4-Hydroxy-3-[3-(2-methoxyphenyl)prop-2-enoyl]chromen-2-one | 57339-76-1

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 香豆素及其衍生物
• 英文名称: 4-Hydroxy-3-[3-(2-methoxyphenyl)prop-2-enoyl]chromen-2-one
• 英文别名: 4-hydroxy-3-[3-(2-methoxyphenyl)prop-2-enoyl]chromen-2-one
• CAS: 57339-76-1
• 化学式: C₁₉H₁₄O₅
• 分子量: 322.317
• InChiKey: LHSIOLHNQCYFSI-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.8
• 重原子数：
  24
• 可旋转键数：
  4
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.05
• 拓扑面积：
  72.8
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  4-Hydroxy-3-[3-(2-methoxyphenyl)prop-2-enoyl]chromen-2-one 、 2-氨基苯硫醇 在 哌啶 作用下， 以 氯仿 为溶剂， 生成 4-Hydroxy-3-[2-(2-methoxyphenyl)-2,3-dihydro-1,5-benzothiazepin-4-yl]chromen-2-one
  参考文献：
  名称：

  Evaluation of Structurally Diverse Benzoazepines Clubbed with Coumarins asMycobacterium tuberculosisAgents

  摘要：

  Tuberculosis caused by Mycobacterium tuberculosis remains a leading cause of mortality worldwide into 21st century. In continuation with our anti‐tuberculosis research programme, in this work, we have prepared molecularly diverse coumarins clubbed with benzothiazepines as well as its aza‐analogues‐benzodiazepines by molecular hybridization. The resulting compounds were screened for their M. tuberculosis activity against H37Rv strains using microplate alamar blue assay. Among the designed diversity, the compounds 5k, 5n and 5o were found significantly active in primary anti‐tuberculosis assay at minimum inhibitory concentration <6.25 μm. Moreover, the IC50 values of 5k and 5o in level‐2 screening were observed as >10 μg/mL and 3.63 μg/mL, respectively. Design and synthesis of more focused library and its three‐dimensional quantitative structure activity relationship analysis are underway.

  DOI：

  10.1111/j.1747-0285.2012.01436.x
• 作为产物：
  描述：

  3-乙酰基-2-羟基苯并吡喃-4-酮 、 邻甲氧基苯甲醛 生成 4-Hydroxy-3-[3-(2-methoxyphenyl)prop-2-enoyl]chromen-2-one
  参考文献：
  名称：

  Evaluation of Structurally Diverse Benzoazepines Clubbed with Coumarins asMycobacterium tuberculosisAgents

  摘要：

  Tuberculosis caused by Mycobacterium tuberculosis remains a leading cause of mortality worldwide into 21st century. In continuation with our anti‐tuberculosis research programme, in this work, we have prepared molecularly diverse coumarins clubbed with benzothiazepines as well as its aza‐analogues‐benzodiazepines by molecular hybridization. The resulting compounds were screened for their M. tuberculosis activity against H37Rv strains using microplate alamar blue assay. Among the designed diversity, the compounds 5k, 5n and 5o were found significantly active in primary anti‐tuberculosis assay at minimum inhibitory concentration <6.25 μm. Moreover, the IC50 values of 5k and 5o in level‐2 screening were observed as >10 μg/mL and 3.63 μg/mL, respectively. Design and synthesis of more focused library and its three‐dimensional quantitative structure activity relationship analysis are underway.

  DOI：

  10.1111/j.1747-0285.2012.01436.x

文献信息

• Evaluation of Structurally Diverse Benzoazepines Clubbed with Coumarins as<i>Mycobacterium tuberculosis</i>Agents
  作者：Kuldip Upadhyay、Atul Manvar、Kena Rawal、Sudhir Joshi、Jalpa Trivedi、Ravi Chaniyara、Anamik Shah

  DOI：10.1111/j.1747-0285.2012.01436.x

  日期：2012.12

  Tuberculosis caused by Mycobacterium tuberculosis remains a leading cause of mortality worldwide into 21st century. In continuation with our anti‐tuberculosis research programme, in this work, we have prepared molecularly diverse coumarins clubbed with benzothiazepines as well as its aza‐analogues‐benzodiazepines by molecular hybridization. The resulting compounds were screened for their M. tuberculosis activity against H37Rv strains using microplate alamar blue assay. Among the designed diversity, the compounds 5k, 5n and 5o were found significantly active in primary anti‐tuberculosis assay at minimum inhibitory concentration <6.25 μm. Moreover, the IC50 values of 5k and 5o in level‐2 screening were observed as >10 μg/mL and 3.63 μg/mL, respectively. Design and synthesis of more focused library and its three‐dimensional quantitative structure activity relationship analysis are underway.