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(2E)-1-(5-chloro-2-hydroxyphenyl)-3-(3,4,5-trimethoxyphenyl)prop-2-en-1-one | 1255189-04-8

中文名称
——
中文别名
——
英文名称
(2E)-1-(5-chloro-2-hydroxyphenyl)-3-(3,4,5-trimethoxyphenyl)prop-2-en-1-one
英文别名
(E)-1-(5-chloro-2-hydroxyphenyl)-3-(3,4,5-trimethoxyphenyl)prop-2-en-1-one
(2E)-1-(5-chloro-2-hydroxyphenyl)-3-(3,4,5-trimethoxyphenyl)prop-2-en-1-one化学式
CAS
1255189-04-8
化学式
C18H17ClO5
mdl
——
分子量
348.783
InChiKey
WLAYUWULDCHEPD-GQCTYLIASA-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):
    4.4
  • 重原子数:
    24
  • 可旋转键数:
    6
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    65
  • 氢给体数:
    1
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    (2E)-1-(5-chloro-2-hydroxyphenyl)-3-(3,4,5-trimethoxyphenyl)prop-2-en-1-one 为溶剂, 反应 8.0h, 以20%的产率得到
    参考文献:
    名称:
    Kamboj, Ramesh C.; Berar, Surinder; Berar, Urmila, Journal of the Indian Chemical Society, 2011, vol. 88, # 6, p. 879 - 885
    摘要:
    DOI:
  • 作为产物:
    描述:
    2-羟基-5-氯苯乙酮3,4,5-三甲氧基苯甲醛 在 barium(II) hydroxide 、 盐酸 作用下, 以 乙醇 为溶剂, 反应 0.33h, 以90%的产率得到(2E)-1-(5-chloro-2-hydroxyphenyl)-3-(3,4,5-trimethoxyphenyl)prop-2-en-1-one
    参考文献:
    名称:
    Kamboj, Ramesh C.; Berar, Surinder; Berar, Urmila, Journal of the Indian Chemical Society, 2011, vol. 88, # 6, p. 879 - 885
    摘要:
    DOI:
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文献信息

  • Compounds exhibiting efflux inhibitor activity and composition and uses thereof
    申请人:Wempe Fitzpatrick Michael
    公开号:US20070254859A1
    公开(公告)日:2007-11-01
    At least one compound chosen from compounds of Formula I: a pharmaceutically acceptable salt or ester thereof, a solvate thereof, a chelate thereof, a non-covalent complex thereof, a prodrug thereof, and mixtures of any of the foregoing, wherein: n is a number from 1 to 900, wherein the individual units may be the same or different; W is chosen from alkyl, substituted alkyl, cycloalkyl, substituted cycloalkyl, aryl, substituted aryl, aralkyl and substituted aralkyl; each of R 2 , R 3 , R 4 and R 5 is independently chosen from —H, alkyl, substituted alkyl, cycloalkyl, substituted cycloalkyl, aryl, substituted aryl, aralkyl and substituted aralkyl; Z′ is chosen from —O—, —N—, —NO—, —NR 4 —, —S—, —SO— and —SO 2 —, wherein R 4 is defined as above; each of X, X′, Y and Z is independently chosen from —CR 4 R 5 —, —NH—, —NR 4 —, —NO—, —O—, —NOR 4 —, —S—, —SO—, —SO 2 —, wherein R 4 and R 5 are defined as above; R 1 is chosen from a tocopherol, a steroid and a flavonoid; and R 6 is chosen from any R 1 , alkyl, substituted alkyl, cycloalkyl, substituted cycloalkyl, aryl, substituted aryl, aralkyl and substituted aralkyl.
  • ESTROGEN RECEPTOR ALPHA COLIGANDS, AND METHODS OF USE THEREOF
    申请人:The Regents of the University of California
    公开号:US20190008797A1
    公开(公告)日:2019-01-10
    Provided herein is a coligand for the estrogen receptor (ER) a subunit, and methods of use thereof in treating conditions associated with ER signaling in an individual. The present ERα coligand may be a cell type-selective, allosteric modulator of ERα signaling. The ERα coligand, when administered to an individual, may modulate ER agonist-dependent signaling in a tissue-selective manner.
  • [EN] ESTROGEN RECEPTOR ALPHA COLIGANDS, AND METHODS OF USE THEREOF<br/>[FR] CO-LIGANDS DES RÉCEPTEURS DES OESTROGÈNES ALPHA ET LEURS PROCÉDÉS D'UTILISATION
    申请人:UNIV CALIFORNIA
    公开号:WO2017132135A1
    公开(公告)日:2017-08-03
    Provided herein is a coligand for the estrogen receptor (ER) α subunit, and methods of use thereof in treating conditions associated with ER signaling in an individual. The present ERα coligand may be a cell type-selective, allosteric modulator of ERα signaling. The ERα coligand, when administered to an individual, may modulate ER agonist-dependent signaling in a tissue-selective manner.
  • Kamboj, Ramesh C.; Berar, Surinder; Berar, Urmila, Journal of the Indian Chemical Society, 2011, vol. 88, # 6, p. 879 - 885
    作者:Kamboj, Ramesh C.、Berar, Surinder、Berar, Urmila、Gupta, Satish C.
    DOI:——
    日期:——
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