4-methyl-3-(3-nitrobenzyl)-7-(pyrimidin-2-yloxy)-2-oxo-2H-1-benzopyran | 393811-59-1

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 香豆素及其衍生物
• 英文名称: 4-methyl-3-(3-nitrobenzyl)-7-(pyrimidin-2-yloxy)-2-oxo-2H-1-benzopyran
• 英文别名: 4-Methyl-3-[(3-nitrophenyl)methyl]-7-pyrimidin-2-yloxychromen-2-one
• CAS: 393811-59-1
• 化学式: C₂₁H₁₅N₃O₅
• 分子量: 389.367
• InChiKey: FBRZJJQDBZRQKO-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.7
• 重原子数：
  29
• 可旋转键数：
  4
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.1
• 拓扑面积：
  107
• 氢给体数：
  0
• 氢受体数：
  7

文献信息

• Coumarin derivatives useful as tnf alpha inhibitors
  申请人：Cheng Fei Jie

  公开号：US20050014705A1

  公开（公告）日：2005-01-20

  Novel compounds composition capable of inhibiting TNFα and having antiimmunoinflammatory and autoimmune properties useful in a pharmaceutical composition, such as for a drug containing this as an active ingredient; and a therapeutic method with the use of these novel compounds.

  一种新型化合物组合，能够抑制TNFα，具有抗免疫炎症和自身免疫性质，在制药组合物中有用，例如作为含有此化合物作为活性成分的药物；以及使用这些新型化合物的治疗方法。
• Coumarin derivatives useful as TNFalpha inhibitors
  申请人：Cheng Fei Jie

  公开号：US20060020138A1

  公开（公告）日：2006-01-26

  Novel compounds composition capable of inhibiting TNFα and having anti immunoinflammatory and autoimmune properties useful in a pharmaceutical composition, such as for a drug containing this as an active ingredient; and a therapeutic method with the use of these novel compounds.

  一种能够抑制TNFα并具有抗免疫炎症和自身免疫特性的新型化合物组合，适用于制备药物组合物，例如含有该化合物作为活性成分的药物；以及使用这些新型化合物的治疗方法。
• COUMARIN DERIVATIVES USEFUL AS TNF ALPHA INHIBITORS
  申请人：Cheng Jie Fei

  公开号：US20100197917A1

  公开（公告）日：2010-08-05

  Novel compounds composition capable of inhibiting TNFα and having antiimmunionflammatory and autoimmune properties useful in a pharmaceutical composition, such as for a drug containing this as an active ingredient; and a therapeutic method with the use of these novel compounds.

  一种能够抑制TNFα并具有抗免疫炎症和自身免疫性质的新型化合物组合，可用于制备药物组合物，例如包含该化合物作为活性成分的药物；以及使用这些新型化合物的治疗方法。
• Novel Coumarin Derivative Having Antitumor Activity
  申请人：Iikura Hitoshi

  公开号：US20110092700A1

  公开（公告）日：2011-04-21

  The present invention provides a compound represented by general formula (1) below or a pharmaceutically acceptable salt thereof: wherein: X is selected from heteroaryl etc., Y 1 and Y 2 are selected from —N═ etc., Y 3 and Y 4 are selected from —CH═ etc., A is selected from sulfamide etc., R 1 is selected from hydrogen etc., and R 2 is selected from C 1-6 alkyl etc. The compound or salt has sufficiently high antitumor activity, and is useful in the treatment of cell proliferative disorders, particularly cancers. The present invention also provides a pharmaceutical composition containing the compound or salt as an active ingredient.

  本发明提供一种由下式（1）或其药学上可接受的盐所表示的化合物：其中，X选自杂环芳基等；Y1和Y2选自—N═等；Y3和Y4选自—CH═等；A选自磺酰胺等；R1选自氢等；R2选自C1-6烷基等。该化合物或盐具有足够高的抗肿瘤活性，并可用于治疗细胞增殖性疾病，特别是癌症。本发明还提供一种含有该化合物或盐作为活性成分的制药组合物。
• p27 Protein Inducer
  申请人：Sakai Toshiyuki

  公开号：US20110009398A1

  公开（公告）日：2011-01-13

  The present invention provides a p27 protein inducing agent comprising a compound represented by general formula (11) below or pharmaceutically acceptable salt thereof as an active ingredient: wherein G 1 , G 2 , G 3 and G 8 are each independently selected from —N═ etc., Ring G 6 is selected from divalent aryl etc., A is selected from amino etc., G 4 is selected from oxygen etc., G 5 is selected from oxygen etc., G 7 is selected from —CH 2 — etc., and R 2 is selected from C 1-6 alkyl etc.

  本发明提供了一种p27蛋白诱导剂，其包含以下通式（11）所表示的化合物或其药学上可接受的盐作为活性成分：其中G1，G2，G3和G8各自独立地选择自—N═等，环G6选择自双价芳基等，A选择自氨基等，G4选择自氧等，G5选择自氧等，G7选择自—CH2—等，R2选择自C1-6烷基等。