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4-chlorocarbonylbutyric acid [2-(4-chlorocarbonylbutyryloxy)ethyl]ester | 909108-33-4

中文名称
——
中文别名
——
英文名称
4-chlorocarbonylbutyric acid [2-(4-chlorocarbonylbutyryloxy)ethyl]ester
英文别名
2-(5-Chloro-5-oxopentanoyl)oxyethyl 5-chloro-5-oxopentanoate
4-chlorocarbonylbutyric acid [2-(4-chlorocarbonylbutyryloxy)ethyl]ester化学式
CAS
909108-33-4
化学式
C12H16Cl2O6
mdl
——
分子量
327.161
InChiKey
QTCNLKKEDKYHRJ-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):
    1.5
  • 重原子数:
    20
  • 可旋转键数:
    13
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.67
  • 拓扑面积:
    86.7
  • 氢给体数:
    0
  • 氢受体数:
    6

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:
    参考文献:
    名称:
    Crosslinking agent, crosslinking method, method of controlling gene expression, and method of examining gene function
    摘要:
    本发明提供了一种交联剂,其在两端具有光降解保护基团,用于交联双链核酸、核酸和蛋白质或多肽,或蛋白质或多肽,特别是双链RNA;一种使用该交联剂交联双链RNA或类似物的方法;一种调节基因表达的方法,可以在任意时机和位置控制目标基因的表达;以及一种检查基因功能的方法。根据本发明,双链核酸之间、核酸和蛋白质或多肽之间,或蛋白质或多肽之间,特别是双链RNA之间的交联可以很容易地形成,此外,交联也可以很容易地去除,因此可以高效地在任意时机和位置轻松控制目标基因的表达。因此,可以执行在特定时机和位置表达的基因的功能检查和/或鉴定。此外,可以抑制传统光遮蔽化合物难以抑制的双链RNA(siRNA)的RNAi效应,并且可以在任意时机和位置轻松控制目标基因的表达。
    公开号:
    US08084625B2
  • 作为产物:
    参考文献:
    名称:
    Crosslinking agent, crosslinking method, method of controlling gene expression, and method of examining gene function
    摘要:
    本发明提供了一种交联剂,其在两端具有光降解保护基团,用于交联双链核酸、核酸和蛋白质或多肽,或蛋白质或多肽,特别是双链RNA;一种使用该交联剂交联双链RNA或类似物的方法;一种调节基因表达的方法,可以在任意时机和位置控制目标基因的表达;以及一种检查基因功能的方法。根据本发明,双链核酸之间、核酸和蛋白质或多肽之间,或蛋白质或多肽之间,特别是双链RNA之间的交联可以很容易地形成,此外,交联也可以很容易地去除,因此可以高效地在任意时机和位置轻松控制目标基因的表达。因此,可以执行在特定时机和位置表达的基因的功能检查和/或鉴定。此外,可以抑制传统光遮蔽化合物难以抑制的双链RNA(siRNA)的RNAi效应,并且可以在任意时机和位置轻松控制目标基因的表达。
    公开号:
    US08084625B2
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文献信息

  • CROSSLINKING AGENT, CROSSLINKING METHOD, METHOD OF CONTROLLING GENE EXPRESSION, AND METHOD OF EXAMINING GENE FUNCTION
    申请人:Furuta Toshiaki
    公开号:US20090023140A1
    公开(公告)日:2009-01-22
    The present invention provides a crosslinking agent which have photodegradable protective groups at two ends to crosslink double-stranded nucleic acid, a nucleic acid and a protein or a polypeptide, or proteins or polypeptides, in particular, double-stranded RNA; a method for crosslinking a double-stranded RNA or the like using the same; a method for regulating gene expression, which can control the expression of a target gene at an arbitrary timing and location; and a method for examining a gene function. According to the present invention, crosslinking between double-stranded nucleic acids between a nucleic acid and a protein or a polypeptide, or between proteins or polypeptides, in particular, between double-stranded RNA can be easily formed, and in addition, the crosslinking can also be easily removed, so that the expression of a target gene can be easily controlled at an arbitrary timing and location with high efficiency. Hence, as a result, function examination and/or identification of a gene that is expressed at a specific timing and location can be performed. In addition, the RNAi effect of a double-stranded RNA (siRNA) that cannot be easily inhibited by a conventional caged compound can be inhibited, and the expression of a target gene can be easily controlled at an arbitrary timing and location.
  • US8084625B2
    申请人:——
    公开号:US8084625B2
    公开(公告)日:2011-12-27
  • Crosslinking agent, crosslinking method, method of controlling gene expression, and method of examining gene function
    申请人:Wako Pure Chemical Industries, Ltd.
    公开号:US08084625B2
    公开(公告)日:2011-12-27
    The present invention provides a crosslinking agent which have photodegradable protective groups at two ends to crosslink double-stranded nucleic acid, a nucleic acid and a protein or a polypeptide, or proteins or polypeptides, in particular, double-stranded RNA; a method for crosslinking a double-stranded RNA or the like using the same; a method for regulating gene expression, which can control the expression of a target gene at an arbitrary timing and location; and a method for examining a gene function. According to the present invention, crosslinking between double-stranded nucleic acids between a nucleic acid and a protein or a polypeptide, or between proteins or polypeptides, in particular, between double-stranded RNA can be easily formed, and in addition, the crosslinking can also be easily removed, so that the expression of a target gene can be easily controlled at an arbitrary timing and location with high efficiency. Hence, as a result, function examination and/or identification of a gene that is expressed at a specific timing and location can be performed. In addition, the RNAi effect of a double-stranded RNA (siRNA) that cannot be easily inhibited by a conventional caged compound can be inhibited, and the expression of a target gene can be easily controlled at an arbitrary timing and location.
    本发明提供了一种交联剂,其在两端具有光降解保护基团,用于交联双链核酸、核酸和蛋白质或多肽,或蛋白质或多肽,特别是双链RNA;一种使用该交联剂交联双链RNA或类似物的方法;一种调节基因表达的方法,可以在任意时机和位置控制目标基因的表达;以及一种检查基因功能的方法。根据本发明,双链核酸之间、核酸和蛋白质或多肽之间,或蛋白质或多肽之间,特别是双链RNA之间的交联可以很容易地形成,此外,交联也可以很容易地去除,因此可以高效地在任意时机和位置轻松控制目标基因的表达。因此,可以执行在特定时机和位置表达的基因的功能检查和/或鉴定。此外,可以抑制传统光遮蔽化合物难以抑制的双链RNA(siRNA)的RNAi效应,并且可以在任意时机和位置轻松控制目标基因的表达。
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