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4-(6-(morpholin-4-yl)pyridin-3-yl)-N-(4-(8-methyl-3,8-diazabicyclo[3.2.1]octan-3-yl)phenyl)pyrimidin-2-amine | 1182185-95-0

中文名称
——
中文别名
——
英文名称
4-(6-(morpholin-4-yl)pyridin-3-yl)-N-(4-(8-methyl-3,8-diazabicyclo[3.2.1]octan-3-yl)phenyl)pyrimidin-2-amine
英文别名
N-[4-(8-methyl-3,8-diazabicyclo[3.2.1]octan-3-yl)phenyl]-4-(6-morpholin-4-ylpyridin-3-yl)pyrimidin-2-amine
4-(6-(morpholin-4-yl)pyridin-3-yl)-N-(4-(8-methyl-3,8-diazabicyclo[3.2.1]octan-3-yl)phenyl)pyrimidin-2-amine化学式
CAS
1182185-95-0
化学式
C26H31N7O
mdl
——
分子量
457.578
InChiKey
MMAAFGGZCPZNED-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):
    3.3
  • 重原子数:
    34
  • 可旋转键数:
    5
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.42
  • 拓扑面积:
    69.6
  • 氢给体数:
    1
  • 氢受体数:
    8

文献信息

  • PYRIMIDINE-2-AMINE COMPOUNDS AND THEIR USE AS INHIBITORS OF JAK KINASES
    申请人:Bhamidipati Somasekhar
    公开号:US20090258864A1
    公开(公告)日:2009-10-15
    This invention is directed to compounds of formula (I): where n, m, Y, R 1 , R 2 , R 3 , R 4 and R 5 are disclosed herein, as isolated stereoisomers or mixtures thereof, or as pharmaceutically acceptable salts thereof; pharmaceutical compositions comprising the compounds of formula (I); and methods of using the compounds and the pharmaceutical compositions in treating diseases or conditions associated with JAK2 activity.
    本发明涉及式(I)的化合物:其中,n、m、Y、R1、R2、R3、R4和R5在此被披露,作为分离的立体异构体或其混合物,或其药学上可接受的盐;包括式(I)化合物的制药组合物;以及使用该化合物和制药组合物治疗与JAK2活性相关的疾病或病症的方法。
  • US8309566B2
    申请人:——
    公开号:US8309566B2
    公开(公告)日:2012-11-13
  • US8735418B2
    申请人:——
    公开号:US8735418B2
    公开(公告)日:2014-05-27
  • US9624229B2
    申请人:——
    公开号:US9624229B2
    公开(公告)日:2017-04-18
  • [EN] A COMBINATION FOR IMMUNE MEDIATED CANCER TREATMENT<br/>[FR] COMBINAISON À MÉDIATION IMMUNITAIRE POUR LE TRAITEMENT DU CANCER
    申请人:RIGEL PHARMACEUTICALS INC
    公开号:WO2017007658A1
    公开(公告)日:2017-01-12
    Disclosed embodiments concern a combination comprising a JAK inhibitor and an immunooncology agent. The immunooncology agent may comprise an anti-PD- 1 antibody, anti- PD-L1 antibody, PI3K inhibitor, indole dioxygenase inhibitor or a combination thereof. The JAK inhibitor may be a pyrimidin-2-amine, 2,4-pyrimidinediamine, or a combination thereof. Also disclosed are embodiments of a method for using the combination to treat a subject, particularly a subject having a cell proliferative disorder. The method may further comprise administering one or more therapeutic agents in addition to the JAK inhibitor and immunooncology agent. Kits comprising the combination are also disclosed.
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