(Z)-(4-((4-((3-(4-Fluorobenzyl)-2,4-dioxothiazolidin-5-ylidene)methyl)phenoxy)methyl)phenyl)boronic acid (Z)-(4-((4-((3-(4-氟苄基)-2,4-二氧代噻唑烷-5-亚基)甲基)苯氧基)甲基苯基)硼酸

CAS 1312201-00-5 MFCD412201005

化学结构图

1312201-00-5
SMILES:

化学属性

Mol. FormulaC24H19BFNO5S

别名和识别编码

Chemical Name(Z)-(4-((4-((3-(4-Fluorobenzyl)-2,4-dioxothiazolidin-5-ylidene)methyl)phenoxy)methyl)phenyl)boronic acid
Chemicalbook IDCB22655402
Chemical Name Translation(Z)-(4-((4-((3-(4-氟苄基)-2,4-二氧代噻唑烷-5-亚基)甲基)苯氧基)甲基苯基)硼酸
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相关文献及参考

  • [2]. Albers HM, et al. Structure-based design of novel boronic acid-based inhibitors of autotaxin. J Med Chem. 2011 Jul 14;54(13):4619-26.
  • [3]. Fulkerson Z, et al. Binding of autotaxin to integrins localizes lysophosphatidic acid production to platelets and mammalian cells. J Biol Chem. 2011 Oct 7;286(40):34654-63.
  • [1]. Albers HM, et al. Chemical Evolution of Autotaxin Inhibitors. Chem Rev. 2012 May 9;112(5):2593-603.
  • [1]. Albers HM, et al. Chemical Evolution of Autotaxin Inhibitors. Chem Rev. 2012 May 9;112(5):2593-603.
  • [2]. Albers HM, et al. Structure-based design of novel boronic acid-based inhibitors of autotaxin. J Med Chem. 2011 Jul 14;54(13):4619-26.
  • [3]. Fulkerson Z, et al. Binding of autotaxin to integrins localizes lysophosphatidic acid production to platelets and mammalian cells. J Biol Chem. 2011 Oct 7;286(40):34654-63.

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