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2-(6-tert-butoxycarbonylmethoxy-3-oxo-3H-xanthen-9-yl)-4-[3-(9H-fluoren-9-ylmethoxycarbonylamino)-propionylamino]-benzoic acid ethyl ester | 886053-27-6

中文名称
——
中文别名
——
英文名称
2-(6-tert-butoxycarbonylmethoxy-3-oxo-3H-xanthen-9-yl)-4-[3-(9H-fluoren-9-ylmethoxycarbonylamino)-propionylamino]-benzoic acid ethyl ester
英文别名
ethyl 4-[3-(9H-fluoren-9-ylmethoxycarbonylamino)propanoylamino]-2-[3-[2-[(2-methylpropan-2-yl)oxy]-2-oxoethoxy]-6-oxoxanthen-9-yl]benzoate
2-(6-tert-butoxycarbonylmethoxy-3-oxo-3H-xanthen-9-yl)-4-[3-(9H-fluoren-9-ylmethoxycarbonylamino)-propionylamino]-benzoic acid ethyl ester化学式
CAS
886053-27-6
化学式
C46H42N2O10
mdl
——
分子量
782.847
InChiKey
COESUHVVTDLLGK-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

物化性质

  • 沸点:
    985.5±65.0 °C(Predicted)
  • 密度:
    1.36±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    6.3
  • 重原子数:
    58
  • 可旋转键数:
    16
  • 环数:
    7.0
  • sp3杂化的碳原子比例:
    0.24
  • 拓扑面积:
    156
  • 氢给体数:
    2
  • 氢受体数:
    10

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:
    2-(6-tert-butoxycarbonylmethoxy-3-oxo-3H-xanthen-9-yl)-4-[3-(9H-fluoren-9-ylmethoxycarbonylamino)-propionylamino]-benzoic acid ethyl ester三氟乙酸 作用下, 以 二氯甲烷 为溶剂, 反应 3.0h, 以95%的产率得到2-(6-carboxymethoxy-3-oxo-3H-xanthen-9-yl)-4-[3-(9H-fluoren-9-ylmethoxycarbonyl-amino)-propionylamino]-benzoic acid ethyl ester
    参考文献:
    名称:
    Fluorescein-based amino acids for solid phase synthesis of fluorogenic protease substrates
    摘要:
    An efficient synthesis of new type fluorescent amino acids is described. The Fmoc-protected dyes can be prepared in a four-step procedure with similar to 30% overall yield from aminofluoresceins and other inexpensive commercially available precursors. The dyes are much more photostable compared to fluorescein and exhibit constant pH-independent fluorescence that is advantageous in biological applications. The Fmoc-protected fluorescent amino acids are ready for use in solid phase peptide synthesis. As a proof of concept, a fluorogenic papain Substrate was synthesized and employed for on-bead detection of the protease activity. By using a novel technique for quantitative analysis of bead fluorescence, a similar to 2.7-fold increase in mean bead brightness was measured and was attributed to Substrate cleavage by papain. The new type fluorescent amino acids seem to be a promising tool for the synthesis of fluorescent peptide ligands and fluorogenic protease substrates. (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2005.11.037
  • 作为产物:
    参考文献:
    名称:
    Fluorescein-based amino acids for solid phase synthesis of fluorogenic protease substrates
    摘要:
    An efficient synthesis of new type fluorescent amino acids is described. The Fmoc-protected dyes can be prepared in a four-step procedure with similar to 30% overall yield from aminofluoresceins and other inexpensive commercially available precursors. The dyes are much more photostable compared to fluorescein and exhibit constant pH-independent fluorescence that is advantageous in biological applications. The Fmoc-protected fluorescent amino acids are ready for use in solid phase peptide synthesis. As a proof of concept, a fluorogenic papain Substrate was synthesized and employed for on-bead detection of the protease activity. By using a novel technique for quantitative analysis of bead fluorescence, a similar to 2.7-fold increase in mean bead brightness was measured and was attributed to Substrate cleavage by papain. The new type fluorescent amino acids seem to be a promising tool for the synthesis of fluorescent peptide ligands and fluorogenic protease substrates. (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2005.11.037
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文献信息

  • Fluorescein-Based Compounds And Their Use For Peptide Synthesis
    申请人:Balakirev Maxim
    公开号:US20080275215A1
    公开(公告)日:2008-11-06
    The present invention is related to new fluorescein derivatives, the method for producing such derivatives and their use for the synthesis of fluorogenic peptides and in particular protease substrates and peptide ligands.
    本发明涉及新的荧光素衍生物,以及制备这些衍生物的方法及其用于合成荧光基肽和特别是蛋白酶底物和肽配体的用途。
  • Fluorescein-based amino acids for solid phase synthesis of fluorogenic protease substrates
    作者:Olga N. Burchak、Laurent Mugherli、François Chatelain、Maxim Y. Balakirev
    DOI:10.1016/j.bmc.2005.11.037
    日期:2006.4
    An efficient synthesis of new type fluorescent amino acids is described. The Fmoc-protected dyes can be prepared in a four-step procedure with similar to 30% overall yield from aminofluoresceins and other inexpensive commercially available precursors. The dyes are much more photostable compared to fluorescein and exhibit constant pH-independent fluorescence that is advantageous in biological applications. The Fmoc-protected fluorescent amino acids are ready for use in solid phase peptide synthesis. As a proof of concept, a fluorogenic papain Substrate was synthesized and employed for on-bead detection of the protease activity. By using a novel technique for quantitative analysis of bead fluorescence, a similar to 2.7-fold increase in mean bead brightness was measured and was attributed to Substrate cleavage by papain. The new type fluorescent amino acids seem to be a promising tool for the synthesis of fluorescent peptide ligands and fluorogenic protease substrates. (c) 2005 Elsevier Ltd. All rights reserved.
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