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N2-isobutyryl-3'-O-(methylthiomethyl)-5'-O-(tert-butyldimethylsilyl)-2'-deoxyguanosine

中文名称
——
中文别名
——
英文名称
N2-isobutyryl-3'-O-(methylthiomethyl)-5'-O-(tert-butyldimethylsilyl)-2'-deoxyguanosine
英文别名
N2-isobutyryl-3'-O-(methylthiomethyl)-5'-O-(tert-butyldimethylsilyl)-2'-deoxyguanosine;N-[9-[(2R,4S,5R)-5-[[tert-butyl(dimethyl)silyl]oxymethyl]-4-(methylsulfanylmethoxy)oxolan-2-yl]-6-oxo-1H-purin-2-yl]-2-methylpropanamide
N<sup>2</sup>-isobutyryl-3'-O-(methylthiomethyl)-5'-O-(tert-butyldimethylsilyl)-2'-deoxyguanosine化学式
CAS
——
化学式
C22H37N5O5SSi
mdl
——
分子量
511.718
InChiKey
ZAJCJTJYZOITAP-ARFHVFGLSA-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):
    3.73
  • 重原子数:
    34
  • 可旋转键数:
    10
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.73
  • 拓扑面积:
    141
  • 氢给体数:
    2
  • 氢受体数:
    8

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
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • [EN] ION SENSOR DNA AND RNA SEQUENCING BY SYNTHESIS USING NUCLEOTIDE REVERSIBLE TERMINATORS<br/>[FR] SÉQUENÇAGE D'ADN ET D'ARN PAR SYNTHÈSE BASÉ SUR LA DÉTECTION D'IONS À L'AIDE DE TERMINATEURS NUCLÉOTIDIQUES RÉVERSIBLES
    申请人:UNIV COLUMBIA
    公开号:WO2017087887A1
    公开(公告)日:2017-05-26
    This disclosure is related to a method for determining the identity of a nucleotide residue of a single-stranded DNA or RNA, or sequencing DNA or RNA, in a solution using an ion-sensing field effect transistor and reversible nucleotide terminators.
    这项披露涉及一种使用离子感应场效应晶体管和可逆核苷酸终止剂在溶液中确定单链DNA或RNA的核苷酸残基身份,或对DNA或RNA进行测序的方法。
  • Methods and compositions for incorporating nucleotides
    申请人:Intelligent BioSystems Inc.
    公开号:US09399799B2
    公开(公告)日:2016-07-26
    The invention provides methods and compositions, including, without limitation, algorithms, computer readable media, computer programs, apparatus, and systems for determining the identity of nucleic acids in nucleotide sequences using, for example, data obtained from sequencing by synthesis methods. The methods of the invention include correcting one or more phenomena that are encountered during nucleotide sequencing, such as using sequencing by synthesis methods. These phenomena include, without limitation, sequence lead, sequence lag, spectral crosstalk, and noise resulting from variations in illumination and/or filter responses.
    该发明提供了一种确定核苷酸序列中核酸的身份的方法和组合物,包括但不限于算法、计算机可读介质、计算机程序、设备和系统,例如使用通过合成方法测序获得的数据。该发明的方法包括纠正在核苷酸测序过程中遇到的一个或多个现象,例如使用合成方法测序。这些现象包括但不限于序列领先、序列滞后、光谱串扰以及由于照明和/或滤波器响应变化而导致的噪声。
  • Hydroxymethyl linkers for labeling nucleotides
    申请人:INTELLIGENT BIOSYSTEMS, INC.
    公开号:US09322050B2
    公开(公告)日:2016-04-26
    The invention provides methods and compositions, including, without limitation, algorithms, computer readable media, computer programs, apparatus, and systems for determining the identity of nucleic acids in nucleotide sequences using, for example, data obtained from sequencing by synthesis methods. The methods of the invention include correcting one or more phenomena that are encountered during nucleotide sequencing, such as using sequencing by synthesis methods. These phenomena include, without limitation, sequence lead, sequence lag, spectral crosstalk, and noise resulting from variations in illumination and/or filter responses.
    本发明提供了用于确定核苷酸序列中核酸的身份的方法和组合物,包括但不限于算法、计算机可读介质、计算机程序、装置和系统,例如使用由合成测序方法获得的数据。本发明的方法包括纠正在核苷酸测序过程中遇到的一个或多个现象,例如使用合成测序方法。这些现象包括但不限于序列引导、序列滞后、光谱串扰以及由照明和/或滤光片响应变化引起的噪声。
  • Methods And Compositions For Incorporating Nucleotides
    申请人:Gordon Steven
    公开号:US20100035253A1
    公开(公告)日:2010-02-11
    The invention provides methods and compositions, including, without limitation, algorithms, computer readable media, computer programs, apparatus, and systems for determining the identity of nucleic acids in nucleotide sequences using, for example, data obtained from sequencing by synthesis methods. The methods of the invention include correcting one or more phenomena that are encountered during nucleotide sequencing, such as using sequencing by synthesis methods. These phenomena include, without limitation, sequence lead, sequence lag, spectral crosstalk, and noise resulting from variations in illumination and/or filter responses.
    本发明提供了用于利用通过合成方法测序获得的数据,确定核酸序列中核苷酸的身份的方法和组合物,包括但不限于算法、计算机可读介质、计算机程序、设备和系统。本发明的方法包括纠正在核苷酸测序中遇到的一个或多个现象,例如使用通过合成方法进行测序。这些现象包括但不限于序列超前、序列滞后、光谱串扰以及由于照明和/或滤光片响应变化而产生的噪声。
  • Methods And Compositions For Base Calling Nucleic Acids
    申请人:GORDON STEVEN
    公开号:US20100063743A1
    公开(公告)日:2010-03-11
    The invention provides methods and compositions, including, without limitation, algorithms, computer readable media, computer programs, apparatus, and systems for determining the identity of nucleic acids in nucleotide sequences using, for example, data obtained from sequencing by synthesis methods. The methods of the invention include correcting one or more phenomena that are encountered during nucleotide sequencing, such as using sequencing by synthesis methods. These phenomena include, without limitation, sequence lead, sequence lag, spectral crosstalk, and noise resulting from variations in illumination and/or filter responses.
    本发明提供了一种确定核酸序列中核苷酸身份的方法和组合物,包括但不限于算法、计算机可读介质、计算机程序、装置和系统,例如使用通过合成方法测序获得的数据。本发明的方法包括纠正在核苷酸测序中遇到的一个或多个现象,例如使用通过合成方法测序。这些现象包括但不限于序列提前、序列滞后、光谱串扰以及由于照明和/或滤波器响应变化而产生的噪声。
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