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N-(2-(naphthalen-2-yl)ethyl)-1H-pyrrole-2-carboxamide | 1569312-39-5

中文名称
——
中文别名
——
英文名称
N-(2-(naphthalen-2-yl)ethyl)-1H-pyrrole-2-carboxamide
英文别名
N-(2-naphthalen-2-ylethyl)-1H-pyrrole-2-carboxamide
N-(2-(naphthalen-2-yl)ethyl)-1H-pyrrole-2-carboxamide化学式
CAS
1569312-39-5
化学式
C17H16N2O
mdl
——
分子量
264.327
InChiKey
NBWVXFRPFCZGCR-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):
    3.5
  • 重原子数:
    20
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    44.9
  • 氢给体数:
    2
  • 氢受体数:
    1

反应信息

  • 作为产物:
    描述:
    2-(三氯乙酰)吡咯2-萘-2-乙胺三乙胺 作用下, 以 乙腈 为溶剂, 反应 24.0h, 以51%的产率得到N-(2-(naphthalen-2-yl)ethyl)-1H-pyrrole-2-carboxamide
    参考文献:
    名称:
    Synthesis and anticancer activity of focused compound libraries from the natural product lead, oroidin
    摘要:
    Oroidin (1), (E)-N-(3-(2-amino-1H-imidazol-4-yl) allyl)-4,5-dibromo-1H-pyrrole-2-carboxamide, is a pyrrole alkaloid isolated from the marine sponge Agelas oroides. Routine screening in a panel of twelve cancer cell lines revealed 1 to be poorly cytotoxic with the 50% growth inhibition concentration (GI(50)) of 42 mu M in MCF-7 (breast) cells and 24 mu M in A2780 (ovarian) cells and >50 mu M in all other cell lines tested. The development of eight focused libraries comprising thirty compounds total identified N-(biphenyl-4-ylmethyl)-1H-pyrrole-2-carboxamide (4l), N-benzyl-4,5-dibromo-1H-pyrrole-2-carboxamide (5a) and N-(biphenyl-4-ylmethyl)-4,5-dibromo-1H-pyrrole-2-carboxamide (5l) as potent inhibitors of cell growth in our panel of cell lines. Of these compounds GI(50) values of <5 mu M were observed with 4l against HT29 (colon) and SW480 (colon); 5a against HT29; and 5l against HT29, SW480, MCF-7, A431 (skin), Du145 (prostate), BE2-C (neuroblastoma) and MIA (pancreas) cell lines. As a cancer class, colon cancer appears to be more sensitive to the oroidin series of compounds, with analogue 5l being the most active. (C) 2014 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2014.01.021
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