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2-hydroxy-1-naphthaldehyde benzenesulfonylhydrazone | 1410954-41-4

中文名称
——
中文别名
——
英文名称
2-hydroxy-1-naphthaldehyde benzenesulfonylhydrazone
英文别名
——
2-hydroxy-1-naphthaldehyde benzenesulfonylhydrazone化学式
CAS
1410954-41-4
化学式
C18H16N2O3S
mdl
——
分子量
340.403
InChiKey
JOBKRGVKGRWJAH-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:
    24.0
  • 可旋转键数:
    4.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.06
  • 拓扑面积:
    69.97
  • 氢给体数:
    1.0
  • 氢受体数:
    4.0

反应信息

  • 作为产物:
    描述:
    参考文献:
    名称:
    一些磺酰胺类和磺酰的抗菌活性,以及​​一系列磺酰的2D-QSAR研究。
    摘要:
    苯磺酸-1-甲基酰肼(1)及其四种芳族磺酰基衍生物(1a-1d),N-(3-氨基-2-羟丙基)苯磺酰胺(2)和N-(2-羟乙基)苯磺酰胺(3)为通过IR,(1)H NMR,(13)C NMR和LCMS技术确定它们的结构。通过微稀释和圆盘扩散法评估了新合成化合物对各种细菌的抗菌活性。实验结果表明,磺酰胺上存在OH基团会降低抗菌活性,磺酰al(1a-1d)的抗菌活性要比母体磺酰胺(1)小,除了白色念珠菌。此外,对28种芳香族磺酰基进行了二维D-QSAR分析,以作为抗大肠杆菌和金黄色葡萄球菌的抗菌剂。
    DOI:
    10.1016/j.saa.2012.08.043
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文献信息

  • Aromatic sulfonyl hydrazides and sulfonyl hydrazones: antimicrobial activity and physical properties
    作者:H. Güzin Aslan、Nurcan Karacan
    DOI:10.1007/s00044-012-0104-0
    日期:2013.3
    A series of novel aromatic sulfonamide derivatives (1-7) were synthesized and characterized by elemental analyses, FT-IR, H-1 NMR, C-13 NMR, and LC/MS techniques. The compounds' quantum mechanical descriptors, surface area, and molecular volume were calculated. All the synthesized compounds were evaluated in vitro as antimicrobial agents against representative strains of gram-positive and gram-negative bacteria and as antifungal agents for yeast by both the disc diffusion and minimal inhibition concentration methods for comparison. All the bacteria and fungi studied were screened against some commercial antibiotics to compare with our chemicals' zone diameters. Quantitative structure-activity relationship studies with multiple linear regression analysis were applied to find the correlation between the different calculated molecular descriptors of the synthesized compounds and biological activity.
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