(E)-2-allyl-6,7-dimethoxy-1-(prop-1-en-1-yl)-1,2,3,4-tetrahydroisoquinoline

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 四氢异喹啉
• 英文名称: (E)-2-allyl-6,7-dimethoxy-1-(prop-1-en-1-yl)-1,2,3,4-tetrahydroisoquinoline
• 英文别名: 6,7-dimethoxy-1-[(E)-prop-1-enyl]-2-prop-2-enyl-3,4-dihydro-1H-isoquinoline
• 化学式: C₁₇H₂₃NO₂
• 分子量: 273.375
• InChiKey: QSWVJRZPBNCWNX-FNORWQNLSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.5
• 重原子数：
  20
• 可旋转键数：
  5
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.41
• 拓扑面积：
  21.7
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  (E)-2-allyl-6,7-dimethoxy-1-(prop-1-en-1-yl)-1,2,3,4-tetrahydroisoquinoline 在 三溴化硼 作用下， 以 二氯甲烷 为溶剂， 反应 2.25h， 以94%的产率得到(E)-2-allyl-1-(prop-1-en-1-yl)-1,2,3,4-tetrahydroisoquinoline-6,7-diol
  参考文献：
  名称：

  Dopaminergic isoquinolines with hexahydrocyclopenta[ ij ]-isoquinolines as D 2 -like selective ligands

  摘要：

  Dopamine receptors (DR) ligands are potential drug candidates for treating neurological disorders including schizophrenia or Parkinson's disease. Three series of isoquinolines: (E)-1-styryl-1,2,3,4-tetrahydroisoquinolines (series 1), 7-phenyl-1,2,3,7,8,8a-hexahydrocyclopenta[ij]-IQs (HCPIQs) (series 2) and (E)-1-(prop-1-en-1-yl)-1,2,3,4- tetrahydroisoquinolines (series 3), were prepared to determine their affinity for both D-1 and D-2-like DR. The effect of different substituents on the nitrogen atom (methyl or allyl), the dioxygenated function (methoxyl or catechol), the substituent at the beta-position of the THIQ skeleton, and the presence or absence of the cyclopentane motif, were studied. We observed that the most active compounds in the three series (2c, 2e, 3a, 3c, 3e, 5c and 5e) possessed a high affinity for D-2-like DR and these remarkable features: a catechol group in the IQ-ring and the N-substitution (methyl or allyl). The series showed the following trend to D-2-RD affinity: HCPIQs > 1-styryl > 1-propenyl. Therefore, the substituent at the beta-position of the THIQ and the cyclopentane ring also modulated this affinity. Among these dopaminergic isoquinolines, HCPIQs stood out for unexpected selectivity to D-2-DR since the Ki D-1/D-2 ratio reached values of 2465, 1010 and 382 for compounds 3a, 3c and 3e, respectively. None of the most active THIQs in D-2 DR displayed relevant cytotoxicity in human neutrophils and HUVEC. Finally, and in agreement with the experimental data, molecular modeling studies on DRs of the most characteristic ligands of the three series revealed stronger molecular interactions with D-2 DR than with D-1 DR, which further supports to the encountered enhanced selectivity to D-2 DR. (C) 2016 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2016.06.009
• 作为产物：
  描述：

  (E)-N-[2-(3,4-dimethoxyphenyl)ethyl]-2-butenamide 在 sodium tetrahydroborate 、 potassium carbonate 、 三氯氧磷 作用下， 以 甲醇 、 乙腈 为溶剂， 反应 17.0h， 生成 (E)-2-allyl-6,7-dimethoxy-1-(prop-1-en-1-yl)-1,2,3,4-tetrahydroisoquinoline
  参考文献：
  名称：

  Dopaminergic isoquinolines with hexahydrocyclopenta[ ij ]-isoquinolines as D 2 -like selective ligands

