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Tert-butyl (1S)-8-hydroxy-1-phenyl-3,4-dihydroisoquinoline-2(1H)-carboxylate | 1085539-50-9

中文名称
——
中文别名
——
英文名称
Tert-butyl (1S)-8-hydroxy-1-phenyl-3,4-dihydroisoquinoline-2(1H)-carboxylate
英文别名
tert-butyl (1S)-8-hydroxy-1-phenyl-3,4-dihydro-1H-isoquinoline-2-carboxylate
Tert-butyl (1S)-8-hydroxy-1-phenyl-3,4-dihydroisoquinoline-2(1H)-carboxylate化学式
CAS
1085539-50-9
化学式
C20H23NO3
mdl
——
分子量
325.408
InChiKey
JUJWWFDQZOJRLP-SFHVURJKSA-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
  • 重原子数:
    24
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.35
  • 拓扑面积:
    49.8
  • 氢给体数:
    1
  • 氢受体数:
    3

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

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文献信息

  • 1-substituted tetrahydroisoquinoline compound
    申请人:Astellas Pharma Inc.
    公开号:US08263607B2
    公开(公告)日:2012-09-11
    Provided is a compound useful as an N-type Ca2+ channel blocker. As a result of intensive studies of compounds having an action of blocking N-type Ca2+ channels, the present inventors found that a tetrahydroisoquinoline compound of the present invention having a substituent at the 1-position has an action of blocking the N-type Ca2+ channels, an antinociceptive pain action, an antineuropathic pain action, an abdominal pain-inhibitory action and an opioid-induced constipation-improving action, and the present invention has been completed based on these findings. The compound of the present invention can be used as a pharmaceutical composition for preventing and/or treating various pains such as neuropathic pain and nociceptive pain, headaches such as migraine and cluster headache, central nervous system diseases such as anxiety, depression, epilepsy, cerebral stroke and restless legs syndrome, abdominal symptoms such as abdominal pain and abdominal distension, stool abnormalities such as diarrhea and constipation, digestive system diseases such as irritable bowel syndrome, urinary system diseases such as overactive bladder and interstitial cystitis, etc.
    提供的是一种作为N型Ca2+通道阻滞剂有用的化合物。由于对具有阻断N型Ca2+通道作用的化合物进行了深入研究,本发明人发现,本发明的四氢异喹啉化合物在1位具有取代基,具有阻断N型Ca2+通道、抗痛觉疼痛作用、抗神经痛作用、抑制腹痛作用和改善阿片类药物引起的便秘作用,基于这些发现完成了本发明。本发明的化合物可用作预防和/或治疗各种疼痛,如神经痛和伤害性疼痛、头痛,如偏头痛和集群头痛、中枢神经系统疾病,如焦虑、抑郁、癫痫、脑卒中和不宁腿综合征、腹部症状,如腹痛和腹胀、大便异常,如腹泻和便秘、消化系统疾病,如肠易激综合征、泌尿系统疾病,如过度活动膀胱和间质性膀胱炎等的药物组成物。
  • 1-SUBSTITUTED TETRAHYDROISOQUINOLINE COMPOUND
    申请人:Astellas Pharma Inc.
    公开号:EP2149560B1
    公开(公告)日:2015-05-13
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