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(R)-4-amino-6-(1-(6-fluoro-1-(pyridin-2-yl)-1H-benzo-[d]imidazol-2-yl)ethylamino)pyrimidine-5-carbonitrile | 1338482-72-6

中文名称
——
中文别名
——
英文名称
(R)-4-amino-6-(1-(6-fluoro-1-(pyridin-2-yl)-1H-benzo-[d]imidazol-2-yl)ethylamino)pyrimidine-5-carbonitrile
英文别名
4-amino-6-[[(1R)-1-(6-fluoro-1-pyridin-2-ylbenzimidazol-2-yl)ethyl]amino]pyrimidine-5-carbonitrile
(R)-4-amino-6-(1-(6-fluoro-1-(pyridin-2-yl)-1H-benzo-[d]imidazol-2-yl)ethylamino)pyrimidine-5-carbonitrile化学式
CAS
1338482-72-6
化学式
C19H15FN8
mdl
——
分子量
374.38
InChiKey
CJJJMUGTTBYKLR-LLVKDONJSA-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):
    2.9
  • 重原子数:
    28
  • 可旋转键数:
    4
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.11
  • 拓扑面积:
    118
  • 氢给体数:
    2
  • 氢受体数:
    8

反应信息

点击查看最新优质反应信息

文献信息

  • HETEROCYCLIC COMPOUNDS AND METHODS OF USE
    申请人:Heald Robert
    公开号:US20120202785A1
    公开(公告)日:2012-08-09
    Formula I compounds, including stereoisomers, geometric isomers, tautomers, metabolites and pharmaceutically acceptable salts thereof, are useful for inhibiting the delta isoform of PI3K, and for treating disorders mediated by lipid kinases such as inflammation, immunological disorders, and cancer. Methods of using compounds of Formula I for in vitro, in situ, and in vivo diagnosis, prevention or treatment of such disorders in mammalian cells, or associated pathological conditions, are disclosed.
    化学式I类化合物,包括立体异构体、几何异构体、互变异构体、代谢物及其药学上可接受的盐,对抑制PI3K的δ异构体以及治疗由脂质激酶介导的疾病,如炎症、免疫性疾病和癌症,具有用途。公开了利用化合物I类进行体外、体内和体内诊断、预防或治疗哺乳动物细胞中的这类疾病,或相关的病理状况的方法。
  • HETEROCYCLIC COMPOUNDS AS PI3 KINASE INHIBITORS
    申请人:F.Hoffmann-La Roche AG
    公开号:EP2673269A1
    公开(公告)日:2013-12-18
  • US8575183B2
    申请人:——
    公开号:US8575183B2
    公开(公告)日:2013-11-05
  • US8653089B2
    申请人:——
    公开号:US8653089B2
    公开(公告)日:2014-02-18
  • [EN] HETEROCYCLIC COMPOUNDS AND THEIR USES<br/>[FR] COMPOSÉS HÉTÉROCYCLIQUES ET LEURS UTILISATIONS
    申请人:AMGEN INC
    公开号:WO2011123751A2
    公开(公告)日:2011-10-06
    Substituted bicyclic heteroaryls and compositions containing them, for the treatment of general inflammation, arthritis, rheumatic diseases, osteoarthritis, inflammatory bowel disorders, inflammatory eye disorders, inflammatory or unstable bladder disorders, psoriasis, skin complaints with inflammatory components, chronic inflammatory conditions, including but not restricted to autoimmune diseases such as systemic lupus erythematosis (SLE), myestenia gravis, rheumatoid arthritis, acute disseminated encephalomyelitis, idiopathic thrombocytopenic purpura, multiples sclerosis, Sjoegren's syndrome and autoimmune hemolytic anemia, allergic conditions including all forms of hypersensitivity, The present invention also enables methods for treating cancers that are mediated, dependent on or associated with p110 activity, including but not restricted to leukemias, such as Acute Myeloid leukaemia (AML) Myelo-dysplastic syndrome (MDS) myelo-proliferative diseases (MPD) Chronic Myeloid Leukemia (CML) T-cell Acute Lymphoblastic leukaemia ( T-ALL) B-cell Acute Lymphoblastic leukaemia (B-ALL) Non Hodgkins Lymphoma (NHL) B-cell lymphoma and solid tumors, such as breast cancer.
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