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N1,N7-bis(2-diethylaminoethyl)-3,9-dimethyl-quinolino[8,7-h]quinoline-1,7-diamine

中文名称
——
中文别名
——
英文名称
N1,N7-bis(2-diethylaminoethyl)-3,9-dimethyl-quinolino[8,7-h]quinoline-1,7-diamine
英文别名
1-N,7-N-bis[2-(diethylamino)ethyl]-3,9-dimethylquinolino[8,7-h]quinoline-1,7-diamine
N1,N7-bis(2-diethylaminoethyl)-3,9-dimethyl-quinolino[8,7-h]quinoline-1,7-diamine化学式
CAS
——
化学式
C30H42N6
mdl
——
分子量
486.7
InChiKey
YDXDIPBVWWLCOL-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:
    12
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.47
  • 拓扑面积:
    56.3
  • 氢给体数:
    2
  • 氢受体数:
    6

文献信息

  • METHODS OF INHIBITING VIRAL INFECTION
    申请人:Functional Genetics, Inc.
    公开号:EP2207801B1
    公开(公告)日:2013-04-17
  • METHOHDS OF INHIBITING VIRAL INFECTION
    申请人:Kinch Michael
    公开号:US20090170890A1
    公开(公告)日:2009-07-02
    A method of inhibiting viral infection in a mammal in need of same, includes administering an effective amount of at least one of the compounds of FGI-103 which are represented by 273, 365 and 510 either prophylactically to prevent viral infection, or therapeutically following viral infection. These compounds appear to selectively inhibit Caspase 8 as a method of preventing infective viral particle release. They can be administered IV, IP, orally or via other conventional administration routes. The compounds are highly effective, requiring relatively low dosages on the order of 1 ng/kg-200 mg/kg of body weight.
  • US8207209B2
    申请人:——
    公开号:US8207209B2
    公开(公告)日:2012-06-26
  • [EN] METHODS OF INHIBITING VIRAL INFECTION<br/>[FR] PROCÉDÉS VISANT À INHIBER UNE INFECTION VIRALE
    申请人:FUNCTIONAL GENETICS INC
    公开号:WO2009055524A1
    公开(公告)日:2009-04-30
    A method of inhibiting viral infection in a mammal in need of same, includes administering an effective amount of at least one of the compounds of FGI- 103 which are represented by 273, 365 and 510 either prophylactically to prevent viral infection, or therapeutically following viral infection. These compounds appear to selectively inhibit Caspase 8 as a method of preventing infective viral particle release. They can be administered IV, IP, orally or via other conventional administration routes. The compounds are highly effective, requiring relatively low dosages on the order of 1 ng/kg - 200 mg/kg of body weight.
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