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2-Hydroxyoxane-2-carboxylic acid | 776255-60-8

中文名称
——
中文别名
——
英文名称
2-Hydroxyoxane-2-carboxylic acid
英文别名
——
2-Hydroxyoxane-2-carboxylic acid化学式
CAS
776255-60-8
化学式
C6H10O4
mdl
——
分子量
146.14
InChiKey
SXTJHIPACWRISC-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):
    -0.2
  • 重原子数:
    10
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.83
  • 拓扑面积:
    66.8
  • 氢给体数:
    2
  • 氢受体数:
    4

文献信息

  • Pharmaceutical composition
    申请人:KAWASAKI INSTITUTE OF INDUSTRIAL PROMOTION
    公开号:US10993960B1
    公开(公告)日:2021-05-04
    A pharmaceutical composition includes polymer units α and β, each having a hydrophilic polymer chain bound to a cationic polymer chain, and a drug. The polymer units α and β are radially arranged such that the cationic polymer chains are directed inward and the hydrophilic polymer chains are directed outward, thereby forming a micelle with the drug encapsulated in the micelle. The cationic polymer chain of the polymer unit α has a phenylboronic acid group in a side chain, and the cationic polymer chain of the polymer unit β has a phenylboronic acid binding site in a side chain. The phenylboronic acid group and the phenylboronic acid binding site form a cross-linked structure that can dissociate in an acidic environment and/or in the presence of a substance capable of competitive binding.
    一种药物组合物包括聚合物单元 α 和 β(每个单元都有一条与阳离子聚合物链结合的亲水聚合物链)以及一种药物。聚合物单元 α 和 β 沿径向排列,使阳离子聚合物链向内,亲水聚合物链向外,从而形成胶束,药物封装在胶束中。聚合物单元 α 的阳离子聚合物链的侧链上有一个苯硼酸基团,聚合物单元 β 的阳离子聚合物链的侧链上有一个苯硼酸结合位点。苯硼酸基团和苯硼酸结合位点形成一种交联结构,在酸性环境中和/或在有竞争性结合物质存在的情况下可以解离。
  • VERFAHREN ZUR HERSTELLUNG VON MIKROPARTIKELN, DIE MIT EINEM AKTIVSTOFF BELADEN SIND
    申请人:BASF SE
    公开号:EP3873658A1
    公开(公告)日:2021-09-08
  • EP300/CREBBP INHIBITOR
    申请人:Daiichi Sankyo Company, Limited
    公开号:US20210171520A1
    公开(公告)日:2021-06-10
    The present invention provides a compound having excellent histone acetyl transferase inhibitory activity against EP300 and/or CREBBP, or a pharmacologically acceptable salt thereof. The compound is represented by the following formula (1) or a pharmacologically acceptable salt thereof: wherein ring Q 1 , ring Q 2 , R 1 , R 2 , R 3 and R 4 respectively have the same meanings as defined in the specification.
  • PHARMACEUTICAL COMPOSITION
    申请人:KAWASAKI INSTITUTE OF INDUSTRIAL PROMOTION
    公开号:US20210187005A1
    公开(公告)日:2021-06-24
    A pharmaceutical composition includes polymer units α and β, each having a hydrophilic polymer chain bound to a cationic polymer chain, and a drug. The polymer units α and β are radially arranged such that the cationic polymer chains are directed inward and the hydrophilic polymer chains are directed outward, thereby forming a micelle with the drug encapsulated in the micelle. The cationic polymer chain of the polymer unit α has a phenylboronic acid group in a side chain, and the cationic polymer chain of the polymer unit β has a phenylboronic acid binding site in a side chain. The phenylboronic acid group and the phenylboronic acid binding site form a cross-linked structure that can dissociate in an acidic environment and/or in the presence of a substance capable of competitive binding.
  • US6120788A
    申请人:——
    公开号:US6120788A
    公开(公告)日:2000-09-19
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