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3,3'-Benzyliden-bis-(6-brom-4-hydroxy-cumarin) und Tautomeres | 95804-56-1

中文名称
——
中文别名
——
英文名称
3,3'-Benzyliden-bis-(6-brom-4-hydroxy-cumarin) und Tautomeres
英文别名
6,6'-dibromo-4,4'-dihydroxy-3,3'-phenylmethanediyl-bis-chromen-2-one;6-Bromo-3-[(6-bromo-4-hydroxy-2-oxochromen-3-yl)-phenylmethyl]-4-hydroxychromen-2-one
3,3'-Benzyliden-bis-(6-brom-4-hydroxy-cumarin) und Tautomeres化学式
CAS
95804-56-1
化学式
C25H14Br2O6
mdl
——
分子量
570.191
InChiKey
IWSWPGSGKPQVRO-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):
    5.4
  • 重原子数:
    33
  • 可旋转键数:
    3
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.04
  • 拓扑面积:
    93.1
  • 氢给体数:
    2
  • 氢受体数:
    6

反应信息

  • 作为产物:
    描述:
    4-溴苯酚哌啶 、 aluminum (III) chloride 、 硫酸三氯氧磷 作用下, 以 乙醇 为溶剂, 反应 18.0h, 生成 3,3'-Benzyliden-bis-(6-brom-4-hydroxy-cumarin) und Tautomeres
    参考文献:
    名称:
    Synthesis, Characterization, and Biological Studies of Metal Complexes of Dicoumarol Derivatives of Gatifloxacin
    摘要:
    Copper(II) complexes were prepared using gatifloxacin and dicoumarin derivatives to investigate their biological activities and to conduct X-ray studies. The complexes were synthesized through classical thermal methods. Biologically potent ligands were synthesized by the reaction of dicoumarin derivative with different aldehydes in ethanol. Cu(II) complexes were formed by mixing ethanolic solution of ligands and gatifloxacin with metal solutions in a 1:1 mole ratio. The structures of the dicoumarin derivatives and their Cu(II) complexes were analyzed by infrared, 1H NMR, 13C NMR, and mass spectrometry. The thermal behavior of the new mixed ligand Cu(II) complexes was investigated by thermogravimetric, fast atom bombardment (FAB) mass, and X-ray analysis. The iron-reducing antioxidant potential (FRAP) (antioxidant activity) of all compounds was evaluated. All the synthesized compounds were screened for antibacterial activity against Escherichia coli; Pseudomonas aeruginosa; Streptococcus pyogenes; minimum inhibitory concentration values for Candida albicans; and Aspergillus niger were determined using the Luria Broth dilution method. The ligands and their complexes were evaluated for antioxidant and antibacterial activity in vitro. The complexes exhibited better results than their respective counterparts.. KEYWORDS :Antimicrobial, Antioxidant, Fast atom bombardment mass, Thermal analysis, Thermo gravimetric analysis, X-ray.
    DOI:
    10.59467/ijhc.2024.34.15
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文献信息

  • NOVEL PRECURSORS OF GLUTAMATE DERIVATIVES
    申请人:Hultsch Christina
    公开号:US20140243532A1
    公开(公告)日:2014-08-28
    This invention relates to novel precursors suitable for 18 F radiolabeling of glutamate derivatives, methods for preparing such compounds and its intermediates, compositions comprising such compounds, kits comprising such compounds or compositions and methods for 18 F radiolabeling of glutamate derivatives wherein the obtained 18 F radiolabeled glutamate derivatives are suitable for diagnostic imaging by Positron Emission Tomography (PET) of proliferative diseases e.g. tumor in mammals.
    本发明涉及适用于18F标记谷酸衍生物的新型前体,制备这种化合物及其中间体的方法,包含这种化合物的组合物,包含这种化合物或组合物的试剂盒以及18F标记谷酸衍生物的方法,其中所得的18F标记谷酸衍生物适用于通过正电子发射断层扫描(PET)对哺乳动物中的增生性疾病例如肿瘤进行诊断成像。
  • Bis-(Coumarin) Compounds With Anti-Inflammatory Activity
    申请人:Mercep Mladen
    公开号:US20080153872A1
    公开(公告)日:2008-06-26
    Certain bis-(coumarin) compounds as well as the products of their intramolecular cyclization including pharmaceutically acceptable salts, hydrates, solvates, clathrates, prodrugs, tautomers and stereoisomers thereof are disclosed. Certain processes and intermediates for the preparation of certain bis-(coumarin) compounds, as well as for the use of these compounds as therapeutically active agents in the prophylaxis and treatment of asthma and other inflammatory diseases and conditions in mammals, especially humans are also disclosed.
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