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dimethyl 4-cyclohexylpyridazine-3,6-dicarboxylate

中文名称
——
中文别名
——
英文名称
dimethyl 4-cyclohexylpyridazine-3,6-dicarboxylate
英文别名
Dimethyl 4-(cyclohexylmethyl)pyridazine-3,6-dicarboxylate
dimethyl 4-cyclohexylpyridazine-3,6-dicarboxylate化学式
CAS
——
化学式
C15H20N2O4
mdl
——
分子量
292.335
InChiKey
MIOFMPQUDLWUQD-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):
    3.2
  • 重原子数:
    21
  • 可旋转键数:
    6
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.6
  • 拓扑面积:
    78.4
  • 氢给体数:
    0
  • 氢受体数:
    6

反应信息

  • 作为反应物:
    描述:
    dimethyl 4-cyclohexylpyridazine-3,6-dicarboxylate戴斯-马丁氧化剂 、 magnesium chloride 作用下, 以 乙腈 为溶剂, 生成
    参考文献:
    名称:
    Heterocyclic α-helix mimetics for targeting protein–protein interactions
    摘要:
    The design and synthesis of alpha-helix peptidomimetics using inverse electron demand Diels-Alder reactions is described. The potency of the resulting pyridazine-based library to disrupt the Bak/Bcl-X-L interaction was tested using an in vitro fluorescence polarization assay. (c) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2007.05.075
  • 作为产物:
    参考文献:
    名称:
    Heterocyclic α-helix mimetics for targeting protein–protein interactions
    摘要:
    The design and synthesis of alpha-helix peptidomimetics using inverse electron demand Diels-Alder reactions is described. The potency of the resulting pyridazine-based library to disrupt the Bak/Bcl-X-L interaction was tested using an in vitro fluorescence polarization assay. (c) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2007.05.075
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文献信息

  • OXAZOLE-PYRIDAZINE-OXAZOLE ALPHA-HELIX MIMETIC
    申请人:Rebek, JR. Julius
    公开号:US20100113466A1
    公开(公告)日:2010-05-06
    There are provided alpha helix scaffolds mimicking i, i+3/i+4, i+7 or i+11 residues having the general structure oxazole-pyridazine-piperidine or oxazole-pyridazine-oxazole. The common pyridazine heterocycle originates from substituted or unsubstituted dimethyl 1,2,4,5-tetrazine-3,6-dicarboxylate. These scaffolds are synthetic counterparts of amphiphilic alpha helices having a hydrophilic face along one side and a hydrophobic face along the other side of the helix.
    提供了模拟i,i+3/i+4,i+7或i+11残基的α螺旋支架,具有氧唑-吡啶嗪-哌啶或氧唑-吡啶嗪-氧唑的一般结构。常见的吡啶嗪杂环起源于取代或未取代的二甲基1,2,4,5-四氮唑-3,6-二羧酸酯。这些支架是具有亲侧面和疏侧面的两栖性α螺旋的合成对应物。
  • [EN] OXAZOLE-PYRIDAZINE-OXAZOLE ALPHA-HELIX MIMETIC<br/>[FR] MIMÉTIQUE DE TYPE HÉLICE ALPHA DE L'OXAZOLE-PYRIDAZINE-OXAZOLE
    申请人:SCRIPPS RESEARCH INST
    公开号:WO2010042758A3
    公开(公告)日:2010-08-12
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