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7-chloro-2-oxo-1,2-dihydroquinoline-4-carboxylic acid | 32431-34-8

中文名称
——
中文别名
——
英文名称
7-chloro-2-oxo-1,2-dihydroquinoline-4-carboxylic acid
英文别名
7-chloro-2-oxo-1H-quinoline-4-carboxylic acid
7-chloro-2-oxo-1,2-dihydroquinoline-4-carboxylic acid化学式
CAS
32431-34-8
化学式
C10H6ClNO3
mdl
——
分子量
223.616
InChiKey
UOGDRGQUIULLFJ-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):
    1.2
  • 重原子数:
    15
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    66.4
  • 氢给体数:
    2
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    7-chloro-2-oxo-1,2-dihydroquinoline-4-carboxylic acid1-羟基苯并三唑盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺三乙胺N,N-二异丙基乙胺 作用下, 以 二氯甲烷N,N-二甲基甲酰胺 为溶剂, 反应 14.0h, 生成 7-chloro-4-(morpholine-4-carbonyl)quinolin-2-yltrifluoromethanesulfonate
    参考文献:
    名称:
    WO2024072870A1
    摘要:
    公开号:
  • 作为产物:
    描述:
    参考文献:
    名称:
    Synthesis and biological evaluation of novel 2-oxo-1,2-dihydroquinoline-4-carboxamide derivatives for the treatment of esophageal squamous cell carcinoma
    摘要:
    No new and effective treatments have been approved for the treatment of esophageal squamous cell carcinoma (ESCC) in the past decade. Cisplatin and 5-fluoruracil are the most commonly used drugs for this disease. In order to develop a new class of drugs effective in our ESCC phenotypic screens, we began a systematic approach to generate novel compounds based on the 2-oxo-1,2-dihydroquinoline-4carboxamide fragment. Herein, we report on the synthesis and initial assessment of 55 new analogues in two ESCC cell lines. Some of the active analogues with 1050 values around 10 mu M were tested in three additional cell lines. Our structure-activity relationships revealed remarkable alterations in the anti proliferative activities upon modest chemical modifications and autophagy modulation is a suggested mechanism of action. (C) 2018 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2018.05.042
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文献信息

  • Enantioselective, Intermolecular [<sub>π</sub>2+<sub>σ</sub>2] Photocycloaddition Reactions of 2(1<i>H</i>)-Quinolones and Bicyclo[1.1.0]butanes
    作者:Morgane de Robichon、Thilo Kratz、Frederike Beyer、Julian Zuber、Christian Merten、Thorsten Bach
    DOI:10.1021/jacs.3c08404
    日期:——
    enantioselectively to 2(1H)-quinolones upon irradiation (λ = 366 nm) in the presence of a chiral complexing agent. A two-point hydrogen bond between the quinolone and the template is responsible for stereocontrol in the photocycloaddition reaction. The reaction leads to the formation of products with a chiral bicyclo[2.1.1]hexane skeleton in high enantiomeric excess (91–99% ee). The chiral template can be almost
    在手性络合剂存在下,经照射 (λ = 366 nm),1-取代的双环[1.1.0]丁烷对映选择性地加成到 2(1 H )-喹诺酮类药物上。喹诺酮和模板之间的两点氢键负责光​​环加成反应中的立体控制。该反应导致形成具有高对映体过量(91-99% ee)的手性双环[2.1.1]己烷骨架的产物。手性模板几乎可以定量(97%)回收并用于另一个反应。可能存在三重态反应途径,如果反应要在可见光 (λ = 420 nm) 下进行,则敏化是一个合适的工具。
  • Synthesis and biological evaluation of novel 2-oxo-1,2-dihydroquinoline-4-carboxamide derivatives for the treatment of esophageal squamous cell carcinoma
    作者:Mai I. Shahin、Joyeeta Roy、Maha Hanafi、Dongyao Wang、Urarika Luesakul、Yifeng Chai、Nongnuj Muangsin、Deena S. Lasheen、Dalal A. Abou El Ella、Khaled A. Abouzid、Nouri Neamati
    DOI:10.1016/j.ejmech.2018.05.042
    日期:2018.7
    No new and effective treatments have been approved for the treatment of esophageal squamous cell carcinoma (ESCC) in the past decade. Cisplatin and 5-fluoruracil are the most commonly used drugs for this disease. In order to develop a new class of drugs effective in our ESCC phenotypic screens, we began a systematic approach to generate novel compounds based on the 2-oxo-1,2-dihydroquinoline-4carboxamide fragment. Herein, we report on the synthesis and initial assessment of 55 new analogues in two ESCC cell lines. Some of the active analogues with 1050 values around 10 mu M were tested in three additional cell lines. Our structure-activity relationships revealed remarkable alterations in the anti proliferative activities upon modest chemical modifications and autophagy modulation is a suggested mechanism of action. (C) 2018 Elsevier Masson SAS. All rights reserved.
  • WO2024072870A1
    申请人:——
    公开号:——
    公开(公告)日:——
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