2-((E)-2-bromovinyl)-3-chloro-1-(methylsulfonyl)-1H-pyrrole | 1255528-97-2

• 分子结构分类: 有机化合物 - 有机卤素化合物 - 芳基卤化物
• 英文名称: 2-((E)-2-bromovinyl)-3-chloro-1-(methylsulfonyl)-1H-pyrrole
• 英文别名: 2-[(E)-2-bromoethenyl]-3-chloro-1-methylsulfonylpyrrole
• CAS: 1255528-97-2
• 化学式: C₇H₇BrClNO₂S
• 分子量: 284.561
• InChiKey: JCFZTOIQKWPUJP-DUXPYHPUSA-N

物化性质

• 沸点：
  407.7±53.0 °C(Predicted)
• 密度：
  1.68±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.1
• 重原子数：
  13
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.14
• 拓扑面积：
  47.4
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  2-((E)-2-bromovinyl)-3-chloro-1-(methylsulfonyl)-1H-pyrrole 、 在 2-((E)-2-bromovinyl)-3-chloro-1-(methylsulfonyl)-1H-pyrrole 作用下， 生成 Rumbrin
  参考文献：
  名称：

  J. Med. Chem. 2010, 53, 7967-7978

  摘要：

  DOI：
• 作为产物：
  描述：

  2-乙酰基-3-氯噻吩 在 吡啶 、 lithium aluminium tetrahydride 、 亚磷酸氢二甲酯 、 碘 、 sodium hydride 、 戴斯-马丁氧化剂 、 三乙胺 、 三苯基膦 、 copper(II) oxide 作用下， 以 四氢呋喃 、 乙醇 、 二氯甲烷 、 N,N-二甲基甲酰胺 、 mineral oil 为溶剂， 反应 20.83h， 生成 2-((Z)-2-bromovinyl)-3-chloro-1-(methylsulfonyl)-1H-pyrrole 、 2-((E)-2-bromovinyl)-3-chloro-1-(methylsulfonyl)-1H-pyrrole
  参考文献：
  名称：

  Synthesis and Biological Evaluation of Polyenylpyrrole Derivatives as Anticancer Agents Acting through Caspases-Dependent Apoptosis

  摘要：

  A class of polyenylpyrroles and their analogues were designed from a hit compound identified in a fungus. The compounds synthesized were evaluated for their cell cytotoxicity against human non-small-cell lung carcinoma cell lines A549. Two compounds were found to exhibit high cytotoxicity against A549 cells with IC50 of 0.6 and 0.01 mu M, respectively. The underlying mechanisms for the anticancer activity were demonstrated as caspases activation dependent apoptosis induction through loss of mitochondrial membrane potential, release of cytochrome c, increase in B-cell lymphoma-2-associated X protein (Bax) level, and decrease in B-cell lymphoma-2 (Bcl-2) level. The two compounds were nontoxic to normal human lung Beas-2b cells (IC50 > 80 mu M), indicating that they are highly selective in their cytotoxicity activities. Furthermore, one compound showed in vivo anticancer activity in human-lung-cancer-cell-bearing mice. These results open promising insights on how these conjugated polyenes mediate cytotoxicity and may provide a molecular rationale for future therapeutic interventions in carcinogenesis.

  DOI：

  10.1021/jm100619x
• 作为试剂：
  描述：

  2-((E)-2-bromovinyl)-3-chloro-1-(methylsulfonyl)-1H-pyrrole 、 在 2-((E)-2-bromovinyl)-3-chloro-1-(methylsulfonyl)-1H-pyrrole 作用下， 生成 Rumbrin
  参考文献：
  名称：

  J. Med. Chem. 2010, 53, 7967-7978

  摘要：

  DOI：

文献信息

• Synthesis and Biological Evaluation of Polyenylpyrrole Derivatives as Anticancer Agents Acting through Caspases-Dependent Apoptosis
  作者：Zhanxiong Fang、Pei-Chun Liao、Yu-Liang Yang、Feng-Ling Yang、Yi-Lin Chen、Yulin Lam、Kuo-Feng Hua、Shih-Hsiung Wu

  DOI：10.1021/jm100619x

  日期：2010.11.25

  A class of polyenylpyrroles and their analogues were designed from a hit compound identified in a fungus. The compounds synthesized were evaluated for their cell cytotoxicity against human non-small-cell lung carcinoma cell lines A549. Two compounds were found to exhibit high cytotoxicity against A549 cells with IC50 of 0.6 and 0.01 mu M, respectively. The underlying mechanisms for the anticancer activity were demonstrated as caspases activation dependent apoptosis induction through loss of mitochondrial membrane potential, release of cytochrome c, increase in B-cell lymphoma-2-associated X protein (Bax) level, and decrease in B-cell lymphoma-2 (Bcl-2) level. The two compounds were nontoxic to normal human lung Beas-2b cells (IC50 > 80 mu M), indicating that they are highly selective in their cytotoxicity activities. Furthermore, one compound showed in vivo anticancer activity in human-lung-cancer-cell-bearing mice. These results open promising insights on how these conjugated polyenes mediate cytotoxicity and may provide a molecular rationale for future therapeutic interventions in carcinogenesis.
• J. Med. Chem. 2010, 53, 7967-7978
  作者：

  DOI：——

  日期：——