formic acid 4-(2-bromoethoxy)-3-methoxyphenyl ester | 1262778-68-6

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 英文名称: formic acid 4-(2-bromoethoxy)-3-methoxyphenyl ester
• 英文别名: [4-(2-Bromoethoxy)-3-methoxyphenyl] formate
• CAS: 1262778-68-6
• 化学式: C₁₀H₁₁BrO₄
• 分子量: 275.099
• InChiKey: SOIZPTYRXAKBBI-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.4
• 重原子数：
  15
• 可旋转键数：
  6
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.3
• 拓扑面积：
  44.8
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  formic acid 4-(2-bromoethoxy)-3-methoxyphenyl ester 在 hydrolysis agent 作用下， 生成 4-(2-bromoethoxy)-3-methoxyphenol
  参考文献：
  名称：

  Suppression of store overload-induced calcium release by hydroxylated metabolites of carvedilol

  摘要：

  Carvedilol is a drug widely used in the treatment of heart failure and associated cardiac arrhythmias. A unique action of carvedilol is its suppression of store overload-induced calcium release (SOICR) through the cardiac ryanodine receptor (RyR2), which can trigger ventricular arrhythmias. Since the effects of carvedilol metabolites on SOICR have not yet been investigated, three carvedilol metabolites hydroxylated at the 3-, 4' and 5'-positions were synthesized and assayed for SOICR inhibition in mutant HEK 293 cells expressing the RyR2 mutant R4496C. This cell line is especially prone to SOICR and calcium release through the defective RyR2 channel was measured with a calcium-sensitive fluorescent dye. These results revealed that the 3- and 4'-hydroxy derivatives are slightly more effective than carvedilol in suppressing SOICR, while the 5'-analog proved slightly less active. Metabolic deactivation of carvedilol via these hydroxylation pathways is therefore insignificant. (C) 2015 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2015.11.008
• 作为产物：
  描述：

  香草醛 在 oxidation agent 作用下， 生成 formic acid 4-(2-bromoethoxy)-3-methoxyphenyl ester
  参考文献：
  名称：

  Suppression of store overload-induced calcium release by hydroxylated metabolites of carvedilol

  摘要：

  Carvedilol is a drug widely used in the treatment of heart failure and associated cardiac arrhythmias. A unique action of carvedilol is its suppression of store overload-induced calcium release (SOICR) through the cardiac ryanodine receptor (RyR2), which can trigger ventricular arrhythmias. Since the effects of carvedilol metabolites on SOICR have not yet been investigated, three carvedilol metabolites hydroxylated at the 3-, 4' and 5'-positions were synthesized and assayed for SOICR inhibition in mutant HEK 293 cells expressing the RyR2 mutant R4496C. This cell line is especially prone to SOICR and calcium release through the defective RyR2 channel was measured with a calcium-sensitive fluorescent dye. These results revealed that the 3- and 4'-hydroxy derivatives are slightly more effective than carvedilol in suppressing SOICR, while the 5'-analog proved slightly less active. Metabolic deactivation of carvedilol via these hydroxylation pathways is therefore insignificant. (C) 2015 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2015.11.008

文献信息

• Synthesis of Active Metabolites of Carvedilol, an Antihypertensive Drug
  作者：N. Senthilkumar、Y. S. Somannavar、Shankar B. Reddy、Brajesh Kumar Sinha、G. K. A. S. S. Narayan、Ramesh Dandala、Kaga Mukkanti

  DOI：10.1080/00397910903534072

  日期：2010.12.22

  A simple synthetic route for active metabolites of carvedilol is reported. The metabolites 4'-hydroxycarvedilol and 5'-hydroxycarvedilol have exhibited high activity for -blockade. We have disclosed syntheses of 4'-hydroxycarvedilol and 5'-hydroxycarvedilol from commercially available vanillin and isovanillin, respectively.