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3,3,5,5-tetramethyl-hexan-2-one | 129583-17-1

中文名称
——
中文别名
——
英文名称
3,3,5,5-tetramethyl-hexan-2-one
英文别名
3,3,5,5-Tetramethyl-hexan-2-on;3,3,5,5-Tetramethyl-2-hexanone;3,3,5,5-tetramethylhexan-2-one
3,3,5,5-tetramethyl-hexan-2-one化学式
CAS
129583-17-1
化学式
C10H20O
mdl
——
分子量
156.268
InChiKey
CTVTYLKKZYFHIL-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:
    70-71 °C(Press: 13 Torr)
  • 密度:
    0.8441 g/cm3

计算性质

  • 辛醇/水分配系数(LogP):
    2.9
  • 重原子数:
    11
  • 可旋转键数:
    3
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.9
  • 拓扑面积:
    17.1
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

点击查看最新优质反应信息

文献信息

  • MONOMERS CAPABLE OF DIMERIZING IN AN AQUEOUS SOLUTION, AND METHODS OF USING SAME
    申请人:Barany Francis
    公开号:US20140194383A1
    公开(公告)日:2014-07-10
    Described herein are monomers capable of forming a biologically useful multimer when in contact with one, two, three or more other monomers in an aqueous media. In one aspect, such monomers may be capable of binding to another monomer in an aqueous media (e.g. in vivo) to form a multimer, (e.g. a dimer). Contemplated monomers may include a ligand moiety, a linker element, and a connector element that joins the ligand moiety and the linker element. In an aqueous media, such contemplated monomers may join together via each linker element and may thus be capable of modulating one or more biomolecules substantially simultaneously, e.g., modulate two or more binding domains on a protein or on different proteins.
    本发明描述了在水中介质中与一个、两个、三个或更多其他单体接触时能够形成具有生物学用途的多聚体的单体。在一方面,这样的单体可能能够在水介质中(例如,体内)与另一个单体结合形成多聚体(例如,二聚体)。考虑的单体可能包括一个配体部分、一个连接元素和一个连接器元素,连接器元素连接配体部分和连接元素。在水介质中,这样的考虑单体可能通过每个连接元素相互连接,因此可能能够实质上同时调节一个或多个生物分子,例如,调节蛋白质上的两个或多个结合域,或者调节不同蛋白质上的结合域。
  • [EN] NOVEL COMPOUNDS AND METHODS OF USING THEM<br/>[FR] COMPOSÉS NOVATEURS ET PROCÉDÉS D'UTILISATION DE CEUX-CI
    申请人:SYNDAX PHARMACEUTICALS INC
    公开号:WO2009015203A1
    公开(公告)日:2009-01-29
    Described herein are novel HDAC modulators, formulations containing them and methods of using them. In some embodiments, the HDAC modulators possess specific stereo chemistry. In other embodiments, the compounds described herein are used in the treatment or prevention of histone deacetylase mediated disorders.
    本文描述了新型HDAC调节剂,含有它们的配方以及使用它们的方法。在某些实施例中,HDAC调节剂具有特定的立体化学结构。在其他实施例中,本文描述的化合物用于治疗或预防组蛋白去乙酰化酶介导的疾病。
  • COFLUORONS AND METHODS OF MAKING AND USING THEM
    申请人:Barany Francis
    公开号:US20140161729A1
    公开(公告)日:2014-06-12
    The present invention is directed to method of using a collection of monomers capable of forming multimers as a fluorescence reporter in different applications such as ligand detection/screening, disease diagnosis, drug discovery or screening, fluorescent labeling and imaging, or other fluorescent methodologies. Each monomer in the collection includes one or more ligand elements useful for binding to a target molecule with a dissociation constant of less than 300 μM and a linker element connected to the ligand elements directly or indirectly through a connector. Association of linker elements of different combinations of monomers, with their ligand elements bound to the target molecule to form a multimer, will generate a unique fluorescent signature different from that produced by those monomers either alone or in association with each other in the absence of the target molecule, when subjected to electromagnetic excitement.
    本发明涉及使用一组能够形成多聚体的单体作为荧光报告物在不同应用中的方法,例如配体检测/筛选、疾病诊断、药物发现或筛选、荧光标记和成像,或其他荧光方法学。该组合中的每个单体均包括一个或多个配体元素,用于与解离常数小于300μM的靶分子结合,并且连接到配体元素的连接器通过直接或间接连接到配体元素。不同单体组合的连接器元素与其配体元素结合到靶分子形成多聚体,将产生一种独特的荧光特征,与那些单体单独或在没有靶分子的情况下相互结合时产生的荧光特征不同,当受到电磁激发时。
  • 1,2,6-SUBSTITUTED BENZIMIDAZOLES AS FLAP MODULATORS
    申请人:JANSSEN PHARMACEUTICA NV
    公开号:US20150119382A1
    公开(公告)日:2015-04-30
    The present invention relates to compounds of Formula (I), and solvates, hydrates, and pharmaceutically acceptable salts thereof, wherein X 1 , X 1 ′, X 1 ″, R 1 , R 2 and R 3 are as defined herein, useful as FLAP modulators. The invention also relates to pharmaceutical compositions comprising compounds of Formula (I). Methods of making and using the compounds of Formula (I) are also within the scope of the invention.
    本发明涉及式(I)化合物及其溶剂合物、水合物和药学上可接受的盐,其中X1、X1'、X1"、R1、R2和R3如本文所定义,其作为FLAP调节剂有用。本发明还涉及包括式(I)化合物的药物组合物。制备和使用式(I)化合物的方法也在本发明范围内。
  • BROMODOMAIN LIGANDS CAPABLE OF DIMERIZING IN AN AQUEOUS SOLUTION, AND METHODS OF USING SAME
    申请人:Coferon, Inc.
    公开号:US20140243286A1
    公开(公告)日:2014-08-28
    Described herein are monomers capable of forming a biologically useful multimer when in contact with one, two, three or more other monomers in an aqueous media. In one aspect, such monomers may be capable of binding to another monomer in an aqueous media (e.g. in vivo) to form a multimer (e.g. a dimer). Contemplated monomers may include a ligand moiety, a linker element, and a connector element that joins the ligand moiety and the linker element. In an aqueous media, such contemplated monomers may join together via each linker element and may thus be capable of modulating one or more biomolecules substantially simultaneously, e.g., modulate two or more binding domains on a protein or on different proteins.
    本文介绍了一种单体,当在水介质中与一个、两个、三个或更多其他单体接触时,能够形成生物上有用的多聚体。在其中一方面,这种单体可以在水介质中(例如在体内)与另一个单体结合形成多聚体(例如二聚体)。考虑到的单体可能包括配体基团、连接元素和连接配体基团和连接元素的连接元素。在水介质中,这些考虑到的单体可以通过每个连接元素连接在一起,因此可以同时调节一个或多个生物分子,例如调节蛋白质或不同蛋白质上的两个或更多结合结构域。
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