Methyl 2-(1-bromo-3-fluoro-6,7,8,9-tetrahydropyrido[1,2-a]indol-9-yl)acetate | 476620-38-9

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吲哚及其衍生物
• 英文名称: Methyl 2-(1-bromo-3-fluoro-6,7,8,9-tetrahydropyrido[1,2-a]indol-9-yl)acetate
• 英文别名: methyl 2-(1-bromo-3-fluoro-6,7,8,9-tetrahydropyrido[1,2-a]indol-9-yl)acetate
• CAS: 476620-38-9
• 化学式: C₁₅H₁₅BrFNO₂
• 分子量: 340.192
• InChiKey: URFCLQCIHGZTBN-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.1
• 重原子数：
  20
• 可旋转键数：
  3
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.4
• 拓扑面积：
  31.2
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  Methyl 2-(1-bromo-3-fluoro-6,7,8,9-tetrahydropyrido[1,2-a]indol-9-yl)acetate 、 4-氯苯甲酰氯 在 三氯化铝 作用下， 以 1,2-二氯乙烷 为溶剂， 生成
  参考文献：
  名称：

  Identification of prostaglandin D2 receptor antagonists based on a tetrahydropyridoindole scaffold

  摘要：

  A new series of indole-based antagonists of the PGD(2) receptor subtype 1 (DP1 receptor) was identified and the progress of the structure-activity relationship study to the identification of potent and selective antagonists is presented. Selective DP1 antagonists with high potency and selectivity were prepared. Of particular interest is the DP1 antagonist 26 with a K-i value of 1 nM for the DP1 receptor and an IC50 value of 4.6 nM in a DP1 functional assay for the inhibition of the PGD(2) induced cAMP production in platelet rich plasma (PRP). (C) 2008 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2008.03.015
• 作为产物：
  描述：

  在 三甲基氯硅烷 、 sodium iodide 作用下， 以 乙醚 、 乙腈 为溶剂， 生成 Methyl 2-(1-bromo-3-fluoro-6,7,8,9-tetrahydropyrido[1,2-a]indol-9-yl)acetate
  参考文献：
  名称：

  Identification of prostaglandin D2 receptor antagonists based on a tetrahydropyridoindole scaffold

  摘要：

  A new series of indole-based antagonists of the PGD(2) receptor subtype 1 (DP1 receptor) was identified and the progress of the structure-activity relationship study to the identification of potent and selective antagonists is presented. Selective DP1 antagonists with high potency and selectivity were prepared. Of particular interest is the DP1 antagonist 26 with a K-i value of 1 nM for the DP1 receptor and an IC50 value of 4.6 nM in a DP1 functional assay for the inhibition of the PGD(2) induced cAMP production in platelet rich plasma (PRP). (C) 2008 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2008.03.015

文献信息

• Identification of prostaglandin D2 receptor antagonists based on a tetrahydropyridoindole scaffold
  作者：Christian Beaulieu、Daniel Guay、Zhaoyin Wang、Yves Leblanc、Patrick Roy、Claude Dufresne、Robert Zamboni、Carl Berthelette、Stephen Day、Nancy Tsou、Danielle Denis、Gillian Greig、Marie-Claude Mathieu、Gary O’Neill

  DOI：10.1016/j.bmcl.2008.03.015

  日期：2008.4

  A new series of indole-based antagonists of the PGD(2) receptor subtype 1 (DP1 receptor) was identified and the progress of the structure-activity relationship study to the identification of potent and selective antagonists is presented. Selective DP1 antagonists with high potency and selectivity were prepared. Of particular interest is the DP1 antagonist 26 with a K-i value of 1 nM for the DP1 receptor and an IC50 value of 4.6 nM in a DP1 functional assay for the inhibition of the PGD(2) induced cAMP production in platelet rich plasma (PRP). (C) 2008 Elsevier Ltd. All rights reserved.