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N-[5-(3,5-difluorobenzyl)-1H-indazol-3-yl]-4-[4-(dimethylamino)piperidin-1-yl]-2-(tetrahydro-2H-pyran-4-ylamino)benzamide | 1108743-77-6

中文名称
——
中文别名
——
英文名称
N-[5-(3,5-difluorobenzyl)-1H-indazol-3-yl]-4-[4-(dimethylamino)piperidin-1-yl]-2-(tetrahydro-2H-pyran-4-ylamino)benzamide
英文别名
N-(5-(3,5-difluorobenzyl)-1H-indazol-3-yl)-4-(4-(dimethylamino)piperidin-1-yl)-2-(tetrahydro-2H-pyran-4-ylamino)benzamide;N-[5-[(3,5-difluorophenyl)methyl]-1H-indazol-3-yl]-4-[4-(dimethylamino)piperidin-1-yl]-2-(oxan-4-ylamino)benzamide
N-[5-(3,5-difluorobenzyl)-1H-indazol-3-yl]-4-[4-(dimethylamino)piperidin-1-yl]-2-(tetrahydro-2H-pyran-4-ylamino)benzamide化学式
CAS
1108743-77-6
化学式
C33H38F2N6O2
mdl
——
分子量
588.701
InChiKey
WJYASLCTLYUHOB-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):
    6.5
  • 重原子数:
    43
  • 可旋转键数:
    8
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.39
  • 拓扑面积:
    85.5
  • 氢给体数:
    3
  • 氢受体数:
    8

文献信息

  • [EN] SUBSTITUTED INDAZOLE DERIVATIVES ACTIVE AS KINASE INHIBITORS<br/>[FR] DÉRIVÉS D'INDAZOLE SUBSTITUÉS ACTIFS COMME INHIBITEURS DE KINASES
    申请人:NERVIANO MEDICAL SCIENCES SRL
    公开号:WO2009013126A1
    公开(公告)日:2009-01-29
    Substituted indazole derivatives of formula (I) and pharmaceutically acceptable salts thereof, as defined in the specification, process for their preparation and pharmaceutical compositions comprising them are disclosed; the compounds of the invention may be useful in therapy in the treatment of diseases associated with a deregulated protein kinase activity, like cancer.
    公开了公式(I)的吲唑生物及其药用盐,如规范中定义的,以及它们的制备方法和包含它们的药物组合物;本发明的化合物可能在治疗与蛋白激酶活性失调相关的疾病,如癌症方面有用。
  • Molecules for administration to ROS1 mutant cancer cells
    申请人:Ignyta, Inc.
    公开号:US10231965B2
    公开(公告)日:2019-03-19
    Substituted indazole derivatives of formula (I) or formula 2.(I) and pharmaceutically acceptable salts thereof, as defined in the specification, process for their preparation and pharmaceutical compositions comprising them are disclosed; the compounds of the invention may be useful in therapy in the treatment of diseases associated with a deregulated protein kinase activity, like cancer.
    公开了公式(I)或公式2的取代吲唑生物以及其药用盐,如规范中所定义,其制备方法和包含它们的药物组合物;该发明的化合物可能在治疗与蛋白激酶活性失调相关的疾病,如癌症方面有用。
  • SUBSTITUTED INDAZOLE DERIVATIVES ACTIVE AS KINASE INHIBITORS
    申请人:LOMBARDI BORGIA Andrea
    公开号:US20130018036A1
    公开(公告)日:2013-01-17
    Substituted indazole derivatives of formula (I) and pharmaceutically acceptable salts thereof, as defined in the specification, process for their preparation and pharmaceutical compositions comprising them are disclosed; the compounds of the invention may be useful in therapy in the treatment of diseases associated with a deregulated protein kinase activity, like cancer.
    本发明披露了式(I)的取代吲唑生物及其药学上可接受的盐,其定义在说明书中,以及其制备过程和包含它们的制药组合物;本发明的化合物可能在治疗与蛋白激酶活性失调相关的疾病,如癌症中有用。
  • N-[5-(3,5-DIFLUOROBENZYL)-1H-INDAZOL-3-YL]-4-(4-METHYL-PIPERAZIN-1-YL)-2-(TETRAHYDRO-2H-PYRAN-4-YLAMINO) BENZAMIDE FOR TREATING PATIENTS WITH ROS1,NTRK1, NTRK2 AND NTRK3 MUTANT CANCER CELLS
    申请人:Ignyta, Inc.
    公开号:EP3834827A1
    公开(公告)日:2021-06-16
    Substituted indazole derivatives of formula (I) or formula 2.(I) and pharmaceutically acceptable salts thereof, as defined in the specification, process for their preparation and pharmaceutical compositions comprising them are disclosed; the compounds of the invention may be useful in therapy in the treatment of diseases associated with a deregulated protein kinase activity, like cancer.
    本发明公开了式(I)或式2.(I)的取代吲唑生物及其药学上可接受的盐类(如说明书中所定义)、其制备工艺和包含它们的药物组合物;本发明的化合物可用于治疗与蛋白激酶活性失调有关的疾病(如癌症)。
  • Substituted indazole derivatives active as kinase inhibitors
    申请人:NERVIANO MEDICAL SCIENCES S.R.L.
    公开号:US10081622B2
    公开(公告)日:2018-09-25
    Substituted indazole derivatives of formula (I) and pharmaceutically acceptable salts thereof, as defined in the specification; the compounds of the invention may be useful in therapy in the treatment of diseases associated with a deregulated protein kinase activity, like cancer.
    如说明书中所定义的式(I)的取代吲唑生物及其药学上可接受的盐;本发明的化合物可用于治疗与蛋白激酶活性失调有关的疾病,如癌症。
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