摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

2'-O-(trans-2-methoxy-cyclohexyl) adenosine | 1097931-66-2

中文名称
——
中文别名
——
英文名称
2'-O-(trans-2-methoxy-cyclohexyl) adenosine
英文别名
2'-O-(trans-2-methoxy-cyclohexyl)adenosine;(2R,3R,4R,5R)-5-(6-aminopurin-9-yl)-2-(hydroxymethyl)-4-[(1R,2R)-2-methoxycyclohexyl]oxyoxolan-3-ol
2'-O-(trans-2-methoxy-cyclohexyl) adenosine化学式
CAS
1097931-66-2
化学式
C17H25N5O5
mdl
——
分子量
379.416
InChiKey
XBARQOPUMSNSEE-MGHJIYOTSA-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):
    0.7
  • 重原子数:
    27
  • 可旋转键数:
    5
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.71
  • 拓扑面积:
    138
  • 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

  • 作为反应物:
    描述:
    2'-O-(trans-2-methoxy-cyclohexyl) adenosine三甲基氯硅烷苯甲酰氯ammonium hydroxide 在 ice water 、 甲醇乙酸乙酯 、 silyl 、 silica gel 、 chloroform methanol 作用下, 以 吡啶 为溶剂, 5.0~30.0 ℃ 、3.55 kPa 条件下, 反应 5.25h, 生成 N6-Benzoyl-2'-O-(trans-2-methoxycyclohexyl) adenosine
    参考文献:
    名称:
    Human RNase H1 oligonucleotide compositions thereof
    摘要:
    本发明提供了可以作为人类2型RNase H底物的寡核苷酸。本发明还涉及使用这些寡核苷酸增强反义寡核苷酸治疗的方法。
    公开号:
    US20070292875A1
  • 作为产物:
    参考文献:
    名称:
    RNA targeted 2′-modified oligonucleotides that are conformationally preorganized
    摘要:
    本文披露了含有2′-O修饰的核糖核苷和含有这种核苷的修饰寡核苷酸。通过分子建模实验表明,本文披露了具有增强结合亲和力的寡核苷酸。本发明的2′-O修饰核苷包括环结构,可将核苷的糖基物质优先定位在3′ endo几何构型中。
    公开号:
    US06271358B1
点击查看最新优质反应信息

文献信息

  • Oligonucleotides having A-DNA form and B-DNA form conformational geometry
    申请人:——
    公开号:US20030096979A1
    公开(公告)日:2003-05-22
    Modified oligonucleotides containing both A-form conformation geometry and B-from conformation geometry nucleotides are disclosed. The B-form geometry allows the oligonucleotide to serve as substrates for RNase H when bound to a target nucleic acid strand. The A-form geometry imparts properties to the oligonucleotide that modulate binding affinity and nuclease resistance. By utilizing C2′ endo sugars or O4′ endo sugars, the B-form characteristics are imparted to a portion of the oligonucleotide. The A-form characteristics are imparted via use of either 2′-O-modified nucleotides that have 3′ endo geometries or use of end caps having particular nuclease stability or by use of both of these in conjunction with each other.
    修改的寡核苷酸同时包含A型构象几何和B型构象几何核苷酸。B型构象允许寡核苷酸在与靶核酸链结合时充当RNase H的底物。A型构象赋予寡核苷酸特定属性,调节结合亲和力和核酸酶抵抗性。通过利用C2′内醛糖或O4′内醛糖,将B型特性赋予寡核苷酸的一部分。通过使用具有3′内醛几何结构的2′-O修饰核苷酸或具有特定核酸酶稳定性的端盖,或者同时使用这两者来赋予A型特性。
  • Human Rnase H1 and oligonucleotide compositions thereof
    申请人:Isis Pharmaceuticals, Inc.
    公开号:US06617442B1
    公开(公告)日:2003-09-09
    The present invention provides oligonucleotides that can serve as substrates for human Type 2 RNase H. The present invention is also directed to methods of using these oligonucleotides in enhancing antisense oligonucleotide therapies.
    本发明提供了可作为人类Type 2 RNase H底物的寡核苷酸。本发明还涉及使用这些寡核苷酸来增强反义寡核苷酸治疗的方法。
  • Human RNase H1 and oligonucleotide compositions thereof
    申请人:ISIS Pharmaceuticals, Inc.
    公开号:US20040102618A1
    公开(公告)日:2004-05-27
    The present invention provides oligonucleotides that can serve as substrates for human Type 2 RNase H. The present invention is also directed to methods of using these oligonucleotides in enhancing antisense oligonucleotide therapies.
    本发明提供了可以作为人类2型RNA酶H底物的寡核苷酸。本发明还涉及使用这些寡核苷酸增强反义寡核苷酸治疗的方法。
  • Oligonucleotdies having A-DNA form and B-DNA form conformational geometry
    申请人:Manoharan Muthiah
    公开号:US20070123702A1
    公开(公告)日:2007-05-31
    Modified oligonucleotides containing both A-form conformation geometry and B-from conformation geometry nucleotides are disclosed. The B-form geometry allows the oligonucleotide to serve as substrates for RNase H when bound to a target nucleic acid strand. The A-form geometry imparts properties to the oligonucleotide that modulate binding affinity and nuclease resistance. By utilizing C2′ endo sugars or O4′ endo sugars, the B-form characteristics are imparted to a portion of the oligonucleotide. The A-form characteristics are imparted via use of either 2′-O-modified nucleotides that have 3′ endo geometries or use of end caps having particular nuclease stability or by use of both of these in conjunction with each other.
    本发明揭示了含有A形构象几何和B形构象几何核苷酸的修饰寡核苷酸。B形几何使寡核苷酸在与靶核酸链结合时可以作为RNase H的底物。A形几何赋予寡核苷酸特定的性质,可以调节结合亲和力和核酸酶抵抗性。通过利用C2′内糖或O4′内糖,将B形特征赋予寡核苷酸的一部分。通过使用具有3′内糖几何的2′-O修饰核苷酸或具有特定核酸酶稳定性的末端盖子或同时使用这两种方法,将A形特征赋予寡核苷酸。
  • Oligonucleotides having A-DNA or B-DNA form
    申请人:ISIS PHARMACEUTICALS, INC.
    公开号:EP1743901A2
    公开(公告)日:2007-01-17
    Modified oligonucleotides containing both A-form conformation geometry and B-form conformation geometry nucleotides are disclosed. The B-form geometry allows the oligonucleotide to serve as substrates for RNase H when bound to a target nucleic acid strand. The A-form geometry imparts properties to the oligonucleotide that modulate binding affinity and nuclease resistance. By utilising C2' endo sugars or O4' endo sugars, the B-form characteristics are imparted to a portion of the oligonucleotide. The A-form characteristics are imparted via use of either 2'-O-modified nucleotides that have 3' endo geometries or use of end caps having particular nuclease stability or by use of both of these in conjunction with each other.
    本研究公开了含有 A 型构象几何和 B 型构象几何核苷酸的修饰寡核苷酸。B 型几何结构可使寡核苷酸在与目标核酸链结合时成为 RNase H 的底物。A 型几何结构赋予了寡核苷酸调节结合亲和力和核酸酶抗性的特性。通过利用 C2'内切糖或 O4'内切糖,可将 B 型特性赋予部分寡核苷酸。通过使用具有 3'内切几何结构的 2'-O 修饰核苷酸,或使用具有特殊核酸酶稳定性的端盖,或通过同时使用这两种核苷酸,可赋予 A 型特性。
查看更多