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5-(3-Amino-propyl)-1-((2R,3R,4R,5R)-4-hydroxy-5-hydroxymethyl-3-methoxy-tetrahydro-furan-2-yl)-1H-pyrimidine-2,4-dione | 289676-19-3

中文名称
——
中文别名
——
英文名称
5-(3-Amino-propyl)-1-((2R,3R,4R,5R)-4-hydroxy-5-hydroxymethyl-3-methoxy-tetrahydro-furan-2-yl)-1H-pyrimidine-2,4-dione
英文别名
5-(3-aminopropyl)-1-[(2R,3R,4R,5R)-4-hydroxy-5-(hydroxymethyl)-3-methoxyoxolan-2-yl]pyrimidine-2,4-dione
5-(3-Amino-propyl)-1-((2R,3R,4R,5R)-4-hydroxy-5-hydroxymethyl-3-methoxy-tetrahydro-furan-2-yl)-1H-pyrimidine-2,4-dione化学式
CAS
289676-19-3
化学式
C13H21N3O6
mdl
——
分子量
315.326
InChiKey
UXHANWSJBOWQHX-DNRKLUKYSA-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):
    -2.1
  • 重原子数:
    22
  • 可旋转键数:
    6
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.69
  • 拓扑面积:
    134
  • 氢给体数:
    4
  • 氢受体数:
    7

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:
    5-(3-Amino-propyl)-1-((2R,3R,4R,5R)-4-hydroxy-5-hydroxymethyl-3-methoxy-tetrahydro-furan-2-yl)-1H-pyrimidine-2,4-dione吡啶盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 34.0h, 生成 Acetic acid (2R,3R,4R,5R)-2-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-5-(5-{3-[2-(1-diphenylcarbamoyl-1H-imidazol-4-yl)-acetylamino]-propyl}-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-4-methoxy-tetrahydro-furan-3-yl ester
    参考文献:
    名称:
    Functionalized nucleoside 5′-triphosphates for in vitro selection of new catalytic ribonucleic acids
    摘要:
    A series of novel 2'-modified nucleoside 5'-triphosphates was synthesized. The amino, imidazole, and carboxylate functionalities were attached to the 5-position of pyrimidine base of these molecules through alkynyl and alkyl spacers, respectively. Two different phosphorylation methods were used to optimize the yields of these highly modified triphosphates. (C) 2000 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(00)00226-2
  • 作为产物:
    描述:
    Acetic acid (2R,3R,4R,5R)-2-acetoxymethyl-5-(5-iodo-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-4-methoxy-tetrahydro-furan-3-yl ester 在 palladium on activated charcoal ammonium hydroxidecopper(l) iodide 、 (Ph3P)4P 、 氢气三乙胺 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 4.0 ℃ 、275.79 kPa 条件下, 反应 56.0h, 生成 5-(3-Amino-propyl)-1-((2R,3R,4R,5R)-4-hydroxy-5-hydroxymethyl-3-methoxy-tetrahydro-furan-2-yl)-1H-pyrimidine-2,4-dione
    参考文献:
    名称:
    Functionalized nucleoside 5′-triphosphates for in vitro selection of new catalytic ribonucleic acids
    摘要:
    A series of novel 2'-modified nucleoside 5'-triphosphates was synthesized. The amino, imidazole, and carboxylate functionalities were attached to the 5-position of pyrimidine base of these molecules through alkynyl and alkyl spacers, respectively. Two different phosphorylation methods were used to optimize the yields of these highly modified triphosphates. (C) 2000 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(00)00226-2
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文献信息

  • Nucleotide triphosphates and their incorporation into oligonucleotides
    申请人:——
    公开号:US20030004122A1
    公开(公告)日:2003-01-02
    The present invention relates to novel nucleotide triphosphates, methods of synthesis and process of incorporating these nucleotide triphosphates into oligonucleotides, and isolation of novel nucleic acid catalysts (e.g., ribozymes or DNAzymes). Also, provided are the use of novel enzymatic nucleic acid molecules to inhibit HER2/neu/ErbB2 gene expression and their applications in human therapy.
    本发明涉及新颖的核苷酸三磷酸盐,合成方法和将这些核苷酸三磷酸盐合成到寡核苷酸中的过程,以及新颖的核酸催化剂(例如核糖酶或DNA酶)的分离。此外,提供了使用新型酶促核酸分子抑制HER2 / neu / ErbB2基因表达的方法,并将其应用于人类治疗。
  • NUCLEIC ACID BASED MODULATORS OF GENE EXPRESSION
    申请人:RIBOZYME PHARMACEUTICALS, INC.
    公开号:EP1212416A2
    公开(公告)日:2002-06-12
  • JP2004512810A
    申请人:——
    公开号:JP2004512810A
    公开(公告)日:2004-04-30
  • US6528640B1
    申请人:——
    公开号:US6528640B1
    公开(公告)日:2003-03-04
  • US6617438B1
    申请人:——
    公开号:US6617438B1
    公开(公告)日:2003-09-09
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