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N-{3-[9-Ethyl-2-(trans-4-hydroxy-cyclo-hexylamino)-9H-purin-6-yl-amino]-phenyl}-4,4-dimethyl-2-pentynylic acid amide | 289479-91-0

中文名称
——
中文别名
——
英文名称
N-{3-[9-Ethyl-2-(trans-4-hydroxy-cyclo-hexylamino)-9H-purin-6-yl-amino]-phenyl}-4,4-dimethyl-2-pentynylic acid amide
英文别名
——
N-{3-[9-Ethyl-2-(trans-4-hydroxy-cyclo-hexylamino)-9H-purin-6-yl-amino]-phenyl}-4,4-dimethyl-2-pentynylic acid amide化学式
CAS
289479-91-0
化学式
C26H33N7O2
mdl
——
分子量
475.594
InChiKey
WNFDAMUJNDGILP-IRJFHVNHSA-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):
    4.29
  • 重原子数:
    35.0
  • 可旋转键数:
    6.0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.46
  • 拓扑面积:
    116.99
  • 氢给体数:
    4.0
  • 氢受体数:
    8.0

文献信息

  • 2-Amino-6-anilino-purines and their use as medicaments
    申请人:——
    公开号:US20020016329A1
    公开(公告)日:2002-02-07
    2-Amino-6-anilino-purine derivatives of the formula I 1 in which the symbols are as defined in claim 1, are described. These compounds inhibit p34 cdc2 /cyclin B cdc13 kinase and protein tyrosine kinase pp60 c-src and can be used for treatment of hyperproliferative diseases, for example tumor diseases, and diseases which respond to inhibition of the activity of protein tyrosine kinase pp60 c-src , in particular osteoporosis.
    公式I中定义的符号如权利要求书1中所定义的那样,描述了1的2-基-6-苯胺嘌呤生物。这些化合物抑制p34 cdc2/cyclin B cdc13激酶和蛋白酪氨酸激酶pp60 c-src,并可用于治疗过度增殖性疾病,例如肿瘤疾病,以及对蛋白酪氨酸激酶pp60 c-src活性抑制有反应的疾病,特别是骨质疏松症。
  • 2-AMINO-6-ANILINO-PURINES AND THEIR USE AS MEDICAMENTS
    申请人:Novartis AG
    公开号:EP1153024B1
    公开(公告)日:2004-04-28
  • JP2002537300A
    申请人:——
    公开号:JP2002537300A
    公开(公告)日:2002-11-05
  • US6767906B2
    申请人:——
    公开号:US6767906B2
    公开(公告)日:2004-07-27
  • [EN] 2-AMINO-6-ANILINO-PURINES AND THEIR USE AS MEDICAMENTS<br/>[FR] 2-AMINO-6-ANILINO-PURINES ET LEUR UTILISATION COMME MEDICAMENTS
    申请人:NOVARTIS AG
    公开号:WO2000049018A1
    公开(公告)日:2000-08-24
    2-Amino-6-anilino-purine derivatives of formula (I) in which R1 is -S(O)k-NR6R7 or-N(aryl lower alkyl) carbamoyl or -NH-S(O)i-R8 or -NH-C(O)-R9; 9 is 1-5; These compounds inhibit p34cdc2/cyclin Bcdc13 kinase and protein tyrosine kinase pp60c-src and can be used for treatment of hyperproliferative diseases, for example tumour diseases, and diseases which respond to inhibition of the activity of protein tyrosine kinase pp60c-src, in particular osteoporosis.
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