6-(2-morpholinoethoxy)-2-(6-fluoropyridin-3-yl)-3-phenyl-1H-inden-1-one | 1274877-55-2

• 分子结构分类: 有机化合物 - 苯类化合物 - 茚和异茚
• 英文名称: 6-(2-morpholinoethoxy)-2-(6-fluoropyridin-3-yl)-3-phenyl-1H-inden-1-one
• 英文别名: 2-(6-Fluoropyridin-3-yl)-6-(2-morpholin-4-ylethoxy)-3-phenylinden-1-one
• CAS: 1274877-55-2
• 化学式: C₂₆H₂₃FN₂O₃
• 分子量: 430.479
• InChiKey: FPNAJMCJWIIQSA-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.7
• 重原子数：
  32
• 可旋转键数：
  6
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.23
• 拓扑面积：
  51.7
• 氢给体数：
  0
• 氢受体数：
  6

文献信息

• [EN] INDENONE DERIVATIVE AND PHARMACEUTICAL COMPOSITION COMPRISING SAME<br/>[FR] DÉRIVÉ D'INDÉNONE ET COMPOSITION PHARMACEUTIQUE LE COMPRENANT
  申请人：KOREA RES INST CHEM TECH

  公开号：WO2011030955A1

  公开（公告）日：2011-03-17

  An indenone derivative of formula (1) is effective in enhancing the activity of osteoblastic cells and inhibiting bone resorption by osteoclastic cells, and a pharmaceutical composition comprising the indenone derivative or a pharmaceutically acceptable salt thereof is useful for preventing or treating bone diseases such as osteoporosis.

  式（1）的吲哚酮衍生物能够增强成骨细胞的活性，抑制破骨细胞的骨吸收作用，含有该吲哚酮衍生物或其药用盐的药用组合物可用于预防或治疗骨质疏松等骨病。
• Indenone Derivative and Pharmaceutical Composition Comprising Same
  申请人：Heo Jung Nyoung

  公开号：US20120214991A1

  公开（公告）日：2012-08-23

  An indenone derivative of formula (1) is effective in enhancing the activity of osteoblastic cells and inhibiting bone resorption by osteoclastic cells, and a pharmaceutical composition comprising the indenone derivative or a pharmaceutically acceptable salt thereof is useful for preventing or treating bone diseases such as osteoporosis.

  式（1）的吲哚酮衍生物能够有效增强成骨细胞的活性，抑制破骨细胞的骨吸收作用，含有该吲哚酮衍生物或其药学上可接受的盐的药物组合物对预防或治疗骨疾病如骨质疏松症具有益处。
• [EN] A METHOD OF TREATING CANCER<br/>[FR] UNE METHODE POUR LE TRAITEMENT DU CANCER
  申请人：MERCK & CO INC

  公开号：WO2000059930A1

  公开（公告）日：2000-10-12

  The present invention relates to methods of treating cancer using a combination of a compound which is a PSA conjugate and a compound which is an inhibitor of prenyl-protein transferase, which methods comprise administering to said mammal, either sequentially in any order or simultaneously, amounts of at least two therapeutic agents selected from a group consisting of a compound which is a PSA conjugate and a compound which is an inhibitor of prenyl-protein transferase. The invention also relates to methods of preparing such compositions.

  本发明涉及使用一种PSA共轭物和一种前尼基蛋白转移酶抑制剂的组合治疗癌症的方法，该方法包括向哺乳动物施用至少两种治疗剂量，所述治疗剂量从以下组合中选择：一种是PSA共轭物，一种是前尼基蛋白转移酶抑制剂，无论是按顺序或同时施用。本发明还涉及制备这种组合物的方法。
• INDENONE DERIVATIVE AND PHARMACEUTICAL COMPOSITION COMPRISING SAME
  申请人：Korea Research Institute Of Chemical Technology

  公开号：EP2475649A1

  公开（公告）日：2012-07-18
• US8877747B2
  申请人：——

  公开号：US8877747B2

  公开（公告）日：2014-11-04