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(E)-1-(3-hydroxyphenyl)-3-[3-(trifluoromethyl)phenyl]prop-2-en-1-one

中文名称
——
中文别名
——
英文名称
(E)-1-(3-hydroxyphenyl)-3-[3-(trifluoromethyl)phenyl]prop-2-en-1-one
英文别名
——
(E)-1-(3-hydroxyphenyl)-3-[3-(trifluoromethyl)phenyl]prop-2-en-1-one化学式
CAS
——
化学式
C16H11F3O2
mdl
——
分子量
292.25
InChiKey
IMPKEYTTWYLUPV-BQYQJAHWSA-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):
    3.6
  • 重原子数:
    21
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.06
  • 拓扑面积:
    37.3
  • 氢给体数:
    1
  • 氢受体数:
    5

文献信息

  • [EN] NUCLEAR RECEPTOR MODULATORS AND THEIR USE FOR THE TREATMENT AND PREVENTION OF CANCER<br/>[FR] MODULATEURS DE RÉCEPTEURS NUCLÉAIRES ET LEUR UTILISATION POUR LE TRAITEMENT ET LA PRÉVENTION D'UN CANCER
    申请人:US HEALTH
    公开号:WO2012174436A1
    公开(公告)日:2012-12-20
    Disclosed are compounds which are nuclear receptor modulators that can act as antagonists to the androgen receptor, for example, a compound of Formula I: wherein R1 to R5 and X1 to X5 are as described herein, as well as pharmaceutically acceptable salts, solvates, and stereoisomers thereof. Pharmaceutical compositions comprising such compounds, as well as methods of use, and treatment for cancers, including prostate cancers, other nuclear receptor mediated cancers, and other conditions, are also disclosed.
    本文披露了一些化合物,它们是核受体调节剂,可以作为雄激素受体的拮抗剂,例如,公式I的化合物:其中R1至R5和X1至X5如本文所述,以及其药用盐、溶剂化合物和立体异构体。还披露了包括这些化合物的药物组合物,以及使用方法和治疗癌症,包括前列腺癌、其他核受体介导的癌症和其他疾病的方法。
  • ANTIBACTERIAL AGENTS AND RELATED SCREENING METHODS USING SMALL MOLECULE MACROARRAYS
    申请人:Blackwell E. Helen
    公开号:US20080009528A1
    公开(公告)日:2008-01-10
    The present invention relates generally to compounds providing antibacterial therapeutic agents and preparations, and related methods of using and making antibacterial compounds. Antibacterial compounds of the present invention include chalcone, alkylpyrimidine, aminopyrimidine and cyanopyridine compounds and derivatives thereof exhibiting minimum inhibitory concentrations (MIC) similar to or less than conventional antibacterial compounds in wide use. For example, the present invention provides chalcone and cyanopyridine compounds, and derivatives thereof, exhibiting high antibacterial activities having multiple electron withdrawing group substituents, such as halogens and fluorinated alky groups, and optionally having hydroxyl and/or alkoxyl groups substituents.
    本发明通常涉及提供抗菌治疗剂和制剂的化合物,以及使用和制备抗菌化合物的相关方法。本发明的抗菌化合物包括香豆素、烷基嘧啶氨基嘧啶氰基吡啶化合物及其衍生物,其最小抑菌浓度(MIC)类似或低于目前广泛使用的传统抗菌化合物。例如,本发明提供具有多个电子吸引基取代基的香豆素氰基吡啶化合物及其衍生物,具有高抗菌活性,可选地具有羟基和/或烷氧基取代基。
  • Antibacterial Agents and Methods of Use Thereof
    申请人:Blackwell Helen E.
    公开号:US20120277252A1
    公开(公告)日:2012-11-01
    The present invention relates generally to compounds providing antibacterial therapeutic agents and preparations, and related methods of using and making antibacterial compounds. Antibacterial compounds of the present invention include chalcone, alkylpyrimidine, aminopyrimidine and cyanopyridine compounds and derivatives thereof exhibiting minimum inhibitory concentrations (MIC) similar to or less than conventional antibacterial compounds in wide use. For example, the present invention provides chalcone and cyanopyridine compounds, and derivatives thereof, exhibiting high antibacterial activities having multiple electron withdrawing group substituents, such as halogens and fluorinated alkyl groups, and optionally having hydroxyl and/or alkoxyl groups substituents.
    本发明涉及提供抗菌治疗剂和制剂的化合物以及相关的使用和制备抗菌化合物的方法。本发明的抗菌化合物包括查尔酮、烷基嘧啶氨基嘧啶氰基吡啶化合物及其衍生物,其最小抑菌浓度(MIC)类似于或小于广泛使用的传统抗菌化合物。例如,本发明提供具有多个电子吸引基取代基,如卤素和代烷基,并且可选地具有羟基和/或烷氧基取代基的查尔酮氰基吡啶化合物及其衍生物,具有高抗菌活性的。
  • ANTIBACTERIAL AGENTS AND METHODS OF USE THEREOF
    申请人:BLACKWELL Helen E.
    公开号:US20100261763A1
    公开(公告)日:2010-10-14
    The present invention relates generally to compounds providing antibacterial therapeutic agents and preparations, and related methods of using and making antibacterial compounds. Antibacterial compounds of the present invention include chalcone, alkylpyrimidine, aminopyrimidine and cyanopyridine compounds and derivatives thereof exhibiting minimum inhibitory concentrations (MIC) similar to or less than conventional antibacterial compounds in wide use. For example, the present invention provides chalcone and cyanopyridine compounds, and derivatives thereof, exhibiting high antibacterial activities having multiple electron withdrawing group substituents, such as halogens and fluorinated alky groups, and optionally having hydroxyl and/or alkoxyl groups substituents.
    本发明涉及提供抗菌治疗剂和制剂的化合物以及使用和制备抗菌化合物的相关方法。本发明的抗菌化合物包括香豆素、烷基嘧啶氨基嘧啶氰基吡啶化合物及其衍生物,其最小抑菌浓度(MIC)类似于或小于广泛使用的传统抗菌化合物。例如,本发明提供具有多个电子吸引基取代基,如卤素和代烷基,并且可选地具有羟基和/或烷氧基取代基的香豆素氰基吡啶化合物及其衍生物,表现出高抗菌活性。
  • US7737164B2
    申请人:——
    公开号:US7737164B2
    公开(公告)日:2010-06-15
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