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2-(1-(4-amino-3-(3-fluoro-4-morpholinophenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)ethyl)-5-fluoro-3-(3-fluorophenyl)-4H-chromen-4-one | 1408085-56-2

中文名称
——
中文别名
——
英文名称
2-(1-(4-amino-3-(3-fluoro-4-morpholinophenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)ethyl)-5-fluoro-3-(3-fluorophenyl)-4H-chromen-4-one
英文别名
2-[1-[4-Amino-3-(3-fluoro-4-morpholin-4-ylphenyl)pyrazolo[3,4-d]pyrimidin-1-yl]ethyl]-5-fluoro-3-(3-fluorophenyl)chromen-4-one
2-(1-(4-amino-3-(3-fluoro-4-morpholinophenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)ethyl)-5-fluoro-3-(3-fluorophenyl)-4H-chromen-4-one化学式
CAS
1408085-56-2
化学式
C32H25F3N6O3
mdl
——
分子量
598.584
InChiKey
FFCKAIJUQUZXJW-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):
    4.8
  • 重原子数:
    44
  • 可旋转键数:
    5
  • 环数:
    7.0
  • sp3杂化的碳原子比例:
    0.19
  • 拓扑面积:
    108
  • 氢给体数:
    1
  • 氢受体数:
    11

文献信息

  • NOVEL COMPOUNDS AS MODULATORS OF PROTEIN KINASES
    申请人:NAGARATHNAM Dhanapalan
    公开号:US20120289496A1
    公开(公告)日:2012-11-15
    The present invention provides PI3K protein kinase modulators, methods of preparing them, pharmaceutical compositions containing them and methods of treatment, prevention and/or amelioration of kinase mediated diseases or disorders with them.
    本发明提供了PI3K蛋白激酶调节剂,其制备方法,含有它们的药物组合物,以及使用它们进行治疗、预防和/或改善激酶介导的疾病或紊乱的方法。
  • [EN] PROCESS FOR PREPARATION OF OPTICALLY PURE AND OPTIONALLY SUBSTITUTED 2- (1 -HYDROXY- ALKYL) - CHROMEN - 4 - ONE DERIVATIVES AND THEIR USE IN PREPARING PHARMACEUTICALS<br/>[FR] PROCÉDÉ DE PRÉPARATION DE DÉRIVÉS OPTIQUEMENT PURS ET ÉVENTUELLEMENT SUBSTITUÉS DE 2- (1 -HYDROXY- ALKYL) - CHROMEN - 4 - ONE ET LEUR UTILISATION DANS LA PRÉPARATION DE PRODUITS PHARMACEUTIQUES
    申请人:RHIZEN PHARMACEUTICALS SA
    公开号:WO2013164801A1
    公开(公告)日:2013-11-07
    The present invention relates to compounds useful as pharmaceutical intermediates, to processes for preparing the intermediates, to intermediates used in the processes, and to the use of the intermediates in the preparation of pharmaceuticals. In particular, the present invention concerns enantiomerically pure optionally substituted 2-(1-hydroxy-alkyl)- chromen-4-one derivatives represented by formula (IA) and (IB), processes for preparing the alcohol derivatives and their use in preparing pharmaceuticals.
    本发明涉及一种作为药物中间体有用的化合物,用于制备中间体的过程,用于该过程的中间体以及中间体在制备药物中的应用。特别地,本发明涉及对映纯的、可选择取代的2-(1-羟基-烷基)-香豆素生物,其化学式为(IA)和(IB),用于制备醇衍生物的过程以及它们在制备药物中的应用。
  • NOVEL PROCESS FOR PREPARATION OF OPTICALLY PURE AND OPTIONALLY SUBSTITUTED 2-(1-HYDROXY-ALKYL)-CHROMEN-4-ONE DERIVATIVES AND THEIR USE IN PREPARING PHARMACEUTICALS
    申请人:Rhizen Pharmaceutical SA
    公开号:US20150087699A1
    公开(公告)日:2015-03-26
    The present invention relates to compounds useful as pharmaceutical intermediates, to processes for preparing the intermediates, to intermediates used in the processes, and to the use of the intermediates in the preparation of pharmaceuticals. In particular, the present invention concerns enantiomerically pure optionally substituted 2-(1-hydroxy-alkyl)-chromen-4-one derivatives represented by formula (IA) and (IB), processes for preparing the alcohol derivatives and their use in preparing pharmaceuticals.
    本发明涉及作为药物中间体有用的化合物,用于制备中间体的过程,用于这些过程中使用的中间体,以及在制备药物中使用这些中间体。具体来说,本发明涉及对映纯的可选取代的2-(1-羟基-烷基)-香豆素生物,其表示为式(IA)和(IB),制备醇衍生物的过程以及它们在制备药物中的使用。
  • PROCESS FOR PREPARATION OF OPTICALLY PURE AND OPTIONALLY SUBSTITUTED 2-(1-HYDROXY-ALKYL)-CHROMEN-4-ONE DERIVATIVES AND THEIR USE IN PREPARING PHARMACEUTICALS
    申请人:Rhizen Pharmaceuticals SA
    公开号:US20170266196A1
    公开(公告)日:2017-09-21
    The present invention relates to compounds useful as pharmaceutical intermediates, to processes for preparing the intermediates, to intermediates used in the processes, and to the use of the intermediates in the preparation of pharmaceuticals. In particular, the present invention concerns enantiomerically pure optionally substituted 2-(1-hydroxy-alkyl)-chromen-4-one derivatives represented by formula (IA) and (IB), processes for preparing the alcohol derivatives and their use in preparing pharmaceuticals.
    本发明涉及用作制药中间体的化合物,制备中间体的过程,用于过程的中间体以及中间体在制备制药品中的应用。特别地,本发明涉及旋光纯的可选取代的2-(1-羟基-烷基)-香豆素生物,其化学式为(IA)和(IB),制备醇衍生物的过程以及它们在制备制药品中的应用。
  • Pharmaceutical compositions containing a PDE4 inhibitor and a PI3 delta or dual PI3 delta-gamma kinase inhibitor
    申请人:Rhizen Pharmaceuticals SA
    公开号:US10058539B2
    公开(公告)日:2018-08-28
    This present invention relates to a method of treating a autoimmune, respiratory and/or inflammatory disease or condition (e.g., psoriasis, rheumatoid arthritis, asthma, COPD). The method comprises administering a PI3K Delta inhibitor or a dual PI3K Delta-Gamma inhibitor and a PDE4 inhibitor. The present invention also relates to pharmaceutical compositions containing a PI3K Delta or dual PI3K Delta-Gamma inhibitor and a PDE4 inhibitor.
    本发明涉及一种治疗自身免疫性、呼吸道和/或炎症性疾病或病症(如屑病、类风湿性关节炎、哮喘、慢性阻塞性肺病)的方法。该方法包括给药 PI3K Delta 抑制剂或双重 PI3K Delta-Gamma 抑制剂和 PDE4 抑制剂。本发明还涉及含有PI3K Delta或双重PI3K Delta-Gamma抑制剂和PDE4抑制剂的药物组合物。
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