制备其合成有用的新中间体的方法,以及制备组合物的方法。该发明还涉及这些化合物和组合物的用途,特别是它们在向患者施用以在涉及CB1受体的疾病中实现治疗效果,或者可以通过操纵这些受体来治疗的疾病中的用途。 这些化合物具有通式(I) 其中符号的含义如规范中所述。
  • 1H-imidazole derivatives as cannabinoid CB2 receptor modulators
    申请人:Lange H.M. Josephus
    公开号:US20060194779A1
    公开(公告)日:2006-08-31
    The invention relates to a group of 1H-imidazole derivatives which are modulators of cannabinoid CB 2 receptors, to methods for the preparation of these compounds, to novel intermediates useful for the synthesis of said imidazole derivatives, to methods for the preparation of these intermediates, to pharmaceutical compositions containing one or more of these 1H-imidazole derivatives as active ingredient, as well as to the use of these pharmaceutical compositions for the treatment of disorders in which cannabinoid CB 2 receptors are involved. The compounds have the general formula (I) wherein R 1 -R 4 have the meanings given in the specification.
    该发明涉及一组1H-咪唑衍生物,它们是大麻素CB2受体调节剂,涉及制备这些化合物的方法,有用于合成该咪唑衍生物的新型中间体,制备这些中间体的方法,含有一种或多种这些1H-咪唑衍生物作为活性成分的药物组合物,以及将这些药物组合物用于治疗涉及大麻素CB2受体的疾病。这些化合物具有通式(I),其中R1-R4具有规范中给出的含义。
  • Cannabinoid receptor inverse agonists and neutral antagonists as therapeutic agents for the treatment of bone disorders
    申请人:Ralston Hamilton Stuart
    公开号:US20060172019A1
    公开(公告)日:2006-08-03
    The present invention pertains to cannabinoid (CB) receptor inverse agonists and neutral antagonists, and especially CB1 and CB2 inverse agonists and neutral antagonists; such as, for example, certain pyrazole compounds; their use in the inhibition of osteoclasts (for example, the inhibition of the survival, formation, and/or activity of osteoclasts), and/or in the inhibition of bone resorption; their use in connection with treatment of bone disorders, such as conditions mediated by osteoclasts (e.g., increased osteoclast activity) and/or characterised by (e.g., increased) bone resorption, such as osteoporosis (e.g., osteoporosis not associated with inflammation; e.g., osteoporosis associated with a genetic predisposition, sex hormone deficiency, or ageing), cancer associated bone disease, and Paget's disease of bone.
    本发明涉及大麻素(CB)受体的反向激动剂和中性拮抗剂,尤其是CB1和CB2的反向激动剂和中性拮抗剂,例如某些吡唑化合物;它们用于抑制破骨细胞(例如抑制破骨细胞的存活、形成和/或活动),和/或抑制骨吸收;它们用于治疗骨疾病,例如由破骨细胞介导的疾病(例如破骨细胞活性增加)和/或以(例如增加的)骨吸收为特征的疾病,例如骨质疏松症(例如与炎症无关的骨质疏松症;例如与遗传倾向、性激素缺乏或衰老有关的骨质疏松症)、癌症相关骨疾病和Paget骨病。
  • Novel Cannabinoid Receptor Ligands, Pharmaceutical Compositions Containing Them, and Process For Their Preparation
    申请人:Muthuppalaniappan Meyyappan
    公开号:US20080234259A1
    公开(公告)日:2008-09-25
    The present invention relates to novel cannabinoid receptor modulators, in particular cannabinoid 1 (CB1) or cannabinoid 2 (CB2) receptor modulators, and uses thereof for treating diseases, conditions and/or disorders modulated by a cannabinoid receptor (such as pain, neurodegenative disorders, eating disorders, weight loss or control, and obesity).
    本发明涉及新型大麻素受体调节剂,特别是大麻素1(CB1)或大麻素2(CB2)受体调节剂,以及它们在治疗由大麻素受体调节的疾病、状况和/或障碍方面的用途(例如疼痛、神经退行性疾病、进食障碍、体重减轻或控制和肥胖症)。
  • NOVEL CANNABINOID RECEPTOR LIGANDS, PHARMACEUTICAL COMPOSITIONS CONTAINING THEM, AND PROCESS FOR THEIR PREPARATION
    申请人:MUTHUPPALANIAPPAN Meyyappan
    公开号:US20120142748A1
    公开(公告)日:2012-06-07
    The present invention relates to novel cannabinoid receptor modulators, in particular cannabinoid 1 (CB1) or cannabinoid 2 (CB2) receptor modulators, and uses thereof for treating diseases, conditions and/or disorders modulated by a cannabinoid receptor.
    本发明涉及新型大麻素受体调节剂,特别是大麻素1(CB1)或大麻素2(CB2)受体调节剂,以及它们用于治疗由大麻素受体调节的疾病、状况和/或障碍的用途。
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