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6-chloro-1-(indol-3-yl)-1,2,3,4-tetrahydro-β-carboline | 1236398-46-1

中文名称
——
中文别名
——
英文名称
6-chloro-1-(indol-3-yl)-1,2,3,4-tetrahydro-β-carboline
英文别名
——
6-chloro-1-(indol-3-yl)-1,2,3,4-tetrahydro-β-carboline化学式
CAS
1236398-46-1
化学式
C19H16ClN3
mdl
——
分子量
321.809
InChiKey
NQIZSICNGOCBGS-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

反应信息

  • 作为反应物:
    描述:
    6-chloro-1-(indol-3-yl)-1,2,3,4-tetrahydro-β-carboline丁酰氯三乙胺 作用下, 以 四氢呋喃 为溶剂, 反应 2.0h, 以67%的产率得到6-chloro-1-(indol-3-yl)-2-butyryl-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
  • 作为产物:
    描述:
    三氟乙酸 作用下, 以 氯仿 为溶剂, 反应 24.0h, 以1.35 g的产率得到6-chloro-1-(indol-3-yl)-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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