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6-methyl-1-(3-hydroxyphenyl)-2-benzyl-1,2,3,4-tetrahydro-β-carboline | 1236397-82-2

中文名称
——
中文别名
——
英文名称
6-methyl-1-(3-hydroxyphenyl)-2-benzyl-1,2,3,4-tetrahydro-β-carboline
英文别名
3-(2-Benzyl-6-methyl-1,3,4,9-tetrahydropyrido[3,4-b]indol-1-yl)phenol
6-methyl-1-(3-hydroxyphenyl)-2-benzyl-1,2,3,4-tetrahydro-β-carboline化学式
CAS
1236397-82-2
化学式
C25H24N2O
mdl
——
分子量
368.478
InChiKey
OQJGJXUXOAVASJ-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):
    5.2
  • 重原子数:
    28
  • 可旋转键数:
    3
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    39.3
  • 氢给体数:
    2
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    1-(3-hydroxyphenyl)-6-methyl-1,2,3,4-tetrahydro-β-carboline hydrochloride 、 苯甲醛甲酸potassium carbonate 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 3.0h, 以77.4%的产率得到6-methyl-1-(3-hydroxyphenyl)-2-benzyl-1,2,3,4-tetrahydro-β-carboline
    参考文献:
    名称:
    Discovery of tetrahydro-β-carbolines as inhibitors of the mitotic kinesin KSP
    摘要:
    Inhibitors of kinesin spindle protein (KSP) are a promising class of anticancer agents that cause mitotic arrest in cells from a failure to form functional bipolar mitotic spindles. Here, we report the synthesis and biological evaluation of a novel series of tetrahydro-beta-carboline analogs based on the structure of the known KSP inhibitor HR22C16. Preferred compounds 11b, 12a and 19b were identified as potent inhibitors in a KSP ATPase assay with good anti-proliferative activity in A549 cells. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2010.05.024
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文献信息

  • Discovery of tetrahydro-β-carbolines as inhibitors of the mitotic kinesin KSP
    作者:Fei Liu、Li-Qin Yu、Cheng Jiang、Lei Yang、Wu-Tong Wu、Qi-Dong You
    DOI:10.1016/j.bmc.2010.05.024
    日期:2010.6.15
    Inhibitors of kinesin spindle protein (KSP) are a promising class of anticancer agents that cause mitotic arrest in cells from a failure to form functional bipolar mitotic spindles. Here, we report the synthesis and biological evaluation of a novel series of tetrahydro-beta-carboline analogs based on the structure of the known KSP inhibitor HR22C16. Preferred compounds 11b, 12a and 19b were identified as potent inhibitors in a KSP ATPase assay with good anti-proliferative activity in A549 cells. (C) 2010 Elsevier Ltd. All rights reserved.
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