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2-(6-Amino-2-methylpurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol | 16526-56-0

中文名称
——
中文别名
——
英文名称
2-(6-Amino-2-methylpurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol
英文别名
——
2-(6-Amino-2-methylpurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol化学式
CAS
16526-56-0
化学式
C11H15N5O4
mdl
——
分子量
281.27
InChiKey
IQZWKGWOBPJWMX-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

物化性质

  • 沸点:
    517.8±60.0 °C(Predicted)
  • 密度:
    1.96±0.1 g/cm3(Predicted)
  • 最大波长(λmax):
    258 (cations); 264 (neutral molecules)

计算性质

  • 辛醇/水分配系数(LogP):
    -0.6
  • 重原子数:
    20
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.55
  • 拓扑面积:
    140
  • 氢给体数:
    4
  • 氢受体数:
    8

SDS

SDS:9662e637fe7b70c7c358a9ea8fcea2ce
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制备方法与用途

2-甲基腺苷是一种腺苷类似物,主要作为平滑肌血管扩张剂使用,并被证实能抑制癌症的进展。这类物质中,磷酸腺苷、阿卡地辛(HY-13417)、氯法拉滨(HY-A0005)、磷酸氟达拉滨(HY-B0028)和维达拉宾(HY-B0277)等产品较为流行。

文献信息

  • MR1 LIGANDS AND PHARMACEUTICAL COMPOSITIONS FOR IMMUNOMODULATION
    申请人:Universität Basel
    公开号:EP3889602A1
    公开(公告)日:2021-10-06
    The invention relates to a method for modulating an interaction between an MR1 polypeptide and an MR1-specific T cell receptor molecule, whereby a MR1 polypeptide is contacted with a MR1 ligand compound that is a nucleobase adduct product reflecting a state of metabolic distress of a eukaryotic cell. The invention further relates to the use of compounds identified as MR1 ligands in vaccination or modulation of an MR1-restricted immune response.
    本发明涉及一种调节MR1多肽与MR1特异性T细胞受体分子之间相互作用的方法,其中MR1多肽与MR1配体化合物接触,MR1配体化合物是反映真核细胞代谢窘迫状态的核碱基加合物产物。 本发明进一步涉及鉴定为 MR1 配体的化合物在疫苗接种或调节 MR1 限制性免疫反应中的用途。
  • Modulators of DUX4 for regulation of muscle function
    申请人:GENEA BIOCELLS USA (HOLDINGS), INC.
    公开号:US10933068B2
    公开(公告)日:2021-03-02
    Disclosed herein are methods and compositions for the treatment of facioscapulohumeral muscular dystrophy and other muscle diseases or disorders. In some cases, the methods and compositions involve the use of methyltransferase inhibitors to inhibit or repress DUX4 expression in muscle cells. Further disclosed herein are methods and cell based assays for screening compounds for the treatment of facioscapulohumeral muscular dystrophy and other muscle diseases.
    本文公开了治疗面肱骨肌营养不良症和其他肌肉疾病或紊乱的方法和组合物。在某些情况下,这些方法和组合物涉及使用甲基转移酶抑制剂来抑制或抑制肌肉细胞中 DUX4 的表达。本文进一步公开了用于筛选治疗面阔肌营养不良症和其他肌肉疾病的化合物的方法和基于细胞的检测方法。
  • Profiling chemically modified DNA/RNA units for disease and cancer diagnosis
    申请人:The Research Foundation for The State University of New York
    公开号:US11339441B2
    公开(公告)日:2022-05-24
    The present invention relates to high-throughput methods comprising direct infusion electrospray ionization mass spectrometry (ESI-MS), multistep tandem mass spectrometry (MSn), consecutive reaction monitoring (CRM), ion mobility spectrometry mass spectrometry (IMS-MS), high-resolution MS, and IMS-MS, for genome-wide (whole cell or tissue) profiling of DNA and RNA nucleotides/nucleosides having a wide variety of variant structural modifications. In particular, these methods are contemplated for providing a specific profile of variant DNA and/or RNA chemically modified nucleic acids (i.e. structures) associated with specific medical conditions. Medical conditions may include, but are not limited to: cancer; including prostate, lung, uterus, larynx, ovary, breast, kidney, and many other types of cancers; specific stages of cancer; bacterial infections; viral infections; genetic and metabolic disorders; and any condition involving changes in DNA and/or RNA structural modifications.
    本发明涉及高通量方法,包括直接注入电喷雾离子化质谱(ESI-MS)、多步串联质谱(MSn)、连续反应监测(CRM)、离子迁移谱质谱(IMS-MS)、高分辨率 MS 和 IMS-MS,用于对具有多种变异结构修饰的 DNA 和 RNA 核苷酸/核苷进行全基因组(全细胞或组织)分析。特别是,这些方法可用于提供与特定病症相关的变异 DNA 和/或 RNA 化学修饰核酸(即结构)的特定概况。病症可包括但不限于:癌症;包括前列腺癌、肺癌、子宫癌、喉癌、卵巢癌、乳腺癌、肾癌和许多其他类型的癌症;癌症的特定阶段;细菌感染;病毒感染;遗传和代谢紊乱;以及任何涉及 DNA 和/或 RNA 结构修饰变化的病症。
  • PROFILING CHEMICALLY MODIFIED DNA/RNA UNITS FOR DISEASE AND CANCER DIAGNOSIS
    申请人:THE RESEARCH FOUNDATION FOR THE STATE UNIVERSITY OF NEW YORK
    公开号:US20170044619A1
    公开(公告)日:2017-02-16
    The present invention relates to high-throughput methods comprising direct infusion electrospray ionization mass spectrometry (ESI-MS), multistep tandem mass spectrometry (MS n ), consecutive reaction monitoring (CRM), ion mobility spectrometry mass spectrometry (IMS-MS), high-resolution MS, and IMS-MS, for genome-wide (whole cell or tissue) profiling of DNA and RNA nucleotides/nucleosides having a wide variety of variant structural modifications. In particular, these methods are contemplated for providing a specific profile of variant DNA and/or RNA chemically modified nucleic acids (i.e. structures) associated with specific medical conditions. Medical conditions may include, but are not limited to: cancer; including prostate, lung, uterus, larynx, ovary, breast, kidney, and many other types of cancers; specific stages of cancer; bacterial infections; viral infections; genetic and metabolic disorders; and any condition involving changes in DNA and/or RNA structural modifications.
  • MODULATORS OF DUX4 FOR REGULATION OF MUSCLE FUNCTION
    申请人:GENEA BIOCELLS USA (HOLDING), INC.
    公开号:US20190298727A1
    公开(公告)日:2019-10-03
    Disclosed herein are methods and compositions for the treatment of facioscapulohumeral muscular dystrophy and other muscle diseases or disorders. In some cases, the methods and compositions involve the use of methyltransferase inhibitors to inhibit or repress DUX4 expression in muscle cells. Further disclosed herein are methods and cell based assays for screening compounds for the treatment of facioscapulohumeral muscular dystrophy and other muscle diseases.
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