4,5-dichloro-thiophene-2-sulfonic acid {3-[5-fluoro-3-methyl-7-(naphthalen-2-yloxy)indol-1-yl]propionyl}amide | 882998-77-8

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 4,5-dichloro-thiophene-2-sulfonic acid {3-[5-fluoro-3-methyl-7-(naphthalen-2-yloxy)indol-1-yl]propionyl}amide
• 英文别名: N-(4,5-dichlorothiophen-2-ylsulfonyl)-3-(5-fluoro-3-methyl-7-(naphthalen-2-yloxy)-1H-indol-1-yl)propanamide；N-(4,5-dichlorothiophen-2-yl)sulfonyl-3-(5-fluoro-3-methyl-7-naphthalen-2-yloxyindol-1-yl)propanamide
• CAS: 882998-77-8
• 化学式: C₂₆H₁₉Cl₂FN₂O₄S₂
• 分子量: 577.484
• InChiKey: NWNFXHAFMZCAEM-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  7.2
• 重原子数：
  37
• 可旋转键数：
  7
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.12
• 拓扑面积：
  114
• 氢给体数：
  1
• 氢受体数：
  6

反应信息

• 作为产物：
  描述：

  2,3-二氯噻吩-5-磺酰胺 、 3-[5-fluoro-3-methyl-7-(naphthalen-2-yloxy)indol-1-yl]propionic acid 在 4-二甲氨基吡啶 、 盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺 作用下， 以 二氯甲烷 为溶剂， 反应 18.0h， 以64.5 mg的产率得到4,5-dichloro-thiophene-2-sulfonic acid {3-[5-fluoro-3-methyl-7-(naphthalen-2-yloxy)indol-1-yl]propionyl}amide
  参考文献：
  名称：

  Structure−Activity Relationship Studies Leading to the Identification of (2E)-3-[l-[(2,4-Dichlorophenyl)methyl]-5-fluoro-3-methyl-lH-indol-7-yl]-N-[(4,5-dichloro-2-thienyl)sulfonyl]-2-propenamide (DG-041), a Potent and Selective Prostanoid EP3 Receptor Antagonist, as a Novel Antiplatelet Agent That Does Not Prolong Bleeding

  摘要：

  The EP(3) receptor on the platelet mediates prostaglandin E(2) potentiation of thrombogenic coagonists including collagen and adenosine diphosphate (ADP). A pharmacophore driven approach led to the identification of diverse peri-substituted heterocycles as potent and selective EP(3) receptor antagonists. A simultaneous chemical optimization and druglike assessment of prioritized molecules converged oil a lead compound 50 (DG-041) that displayed favorable in vitro and functional activities as an inhibitor of human platelet aggregation. This agent is currently in human clinical trials for the treatment of atherothrombosis.

  DOI：

  10.1021/jm9005912