1-(4-Methoxy-phenyl)-3-methyl-1-{1-[5-methyl-2-(4-trifluoromethyl-phenyl)-1H-imidazol-4-ylmethyl]-piperidin-4-yl}-urea | 466665-38-3

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: 1-(4-Methoxy-phenyl)-3-methyl-1-{1-[5-methyl-2-(4-trifluoromethyl-phenyl)-1H-imidazol-4-ylmethyl]-piperidin-4-yl}-urea
• 英文别名: 1-(4-methoxyphenyl)-3-methyl-1-[1-[[5-methyl-2-[4-(trifluoromethyl)phenyl]-1H-imidazol-4-yl]methyl]piperidin-4-yl]urea
• CAS: 466665-38-3
• 化学式: C₂₆H₃₀F₃N₅O₂
• 分子量: 501.552
• InChiKey: GENJYJVJSCQZSO-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.3
• 重原子数：
  36
• 可旋转键数：
  6
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.38
• 拓扑面积：
  73.5
• 氢给体数：
  2
• 氢受体数：
  7

文献信息

• Amino piperidine derivatives
  申请人：——

  公开号：US20030069276A1

  公开（公告）日：2003-04-10

  The invention comprises novel aminopiperidine derivatives, a process for their manufacture, pharmaceutical compositions and the use of such compounds in medicine. In particular, the compounds of formula I prevent the human immunodeficiency virus (HIV) from entering cells by blocking interaction of the viral envelope protein gp120 with a chemokine receptor on the cell surface. The compounds of this invention may be advantageously used as therapeutic agents for the treatment of diseases mediated by the human immunodeficiency virus (HIV), either alone or in combination with other inhibitors of HIV viral replication or with pharmacoenhancers.

  该发明涉及新颖的氨基哌啶衍生物，其制备方法，药物组合物以及在医学中使用这些化合物。具体而言，公式I的化合物通过阻断病毒包膜蛋白gp120与细胞表面的趋化因子受体的相互作用，防止人类免疫缺陷病毒（HIV）进入细胞。本发明的化合物可优势地用作治疗由人类免疫缺陷病毒（HIV）介导的疾病的治疗剂，可以单独使用，也可以与其他HIV病毒复制抑制剂或药物增效剂联合使用。
• AMINOPIPERIDINE DERIVATIVES AS MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY
  申请人：F. HOFFMANN-LA ROCHE AG

  公开号：EP1417202A2

  公开（公告）日：2004-05-12
• [EN] AMINOPIPERIDINE DERIVATIVES<br/>[FR] DERIVES D'AMINOPIPERIDINE
  申请人：HOFFMANN LA ROCHE

  公开号：WO2002079186A2

  公开（公告）日：2002-10-10

  The invention is concerned with novel aminopiperidine derivatives, a process for their manufacture, pharmaceutical compositions and the use of such compounds in medicine. In particular, the compounds of Formula (I) prevent the human immunodeficiency virus (HIV) from entering cells by blocking interaction of the viral envelope protein gp120 with a chemokine receptor on the cell surface. Consequently the compounds of this invention may be advantageously used as therapeutic agents for the treatment of diseases mediated by the human immunodeficiency virus (HIV), either alone or in combination with other inhibitors of HIV viral replication or with pharmacoenhancers. Disclosed are compounds of general formula (I) wherein R?1, R2, R3¿, X and A are as defined in the description.