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Benzenamine, 2-methoxy-N-(3-pyridinylmethylene)- | 41855-67-8

中文名称
——
中文别名
——
英文名称
Benzenamine, 2-methoxy-N-(3-pyridinylmethylene)-
英文别名
N-(2-methoxyphenyl)-1-pyridin-3-ylmethanimine
Benzenamine, 2-methoxy-N-(3-pyridinylmethylene)-化学式
CAS
41855-67-8
化学式
C13H12N2O
mdl
——
分子量
212.251
InChiKey
ZCCHUQACOQUSSB-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):
    2.1
  • 重原子数:
    16
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.08
  • 拓扑面积:
    34.5
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    Benzenamine, 2-methoxy-N-(3-pyridinylmethylene)- 在 sodium tetrahydroborate 作用下, 以 1,4-二氧六环 为溶剂, 生成
    参考文献:
    名称:
    Design and Optimization of Novel Hydroxamate-Based Histone Deacetylase Inhibitors of Bis-Substituted Aromatic Amides Bearing Potent Activities against Tumor Growth and Metastasis
    摘要:
    Histone deacetylases (HDACs) are one of the most promising drug targets for cancer therapy, and since more than 90% of all cancer-related deaths are associated with tumor metastasis, developing strategies to inhibit tumor metastasis while retaining anti-tumor growth activity are of great interest. Herein we demonstrated the design and identification of a series of novel hydroxamate-based HDAC inhibitors bearing potent activities against tumor growth and metastasis. Optimization of the initial hit resulted in the discovery of new HDAC inhibitors through studying the structureactivity relationship. Among them, compound 11b, one of the most potent leads, exhibited nanomolar IC50 values toward inhibition of class I and IIb HDACs as well as sub-micromolar activity against proliferation and migration of breast cancer cells in vitro. More importantly, it also significantly suppressed tumor growth in a breast tumor xenograft mouse model and dose-dependently blocked in vivo tumor metastasis in a mouse pulmonary metastasis model.
    DOI:
    10.1021/jm5012148
  • 作为产物:
    描述:
    3-吡啶甲醛N-sulfinyl-2-methoxyaniline 在 10V/SiO2-25 作用下, 以 正庚烷 为溶剂, 反应 1.5h, 以91%的产率得到Benzenamine, 2-methoxy-N-(3-pyridinylmethylene)-
    参考文献:
    名称:
    二氧化硅负载的氯氧化钒催化N-亚磺胺和羰基化合物的氧/亚氨基异复分解
    摘要:
    通过无水接枝VOCl 3到二氧化硅表面上,制备了一系列二氧化硅负载的钒氧杂配合物。获得的材料已通过拉曼,漫反射FTIR(DRIFT)和UV-vis,51 V固态NMR和X射线光电子能谱,元素分析和N 2物理吸附进行了表征。发现低钒含量(1-5%)的样品主要由分离的四面体d 0单元(SiO)V(O)Cl 2组成,而钒含量较高的材料则被显着污染。 d 1的量钒物种。二氧化硅负载的钒络合物充当N-亚磺酰基胺与提供亚胺和SO 2的羰基化合物之间的羰基/亚胺基异位复分解反应的非均相催化剂。将VOCl 3接枝到二氧化硅上可大大提高其催化活性。已开发出一种新型的无水表达方法,用于制备多种醛和某些酮的亚胺。值得注意的是,这是过渡金属介导的酮的异复酰亚胺化的第一个例子。
    DOI:
    10.1016/j.jcat.2011.07.011
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文献信息

  • Design and Optimization of Novel Hydroxamate-Based Histone Deacetylase Inhibitors of Bis-Substituted Aromatic Amides Bearing Potent Activities against Tumor Growth and Metastasis
    作者:Feifei Yang、Tao Zhang、Haigang Wu、Yang Yang、Ning Liu、Ang Chen、Qiang Li、Jingjie Li、Liwen Qin、Beier Jiang、Xin Wang、Xiufeng Pang、Zhengfang Yi、Mingyao Liu、Yihua Chen
    DOI:10.1021/jm5012148
    日期:2014.11.26
    Histone deacetylases (HDACs) are one of the most promising drug targets for cancer therapy, and since more than 90% of all cancer-related deaths are associated with tumor metastasis, developing strategies to inhibit tumor metastasis while retaining anti-tumor growth activity are of great interest. Herein we demonstrated the design and identification of a series of novel hydroxamate-based HDAC inhibitors bearing potent activities against tumor growth and metastasis. Optimization of the initial hit resulted in the discovery of new HDAC inhibitors through studying the structureactivity relationship. Among them, compound 11b, one of the most potent leads, exhibited nanomolar IC50 values toward inhibition of class I and IIb HDACs as well as sub-micromolar activity against proliferation and migration of breast cancer cells in vitro. More importantly, it also significantly suppressed tumor growth in a breast tumor xenograft mouse model and dose-dependently blocked in vivo tumor metastasis in a mouse pulmonary metastasis model.
  • Oxo/imido heterometathesis of N-sulfinylamines and carbonyl compounds catalyzed by silica-supported vanadium oxochloride
    作者:Pavel A. Zhizhko、Anton A. Zhizhin、Dmitry N. Zarubin、Nikolai A. Ustynyuk、Dmitry A. Lemenovskii、Boris N. Shelimov、Leonid M. Kustov、Olga P. Tkachenko、Gayane A. Kirakosyan
    DOI:10.1016/j.jcat.2011.07.011
    日期:2011.10
    with a higher vanadium content are contaminated with a significant amount of d1 vanadium species. The silica-supported vanadium complexes act as heterogeneous catalysts for oxo/imido heterometathesis between N-sulfinylamines and carbonyl compounds affording imines and SO2. Grafting VOCl3 onto silica leads to a dramatic enhancement of its catalytic activity. A novel water-free express method for preparation
    通过无水接枝VOCl 3到二氧化硅表面上,制备了一系列二氧化硅负载的钒氧杂配合物。获得的材料已通过拉曼,漫反射FTIR(DRIFT)和UV-vis,51 V固态NMR和X射线光电子能谱,元素分析和N 2物理吸附进行了表征。发现低钒含量(1-5%)的样品主要由分离的四面体d 0单元(SiO)V(O)Cl 2组成,而钒含量较高的材料则被显着污染。 d 1的量钒物种。二氧化硅负载的钒络合物充当N-亚磺酰基胺与提供亚胺和SO 2的羰基化合物之间的羰基/亚胺基异位复分解反应的非均相催化剂。将VOCl 3接枝到二氧化硅上可大大提高其催化活性。已开发出一种新型的无水表达方法,用于制备多种醛和某些酮的亚胺。值得注意的是,这是过渡金属介导的酮的异复酰亚胺化的第一个例子。
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