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Acetic acid;cyclohexane-1,2-diamine | 957771-42-5

中文名称
——
中文别名
——
英文名称
Acetic acid;cyclohexane-1,2-diamine
英文别名
——
Acetic acid;cyclohexane-1,2-diamine化学式
CAS
957771-42-5
化学式
C8H18N2O2
mdl
——
分子量
174.24
InChiKey
NLXWRANDNXTOJJ-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):
    0.31
  • 重原子数:
    12
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.88
  • 拓扑面积:
    89.3
  • 氢给体数:
    3
  • 氢受体数:
    4

文献信息

  • STABILIZED NUCLEIC ACID DARK QUENCHER-FLUOROPHORE PROBES
    申请人:Cook Ronald M.
    公开号:US20090259030A1
    公开(公告)日:2009-10-15
    The present invention provides a new class of solids supports for synthesis of modified oligomers of nucleic acids, and nucleic acid probes that have a format expediently synthesized on the new supports. Exemplary solid supports include at least one quencher bound through a linker to the solid support. Various exemplary embodiments include a moiety that stabilizes a duplex, triplex or higher order aggregation (e.g., hybridization) of nucleic acids of which the oligomer of the invention is a component. Other components of the solid support include moieties that stabilize aggregations of nucleic acids, e.g., intercalators, minor groove binding moieties, bases modified with a stabilizing moiety (e.g., alkynyl moieties, and fluoroalkyl moieties), and conformational stabilizing moieties, such as those described in commonly owned U.S. Patent Application Publication No. 2007/0059752.
    本发明提供了一种新型固体支持体,用于合成修饰寡核苷酸的新类固体支持体以及具有在新支持体上方便合成的核酸探针。示例固体支持体包括至少通过连接剂与固体支持体结合的一个猝灭剂。各种示例实施例包括稳定双链、三链或更高级别聚集(例如,杂交)的基团,其中该发明的寡聚物是其中的一个组分的基团。固体支持体的其他组分包括稳定核酸聚集的基团,例如,插入剂、小沟结合基团、经过稳定基团修饰的碱基(例如,炔基基团和氟烷基团)和构象稳定基团,例如,如同在共同拥有的美国专利申请公开号2007/0059752中描述的那样。
  • Enhanced triple-helix and double-helix formation with oligomers containing modified pyrimidines
    申请人:——
    公开号:US20030170680A1
    公开(公告)日:2003-09-11
    Novel oligomers are disclosed which have enhanced ability with respect to forming duplexes or triplexes compared with oligomers containing only conventional bases. The oligomers contain the bases 5-(1-propynyl)uracil, 5-(1-propynyl)cytosine or related analogs. The oligomers of the invention are capable of (i) forming triplexes with various target sequences such as virus or oncogene sequences by coupling into the major groove of a target DNA duplex at physiological pH or (ii) forming duplexes by binding to single-stranded DNA or to RNA encoded by target genes. The oligomers of the invention can be incorporated into pharmaceutically acceptable carriers and can be constructed to have any desired sequence, provided the sequence normally includes one or more bases that is replaced with the analogs of the invention. Compositions of the invention can be used as pharmaceutical agents to treat various diseases such as those caused by viruses and can be used for diagnostic purposes in order to detect viruses or disease conditions.
    本发明揭示了一种新型寡聚物,与仅含传统碱基的寡聚物相比,具有增强的形成双链或三链的能力。该寡聚物包含5-(1-丙炔基)尿嘧啶,5-(1-丙炔基)胞嘧啶或相关类似物的碱基。本发明的寡聚物能够(i)通过在生理pH值下与靶DNA双链的主沟结合,形成与各种靶序列(如病毒或癌基因序列)的三链,或(ii)通过结合单链DNA或靶基因编码的RNA而形成双链。本发明的寡聚物可以被纳入药学可接受的载体中,并且可以构建任何所需的序列,只要序列通常包括一个或多个被本发明类似物替换的碱基。本发明的组合物可以用作制药剂治疗各种由病毒引起的疾病,并可用于诊断目的,以检测病毒或疾病情况。
  • ENHANCED TRIPLE-HELIX AND DOUBLE-HELIX FORMATION WITH OLIGOMERS CONTAINING MODIFIED PYRIMIDINES
    申请人:——
    公开号:US20040265802A9
    公开(公告)日:2004-12-30
