methyl 2-(phenoxymethyl)-1H-benzo[d]imidazole-5-carboxylate

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并咪唑类
• 英文名称: methyl 2-(phenoxymethyl)-1H-benzo[d]imidazole-5-carboxylate
• 英文别名: methyl 2-(phenoxymethyl)-3H-benzimidazole-5-carboxylate
• 化学式: C₁₆H₁₄N₂O₃
• 分子量: 282.299
• InChiKey: SOQRKXCKLPEZGF-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.8
• 重原子数：
  21
• 可旋转键数：
  5
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.12
• 拓扑面积：
  64.2
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  methyl 2-(phenoxymethyl)-1H-benzo[d]imidazole-5-carboxylate 在 盐酸 、 溶剂黄146 作用下， 以 水 为溶剂， 反应 4.0h， 生成 2-(phenoxymethyl)-1H-benzo[d]imidazole-5-carboxylic acid
  参考文献：
  名称：

  Discovery of a novel series of benzimidazole derivatives as diacylglycerol acyltransferase inhibitors

  摘要：

  A novel series of benzimidazole derivatives was prepared and evaluated for their diacylglycerol acyltransferase (DGAT) inhibitory activity using microsome from rat liver. Among the newly synthesized compounds, furfurylamine containing benzimidazole carboxamide 10j showed the most potent DGAT inhibitory effect (IC50 = 4.4 mu M) and inhibited triglyceride formation in HepG2 cells. Furthermore, compound 10j reduced body weight gain of Institute of Cancer Research mice on a high-fat diet and decreased levels of total triglyceride, total cholesterol, and LDL-cholesterol in the blood accompanied with a significant increase in HDL-cholesterol level. (C) 2012 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2012.10.046
• 作为产物：
  描述：

  苯氧乙酸乙酯 在 lithium hydroxide monohydrate 作用下， 以 四氢呋喃 、 水 为溶剂， 反应 13.0h， 生成 methyl 2-(phenoxymethyl)-1H-benzo[d]imidazole-5-carboxylate
  参考文献：
  名称：

  Discovery of a novel series of benzimidazole derivatives as diacylglycerol acyltransferase inhibitors

  摘要：

  A novel series of benzimidazole derivatives was prepared and evaluated for their diacylglycerol acyltransferase (DGAT) inhibitory activity using microsome from rat liver. Among the newly synthesized compounds, furfurylamine containing benzimidazole carboxamide 10j showed the most potent DGAT inhibitory effect (IC50 = 4.4 mu M) and inhibited triglyceride formation in HepG2 cells. Furthermore, compound 10j reduced body weight gain of Institute of Cancer Research mice on a high-fat diet and decreased levels of total triglyceride, total cholesterol, and LDL-cholesterol in the blood accompanied with a significant increase in HDL-cholesterol level. (C) 2012 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2012.10.046

文献信息

• Synthesis and structure–activity relationships of new antimicrobial active multisubstituted benzazole derivatives
  作者：Ilkay Yildiz-Oren、Ismail Yalcin、Esin Aki-Sener、Nejat Ucarturk

  DOI：10.1016/j.ejmech.2003.11.014

  日期：2004.3

  benzothiazole ring system enhanced the antimicrobial activity against Staphylococcus aureus. In these sets of non-nucleoside fused heterocyclic compounds electron withdrawing groups at position 5 of the benzazoles increased the activity against C. albicans.

  合成了一系列多取代的苯并恶唑，苯并咪唑和苯并噻唑（5-7）作为非核苷稠合的等排杂环化合物，并测试了它们对各种革兰氏阳性和革兰氏阴性细菌的抗菌活性以及对白色念珠菌的抗菌活性。微生物学结果表明，所合成的化合物在MIC值为100至3.12 microg / ml的范围内具有针对被测微生物的广谱活性。结构-活性关系（SAR）研究表明，苯并噻唑环系统增强了对金黄色葡萄球菌的抗菌活性。在这些非核苷稠合的杂环化合物中，苯并恶唑的5位吸电子基团增加了对白色念珠菌的活性。
• Discovery of a novel series of benzimidazole derivatives as diacylglycerol acyltransferase inhibitors
  作者：Kyeong Lee、Ja-Il Goo、Hwa Young Jung、Minkyoung Kim、Shanthaveerappa K. Boovanahalli、Hye Ran Park、Mun-Ock Kim、Dong-Hyun Kim、Hyun Sun Lee、Yongseok Choi

  DOI：10.1016/j.bmcl.2012.10.046

  日期：2012.12

  A novel series of benzimidazole derivatives was prepared and evaluated for their diacylglycerol acyltransferase (DGAT) inhibitory activity using microsome from rat liver. Among the newly synthesized compounds, furfurylamine containing benzimidazole carboxamide 10j showed the most potent DGAT inhibitory effect (IC50 = 4.4 mu M) and inhibited triglyceride formation in HepG2 cells. Furthermore, compound 10j reduced body weight gain of Institute of Cancer Research mice on a high-fat diet and decreased levels of total triglyceride, total cholesterol, and LDL-cholesterol in the blood accompanied with a significant increase in HDL-cholesterol level. (C) 2012 Elsevier Ltd. All rights reserved.