[2-[4-[Bis[(2-methylpropan-2-yl)oxycarbonylamino]methylideneamino]phenyl]-1-(naphthalen-1-ylsulfonylamino)ethyl]phosphonic acid

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: [2-[4-[Bis[(2-methylpropan-2-yl)oxycarbonylamino]methylideneamino]phenyl]-1-(naphthalen-1-ylsulfonylamino)ethyl]phosphonic acid
• 英文别名: [2-[4-[bis[(2-methylpropan-2-yl)oxycarbonylamino]methylideneamino]phenyl]-1-(naphthalen-1-ylsulfonylamino)ethyl]phosphonic acid
• 化学式: C₂₉H₃₇N₄O₉PS
• 分子量: 648.7
• InChiKey: XUXMBJMLPOALMS-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.2
• 重原子数：
  44
• 可旋转键数：
  13
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.34
• 拓扑面积：
  201
• 氢给体数：
  5
• 氢受体数：
  10

文献信息

• Novel Urokinase Inhibitors
  申请人：Augustyns Koen

  公开号：US20080312191A1

  公开（公告）日：2008-12-18

  The present invention relates to novel compounds with inhibitory activity towards urokinase plasminogen activator (uPA); to methods for preparation of said uPA inhibitor compounds; to pharmaceutical compositions comprising said uPA inhibitor compounds; to the use of said uPA inhibitor compounds as a medicament and the use of said uPA inhibitor compounds for the preparation of a medicament for the treatment of conditions chosen from the group comprising cancer, tumour growth, tumour invasion, tumour metastasis, diabetic retinopathy, hemorrhagic atherosclerosis and inflammatory conditions, such as rheumatoid arthritis and psoriasis.

  本发明涉及具有抑制尿激酶纤溶酶原活化物（uPA）活性的新化合物；制备所述uPA抑制剂化合物的方法；包括所述uPA抑制剂化合物的药物组合物；将所述uPA抑制剂化合物用作药物的用途以及将所述uPA抑制剂化合物用于制备用于治疗癌症、肿瘤生长、肿瘤侵袭、肿瘤转移、糖尿病视网膜病变、出血性动脉粥样硬化和类风湿性关节炎和银屑病等条件的药物的用途。
• NOVEL UROKINASE INHIBITORS
  申请人：Universiteit Antwerpen

  公开号：EP1940856B1

  公开（公告）日：2014-10-08
• US8003627B2
  申请人：——

  公开号：US8003627B2

  公开（公告）日：2011-08-23