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1-(4-ethyl-phenyl)-4-phenyl-piperazine | 14960-83-9

中文名称
——
中文别名
——
英文名称
1-(4-ethyl-phenyl)-4-phenyl-piperazine
英文别名
1-(4-Ethylphenyl)-4-phenylpiperazine
1-(4-ethyl-phenyl)-4-phenyl-piperazine化学式
CAS
14960-83-9
化学式
C18H22N2
mdl
——
分子量
266.386
InChiKey
MPQWEUKWOZKWFV-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):
    4.4
  • 重原子数:
    20
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    6.5
  • 氢给体数:
    0
  • 氢受体数:
    2

文献信息

  • BRIDGED BICYCLIC ARYL AND BRIDGED BICYCLIC HETEROARYL SUBSTITUTED TRIAZOLES USEFUL AS AXL INHIBITORS
    申请人:Goff Dane
    公开号:US20080176847A1
    公开(公告)日:2008-07-24
    Bridged bicyclic aryl or heteroaryl substituted triazoles and pharmaceutical compositions containing the compounds are disclosed as being useful in inhibiting the activity of the receptor protein tyrosine kinase Axl. Methods of using the compounds in treating diseases or conditions associated with Axl activity are also disclosed.
    本发明公开了桥接的双环芳基或杂环芳基取代的三唑化合物和含有这些化合物的制药组合物,其被用于抑制受体蛋白酪氨酸激酶Axl的活性。本发明还公开了使用这些化合物治疗与Axl活性相关的疾病或病状的方法。
  • AMINE DERIVATIVES HAVING NPY Y5 RECEPTOR ANTAGONISTIC ACTIVITY AND THE USES THEREOF
    申请人:OKUNO Takayuki
    公开号:US20100273842A1
    公开(公告)日:2010-10-28
    This invention provides an anorectic or anti-obesity composition comprising a compound of the formula (I): a pharmaceutically acceptable salt or solvate thereof, wherein R 1 is optionally substituted lower alkyl, Y is —S(O) n — wherein n is 1 or 2, or —CO—, R 2 is hydrogen or lower alkyl, R 7 is hydrogen or lower alkyl, X is lower alkylene, lower alkenylene, arylene, cycloalkylene or the like, and Z is lower alkyl, optionally substituted carbocyclyl, optionally substituted heterocyclyl or the like.
  • AMINE DERIVATIVE HAVING NPY Y5 RECEPTOR ANTAGONISTIC ACTIVITY
    申请人:Okuno Takayuki
    公开号:US20100267945A1
    公开(公告)日:2010-10-21
    A compound of the formula (I): a pharmaceutically acceptable salt or solvate thereof, where R 1 is optionally substituted lower alkyl, Y is —S(O) 2 —, R 2 is hydrogen or optionally substituted lower alkyl, R 7 is hydrogen or optionally substituted lower alkyl, X is a group of the formula: where R 5 and R 6 are each independently hydrogen, a group of the formula: is optionally substituted cycloalkylene, p is 0, and q is 1 or 2, Z is optionally substituted carbocyclyl or optionally substituted heterocyclyl, and provided that a compound wherein Z is fused heterocyclyl consisting of three rings or optionally substituted pyrimidinyl is excluded.
  • US8012965B2
    申请人:——
    公开号:US8012965B2
    公开(公告)日:2011-09-06
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