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benzyl 3-((2-(4-(4-acetylpiperazin-1-yl)phenylamino)-5-carbamoylpyrimidin-4-ylamino)methyl)piperidine-1-carboxylate | 1198300-33-2

中文名称
——
中文别名
——
英文名称
benzyl 3-((2-(4-(4-acetylpiperazin-1-yl)phenylamino)-5-carbamoylpyrimidin-4-ylamino)methyl)piperidine-1-carboxylate
英文别名
benzyl 3-[[[2-[4-(4-acetylpiperazin-1-yl)anilino]-5-carbamoylpyrimidin-4-yl]amino]methyl]piperidine-1-carboxylate
benzyl 3-((2-(4-(4-acetylpiperazin-1-yl)phenylamino)-5-carbamoylpyrimidin-4-ylamino)methyl)piperidine-1-carboxylate化学式
CAS
1198300-33-2
化学式
C31H38N8O4
mdl
——
分子量
586.694
InChiKey
HDCIPVZAKAAPAU-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):
    3.4
  • 重原子数:
    43
  • 可旋转键数:
    10
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.39
  • 拓扑面积:
    146
  • 氢给体数:
    3
  • 氢受体数:
    9

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • Inhibitors of protein kinases
    申请人:Bauer Shawn M.
    公开号:US20090318407A1
    公开(公告)日:2009-12-24
    The present invention is directed to compounds of formula I-II and pharmaceutically acceptable tautomers, salts, or stereoisomers thereof which are inhibitors of syk and/or JAK kinase. The present invention is also directed to intermediates used in making such compounds, the preparation of such a compound, pharmaceutical compositions containing such a compound, methods of inhibition syk and/or JAK kinase activity, methods of inhibition the platelet aggregation, and methods to prevent or treat a number of conditions mediated at least in part by syk and/or JAK kinase activity, such as undesired thrombosis and Non Hodgkin's Lymphoma.
    本发明涉及式I-II化合物及其药学上可接受的互变异构体、盐或立体异构体,其是SYK和/或JAK激酶的抑制剂。本发明还涉及用于制备这种化合物的中间体,该化合物的制备,含有该化合物的制药组合物,抑制SYK和/或JAK激酶活性的方法,抑制血小板聚集的方法,以及预防或治疗由SYK和/或JAK激酶活性至少部分介导的多种疾病,如不良血栓和非霍奇金淋巴瘤的方法。
  • INHIBITORS OF PROTEIN KINASES
    申请人:Bauer Shawn M.
    公开号:US20120129867A1
    公开(公告)日:2012-05-24
    The present invention is directed to compounds of formula I-II and pharmaceutically acceptable tautomers, salts, or stereoisomers thereof which are inhibitors of syk and/or JAK kinase. The present invention is also directed to intermediates used in making such compounds, the preparation of such a compound, pharmaceutical compositions containing such a compound, methods of inhibition syk and/or JAK kinase activity, methods of inhibition the platelet aggregation, and methods to prevent or treat a number of conditions mediated at least in part by syk and/or JAK kinase activity, such as undesired thrombosis and Non Hodgkin's Lymphoma.
    本发明涉及式I-II化合物及其药学上可接受的互变异构体、盐或立体异构体,其为syk和/或JAK激酶的抑制剂。本发明还涉及用于制备这种化合物的中间体,制备这种化合物的方法,包含这种化合物的制药组合物,抑制syk和/或JAK激酶活性的方法,抑制血小板聚集的方法,以及预防或治疗至少部分由syk和/或JAK激酶活性介导的多种情况的方法,例如不良血栓形成和非何杰金淋巴瘤。
  • 2,6-DIAMINO-PYRIMIDIN-5-YL-CARBOXAMIDES AS SYK OR JAK KINASES INHIBITORS
    申请人:Portola Pharmaceuticals, Inc.
    公开号:EP2321283B1
    公开(公告)日:2016-07-13
  • 2, 6-DIAMINO-PYRIMIDIN- 5-YL-CARBOXAMIDES AS SYK OR JAK KINASES INHIBITORS
    申请人:Portola Pharmaceuticals, Inc.
    公开号:EP2321283A1
    公开(公告)日:2011-05-18
  • US8138339B2
    申请人:——
    公开号:US8138339B2
    公开(公告)日:2012-03-20
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