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4-{2-[2-(4-tert-Butoxycarbonylamino-butylcarbamoyl)-1-methyl-1H-imidazol-4-ylcarbamoyl]-1-methyl-1H-imidazol-4-ylcarbamoyl}-butyric acid | 489457-55-8

中文名称
——
中文别名
——
英文名称
4-{2-[2-(4-tert-Butoxycarbonylamino-butylcarbamoyl)-1-methyl-1H-imidazol-4-ylcarbamoyl]-1-methyl-1H-imidazol-4-ylcarbamoyl}-butyric acid
英文别名
5-[[1-Methyl-2-[[1-methyl-2-[4-[(2-methylpropan-2-yl)oxycarbonylamino]butylcarbamoyl]imidazol-4-yl]carbamoyl]imidazol-4-yl]amino]-5-oxopentanoic acid;5-[[1-methyl-2-[[1-methyl-2-[4-[(2-methylpropan-2-yl)oxycarbonylamino]butylcarbamoyl]imidazol-4-yl]carbamoyl]imidazol-4-yl]amino]-5-oxopentanoic acid
4-{2-[2-(4-tert-Butoxycarbonylamino-butylcarbamoyl)-1-methyl-1H-imidazol-4-ylcarbamoyl]-1-methyl-1H-imidazol-4-ylcarbamoyl}-butyric acid化学式
CAS
489457-55-8
化学式
C24H36N8O7
mdl
——
分子量
548.599
InChiKey
RPBORCDLVIZKAH-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):
    -0.1
  • 重原子数:
    39
  • 可旋转键数:
    15
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.54
  • 拓扑面积:
    199
  • 氢给体数:
    5
  • 氢受体数:
    9

反应信息

  • 作为反应物:
    描述:
    4-{2-[2-(4-tert-Butoxycarbonylamino-butylcarbamoyl)-1-methyl-1H-imidazol-4-ylcarbamoyl]-1-methyl-1H-imidazol-4-ylcarbamoyl}-butyric acid 在 palladium on activated charcoal 氢气1-羟基苯并三唑盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺 作用下, 以 四氢呋喃N,N-二甲基甲酰胺 为溶剂, 生成 [4-({4-[(4-{4-[2-(3-Chloromethyl-6-hydroxy-2,3-dihydro-indole-1-carbonyl)-benzofuran-5-ylcarbamoyl]-butyrylamino}-1-methyl-1H-imidazole-2-carbonyl)-amino]-1-methyl-1H-imidazole-2-carbonyl}-amino)-butyl]-carbamic acid tert-butyl ester
    参考文献:
    名称:
    Sequence selective recognition of DNA by hairpin conjugates of a racemic seco-cyclopropaneindoline-2-benzofurancarboxamide and polyamides
    摘要:
    Conjugates of racemic seco-cyclopropaneindoline-2-benzofurancarboxamide (CI-Bf) and four diamides (ImIm 1, ImPy 2, PyIm 3, and PyPy 4, where Py is pyrrole, and Im is imidazole), linked by a gamma-aminobutyrate group were synthesized. In addition to alkylating at adenine-N3 positions within an A(5) sequence, the imidazole-containing compounds 1 and 2 were found to also alkylate purine-N3 positions within a sequence 3'-GGGGGGA(888)CTGCTC(894)-5'. A model for the binding of hairpin conjugates I and 2 with the 3'-GACT-5' sequence is proposed. (C) 2002 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(02)00341-4
  • 作为产物:
    描述:
    [4-({1-Methyl-4-[(1-methyl-4-nitro-1H-imidazole-2-carbonyl)-amino]-1H-imidazole-2-carbonyl}-amino)-butyl]-carbamic acid tert-butyl ester 在 palladium on activated charcoal 吡啶4-二甲氨基吡啶氢气 作用下, 以 甲醇 为溶剂, 生成 4-{2-[2-(4-tert-Butoxycarbonylamino-butylcarbamoyl)-1-methyl-1H-imidazol-4-ylcarbamoyl]-1-methyl-1H-imidazol-4-ylcarbamoyl}-butyric acid
    参考文献:
    名称:
    Sequence selective recognition of DNA by hairpin conjugates of a racemic seco-cyclopropaneindoline-2-benzofurancarboxamide and polyamides
    摘要:
    Conjugates of racemic seco-cyclopropaneindoline-2-benzofurancarboxamide (CI-Bf) and four diamides (ImIm 1, ImPy 2, PyIm 3, and PyPy 4, where Py is pyrrole, and Im is imidazole), linked by a gamma-aminobutyrate group were synthesized. In addition to alkylating at adenine-N3 positions within an A(5) sequence, the imidazole-containing compounds 1 and 2 were found to also alkylate purine-N3 positions within a sequence 3'-GGGGGGA(888)CTGCTC(894)-5'. A model for the binding of hairpin conjugates I and 2 with the 3'-GACT-5' sequence is proposed. (C) 2002 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(02)00341-4
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