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3,5-diiodo-N-(naphthalen-2-yl)benzamide | 1613336-72-3

中文名称
——
中文别名
——
英文名称
3,5-diiodo-N-(naphthalen-2-yl)benzamide
英文别名
3,5-diiodo-N-naphthalen-2-ylbenzamide
3,5-diiodo-N-(naphthalen-2-yl)benzamide化学式
CAS
1613336-72-3
化学式
C17H11I2NO
mdl
——
分子量
499.089
InChiKey
XKIPHAKMUBNTGX-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):
    5.3
  • 重原子数:
    21
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    29.1
  • 氢给体数:
    1
  • 氢受体数:
    1

反应信息

  • 作为产物:
    描述:
    3,5-二碘苯甲酸2-萘胺 在 O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate 、 N,N-二异丙基乙胺 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 0.25h, 以45%的产率得到3,5-diiodo-N-(naphthalen-2-yl)benzamide
    参考文献:
    名称:
    Dual Protonophore–Chitinase Inhibitors Dramatically Affect O. volvulus Molting
    摘要:
    The L3-stage-specific chitinase OvCHT1 has been implicated in the development of Onchocerca volvulus, the causative agent of ondiocerciasis. Closantel, a known anthelmintic drug, was previously discovered as a potent and specific OvCHT1 inhibitor. As closantel is also a known protonophore, we performed a simple scaffold modulation to map out the structural features that are relevant for its individual or dual biochemical roles. Furthermore, we present that either OvCHT1 inhibition or protonophoric activity was capable of affecting O. volvulus L3 molting and that the presence of both activities in a single molecule yielded more potent inhibition of the nematode's developmental process.
    DOI:
    10.1021/jm5006435
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文献信息

  • Dual Protonophore–Chitinase Inhibitors Dramatically Affect <i>O. volvulus</i> Molting
    作者:Major Gooyit、Nancy Tricoche、Sara Lustigman、Kim D. Janda
    DOI:10.1021/jm5006435
    日期:2014.7.10
    The L3-stage-specific chitinase OvCHT1 has been implicated in the development of Onchocerca volvulus, the causative agent of ondiocerciasis. Closantel, a known anthelmintic drug, was previously discovered as a potent and specific OvCHT1 inhibitor. As closantel is also a known protonophore, we performed a simple scaffold modulation to map out the structural features that are relevant for its individual or dual biochemical roles. Furthermore, we present that either OvCHT1 inhibition or protonophoric activity was capable of affecting O. volvulus L3 molting and that the presence of both activities in a single molecule yielded more potent inhibition of the nematode's developmental process.
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