2-(3-Phenyl-ureido)-4,5,6,7,8,9-hexahydro-cycloocta[b]thiophene-3-carboxylic acid methyl ester

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 2-(3-Phenyl-ureido)-4,5,6,7,8,9-hexahydro-cycloocta[b]thiophene-3-carboxylic acid methyl ester
• 英文别名: Methyl 2-[(anilinocarbonyl)amino]-4,5,6,7,8,9-hexahydrocycloocta[b]thiophene-3-carboxylate；methyl 2-(phenylcarbamoylamino)-4,5,6,7,8,9-hexahydrocycloocta[b]thiophene-3-carboxylate
• 化学式: C₁₉H₂₂N₂O₃S
• mdl: MFCD01342304
• 分子量: 358.461
• InChiKey: FLGBAPKSXVYEOA-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.2
• 重原子数：
  25
• 可旋转键数：
  4
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.37
• 拓扑面积：
  95.7
• 氢给体数：
  2
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  环辛酮 在 吗啉 、 吡啶 、 sulfur 作用下， 以 甲醇 为溶剂， 反应 36.0h， 生成 2-(3-Phenyl-ureido)-4,5,6,7,8,9-hexahydro-cycloocta[b]thiophene-3-carboxylic acid methyl ester
  参考文献：
  名称：

  A new class of small molecule RNA polymerase inhibitors with activity against Rifampicin-resistant Staphylococcus aureus1

  摘要：

  The RNA polymerase holoenzyme is a proven target for antibacterial agents. A high-throughput screening program based on this enzyme from Staphylococcus aureus had previously identified a 2-ureidothiophene-3-carboxylate as a low micromolar inhibitor. An investigation of the relationships between the structures of this class of compounds and their inhibitory- and antibacterial activities is described here, leading to a set of potent RNA polymerase inhibitors with antibacterial activity. Characterization of this bioactivity, including studies of the mechanism of action, is provided, highlighting the power of the reverse chemical genetics approach in providing tools to inhibit the bacterial RNA polymerase. (c) 2006 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2006.05.035

文献信息

• A new class of small molecule RNA polymerase inhibitors with activity against Rifampicin-resistant Staphylococcus aureus1
  作者：Francis Arhin、Odette Bélanger、Stéphane Ciblat、Mohammed Dehbi、Daniel Delorme、Evelyne Dietrich、Dilip Dixit、Yanick Lafontaine、Dario Lehoux、Jing Liu、Geoffrey A. McKay、Greg Moeck、Ranga Reddy、Yannick Rose、Ramakrishnan Srikumar、Kelly S.E. Tanaka、Daniel M. Williams、Philippe Gros、Jerry Pelletier、Thomas R. Parr、Adel Rafai Far

  DOI：10.1016/j.bmc.2006.05.035

  日期：2006.9

  The RNA polymerase holoenzyme is a proven target for antibacterial agents. A high-throughput screening program based on this enzyme from Staphylococcus aureus had previously identified a 2-ureidothiophene-3-carboxylate as a low micromolar inhibitor. An investigation of the relationships between the structures of this class of compounds and their inhibitory- and antibacterial activities is described here, leading to a set of potent RNA polymerase inhibitors with antibacterial activity. Characterization of this bioactivity, including studies of the mechanism of action, is provided, highlighting the power of the reverse chemical genetics approach in providing tools to inhibit the bacterial RNA polymerase. (c) 2006 Elsevier Ltd. All rights reserved.