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1-(4-Ethylpiperazin-1-yl)-2-methylpropan-1-one

中文名称
——
中文别名
——
英文名称
1-(4-Ethylpiperazin-1-yl)-2-methylpropan-1-one
英文别名
——
1-(4-Ethylpiperazin-1-yl)-2-methylpropan-1-one化学式
CAS
——
化学式
C10H20N2O
mdl
MFCD03390598
分子量
184.28
InChiKey
ISKJMLDSTMHQTH-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):
    0.9
  • 重原子数:
    13
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.9
  • 拓扑面积:
    23.6
  • 氢给体数:
    0
  • 氢受体数:
    2

文献信息

  • [EN] BROMODOMAIN LIGANDS CAPABLE OF DIMERIZING IN AN AQUEOUS SOLUTION<br/>[FR] LIGANDS DE BROMODOMAINE POUVANT SE DIMÉRISER DANS UNE SOLUTION AQUEUSE
    申请人:COFERON INC
    公开号:WO2015081280A1
    公开(公告)日:2015-06-04
    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.
    本文描述的是一种单体,当与性介质中的一个、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。在一个方面,这些单体可能能够在性介质中(例如体内)与另一个单体结合,形成一个多聚体(例如二聚体)。考虑到的单体可能包括一个配体基团、一个连接元素和连接配体基团与连接元素的连接元素。在性介质中,这些考虑到的单体可以通过每个连接元素相互结合,因此可以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更多结合结构域或不同蛋白质上的结合结构域。
  • [EN] SERINE BIOSYNTHETIC PATHWAY INHIBITORS<br/>[FR] INHIBITEURS DE LA VOIE DE BIOSYNTHÈSE DE LA SÉRINE
    申请人:UNIV CATHOLIQUE LOUVAIN
    公开号:WO2017157882A1
    公开(公告)日:2017-09-21
    The present invention relates to a compound of formula (I), a stereoisomer thereof, an enantiomer thereof, a racemic thereof, or a tautomer thereof as defined in claim 1 (I) the present invention also relates to a compound of formula (I), a stereoisomer thereof, an 5 enantiomer thereof, a racemic thereof, or a tautomer thereof, as defined in the claims for use as a medicament, in particular for use in the prevention or treatment of a cellular proliferative disease.
    本发明涉及公式(I)的化合物,其立体异构体,对映异构体,消旋体或互变异构体,如权利要求1中定义的(I)。本发明还涉及公式(I)的化合物,其立体异构体,对映异构体,消旋体或互变异构体,如权利要求中定义的用作药物,特别是用于预防或治疗细胞增殖性疾病。
  • Substituted pyrazoles as p38 kinase inhibitors
    申请人:Naraian S. Ashok
    公开号:US20070078146A1
    公开(公告)日:2007-04-05
    A class of pyrazole derivatives is described for use in treating p38 kinase medicated disorders. Compounds of particular interest are defined by Formula IA wherein R 1 , R 2 , R 3 and R 4 are as described in the specification.
    描述了一类吡唑生物,用于治疗p38激酶介导的疾病。特别感兴趣的化合物由公式IA定义,其中R1、R2、R3和R4如规范中所述。
  • GLUCOKINASE ACTIVATORS
    申请人:Aicher Thomas D.
    公开号:US20090247526A1
    公开(公告)日:2009-10-01
    Provided are compounds of formula I wherein R 2 , L, Z, Y, G and R 1 are as defined herein, that are useful in the treatment and/or prevention of diseases or disorders mediated by deficient levels of glucokinase activity or which can be treated by activating glucokinase including, but not limited to, diabetes mellitus, impaired glucose tolerance, IFG (impaired fasting glucose) and IFG (impaired fasting glycemia), as well as other diseases and disorders such as those discussed herein.
    提供了化合物I的公式,其中R2、L、Z、Y、G和R1的定义如此处所述,这些化合物在治疗和/或预防由葡萄糖激酶活性不足介导的疾病或疾病中有用,或者可以通过激活葡萄糖激酶来治疗,包括但不限于糖尿病、糖耐量受损、IFG(空腹血糖受损)和IFG(空腹高血糖)以及其他疾病和疾病,如本文所讨论的。
  • 2-AMINOPYRIDINE DERIVATIVES AS GLUCOKINASE ACTIVATORS
    申请人:Aicher Thomas Daniel
    公开号:US20100099713A1
    公开(公告)日:2010-04-22
    Provided are compounds having the Formula I or salts thereof, wherein R 2 , L, R 3 , R 11 , D 2 and R 13 are as defined herein, that are useful in the treatment and/or prevention of diseases mediated by deficient levels of glucokinase activity, such as diabetes mellitus. Also provided are methods of treating or preventing diseases and disorders characterized by underactivity of glucokinase or which can be treated by activating glucokinase.
    提供的化合物具有I式或其盐,其中R2、L、R3、R11、D2和R13的定义如本文所述,可用于治疗和/或预防由葡萄糖激酶活性不足引起的疾病,如糖尿病。还提供了治疗或预防由葡萄糖激酶活性不足或可以通过激活葡萄糖激酶治疗的疾病和疾病的方法。
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