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Methyl 2-(3-phenylpropanoyl)-1,3,4,9-tetrahydropyrido[3,4-b]indole-1-carboxylate | 1206876-23-4

中文名称
——
中文别名
——
英文名称
Methyl 2-(3-phenylpropanoyl)-1,3,4,9-tetrahydropyrido[3,4-b]indole-1-carboxylate
英文别名
——
Methyl 2-(3-phenylpropanoyl)-1,3,4,9-tetrahydropyrido[3,4-b]indole-1-carboxylate化学式
CAS
1206876-23-4
化学式
C22H22N2O3
mdl
——
分子量
362.428
InChiKey
SONYNSGGFBITQQ-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):
    3.4
  • 重原子数:
    27
  • 可旋转键数:
    5
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.27
  • 拓扑面积:
    62.4
  • 氢给体数:
    1
  • 氢受体数:
    3

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

反应信息

  • 作为反应物:
    描述:
    Methyl 2-(3-phenylpropanoyl)-1,3,4,9-tetrahydropyrido[3,4-b]indole-1-carboxylate 、 lithium hydroxide 作用下, 以 四氢呋喃 为溶剂, 以95%的产率得到
    参考文献:
    名称:
    Substituted tetrahydro-β-carbolines as potential agents for the treatment of human papillomavirus infection
    摘要:
    The identification and optimization of a series of substituted tetrahydro-beta-carbolines with potent activity against human papillomavirus is described. Structure-activity studies focused on the substitution pattern and chirality of the beta-carboline ring system are discussed. Optimization of these parameters led to compounds with antiviral activities in the low nanomolar range. (c) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2009.10.123
  • 作为产物:
    描述:
    2,3,4,9-四氢-1H-beta-咔啉-1-羧酸甲酯3-苯丙酰氯N,N-二异丙基乙胺 作用下, 以 二氯甲烷 为溶剂, 以66%的产率得到Methyl 2-(3-phenylpropanoyl)-1,3,4,9-tetrahydropyrido[3,4-b]indole-1-carboxylate
    参考文献:
    名称:
    Substituted tetrahydro-β-carbolines as potential agents for the treatment of human papillomavirus infection
    摘要:
    The identification and optimization of a series of substituted tetrahydro-beta-carbolines with potent activity against human papillomavirus is described. Structure-activity studies focused on the substitution pattern and chirality of the beta-carboline ring system are discussed. Optimization of these parameters led to compounds with antiviral activities in the low nanomolar range. (c) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2009.10.123
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文献信息

  • Substituted tetrahydro-β-carbolines as potential agents for the treatment of human papillomavirus infection
    作者:John F. Miller、Elizabeth M. Turner、Ronald G. Sherrill、Kristjan Gudmundsson、Andrew Spaltenstein、Phiroze Sethna、Kevin W. Brown、Robert Harvey、Karen R. Romines、Pamela Golden
    DOI:10.1016/j.bmcl.2009.10.123
    日期:2010.1
    The identification and optimization of a series of substituted tetrahydro-beta-carbolines with potent activity against human papillomavirus is described. Structure-activity studies focused on the substitution pattern and chirality of the beta-carboline ring system are discussed. Optimization of these parameters led to compounds with antiviral activities in the low nanomolar range. (c) 2009 Elsevier Ltd. All rights reserved.
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