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4-Hydroxy-6-phenylcarbostyril | 14300-44-8

中文名称
——
中文别名
——
英文名称
4-Hydroxy-6-phenylcarbostyril
英文别名
4-hydroxy-6-phenyl-1H-quinolin-2-one;4-Hydroxy-6-phenyl-carbostyril;4-hydroxy-6-phenyl-1H-quinolin-2-one
4-Hydroxy-6-phenylcarbostyril化学式
CAS
14300-44-8
化学式
C15H11NO2
mdl
——
分子量
237.258
InChiKey
UFPMMKWAGDIAJJ-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):
    3
  • 重原子数:
    18
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    49.3
  • 氢给体数:
    2
  • 氢受体数:
    3

文献信息

  • Small Molecule Inhibitors of Toll-Like Receptor 9
    申请人:Lipford Grayson B.
    公开号:US20100160314A1
    公开(公告)日:2010-06-24
    Small molecule compounds and compositions containing said compounds useful for inhibiting signaling by certain Toll-like receptors (TLRs), particularly TLR9, are provided. The compounds and compositions can be used to inhibit immune responses, including unwanted immune responses in particular. Compounds, compositions, and methods are provided to treat a variety of conditions involving unwanted immune responses, including for example autoimmune disease, inflammation, transplant rejection, and sepsis.
    提供小分子化合物和包含所述化合物的组合物,用于抑制某些Toll样受体(TLRs)的信号传导,特别是TLR9。这些化合物和组合物可用于抑制免疫反应,包括特别是非所需的免疫反应。提供的化合物、组合物和方法可用于治疗涉及非所需免疫反应的各种病症,例如自身免疫病、炎症、移植排斥和败血症。
  • 6-Aryl aminomethyl quinoline derivatives and their use as anti-tumour agents
    申请人:IMPERIAL CHEMICAL INDUSTRIES PLC
    公开号:EP0318225A2
    公开(公告)日:1989-05-31
    The invention relates to a quinoline of the formula:- wherein each of R¹ and R², which may be the same or different, is hydrogen, halogeno, hydroxy, cyano, carbamoyl, nitro or amino, alkyl, alkoxy, alkylthio, alkylamino, dialkylamino or alkanoylamino each of up to 4 carbon atoms, or substituted alkyl or alkoxy each of up to 3 carbon atoms, provided that both R¹ and R² are not hydrogen; the quinoline ring may bear further substituents; R³ is hydrogen or alkyl of up to 4 carbon atoms; R⁴ is hydrogen, alkyl, alkenyl or alkynyl each of up to 4 carbon atoms or substituted alkyl of up to 3 carbon atoms; Ar is phenylene, naphthylene or heterocyclene which is unsubstituted or which bears one or more substituents; R⁵ is such that R⁵-NH₂ is an amino acid; or a pharmaceutically-acceptable salt or ester thereof. The compounds possess anti-tumour activity.
    本发明涉及一种式如下的喹啉 其中R¹和R²可以相同或不同,各自为氢、卤素、羟基、基、基甲酰基、硝基或基、烷基、烷氧基、烷基、烷基基、二烷基基或烷酰基,各自最多为4个碳原子,或取代的烷基或烷氧基,各自最多为3个碳原子,条件是R¹和R²都不是氢; 喹啉环可带有其他取代基; R³ 是氢或最多 4 个碳原子的烷基; R⁴ 是氢、各含最多 4 个碳原子的烷基、烯基或炔基或含最多 3 个碳原子的取代烷基; Ar 是未取代的苯基、基或杂环基,或带有一个或多个取代基; R⁵ 是 R⁵-NH₂ 是氨基酸; 或其药学上可接受的盐或酯。 这些化合物具有抗肿瘤活性。
  • SMALL MOLECULE INHIBITORS OF TOLL-LIKE RECEPTOR 9
    申请人:Coley Pharmaceutical Group, Inc.
    公开号:EP2081924A2
    公开(公告)日:2009-07-29
  • US5112837A
    申请人:——
    公开号:US5112837A
    公开(公告)日:1992-05-12
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