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ethyl 3-(4-chlorophenoxy)-2-(4-chlorophenyl)-1H-indole-5-carboxylate | 1330540-11-8

中文名称
——
中文别名
——
英文名称
ethyl 3-(4-chlorophenoxy)-2-(4-chlorophenyl)-1H-indole-5-carboxylate
英文别名
——
ethyl 3-(4-chlorophenoxy)-2-(4-chlorophenyl)-1H-indole-5-carboxylate化学式
CAS
1330540-11-8
化学式
C23H17Cl2NO3
mdl
——
分子量
426.299
InChiKey
TYUPJWKMPQMPFY-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):
    6.7
  • 重原子数:
    29
  • 可旋转键数:
    6
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.09
  • 拓扑面积:
    51.3
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为产物:
    参考文献:
    名称:
    Antiproliferative activity of 2,3-disubstituted indoles toward apoptosis-resistant cancers cells
    摘要:
    Many types of cancer, including glioma, melanoma, NSCLC, among others, are resistant to apoptosis induction and poorly responsive to current therapies with propaptotic agents. We describe a series of 2,3-disubstituted indoles, which display cytostatic rather than cytotoxic effects in cancer cells, and serve as a new chemical scaffold to develop anticancer agents capable of combating apoptosis-resistant cancers associated with dismal prognoses. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2013.03.110
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文献信息

  • Antibiotic sensitivity-restoring and photosensitive agents
    申请人:NEW MEXICO TECH UNIVERSITY RESEARCH PARK CORPORATION
    公开号:US10239834B2
    公开(公告)日:2019-03-26
    The present disclosure describes a method to treat conditions, including bacterial infections and cancer, using a photosensitive compound that, upon exposure to white light, can be activated. The photosensitive compound can also interact synergistically with antibiotics used concomitantly to kill drug-resistant bacteria. The photosensitive compounds can also be used to inhibit the proliferation of cancer cells.
    本公开描述了一种使用光敏化合物治疗细菌感染和癌症等疾病的方法,该化合物在白光照射下可被激活。光敏化合物还能与同时使用的抗生素产生协同作用,杀死耐药细菌。光敏化合物还可用于抑制癌细胞的增殖。
  • ANTIBIOTIC SENSITIVITY-RESTORING AND PHOTOSENSITIVE AGENTS
    申请人:New Mexico Tech Research Foundation
    公开号:US20180155286A1
    公开(公告)日:2018-06-07
    The present disclosure describes a method to treat conditions, including bacterial infections and cancer, using a photosensitive compound that, upon exposure to white light, can be activated. The photosensitive compound can also interact synergistically with antibiotics used concomitantly to kill drug-resistant bacteria. The photosensitive compounds can also be used to inhibit the proliferation of cancer cells.
  • US9834514B2
    申请人:——
    公开号:US9834514B2
    公开(公告)日:2017-12-05
  • [EN] ANTIBIOTIC SENSITIVITY-RESTORING AND PHOTOSENSITIVE AGENTS<br/>[FR] AGENTS PHOTOSENSIBLES ET DE RÉTABLISSEMENT DE LA SENSIBILITÉ AUX ANTIBIOTIQUES
    申请人:NEW MEXICO TECH RES FOUND
    公开号:WO2016172193A1
    公开(公告)日:2016-10-27
    The present disclosure describes a method to treat conditions, including bacterial infections and cancer, using a photosensitive compound that, upon exposure to white light, can be activated. The photosensitive compound can also interact synergistically with antibiotics used concomitantly to kill drug-resistant bacteria. The photosensitive compounds can also be used to inhibit the proliferation of cancer cells.
  • Antiproliferative activity of 2,3-disubstituted indoles toward apoptosis-resistant cancers cells
    作者:Igor V. Magedov、Florence Lefranc、Liliya V. Frolova、Laetitia Moreno Y. Banuls、Amanda S. Peretti、Snezna Rogelj、Véronique Mathieu、Robert Kiss、Alexander Kornienko
    DOI:10.1016/j.bmcl.2013.03.110
    日期:2013.6
    Many types of cancer, including glioma, melanoma, NSCLC, among others, are resistant to apoptosis induction and poorly responsive to current therapies with propaptotic agents. We describe a series of 2,3-disubstituted indoles, which display cytostatic rather than cytotoxic effects in cancer cells, and serve as a new chemical scaffold to develop anticancer agents capable of combating apoptosis-resistant cancers associated with dismal prognoses. (C) 2013 Elsevier Ltd. All rights reserved.
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