(2E)-N-(6-nitro-1,3-benzothiazol-2-yl)-3-phenylprop-2-enamide | 1374874-62-0

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 肉桂酸及其衍生物
• 英文名称: (2E)-N-(6-nitro-1,3-benzothiazol-2-yl)-3-phenylprop-2-enamide
• 英文别名: (E)-N-(6-nitro-1,3-benzothiazol-2-yl)-3-phenylprop-2-enamide
• CAS: 1374874-62-0
• 化学式: C₁₆H₁₁N₃O₃S
• 分子量: 325.348
• InChiKey: JJNAOWYXQWCSGU-RMKNXTFCSA-N

物化性质

• 密度：
  1.478±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.8
• 重原子数：
  23
• 可旋转键数：
  3
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  116
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为产物：
  描述：

  肉桂酸 在 氯化亚砜 、 三乙胺 作用下， 以 二氯甲烷 为溶剂， 反应 14.0h， 生成 (2E)-N-(6-nitro-1,3-benzothiazol-2-yl)-3-phenylprop-2-enamide
  参考文献：
  名称：

  Exploring the anti-biofilm activity of cinnamic acid derivatives in Candida albicans

  摘要：

  Some compounds, characterized by phenylethenyl moiety, such as methyl cinnamate and caffeic acid phenethyl ester, are able to inhibit C. albicans biofilm formation. On these bases, and as a consequence of our previous work, we synthesized a series of cinnamoyl ester and amide derivatives in order to evaluate them for the activity against C. albicans biofilm and planlctonically grown cells.The most active compounds 7 and 8 showed >> 50% biofilm inhibition concentrations (BMIC50) of 2 mu g/mL and 4 mu g/mL respectively, against C albicans biofilm formation; otherwise, 7 showed an interesting activity also against mature biofilm, with BMIC50 of 8 mu g/mL. (C) 2016 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2016.10.091

文献信息

• Exploring the anti-biofilm activity of cinnamic acid derivatives in Candida albicans
  作者：Daniela De Vita、Giovanna Simonetti、Fabiana Pandolfi、Roberta Costi、Roberto Di Santo、Felicia Diodata D’Auria、Luigi Scipione

  DOI：10.1016/j.bmcl.2016.10.091

  日期：2016.12

  Some compounds, characterized by phenylethenyl moiety, such as methyl cinnamate and caffeic acid phenethyl ester, are able to inhibit C. albicans biofilm formation. On these bases, and as a consequence of our previous work, we synthesized a series of cinnamoyl ester and amide derivatives in order to evaluate them for the activity against C. albicans biofilm and planlctonically grown cells.The most active compounds 7 and 8 showed >> 50% biofilm inhibition concentrations (BMIC50) of 2 mu g/mL and 4 mu g/mL respectively, against C albicans biofilm formation; otherwise, 7 showed an interesting activity also against mature biofilm, with BMIC50 of 8 mu g/mL. (C) 2016 Elsevier Ltd. All rights reserved.