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1-[8-(2-chlorophenyl)-9-(4-chlorophenyl)-9H-purin-6-yl]-4-phenylpiperidin-4-amine | 1408074-84-9

中文名称
——
中文别名
——
英文名称
1-[8-(2-chlorophenyl)-9-(4-chlorophenyl)-9H-purin-6-yl]-4-phenylpiperidin-4-amine
英文别名
1-[8-(2-Chlorophenyl)-9-(4-chlorophenyl)-9H-purin-6-yl]-4-phenyl-4-piperidinamine;1-[8-(2-chlorophenyl)-9-(4-chlorophenyl)purin-6-yl]-4-phenylpiperidin-4-amine
1-[8-(2-chlorophenyl)-9-(4-chlorophenyl)-9H-purin-6-yl]-4-phenylpiperidin-4-amine化学式
CAS
1408074-84-9
化学式
C28H24Cl2N6
mdl
——
分子量
515.445
InChiKey
XQBGHGICHOVVTE-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

计算性质

  • 辛醇/水分配系数(LogP):
    6
  • 重原子数:
    36
  • 可旋转键数:
    4
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.18
  • 拓扑面积:
    72.9
  • 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
  • 下游产品
    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

  • PERIPHERALLY RESTRICTED DIPHENYL PURINE DERIVATIVES
    申请人:RESEARCH TRIANGLE INSTITUTE
    公开号:US20150031689A1
    公开(公告)日:2015-01-29
    The invention provides compounds capable of acting as antagonists at cannabanoid receptors according to the following formula: Such compounds may be used to treat conditions for which the cannabinoid receptor system has been implicated, such as obesity, liver disease, diabetes, pain, and inflammation.
    该发明提供了能够作为大麻素受体拮抗剂的化合物,其化学式如下:这些化合物可用于治疗大麻素受体系统被涉及的疾病,如肥胖症、肝病、糖尿病、疼痛和炎症等。
  • Peripherally restricted diphenyl purine derivatives
    申请人:RESEARCH TRIANGLE INSTITUTE
    公开号:US09187480B2
    公开(公告)日:2015-11-17
    The invention provides compounds capable of acting as antagonists at cannabanoid receptors according to the following formula: Such compounds may be used to treat conditions for which the cannabinoid receptor system has been implicated, such as obesity, liver disease, diabetes, pain, and inflammation.
    该发明提供了一些化合物,其能够作为大麻素受体拮抗剂,其化学式如下:这些化合物可用于治疗大麻素受体系统被牵涉的疾病,如肥胖症、肝病、糖尿病、疼痛和炎症等疾病。
  • Diphenyl Purine Derivatives as Peripherally Selective Cannabinoid Receptor 1 Antagonists
    作者:Alan Fulp、Katherine Bortoff、Yanan Zhang、Herbert Seltzman、James Mathews、Rodney Snyder、Tim Fennell、Rangan Maitra
    DOI:10.1021/jm301181r
    日期:2012.11.26
    Cannabinoid receptor 1 (CB1) antagonists are potentially useful for the treatment of several diseases. However, clinical development of several CB1 antagonists was halted due to central nervous system (CNS)-related side effects including depression and suicidal ideation in some users. Recently, studies have indicated that selective regulation of CB1 receptors in the periphery is a viable strategy for treating several important disorder. Past efforts to develop peripherally selective antagonists of CB1 have largely targeted rimonabant, an inverse agonist of CB1. Reported here are out efforts toward developing a peripherally selective CB1 antagonist based on the otenabant scaffold. Even though otenabant penetrates the CNS, it is unique among CB1 antagonists that have been clinically tested because it has properties that are normally associated with peripherally selective compounds. Our efforts have resulted in an orally absorbed compound that is a potent and selective CB1 antagonist with limited penetration into the CNS.
  • US9187480B2
    申请人:——
    公开号:US9187480B2
    公开(公告)日:2015-11-17
  • US9458160B2
    申请人:——
    公开号:US9458160B2
    公开(公告)日:2016-10-04
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