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6-[8-(4-dimethylamino-phenyl)-1,2-dimethyl-7-oxo-7H-pyrano[3,2-e]indol-3-yl]-hexanoic acid 4-(2-amino-9H-purin-6-yloxymethyl)-benzylamide | 1291090-25-9

中文名称
——
中文别名
——
英文名称
6-[8-(4-dimethylamino-phenyl)-1,2-dimethyl-7-oxo-7H-pyrano[3,2-e]indol-3-yl]-hexanoic acid 4-(2-amino-9H-purin-6-yloxymethyl)-benzylamide
英文别名
N-[[4-[(2-amino-7H-purin-6-yl)oxymethyl]phenyl]methyl]-6-[8-[4-(dimethylamino)phenyl]-1,2-dimethyl-7-oxopyrano[3,2-e]indol-3-yl]hexanamide
6-[8-(4-dimethylamino-phenyl)-1,2-dimethyl-7-oxo-7H-pyrano[3,2-e]indol-3-yl]-hexanoic acid 4-(2-amino-9H-purin-6-yloxymethyl)-benzylamide化学式
CAS
1291090-25-9
化学式
C40H42N8O4
mdl
——
分子量
698.825
InChiKey
GEFQTFDWWNZVPB-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):
    5.9
  • 重原子数:
    52
  • 可旋转键数:
    13
  • 环数:
    7.0
  • sp3杂化的碳原子比例:
    0.28
  • 拓扑面积:
    153
  • 氢给体数:
    3
  • 氢受体数:
    9

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

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文献信息

  • Syntheses and characterizations of novel pyrrolocoumarin probes for SNAP-tag labeling technology
    作者:De-Sheng Mei、Yi Qu、Jin-Xiang He、Lei Chen、Zhu-Jun Yao
    DOI:10.1016/j.tet.2011.01.075
    日期:2011.3
    SNAP-tag technology is a revolutionary protein labeling technology employing in various biological studies. Since low signal/noise ratio and severe overlap between the FRET donors/acceptors often occurred in applying present fluorescent probes and thus limited the further applications, development of new fluorescent probes with excellent fluorescent properties is still of request by today's SNAP-tag technology. In this paper, a number of SNAP-tag protein probes have been developed by incorporating a novel pyrrolocoumarin fluorophore recently developed by our group. Examination of these novel synthetic compounds shows all these materials possess satisfactory fluorescent properties. Among these, probe 7 exhibits the most excellent characters, and its quantum yield, maximum emission wavelength and Stocks shift reach to 0.44, 534 nm and 112 nm, respectively. Further analysis of structure-property relationship indicates that the probes with a longer C3-substituted alkyl (such as pentyl) give stronger fluorescence. (C) 2011 Elsevier Ltd. All rights reserved.
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