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Eu(DPM)3

中文名称
——
中文别名
——
英文名称
Eu(DPM)3
英文别名
Resolve-A1;europium;2,2,6,6-tetramethylheptane-3,5-dione
Eu(DPM)3化学式
CAS
——
化学式
C33H60EuO6
mdl
——
分子量
704.796
InChiKey
LTMLYJXKFUNAJT-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):
    7.82
  • 重原子数:
    40
  • 可旋转键数:
    6
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.82
  • 拓扑面积:
    102
  • 氢给体数:
    0
  • 氢受体数:
    6

反应信息

  • 作为反应物:
    描述:
    Eu(DPM)3二-n-己基亚砜乙醇 为溶剂, 生成 Eu(DPM)3(DHSO)
    参考文献:
    名称:
    Karasev, V. E.; Botova, I. N.; Kovalenko, V. N., Russian Journal of Inorganic Chemistry, 1988, vol. 33, p. 637 - 640
    摘要:
    DOI:
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文献信息

  • CYCLIC ETHER PYRAZOL-4-YL-HETEROCYCLYL-CARBOXAMIDE COMPOUNDS AND METHODS OF USE
    申请人:Genentech, Inc.
    公开号:US20140088117A1
    公开(公告)日:2014-03-27
    Cyclic ether pyrazol-4-yl-heterocyclyl-carboxamide compounds of Formula I, including stereoisomers, geometric isomers, tautomers, and pharmaceutically acceptable salts thereof, wherein R 2 is a cyclic ether and X is thiazolyl, pyrazinyl, pyridinyl, or pyrimidinyl, are useful for inhibiting Pim kinase, and for treating disorders such as cancer mediated by Pim kinase. Methods of using compounds of Formula I for in vitro, in situ, and in vivo diagnosis, prevention or treatment of such disorders in mammalian cells, or associated pathological conditions, are disclosed.
    公式I中的环氧杂环基卡氧酰胺化合物,包括立体异构体、几何异构体、互变异构体和其药学上可接受的盐,其中R2是环氧杂环基,X是噻唑基、吡嗪基、吡啶基或嘧啶基,可用于抑制Pim激酶,并用于治疗由Pim激酶介导的癌症等疾病。公开了使用公式I中的化合物进行哺乳动物细胞中的体外、体内和原位诊断、预防或治疗此类疾病或相关病理条件的方法。
  • Cyclic Ether Pyrazol-4-YL-Heterocyclyl-Carboxamide Compounds And Methods Of Use
    申请人:Genentech, Inc.
    公开号:US20160213652A1
    公开(公告)日:2016-07-28
    Cyclic ether pyrazol-4-yl-heterocyclyl-carboxamide compounds of Formula I, including stereoisomers, geometric isomers, tautomers, and pharmaceutically acceptable salts thereof, wherein R 2 is a cyclic ether and X is thiazolyl, pyrazinyl, pyridinyl, or pyrimidinyl, are useful for inhibiting Pim kinase, and for treating disorders such as cancer mediated by Pim kinase. Methods of using compounds of Formula I for in vitro, in situ, and in vivo diagnosis, prevention or treatment of such disorders in mammalian cells, or associated pathological conditions, are disclosed.
    公式I中的环氧杂环基卡氧酰胺化合物,包括立体异构体、几何异构体、互变异构体和其药学上可接受的盐,其中R2是环氧杂环基,X是噻唑基、吡嗪基、吡啶基或嘧啶基,可用于抑制Pim激酶,并用于治疗由Pim激酶介导的癌症等疾病。公开了使用公式I中的化合物进行哺乳动物细胞中的体外、原位和体内诊断、预防或治疗此类疾病或相关病理条件的方法。
  • Cyclic ether pyrazol-4-yl-heterocyclyl-carboxamide compounds and methods of use
    申请人:Genentech, Inc.
    公开号:US09328106B2
    公开(公告)日:2016-05-03
    Cyclic ether pyrazol-4-yl-heterocyclyl-carboxamide compounds of Formula I, including stereoisomers, geometric isomers, tautomers, and pharmaceutically acceptable salts thereof, wherein R2 is a cyclic ether and X is thiazolyl, pyrazinyl, pyridinyl, or pyrimidinyl, are useful for inhibiting Pim kinase, and for treating disorders such as cancer mediated by Pim kinase. Methods of using compounds of Formula I for in vitro, in situ, and in vivo diagnosis, prevention or treatment of such disorders in mammalian cells, or associated pathological conditions, are disclosed.
    公式I中的环氧杂环基羧酰胺化合物,包括立体异构体、几何异构体、互变异构体和其药学上可接受的盐,其中R2是一个环氧杂环基,X是噻唑基、吡嗪基、吡啶基或嘧啶基,用于抑制Pim激酶,并用于治疗由Pim激酶介导的癌症等疾病。本文介绍了利用公式I中的化合物在哺乳动物细胞中进行体外、原位和体内诊断、预防或治疗此类疾病或相关病理条件的方法。
  • PREPARATION AND CHARACTERIZATION OF SOME RARE-EARTH COMPLEXES OF THE PHTHALOCYANINE RADICAL
    作者:Hiroshi Sugimoto、Teruaki Higashi、Masayasu Mori
    DOI:10.1246/cl.1983.1167
    日期:1983.8.5
    5-heptanedionato) complexes of rare-earth elements, M3+(dpm)3 (M = Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu, and Y) with lithium phthalocyanine Li2(Pc2−) in tetrahydrofuran gave new stable phthalocyanine radical complexes [M3+(Pc−·)(dpm)2].
    稀土元素三(2,2,6,6-四甲基-3,5-庚二酮)配合物的反应,M3+(dpm)3 (M = Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er、Tm、Yb、Lu 和 Y) 与四氢呋喃中的酞菁 Li2(Pc2-) 生成新的稳定的酞菁自由基复合物 [M3+(Pc-·)(dpm)2]。
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