    Novel oligomers are disclosed which have enhanced ability with respect to forming duplexes or triplexes compared with oligomers containing only conventional bases. The oligomers contain the bases 5-(1-propynyl)uracil, 5-(1-propynyl)cytosine or related analogs. The oligomers of the invention are capable of (i) forming triplexes with various target sequences such as virus or oncogene sequences by coupling into the major groove of a target DNA duplex at physiological pH or (ii) forming duplexes by binding to single-stranded DNA or to RNA encoded by target genes. The oligomers of the invention can be incorporated into pharmaceutically acceptable carriers and can be constructed to have any desired sequence, provided the sequence normally includes one or more bases that is replaced with the analogs of the invention. Compositions of the invention can be used as pharmaceutical agents to treat various diseases such as those caused by viruses and can be used for diagnostic purposes in order to detect viruses or disease conditions.
    本发明披露了一种新型寡聚物,与仅含传统碱基的寡聚物相比,其具有增强的双链或三链形成能力。该寡聚物包含碱基5-(1-丙炔基)尿嘧啶,5-(1-丙炔基)胞嘧啶或相关类似物。本发明的寡聚物能够(i)在生理pH下通过耦合到目标DNA双链的主沟槽形成三链,如病毒或癌基因序列,或(ii)通过结合到单链DNA或由目标基因编码的RNA形成双链。本发明的寡聚物可以被纳入到药学可接受的载体中,并且可以构建任何所需的序列,只要该序列通常包括一个或多个被本发明的类似物替换的碱基。本发明的组合物可以用作制药剂治疗各种疾病,如由病毒引起的疾病,并且可以用于诊断目的,以检测病毒或疾病情况。
  • Oligomers containing modified pyrimidines
    申请人:ISIS PHARMACEUTICALS, INC.
    公开号:EP1256589A2
    公开(公告)日:2002-11-13
    An oligomer comprising at least two nucleomonomers and pharmaceutically acceptable salts thereof wherein at least one of said nucleomonomers comprises a base of formula (1) or (2): wherein each X is independently O or S; R2 is a group comprising at least one pi bond connected to the carbon atom attached to the base; Pr is (H)2 or a protecting group;    with the proviso that when at least one of said nucleomonomers of said oligomer comprises deoxyuridine 5-substituted by vinyl, 1-butenyl, 1-pentenyl, 1-hexenyl, 1-heptenyl, 1-octenyl, 1-propynyl, 1-butynyl, 1-hexynyl, 1-heptynyl, or 1-octynyl, then the remainder of the nucleomonomers comprising said oligomer are not solely comprised of phosphodiester linked 2'-deoxyadenosine, 2'deoxyguanosine, 2'-deoxycytidine, thymidine or a combination thereof; and wherein said oligomer includes at least one unit having one of thirteen specific formulas.
    由至少两种核单体及其药学上可接受的盐组成的低聚物,其中至少一种核单体包括式 (1) 或 (2) 的碱: 其中每个 X 独立地为 O 或 S; R2 是一个基团,包含至少一个与连接到碱的碳原子相连的π键; Pr 是 (H)2 或保护基团; 1-庚炔基、1-庚炔基、1-辛炔基、1-丙炔基、1-丁炔基、1-己炔基、1-庚炔基或 1-辛炔基,则组成所述低聚物的核单体的其余部分并非仅由磷酸二酯连接的 2'-脱氧腺苷2'-脱氧鸟苷、2'-脱氧胞苷、胸腺嘧啶或其组合组成;其中所述低聚物包括至少一个具有十三种特定公式之一的单元。
  • Stabilized Nucleic Acid Dark Quencher-Fluorophore Probes
    申请人:Biosearch Technologies, Inc.
    公开号:EP2757091A1
    公开(公告)日:2014-07-23
    The present invention provides a new class of solids supports for synthesis of modified oligomers of nucleic acids, and nucleic acid probes that have a format expediently synthesized on the new supports. Exemplary solid supports include at least one quencher bound through a linker to the solid support. Various exemplary embodiments include a moiety that stabilizes a duplex, triplex, or higher order aggregation (e.g. hybridization) of nucleic acids of which the oligomer of the invention is a component. Other components of the solid support include moieties that stabilize aggregations of nucleic acids, e.g. intercalators, minor groove binding moieties, bases modified with a stabilizing moiety (e.g. alkynyl moieties, and fluoroalkyl moieties), and conformational stabilizing moieties, such as those described in commonly owned U.S. Patent Application Publication No. 2007/0059752.
    本发明提供了一类新的固体支持物,用于合成经修饰的核酸寡聚体,以及可在新支持物上方便合成的核酸探针。示例性固体支持物包括至少一种通过连接体与固体支持物结合的淬灭剂。各种示例性实施方案包括一种分子,它能稳定本发明寡聚体作为其组成部分的核酸的双工、三工或高阶聚合(如杂交)。固体支持物的其他成分包括可稳定核酸聚集的分子,如插入物、小槽结合分子、用稳定分子修饰的碱基(如炔基分子和氟烷基分子),以及构象稳定分子,如共同拥有的美国专利申请公开号 2007/0059752 中所述的分子。
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