  摘要：

  Dopamine receptors (DR) ligands are potential drug candidates for treating neurological disorders including schizophrenia or Parkinson's disease. Three series of isoquinolines: (E)-1-styryl-1,2,3,4-tetrahydroisoquinolines (series 1), 7-phenyl-1,2,3,7,8,8a-hexahydrocyclopenta[ij]-IQs (HCPIQs) (series 2) and (E)-1-(prop-1-en-1-yl)-1,2,3,4- tetrahydroisoquinolines (series 3), were prepared to determine their affinity for both D-1 and D-2-like DR. The effect of different substituents on the nitrogen atom (methyl or allyl), the dioxygenated function (methoxyl or catechol), the substituent at the beta-position of the THIQ skeleton, and the presence or absence of the cyclopentane motif, were studied. We observed that the most active compounds in the three series (2c, 2e, 3a, 3c, 3e, 5c and 5e) possessed a high affinity for D-2-like DR and these remarkable features: a catechol group in the IQ-ring and the N-substitution (methyl or allyl). The series showed the following trend to D-2-RD affinity: HCPIQs > 1-styryl > 1-propenyl. Therefore, the substituent at the beta-position of the THIQ and the cyclopentane ring also modulated this affinity. Among these dopaminergic isoquinolines, HCPIQs stood out for unexpected selectivity to D-2-DR since the Ki D-1/D-2 ratio reached values of 2465, 1010 and 382 for compounds 3a, 3c and 3e, respectively. None of the most active THIQs in D-2 DR displayed relevant cytotoxicity in human neutrophils and HUVEC. Finally, and in agreement with the experimental data, molecular modeling studies on DRs of the most characteristic ligands of the three series revealed stronger molecular interactions with D-2 DR than with D-1 DR, which further supports to the encountered enhanced selectivity to D-2 DR. (C) 2016 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2016.06.009

文献信息

• Dopaminergic isoquinolines with hexahydrocyclopenta[ ij ]-isoquinolines as D 2 -like selective ligands
  作者：Javier Párraga、Sebastián A. Andujar、Sebastián Rojas、Lucas J. Gutierrez、Noureddine El Aouad、M. Jesús Sanz、Ricardo D. Enriz、Nuria Cabedo、Diego Cortes

  DOI：10.1016/j.ejmech.2016.06.009

  日期：2016.10

  Dopamine receptors (DR) ligands are potential drug candidates for treating neurological disorders including schizophrenia or Parkinson's disease. Three series of isoquinolines: (E)-1-styryl-1,2,3,4-tetrahydroisoquinolines (series 1), 7-phenyl-1,2,3,7,8,8a-hexahydrocyclopenta[ij]-IQs (HCPIQs) (series 2) and (E)-1-(prop-1-en-1-yl)-1,2,3,4- tetrahydroisoquinolines (series 3), were prepared to determine their affinity for both D-1 and D-2-like DR. The effect of different substituents on the nitrogen atom (methyl or allyl), the dioxygenated function (methoxyl or catechol), the substituent at the beta-position of the THIQ skeleton, and the presence or absence of the cyclopentane motif, were studied. We observed that the most active compounds in the three series (2c, 2e, 3a, 3c, 3e, 5c and 5e) possessed a high affinity for D-2-like DR and these remarkable features: a catechol group in the IQ-ring and the N-substitution (methyl or allyl). The series showed the following trend to D-2-RD affinity: HCPIQs > 1-styryl > 1-propenyl. Therefore, the substituent at the beta-position of the THIQ and the cyclopentane ring also modulated this affinity. Among these dopaminergic isoquinolines, HCPIQs stood out for unexpected selectivity to D-2-DR since the Ki D-1/D-2 ratio reached values of 2465, 1010 and 382 for compounds 3a, 3c and 3e, respectively. None of the most active THIQs in D-2 DR displayed relevant cytotoxicity in human neutrophils and HUVEC. Finally, and in agreement with the experimental data, molecular modeling studies on DRs of the most characteristic ligands of the three series revealed stronger molecular interactions with D-2 DR than with D-1 DR, which further supports to the encountered enhanced selectivity to D-2 DR. (C) 2016 Elsevier Masson SAS. All rights reserved.