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(E)-1-(2-methoxyphenyl)-3-(3-cyanophenyl)prop-2-en-1-one | 1365644-22-9

中文名称
——
中文别名
——
英文名称
(E)-1-(2-methoxyphenyl)-3-(3-cyanophenyl)prop-2-en-1-one
英文别名
3-[(E)-3-(2-methoxyphenyl)-3-oxoprop-1-enyl]benzonitrile
(E)-1-(2-methoxyphenyl)-3-(3-cyanophenyl)prop-2-en-1-one化学式
CAS
1365644-22-9
化学式
C17H13NO2
mdl
——
分子量
263.296
InChiKey
MDQIANFIPJOBRL-MDZDMXLPSA-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):
    3.4
  • 重原子数:
    20
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.06
  • 拓扑面积:
    50.1
  • 氢给体数:
    0
  • 氢受体数:
    3

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    2'-甲氧基苯乙酮3-氰基苯甲醛lithium hydroxide monohydrate 作用下, 以 乙醇 为溶剂, 反应 2.17h, 以50%的产率得到(E)-1-(2-methoxyphenyl)-3-(3-cyanophenyl)prop-2-en-1-one
    参考文献:
    名称:
    Methoxychalcone inhibitors of androgen receptor translocation and function
    摘要:
    Androgen receptor activity drives incurable castrate-resistant prostate cancer. All approved antiandrogens inhibit androgen receptor-driven transcription, and in addition the second-generation antiandrogen MDV3100 inhibits ligand-activated androgen receptor nuclear translocation, via an unknown mechanism. Here, we report methoxychalcones that lock the heat shock protein 90-androgen receptor complex in the cytoplasm in an androgen-non-responsive state, thus demonstrating a novel chemical scaffold for antiandrogen development and a unique mechanism of antiandrogen activity. Published by Elsevier Ltd.
    DOI:
    10.1016/j.bmcl.2011.12.141
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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。
  • NUCLEAR RECEPTOR MODULATORS AND THEIR USE FOR THE TREATMENT AND PREVENTION OF CANCER
    申请人:The U.S.A. as represented by the Secretary, Department of Health and Human Services
    公开号:EP3333153A1
    公开(公告)日:2018-06-13
    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.
    所公开的化合物是核受体调节剂,可作为雄激素受体的拮抗剂,例如,式 I 的化合物: 其中 R1 至 R5 和 X1 至 X5 如本文所述,以及其药学上可接受的盐、溶剂和立体异构体。此外,还公开了包含此类化合物的药物组合物,以及使用方法和癌症(包括前列腺癌、其他核受体介导的癌症和其他疾病)的治疗方法。
  • Nuclear receptor modulators and their use for the treatment and prevention of cancer
    申请人:The United States of America, as represented by the Secretary, Department of Health and Human Services
    公开号:US10737995B2
    公开(公告)日:2020-08-11
    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.
    所公开的化合物是核受体调节剂,可作为雄激素受体的拮抗剂,例如,式 I 的化合物: 其中 R1 至 R5 和 X1 至 X5 如本文所述,以及其药学上可接受的盐、溶剂和立体异构体。此外,还公开了包含此类化合物的药物组合物、使用方法以及癌症(包括前列腺癌)、其他核受体介导的癌症和其他疾病的治疗方法。
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