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(E)-N-(4-(6-amino-7-(4-chlorophenyl)-8-oxo-7H-purin-9(8H)-yl)phenyl)-4-(dimethylamino)-N-methylbut-2-enamide | 1448444-90-3

中文名称
——
中文别名
——
英文名称
(E)-N-(4-(6-amino-7-(4-chlorophenyl)-8-oxo-7H-purin-9(8H)-yl)phenyl)-4-(dimethylamino)-N-methylbut-2-enamide
英文别名
(E)-N-[4-[6-amino-7-(4-chlorophenyl)-8-oxopurin-9-yl]phenyl]-4-(dimethylamino)-N-methylbut-2-enamide
(E)-N-(4-(6-amino-7-(4-chlorophenyl)-8-oxo-7H-purin-9(8H)-yl)phenyl)-4-(dimethylamino)-N-methylbut-2-enamide化学式
CAS
1448444-90-3
化学式
C24H24ClN7O2
mdl
——
分子量
477.953
InChiKey
DIGKUDHIIBVQCW-SNAWJCMRSA-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:
    34
  • 可旋转键数:
    6
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    98.9
  • 氢给体数:
    1
  • 氢受体数:
    6

文献信息

  • PURINONE COMPOUNDS AS KINASE INHIBITORS
    申请人:CHEN Wei
    公开号:US20130197014A1
    公开(公告)日:2013-08-01
    Disclosed herein are compounds that form covalent bonds with Bruton's tyrosine kinase (Btk). Also described are irreversible inhibitors of Btk. In addition, reversible inhibitors of Btk are also described. Also disclosed are pharmaceutical compositions that include the compounds. Methods of using the Btk inhibitors are disclosed, alone or in combination with other therapeutic agents, for the treatment of autoimmune diseases or conditions, heteroimmune diseases or conditions, cancer, including lymphoma, and inflammatory diseases or conditions.
    本文披露了与布鲁顿氏酪氨酸激酶(Btk)形成共价键的化合物。还描述了Btk的不可逆抑制剂。此外,还描述了Btk的可逆抑制剂。还披露了包括这些化合物的药物组合物。披露了使用Btk抑制剂的方法,单独或与其他治疗剂联合治疗自身免疫疾病或症状、异源免疫疾病或症状、癌症(包括淋巴瘤)和炎症性疾病或症状。
  • US8501724B1
    申请人:——
    公开号:US8501724B1
    公开(公告)日:2013-08-06
  • US9469642B2
    申请人:——
    公开号:US9469642B2
    公开(公告)日:2016-10-18
  • [EN] PURINONE COMPOUNDS AS KINASE INHIBITORS<br/>[FR] COMPOSÉS PURINONES COMME INHIBITEURS DE KINASE
    申请人:PHARMACYCLICS INC
    公开号:WO2013116382A1
    公开(公告)日:2013-08-08
    Disclosed herein are compounds that form covalent bonds with Bruton's tyrosine kinase (Btk). Also described are irreversible inhibitors of Btk. In addition, reversible inhibitors of Btk are also described. Also disclosed are pharmaceutical compositions that include the compounds. Methods of using the Btk inhibitors are disclosed, alone or in combination with other therapeutic agents, for the treatment of autoimmune diseases or conditions, heteroimmune diseases or conditions, cancer, including lymphoma, and inflammatory diseases or conditions.
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