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(3-氯-4-氟苯基)(环丙基)甲酮 | 898790-09-5

中文名称
(3-氯-4-氟苯基)(环丙基)甲酮
中文别名
3-氯-4-氟-苯基环丙基甲基酮
英文名称
3-Chloro-4-fluorophenyl cyclopropyl ketone
英文别名
(3-chloro-4-fluorophenyl)-cyclopropylmethanone
(3-氯-4-氟苯基)(环丙基)甲酮化学式
CAS
898790-09-5
化学式
C10H8ClFO
mdl
——
分子量
198.62
InChiKey
UWLYSHCUFNFEPS-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

物化性质

  • 沸点:
    300.8±27.0 °C(Predicted)
  • 密度:
    1.356±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.9
  • 重原子数:
    13
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.3
  • 拓扑面积:
    17.1
  • 氢给体数:
    0
  • 氢受体数:
    2

文献信息

  • KYNURENINE-3-MONOOXYGENASE INHIBITORS, PHARMACEUTICAL COMPOSITIONS, AND METHODS OF USE THEREOF
    申请人:CHDI FOUNDATION, INC.
    公开号:US20150057238A1
    公开(公告)日:2015-02-26
    Certain compounds, or pharmaceutically acceptable salts or prodrugs thereof, are provided herein. Also provided are pharmaceutical compositions comprising at least one compound, or pharmaceutically acceptable salt or prodrug thereof, described herein and one or more pharmaceutically acceptable vehicle. Methods of treating patients suffering from certain diseases and disorders responsive to the inhibition of KMO activity are described, which comprise administering to such patients an amount of at least one compound, or pharmaceutically acceptable salt or prodrug thereof, described herein effective to reduce signs or symptoms of the disease or disorder are disclosed. These diseases include neurodegenerative disorders such as Huntington's disease. Also described are methods of treatment include administering at least one compound, or pharmaceutically acceptable salt or prodrug thereof, described herein as a single active agent or administering at least one compound, or pharmaceutically acceptable salt or prodrug thereof, described herein in combination with one or more other therapeutic agents. Also provided are methods for screening compounds capable of inhibiting KMO activity.
    本文提供了某些化合物,或其药学上可接受的盐或前药。还提供了包含至少一种化合物或其药学上可接受的盐或前药及一种或多种药学上可接受的载体的制药组合物。本文描述了治疗对KMO活性抑制有反应的某些疾病和障碍的患者的方法,包括向这些患者施用至少一种本文所述的化合物或其药学上可接受的盐或前药的有效量,以减少疾病或障碍的症状。这些疾病包括神经退行性疾病,如亨廷顿病。本文还描述了治疗方法,包括将至少一种本文所述的化合物或其药学上可接受的盐或前药作为单一活性剂施用,或将至少一种本文所述的化合物或其药学上可接受的盐或前药与一种或多种其他治疗剂联合施用。还提供了筛选能够抑制KMO活性的化合物的方法。
  • Kynurenine-3-monooxygenase inhibitors, pharmaceutical compositions, and methods of use thereof
    申请人:CHDI Foundation, Inc.
    公开号:US10442782B2
    公开(公告)日:2019-10-15
    Certain compounds, or pharmaceutically acceptable salts or prodrugs thereof, are provided herein. Also provided are pharmaceutical compositions comprising at least one compound, or pharmaceutically acceptable salt or prodrug thereof, described herein and one or more pharmaceutically acceptable vehicle. Methods of treating patients suffering from certain diseases and disorders responsive to the inhibition of KMO activity are described, which comprise administering to such patients an amount of at least one compound, or pharmaceutically acceptable salt or prodrug thereof, described herein effective to reduce signs or symptoms of the disease or disorder are disclosed. These diseases include neurodegenerative disorders such as Huntington's disease. Also described are methods of treatment include administering at least one compound, or pharmaceutically acceptable salt or prodrug thereof, described herein as a single active agent or administering at least one compound, or pharmaceutically acceptable salt or prodrug thereof, described herein in combination with one or more other therapeutic agents. Also provided are methods for screening compounds capable of inhibiting KMO activity.
    本文提供了某些化合物或其药学上可接受的盐或原药。还提供了包含至少一种本文所述化合物或其药学上可接受的盐或原药以及一种或多种药学上可接受的载体的药物组合物。描述了治疗对抑制 KMO 活性有反应的某些疾病和失调患者的方法,其中包括向此类患者施用一定量的本文所述的至少一种化合物或其药学上可接受的盐或原药,以有效减少疾病或失调的体征或症状。这些疾病包括神经退行性疾病,如亨廷顿氏病。还描述了治疗方法,包括将本文所述的至少一种化合物或其药学上可接受的盐或原药作为单一活性剂给药,或将本文所述的至少一种化合物或其药学上可接受的盐或原药与一种或多种其它治疗剂联合给药。还提供了筛选能够抑制 KMO 活性的化合物的方法。
  • US9822058B2
    申请人:——
    公开号:US9822058B2
    公开(公告)日:2017-11-21
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