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(2S,6S)-2,6-Dimethyl-7-oxo-6-{2-[(quinoxaline-2-carbonyl)-amino]-ethoxy}-1,4-diaza-bicyclo[3.2.0]heptane-2-carboxylic acid methyl ester | 544481-15-4

中文名称
——
中文别名
——
英文名称
(2S,6S)-2,6-Dimethyl-7-oxo-6-{2-[(quinoxaline-2-carbonyl)-amino]-ethoxy}-1,4-diaza-bicyclo[3.2.0]heptane-2-carboxylic acid methyl ester
英文别名
methyl (2S,6S)-2,6-dimethyl-7-oxo-6-[2-(quinoxaline-2-carbonylamino)ethoxy]-1,4-diazabicyclo[3.2.0]heptane-2-carboxylate
(2S,6S)-2,6-Dimethyl-7-oxo-6-{2-[(quinoxaline-2-carbonyl)-amino]-ethoxy}-1,4-diaza-bicyclo[3.2.0]heptane-2-carboxylic acid methyl ester化学式
CAS
544481-15-4
化学式
C20H23N5O5
mdl
——
分子量
413.433
InChiKey
QPGMGFGZWZRZMR-RFFXKOPCSA-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):
    -0.2
  • 重原子数:
    30
  • 可旋转键数:
    7
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.45
  • 拓扑面积:
    123
  • 氢给体数:
    2
  • 氢受体数:
    8

反应信息

  • 作为反应物:
    描述:
    (2S,6S)-2,6-Dimethyl-7-oxo-6-{2-[(quinoxaline-2-carbonyl)-amino]-ethoxy}-1,4-diaza-bicyclo[3.2.0]heptane-2-carboxylic acid methyl ester 在 camphor-10-sulfonic acid 作用下, 以 二氯甲烷 为溶剂, 反应 15.0h, 生成 (4E,11E)-(2S,6S,9S,13S)-2,6,9,13-Tetramethyl-7,14-dioxo-6,13-bis-{2-[(quinoxaline-2-carbonyl)-amino]-ethoxy}-1,4,8,11-tetraaza-cyclotetradeca-4,11-diene-2,9-dicarboxylic acid dimethyl ester
    参考文献:
    名称:
    Synthesis of 5,12-Dioxocyclam Nickel (II) Complexes Having Quinoxaline Substituents at the 6 and 13 Positions as Potential DNA Bis-Intercalating and Cleaving Agents
    摘要:
    Several dioxocyclams containing quinoxaline moieties, as well as their nickel(II) complexes were synthesized and studied for their ability to bind and oxidatively cleave DNA. Although no evidence for binding by intercalation was found, the ability of the Ni(II) complexes to cleave DNA in the presence of Oxone was strongly dependent on both the nature and the spatial orientation of the quinoxaline moieties, suggesting at least transient association of these complexes with DNA.
    DOI:
    10.1021/jo020708r
  • 作为产物:
    参考文献:
    名称:
    Synthesis of 5,12-Dioxocyclam Nickel (II) Complexes Having Quinoxaline Substituents at the 6 and 13 Positions as Potential DNA Bis-Intercalating and Cleaving Agents
    摘要:
    Several dioxocyclams containing quinoxaline moieties, as well as their nickel(II) complexes were synthesized and studied for their ability to bind and oxidatively cleave DNA. Although no evidence for binding by intercalation was found, the ability of the Ni(II) complexes to cleave DNA in the presence of Oxone was strongly dependent on both the nature and the spatial orientation of the quinoxaline moieties, suggesting at least transient association of these complexes with DNA.
    DOI:
    10.1021/jo020708r
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文献信息

  • Synthesis of 5,12-Dioxocyclam Nickel (II) Complexes Having Quinoxaline Substituents at the 6 and 13 Positions as Potential DNA Bis-Intercalating and Cleaving Agents
    作者:Louis S. Hegedus、Marc M. Greenberg、Jory J. Wendling、Joseph P. Bullock
    DOI:10.1021/jo020708r
    日期:2003.5.1
    Several dioxocyclams containing quinoxaline moieties, as well as their nickel(II) complexes were synthesized and studied for their ability to bind and oxidatively cleave DNA. Although no evidence for binding by intercalation was found, the ability of the Ni(II) complexes to cleave DNA in the presence of Oxone was strongly dependent on both the nature and the spatial orientation of the quinoxaline moieties, suggesting at least transient association of these complexes with DNA.
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