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1-methyl-2,6-dioxo-3-pentyl-7-(2-propen-1-yl)-2,3,6,7-tetrahydro-1H-purine-8-carbaldehyde | 862893-48-9

中文名称
——
中文别名
——
英文名称
1-methyl-2,6-dioxo-3-pentyl-7-(2-propen-1-yl)-2,3,6,7-tetrahydro-1H-purine-8-carbaldehyde
英文别名
1-methyl-2,6-dioxo-3-pentyl-7-prop-2-enylpurine-8-carbaldehyde
1-methyl-2,6-dioxo-3-pentyl-7-(2-propen-1-yl)-2,3,6,7-tetrahydro-1H-purine-8-carbaldehyde化学式
CAS
862893-48-9
化学式
C15H20N4O3
mdl
——
分子量
304.349
InChiKey
VAGQWHCVIHDRDI-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):
    1.9
  • 重原子数:
    22
  • 可旋转键数:
    7
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.47
  • 拓扑面积:
    75.5
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

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文献信息

  • Medicaments with hm74a receptor activity
    申请人:Pinto Leo Ivan
    公开号:US20070135456A1
    公开(公告)日:2007-06-14
    The present invention provides therapeutically active compounds which are xanthine derivatives, processes for the manufacture of said derivatives, pharmaceutical formulations containing the active compounds and the use of the compounds in therapy, particularly in the treatment of diseases where under-activation of the HM74A receptor contributes to the disease or where activation of the receptor will be beneficial, having the formula (II): wherein R 1 is selected from: hydrogen and C 1-4 alkyl which may be optionally substituted with one or more groups selected from CN and CF 3 , R 2 is selected from: C 2-10 unsubstituted alkyl, C 1-10 alkyl substituted with one or more groups selected from fluorine and CN, C 5 alkenyl, unbranched C 4 alkenyl, and C 1-4 alkyl substituted with cycloalkyl, and R 3 is selected from halogen and CN.
    本发明提供了治疗活性化合物,其为黄嘌呤生物,制备该衍生物的方法,含有活性化合物的药物制剂以及化合物在治疗中的用途,特别是在HM74A受体欠活化导致疾病或激活受体将有益的疾病治疗中,其具有以下式子(II):其中,R1选自:氢和C1-4烷基,其可以选择性地被一个或多个CN和CF3基团取代,R2选自:C2-10未取代烷基,C1-10烷基,其被一个或多个和CN基团取代,C5烯基,直链C4烯基和被环烷基取代的C1-4烷基,R3选自卤素和CN。
  • NOVEL COMPOUNDS
    申请人:Pinto Ivan Leo
    公开号:US20100010021A1
    公开(公告)日:2010-01-14
    The present invention relates to therapeutically active xanthine derivative compounds of Formula (I): corresponding processes for manufacture of said derivatives, pharmaceutical formulations containing and uses of such compounds in therapy, particularly in treatment of diseases where under-activation of the HM74A receptor contributes to the disease or where activation of the receptor will be beneficial.
    本发明涉及公式(I)的治疗活性黄嘌呤生物化合物,相应的制备该衍生物的过程,含有该化合物的药物制剂以及该化合物在治疗中的用途,特别是在治疗HM74A受体低活化导致疾病或激活该受体将有益的疾病治疗中的应用。
  • Xanthine Derivatives with HM74A Receptor Activity
    申请人:Hatley Richard Jonathan Daniel
    公开号:US20090209561A1
    公开(公告)日:2009-08-20
    The present invention relates to therapeutically active xanthine compound derivatives, corresponding pharmaceutical formulations containing, processes for making or manufacture and the use of the aforementioned compounds in therapy, particularly in the treatment of diseases where under-activation of the HM74A receptor contributes to the disease or where activation of the receptor will be beneficial.
    本发明涉及治疗活性黄嘌呤化合物衍生物,相应的制药配方,制造或制造过程以及上述化合物在治疗中的使用,特别是在治疗HM74A受体欠活化导致疾病或激活受体有益的疾病中的治疗。
  • Xanthines with HM74A receptor activity
    申请人:Smithkline Beecham Corporation
    公开号:US07713982B2
    公开(公告)日:2010-05-11
    The present invention relates to a therapeutically active xanthine derivative compound of formula (I): corresponding pharmaceutical formulations containing, manufacture processes for, methods or uses of such compounds in therapy, in particular for treatment of diseases where under-activation of the HM74A receptor contributes to such diseases or where activation of the HM74A receptor will be beneficial.
    本发明涉及公式(I)的治疗活性黄嘌呤生物化合物,包括相应的制药配方,制造该化合物的过程,以及在治疗中使用该化合物的方法或用途,特别是用于治疗HM74A受体欠活化导致的疾病或激活HM74A受体有益的疾病。
  • MEDICAMENTS WITH HM74A RECEPTOR ACTIVITY
    申请人:SMITHKLINE BEECHAM CORPORATION
    公开号:EP1781657A2
    公开(公告)日:2007-05-09
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