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5-Cyano-3,6-dihydro-4-methyl-6-cyclohexyl-2-oxo-1-(2H)-pyrimidinecarboxylic acid, 1-ethyl ester | 464191-30-8

中文名称
——
中文别名
——
英文名称
5-Cyano-3,6-dihydro-4-methyl-6-cyclohexyl-2-oxo-1-(2H)-pyrimidinecarboxylic acid, 1-ethyl ester
英文别名
5Cyano-3,6-dihydro-4-methyl-6-cyclohexyl-2-oxo-1-(2H)-pyrimidinecarboxylic acid, 1-ethyl ester;ethyl 5-cyano-4-cyclohexyl-6-methyl-2-oxo-1,4-dihydropyrimidine-3-carboxylate
5-Cyano-3,6-dihydro-4-methyl-6-cyclohexyl-2-oxo-1-(2H)-pyrimidinecarboxylic acid, 1-ethyl ester化学式
CAS
464191-30-8
化学式
C15H21N3O3
mdl
——
分子量
291.35
InChiKey
XINZSROVULFHAM-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):
    2.3
  • 重原子数:
    21
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.67
  • 拓扑面积:
    82.4
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    环己氯化镁氯化铵吡啶氯甲酸乙酯三氟乙酸碳酸氢钠乙腈乙酸乙酯 、 silica gel 、 Sodium sulfate-III 作用下, 以 四氢呋喃二氯甲烷乙酸乙酯 为溶剂, 反应 2.83h, 以to give 35 mg of desired product as yellow foam (60%)的产率得到5-Cyano-3,6-dihydro-4-methyl-6-cyclohexyl-2-oxo-1-(2H)-pyrimidinecarboxylic acid, 1-ethyl ester
    参考文献:
    名称:
    Cyano-substituted dihydropyrimidine compounds and their use to treat diseases
    摘要:
    本发明提供了I式化合物及其药学上可接受的盐。I式化合物能够诱导有丝分裂阻滞,因此它们可用作抗癌剂。I式化合物也可用于治疗其他可以通过诱导有丝分裂阻滞来治疗的疾病。
    公开号:
    US06900214B2
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文献信息

  • Novel cyano-substituted dihydropyrimidine compounds and their use to treat diseases
    申请人:——
    公开号:US20030008888A1
    公开(公告)日:2003-01-09
    The present invention provides compounds of formula I 1 and pharmaceutically acceptable salts thereof. The formula I compounds induce mitotic arrest thereby making them useful as anti-cancer agents. The formula I compounds are also useful for the treatment of other diseases which can be treated by inducing mitotic arrest.
    本发明提供了I1式化合物及其药学上可接受的盐。I式化合物诱导有丝分裂停滞,因此它们可用作抗癌剂。I式化合物还可用于治疗其他可以通过诱导有丝分裂停滞来治疗的疾病。
  • Cyano-substituted dihydropyrimidine compounds and their use to treat diseases
    申请人:——
    公开号:US20020143026A1
    公开(公告)日:2002-10-03
    The present invention provides compounds of formula I 1 and pharmaceutically acceptable salts thereof. The formula I compounds induce mitotic arrest thereby making them useful as anti-cancer agents. The formula I compounds are also useful for the treatment of other diseases which can be treated by inducing mitotic arrest.
    本发明提供了I1式化合物及其药学上可接受的盐。I式化合物诱导有丝分裂阻滞,因此它们可用作抗癌剂。I式化合物还可用于治疗其他可以通过诱导有丝分裂阻滞治疗的疾病。
  • Method of treating proliferative diseases using Eg5 inhibitors
    申请人:——
    公开号:US20020165240A1
    公开(公告)日:2002-11-07
    The invention provides a method for treating a condition via modulation of the Eg5 protein activity comprising administering to a mammalian species in need of such treatment an effective amount of at least one small molecule Eg5 protein inhibitor. The invention also provides a method for treating a condition via modulation of the Eg5 protein activity comprising administering to a mammalian species in need of such treatment an effective amount of at least one small molecule Eg5 protein inhibitor in combination with at least one other anti-cancer agent.
    本发明提供了一种通过调节Eg5蛋白活性治疗疾病的方法,包括向需要此类治疗的哺乳动物物种中给予至少一种小分子Eg5蛋白抑制剂的有效量。本发明还提供了一种通过调节Eg5蛋白活性治疗疾病的方法,包括向需要此类治疗的哺乳动物物种中给予至少一种小分子Eg5蛋白抑制剂和至少一种其他抗癌剂的有效量。
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