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1KAO009 | 58811-19-1

中文名称
——
中文别名
——
英文名称
1KAO009
英文别名
3,3'-dibromo-4,4'-pentanediyldioxy-bis-benzamidine;3,3'-Dibrom-4,4'-pentandiyldioxy-bis-benzamidin;1.5-Bis-(2-brom-4-carbamimidoyl-phenoxy)-pentan;Benzenecarboximidamide, 4,4'-(1,5-pentanediylbis(oxy))bis(3-bromo-;3-bromo-4-[5-(2-bromo-4-carbamimidoylphenoxy)pentoxy]benzenecarboximidamide
1KAO009化学式
CAS
58811-19-1
化学式
C19H22Br2N4O2
mdl
——
分子量
498.217
InChiKey
ZXPCUEQZOSZFTK-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):
    3.9
  • 重原子数:
    27
  • 可旋转键数:
    10
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.26
  • 拓扑面积:
    118
  • 氢给体数:
    4
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    3,3'-dibromo-4,4'-pentanediyldioxy-di-benzonitrile 生成 1KAO009
    参考文献:
    名称:
    138.寻找化学am。部X.替补4:4'-脒基α ω -diphenoxyalkanes和二苯基醚类
    摘要:
    DOI:
    10.1039/jr9490000642
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文献信息

  • 138. The search for chemotherapeutic amidines. Part X. Substituted 4 : 4′-diamidino-αω-diphenoxyalkanes and -diphenyl ethers
    作者:S. S. Berg、G. Newbery
    DOI:10.1039/jr9490000642
    日期:——
  • Analogs of 1,5-bis(4-amidinophenoxy)pentane (pentamidine) in the treatment of experimental Pneumocystis carinii pneumonia
    作者:Richard R. Tidwell、Susan Kilgore Jones、J. Dieter Geratz、Kwasi A. Ohemeng、Michael Cory、James Edwin Hall
    DOI:10.1021/jm00166a026
    日期:1990.4
    A series of 33 analogues of the anti-Pneumocystis carinii drug 1,5-bis(4-amidinophenoxy)pentane (pentamidine) was synthesized for screening against a rat model of P. carinii pneumonia (PCP). Twenty-five of the compounds showed efficacy against PCP when compared to a saline-treated control group. Two compounds, 1,4-bis(4-amidinophenoxy)butane (butamidine, 6) and 1,3-bis(4-amidino-2-methoxyphenoxy)propane (DAMP, 16), were statistically more effective than the parent drug in treating PCP in the rat model of infection. In addition to their activity against PCP, the compounds were also evaluated for antitrypsin activity, ability to inhibit thymidylate synthetase, affinity for DNA, and toxicity. No correlation was observed between the tested molecular interactions of the diamidines and their effectiveness against PCP.
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