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(S)-2-(4-fluoro-phenyl)-4-oxo-3,4-dihydro-2H-pyridine-1-carboxylic acid quinolin-5-ylamide | 1232688-17-3

中文名称
——
中文别名
——
英文名称
(S)-2-(4-fluoro-phenyl)-4-oxo-3,4-dihydro-2H-pyridine-1-carboxylic acid quinolin-5-ylamide
英文别名
(2S)-2-(4-fluorophenyl)-4-oxo-N-quinolin-5-yl-2,3-dihydropyridine-1-carboxamide
(S)-2-(4-fluoro-phenyl)-4-oxo-3,4-dihydro-2H-pyridine-1-carboxylic acid quinolin-5-ylamide化学式
CAS
1232688-17-3
化学式
C21H16FN3O2
mdl
——
分子量
361.375
InChiKey
ZREAHQPXWUVTDX-FQEVSTJZSA-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):
    2.6
  • 重原子数:
    27
  • 可旋转键数:
    2
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.1
  • 拓扑面积:
    62.3
  • 氢给体数:
    1
  • 氢受体数:
    4

文献信息

  • DIHYDROPYRIDONE UREAS AS P2X7 MODULATORS
    申请人:Brotherton-Pleiss Christine E.
    公开号:US20100160388A1
    公开(公告)日:2010-06-24
    Compounds of the formula I: or pharmaceutically acceptable salts thereof, wherein m, n, R 1 , R 2 , R 3 , R 4 and R 5 are as defined herein. Also disclosed are methods of making the compounds and using the compounds for treatment of diseases associated with the P2X7 purinergic receptor.
    公式I的化合物:或其药用可接受的盐,其中m、n、R1、R2、R3、R4和R5按本文件定义。还公开了制造这些化合物的方法以及使用这些化合物治疗与P2X7嘌呤能受体相关疾病的方法。
  • Methods of modulating immune activity
    申请人:Flagship Pioneering Innovations V, Inc.
    公开号:US11376272B2
    公开(公告)日:2022-07-05
    In one aspect, the invention provides methods of increasing immune response by administering postcellular signaling factors produced by cells exposed to a stress condition. In one aspect, the invention provides methods of increasing immune response by administering in combination (a) a Stimulator of Interferon Genes (STING) agonist and (b) a purinergic receptor agonist. The increase in immune response may be used, for example, for treatment of infection or cancer. The invention also provides screening assays for identification of compounds that induce production of postcellular signaling factors which are also immunostimulatory agents. The invention further provides methods for identifying postcellular signaling factors with immunostimulatory activity. In another aspect, the invention provides methods of decreasing immune response by administering to a cell, tissue or subject a purinergic receptor antagonist alone or in combination with a Stimulator of Interferon Genes (STING) antagonist.
    一方面,本发明提供了通过施用暴露于应激条件下的细胞产生的细胞后信号因子来提高免疫应答的方法。在一个方面,本发明提供了通过联合施用(a)干扰素基因刺激剂(STING)激动剂和(b)嘌呤能受体激动剂来增加免疫反应的方法。免疫反应的增强可用于治疗感染或癌症等。本发明还提供了筛选测定法,用于鉴定能诱导产生细胞后信号因子的化合物,这些细胞后信号因子也是免疫刺激剂。本发明进一步提供了鉴定具有免疫刺激活性的细胞后信号因子的方法。在另一方面,本发明提供了通过向细胞、组织或受试者单独施用嘌呤能受体拮抗剂或与干扰素基因刺激剂(STING)拮抗剂联合施用来降低免疫反应的方法。
  • METHODS OF MODULATING IMMUNE ACTIVITY
    申请人:Flagship Pioneering Innovations V, Inc.
    公开号:US20210299155A1
    公开(公告)日:2021-09-30
    In one aspect, the invention provides methods of increasing immune response by administering posteellular signaling factors produced by cells exposed to a stress condition. In one aspect, the invention provides methods of increasing immune response by administering in combination (a) a Stimulator of Interferon Genes (STING) agonist and (b) a purinergic receptor agonist. The increase in immune response may be used, for example, for treatment of infection or cancer. The invention also provides screening assays for identification of compounds that induce production of postcellular signaling factors which are also immunostimulatory agents. The invention further provides methods for identifying postcellular signaling factors with immunostimulatory activity. In another aspect, the invention provides methods of decreasing immune response by administering to a cell, tissue or subject a purinergic receptor antagonist alone or in combination with a Stimulator of Interferon Genes (STING) antagonist.
  • US8153809B2
    申请人:——
    公开号:US8153809B2
    公开(公告)日:2012-04-10
  • [EN] DIHYDROPYRIDONE UREAS AS P2X7 MODULATORS<br/>[FR] DIHYDROPYRIDONE URÉES EN TANT QUE MODULATEURS DE P2X7
    申请人:HOFFMANN LA ROCHE
    公开号:WO2010072599A1
    公开(公告)日:2010-07-01
    Compounds of the formula (I) or pharmaceutically acceptable salts thereof, wherein m, n, R1, R2, R3, R4 and R5 are as defined herein. Also disclosed are methods of making the compounds and using the compounds for treatment of diseases associated with the P2X7 purinergic receptor.
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