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(4R,4aR,7S,7aR,12bS)-3,6-dimethyl-2,4,4a,7,7a,13-hexahydro-1H-4,12-methanobenzofuro[3,2-e]isoquinoline-7,9-diol

中文名称
——
中文别名
——
英文名称
(4R,4aR,7S,7aR,12bS)-3,6-dimethyl-2,4,4a,7,7a,13-hexahydro-1H-4,12-methanobenzofuro[3,2-e]isoquinoline-7,9-diol
英文别名
——
(4R,4aR,7S,7aR,12bS)-3,6-dimethyl-2,4,4a,7,7a,13-hexahydro-1H-4,12-methanobenzofuro[3,2-e]isoquinoline-7,9-diol化学式
CAS
——
化学式
C18H21NO3
mdl
——
分子量
299.4
InChiKey
XPNQFJCQYHMGGC-LTHWPDAASA-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):
    0.7
  • 重原子数:
    22
  • 可旋转键数:
    0
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.56
  • 拓扑面积:
    52.9
  • 氢给体数:
    2
  • 氢受体数:
    4

文献信息

  • Abuse resistant capsule
    申请人:R.P. Scherer Technologies, LLC
    公开号:US10420729B2
    公开(公告)日:2019-09-24
    The present invention is directed to an immediate release and extended release capsule or capsule fill which mitigates the abuse of abuse-susceptible active pharmaceutical ingredients by direct intravenous injection. The fill comprises a parenteral abuse resistant liquid formulation which when mixed with water and heated, results in a turbid, viscous or bubbling mixture that is not injectable with a standard insulin syringe. The abuse-susceptible active pharmaceutical ingredient is selected from the group consisting of opiates, opioids, tranquilizers, stimulants and narcotics.
    本发明涉及一种速释和缓释胶囊或胶囊填充剂,它可减少通过直接静脉注射滥用易滥用的活性药物成分。填充物包括一种肠外抗滥用液体制剂,当与混合并加热时,会产生一种浑浊、粘稠或起泡的混合物,不能用标准胰岛素注射器注射。抗滥用活性药物成分选自阿片类、阿片类、镇静剂、兴奋剂和麻醉剂
  • ABUSE RESISTANT CAPSULE
    申请人:R.P. Scherer Technologies, LLC
    公开号:EP2968129A1
    公开(公告)日:2016-01-20
  • EP3446681B1
    申请人:——
    公开号:EP3446681B1
    公开(公告)日:2020-12-23
  • US20140271835A1
    申请人:——
    公开号:US20140271835A1
    公开(公告)日:2014-09-18
  • [EN] ABUSE RESISTANT CAPSULE<br/>[FR] CAPSULE RÉSISTANTE AUX ABUS
    申请人:WENGNER SIMONE
    公开号:WO2014140231A1
    公开(公告)日:2014-09-18
    The present invention is directed to an immediate release and extended release capsule or capsule fill which mitigates the abuse of abuse-susceptible active pharmaceutical ingredients by direct intravenous injection. The fill comprises a parenteral abuse resistant liquid formulation which when mixed with water and heated, results in a turbid, viscous or bubbling mixture that is not injectable with a standard insulin syringe. The abuse-susceptible active pharmaceutical ingredient is selected from the group consisting of opiates, opioids, tranquillizers, stimulants and narcotics.
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