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4-(4-((2-(4-(6-bromo-2-oxo-2H-chromen-3-yl)thiazol-2-yl)hydrazineylidene)methyl)-3-(p-tolyl)-1H-pyrazol-1-yl)benzenesulfonamide | 1620486-00-1

中文名称
——
中文别名
——
英文名称
4-(4-((2-(4-(6-bromo-2-oxo-2H-chromen-3-yl)thiazol-2-yl)hydrazineylidene)methyl)-3-(p-tolyl)-1H-pyrazol-1-yl)benzenesulfonamide
英文别名
——
4-(4-((2-(4-(6-bromo-2-oxo-2H-chromen-3-yl)thiazol-2-yl)hydrazineylidene)methyl)-3-(p-tolyl)-1H-pyrazol-1-yl)benzenesulfonamide化学式
CAS
1620486-00-1
化学式
C29H21BrN6O4S2
mdl
——
分子量
661.56
InChiKey
PPHITHNLCOUDOY-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):
    5.93
  • 重原子数:
    42.0
  • 可旋转键数:
    7.0
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.03
  • 拓扑面积:
    145.47
  • 氢给体数:
    2.0
  • 氢受体数:
    10.0

反应信息

  • 作为产物:
    描述:
    2-({1-[4-(aminosulfonyl)phenyl]-3-(4-methylphenyl)-1H-pyrazol-4-yl}methylidene)-1-hydrazinecarbothioamide 、 6-bromo-3-(2-bromoacetyl)-2H-chromen-2-onesodium acetate 作用下, 以 四氢呋喃乙醇 为溶剂, 反应 2.0h, 生成 4-(4-((2-(4-(6-bromo-2-oxo-2H-chromen-3-yl)thiazol-2-yl)hydrazineylidene)methyl)-3-(p-tolyl)-1H-pyrazol-1-yl)benzenesulfonamide
    参考文献:
    名称:
    Dual evaluation of some novel 2-amino-substituted coumarinylthiazoles as anti-inflammatory–antimicrobial agents and their docking studies with COX-1/COX-2 active sites
    摘要:
    Synthesis of total eighteen 2-amino-substituted 4-coumarinylthiazoles including sixteen new compounds (3a-o and 5b) bearing the benzenesulfonamide moiety is described in the present report. All the synthesized target compounds were examined for their in vivo anti-inflammatory (AI) activity and in vitro antimicrobial activity. Results revealed that six compounds (3d, 3f, 3g, 3h, 3j and 3n) exhibited pronounced anti-inflammatory activity comparable to the standard drug indomethacin. AI results were further confirmed by the docking studies of the most active (3n) and the least active compound (3a) with COX-1 and COX-2 active sites. In addition, most of the compounds exhibited moderate antimicrobial activity against Gram-positive bacteria as well as fungal yeast, S. cervisiae. Comparison between 3 and 5 indicated that incorporation of additional substituted pyrazole nucleus into the scaffold significantly enhanced AI activity.
    DOI:
    10.3109/14756366.2013.805755
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